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Characterization of complexes synthesized using Schiff base ligands and their screening for toxicity two fungal and one bacterial species on rice pathogens.

1. Introduction

Ever since the Italian chemist, Hugo Schiff used imines to make several "metallo-imines", numbers of variants of the condensation products of imines and aldehydes or ketones such as RCH=NR7--where R & R7 are alkyl and/or aryl substituent's, are popularized. They are also known as Schiff bases (SBs), anils, imines or azomethines. They are also known as anils, imines, or azomethines. These have several applications in organic studies, such as for building new heterocyclic systems, for identification, detection, and determination of aldehydes and ketones, for purification of carbonyl or amino compounds, or for the protection of these groups during the complex formation or such sensitive reactions [1]. They have other side applications in various other fields, coordination chemistry [2-9], analytical chemistry [10-16], pigments and dyes [17], and polymer industries [18], in vitamins and enzymes [4] for model biomolecules. There is a special mention of these complexes in agriculture [4] as fungicides, pesticides, and bacteriocides.

Survey of the literature for SB metal complexes and their applications showed excellent review articles [19, 20] for the detailed understanding of this class of compounds in all respects and one more especially dedicated to copper complexes [21]. They provide several details on number of metal complexes derived from SBs used widely for applications in food and dye industry, analytical chemistry, catalysis, polymers, antifertility, agrochemical, anti-inflammatory activity, antiradical activities, and biological systems as enzymatic agents. Several have reviewed them in light of their antimicrobial, antibacterial, antifungal, antitumor, and cytotoxic activities [19, 20]. There are some individual articles too not mentioned in them with studies on the above mentioned types of activities with some metals ions such as Cu(II), Ni(II), and Co(II) with SB derived from salicylaldehyde and 2-substituted aniline [22]; Cu(II), Ni(II), and Zn(II) complexes with SB from p-chlorobenzaldehyde with p-chloroaniline [23]; Mn(II), Fe(II), Ni(II), and Cu(II) complexes with SB from 5-acetamido-1,3,4-thiodiazole-2-sulphonamide and their biological activity [24]; Zn(II), Ni(II), and Cu(II) complexes with SB from dicinnamoylmethane and aromatic amines [25]; Zn(II), Mn(II), Ni(II), and Cu(II) complexes with SB from 2-hydroxy-1-naphthaldehyde and 5-amino-1-naphthol and their antibacterial activities [26]; Co(II), Ni(II), and Cu(II) complexes with SB from 1,4-dicarbonylphenyldihydrazide with 2,6-diformyl-4-methylphenol [27]; Co(II), Ni(II), and Cu(II) complexes with SB from 2-H/Cl/Br-6-(4fluorophenyliminomethyl)phenol [28]; Co(II), Ni(II), and Cu(II) complexes with SB from pyrazolealdehyde with 2-aminophenol [29]; Co(II), Ni(II), Zn(II), Cd(II), Hg(II), and Cu(II) complexes with SB from benzofuran-2-carbohydrazide and 4-methyl-thio-benzaldehyde and their antifungal, antibacterial activities being screened [30]; Ni(II) and Cu(II) complexes of SB derived from 1naphthylamine and 2-hydroxy-naphthalene-1-carbaldehyde [31]; Fe(III), Ni(II), Cu(II), Co(II), Zn(II), and U[O.sub.2](II) complexes of SB derived from 2-furancarboxaldehyde and ophenylenediamine [32]; VO(II), Co(II), Rh(III), Pd(II), and Au(III) complexes of SB derived from 4-nitrobenzoic acid and thiosemicarbazide and their antibacterial activity [33]; VO(IV), Cu(II), and Ru(II) complexes of SB derived from 3-hydroxyquinoxaline-2-carboxaldehyde and several amines 1,8-diaminonaphthalene, 2,3-diamine maleonitrile, 1,2-diaminocyclohexane, 2-iminophenol, and 4-aminoantipyrine [34]; Mn(II), Co(II), Ni(II), Cu(II), and Zn(II) complexes of SB derived from 1, 10-phenanthroline and o-vanillidene-2-aminobenzothiazole and o-vanillidene-2-quino-N-(2-pyridyl)-benzenesulfonamide [35]; Hg(II), Zn(II), and VO(IV) complexes of SB from S-aminosulfonyl-4-chloro-N-2,6-dimethylphenyl-2-hydroxybenzamide with salicylamide [36]; Co(II), Cu(II), Ni(II), and Zn(II) complexes of SB derived from several substituted pyridines with salicylaldehyde [37]. Recently new series of Co(II), Ni(II), Cu(II), Cd(II), and Hg(II) complexes were synthesized by the condensation of naphthofuran-2carbohydrazide and diacetylmonoxime. The ligand along with its metal complexes has been characterized on the basis of analytical data, IR, electronic, mass, *HNMR, ESR spectral data, thermal studies, magnetic susceptibility, and molar conductance measurements. In order to evaluate the effect of metal ions upon chelation, both the ligand and its metal complexes were screened for their antibacterial and antifungal activities by minimum inhibitory concentration (MIC) method [38]. Metal chelates, [M[(HL).sub.2][([H.sub.2]O).sub.2]][X.sub.2] (where M = Mn(II), Co(II), Cu(II), Ni(II), or Zn(II), X = N[O.sup.-.sub.3] or Cl-, and HL = SB moiety), have been prepared and characterized by elemental analysis, magnetic and spectroscopic measurements (infrared, X-ray powder diffraction, and scanning electron microscopy). The SB and its metal chelates have been screened for their in vitro antibacterial activity against four bacteria, gram-positive (Staphylococcus aureus) and gram-negative (Escherichia coli), and two strains of fungus (Aspergillus flavus and Candida albicans). The metal chelates were shown to possess more antibacterial activity than the free SB chelate [39].

Metal complexes of SBs derived from 2-furancarboxaldehyde and o-phenylenediamine (L1), and 2-thiophenecarboxaldehyde and 2-aminothiophenol (HL2) are reported and characterized based on elemental analyses, IR 1H NMR, solid reflectance, magnetic moment, molar conductance, and thermal analysis (TGA). Consider M = Fe(III), Ni(II), Cu(II), Co(II), Zn(II), and UO2(II). The synthesized ligands, in comparison to their metal complexes, were also screened for their antibacterial activity against bacterial species, Escherichia coli, Pseudomonas aeruginosa, and Staphylococcus Pyogenes, as well as fungi (Candida). The activity data show the metal complexes to be more potent antibacterials than the parent SB ligand against one or more bacterial species [32].

Synthesis and characterisation of new transition metal complexes of SBs derived from 3-hydroxyquinoxaline-2carboxaldehyde and application of some of these complexes as hydrogenation and oxidation catalysts. The subnormal magnetic moment values substantiate a binuclear structure for all the Cu(II) complexes favouring square-planar geometry and those with magnetic moment of 1.76 BM favoured octahedral geometry with mononuclear complex formation with this SB ligand [34].

It is found that the SBs selected for synthesis for this study have not been found in the literature. It is also noticed that many of the tridentate ligands are found to show striking biochemical characters where the azomethine linkage are blended into stable structured inorganic metal chelates. In a delicately balanced living system, physiological activity is a result of several chemical and physical processes. In such processes, the metal complexes furnished useful drugs and other substances as described by selective toxicity in pharmacology [40-42]. They function by upsetting this delicate balance in two ways: (a) by reinforcing the toxicity of a heavy metal and/or (b) by withdrawing the essential metal content from the system. For example, in highly basic iron rich soils, the metal ion, not available to the rootlets of plants, is extracted by spraying Ethylenediaminetetraacetic acid--(edta) in the form of a soluble complex. Such a mechanism for many fungicides and bactericides is described as a partition effect or cooperative effect [43]. Thus, to evaluate the chemical substances as fungicides and bactericides, the following methods are used commonly: (1) slide germination method [44-46], (2) test-tube dilution method [47], (3) cell-volume assay method [48], (4) inhibition-zone or modified paper disc method [49-51], and (5) poisoned food technique [50].

Three important rice pathogens were selected for the present study: two fungal species and a bacterium. The reasons for selecting these species are given in brief. (1) Rhizoctonia solani causes sheath blight [52, 53] which is a serious disease of the rice-crop. The symptoms are (a) grayish white patches and (b) yellowing of leaves. This spreads very quickly and causes enormous loss. It also causes several other diseases on many economically important commercial crops. (2) Acrocylindrium oryzae causes sheath rot of paddy decaying the sheath and was first reported [54-56] in India. A large number of fungicides are evaluated against this organism, in vitro and in vivo. A few of them are in use to arrest thedisease yetitisquite uncontrolled. (3) Xanthomonas oryzae causes bacterial-leaf-blight and is usually noticed [54-56] in the field at the heading stage. The young seedlings, after transplanting, are affected when the upper leaves are rolled along the mid-rib to wither away. Subsequently, the disease extends to the whole field giving a burnt appearance. Applications of heavy doses of nitrogenous fertilizers are said to be the cause of this disease.

In this paper we report the synthesis of new SBs and their metal complexes. They were characterized by C, H, N, Cl and metal analyses, Infra-red (IR), UV-Visible (UV-Vis), thermogravimetric analysis (TGA) for estimating coordinated water, and magnetic susceptibility measurements. By using the appropriate techniques or methods, these were screened for their toxicity against the chosen fungal and bacterial organisms. The results are summarized in the light of their observed physiological activity and a scope for future development.

2. Materials and Methods

2.1. Solvents and Reagents. Solvents were purified and distilled as per standard procedures [57]. Benzoic acid hydrazide orbenzohydrazide [58,59],2-hydroxybenzohydrazide or salicylhydrazide [60, 61], and 1-(2,4-dihydroxyphenyl)ethanone or resacetophenone [62] were prepared as per reported procedures. Hydrazine carbothioamide or thiosemicarbazide was recrystallized from water. The sodium salt of dehydroacetic acid or 3-acetyl-2-hydroxy-6-methyl-4H-pyran-4-one [63] was used as a white solid after treating with dil HCl.

2.2. SBs Ligands Synthesized Are the Following (Scheme 1)

(1) BHFH or Ligand 1 (L1) = N'-((furan-2-yl) methylene)-2-hydroxybenzohydrazide was obtained by condensing salicylhydrazide or 2-hydroxybenzohydrazide and furfuraldehyde or furan-2-carbaldehyde.

(2) BHEH or Ligand 2 (L2) = 2-hydroxy-N,-(1-(2,4-dihydroxyphenyl)ethylidene) benzohydrazide) was obtained from salicylhydrazide or 2-hydroxybenzohydrazide and resacetophenone or 1-(2,4-dihydroxyphenyl)ethanone.

(3) HAEP or Ligand 3 (L3) = 1-(1-(2, 4-dihydroxyphenyl) ethylidene thiosemicarbazide was obtained from hydrazinecarbothioamide or thiosemicarbazide and resacetophenone or 1-(2,4-dihydroxy phenyl)ethanone.

(4) BFH or Ligand 4 (L4) = N'-((furan-2-yl) methylene)benzohydrazide was obtained from benzohydrazide and furfuraldehyde or furan-2-carbaldehyde.

(5) BHDH or Ligand 5 (L5) = 2-hydroxyl-N'-(1-(2-hydroxy-6-methyl-4-oxo-4H-pyran-3-yl)ethylidene) benzohydrazide was obtained from salicylhydrazide or 2-hydroxybenzohydrazide and dehydroacetic acid or 3-acetyl-2-hydroxy-6-methyl-4H-pyran-4-one.

(6) DHA or Ligand 6 (L6) = 3-acetyl-2-hydroxy-6-methyl-4H-pyran-4-one or dehydroacetic acid was used as it is.

2.3. Physical Measurements. C, H, and N analyses were done on Perkin-Elmer 240C analyzer. IR spectra were recorded on Perkin-Elmer grating spectrophotometer 577, near IR-VisUV spectra were recorded on DMR-21 in absorbance range of 300-2000 nm. Magnetic susceptibilities were determined at RT on Faraday's balance. The metal and chloride were estimated by gravimetry [64]. The TGA were analyzed in static air, using limiting temperature of 500[degrees]C and heating rate of 10[degrees]C/min.

2.4. Preparation of the Complexes. All the complexes were prepared by a very similar procedure: to the metal chloride (except VO(II) being a sulfate) in methanol, respective ligand dissolved in methanol is added slowly while stirring. This mixture was either refluxed for 30 min to 3 hrs or digested for 1-2 h for different complexes [52]. Some complexes were obtained at pH 5.5 and some around 8.5 depending on the basicity of the ligand in use. Quantitative precipitates were collected, washed, and dried.

The relevant physical data such as C, H, N, Cl, melting points or decomposition temperatures, colour, and metal analyses are compiled for each ligand and its complexes in Tables 1, 2, 3, 4, 5, and 6. For easy comparison and prediction of the complex formation with clarity on the denticity of the ligand, interpretation of the IR data of each ligand and its complexes are presented separately in Tables 7-12 with all the relevant explanation and references. The analysis of the magnetic susceptibility measurements, the bands obtained using the UV-Vis spectra, their transitions, the predicted geometries, and the interpreted molecular structures are discussed separately, for convenience, in Tables 13-19 for each metal ion forming complex with different ligands.

2.5. Physiological Activity. For the fungal species liquid broth method [52] was followed: peeled and cooked potato (350 g) was collected into which dextrose (35 g) was dissolved and made up to 1750 mL by distilled water (PDA medium). pH was adjusted to 7.0 by adding drops of NaOH solution. It was distributed as 100 mL each into seventeen 250 mL conical flasks containing 2 g of agar-agar and 100 mg metal complex for the organism Rhizoctonia solani. For the Acrocylindrium oryzae, it was distributed as 25 mL each into 70 (150 mL) conical flasks containing 25 mg of the metal complex (1000 ppm).

All the flasks were tightly plugged with cotton and paper. They were all sterilized in the autoclave at 15 lbs pressure and 121[degrees]C for 20 min. The sterilized molten PDA medium from each flask, with the metal complex suspended uniformly, was poured into five petri dishes (90 mm diameter and 20 mL each) and all the replicates were numbered and labeled immediately. All theses pecimens were inoculated and incubated along with a standard fungicide, Dithane M-45, for comparison. Control flasks without chemical were also inoculated and incubated simultaneously.

In the case of the bacterium well-zone or inhibition-zone technique [49, 51] was adopted. To hot 1L distilled water, Hayward's medium [49-52] was added while stirring. The solution was made up to 2 L and pH adjusted to 7.0 by adding drops of NaOH solution. It was distributed equally as 200 mL into 10 (500 mL) conical flasks containing 2g of agar-agar each. All were inoculated and incubated. A set of plates with a standard bactericide, 2-bromo-2-nitro-1, 3-propanediol (Bronidiol), for comparison and another set of control plates with distilled water were kept for evaluation of results. All the data are consolidated in Table 20.

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3. Results and Discussion

Five new ligands were synthesized by mixing the appropriate amine and the aldehyde condensation via a Schiff base reaction (Scheme 1). All of the SBs, thus formed, are crystalline powders white or pale-yellow in colour and are stable to air and moisture. They are found to be soluble in most of the polar solvents like ethanol, methanol, acetone, and so forth and also in bases. All of them were characterized by elemental analyses, melting points (Tables 1-6), and IR spectra (Tables 7-12). The elemental analyses of the ligands show that there is a loss of a few molecules during the CHN analyses, probably due to the low melting points of the synthesized ligands and the details are given in the remarks column of the Tables 1-6, while the IR spectra show all the expected structural peaks. From the IR data in Table 7, it was analyzed that L1 acts as a tridentate ligand by coordinating through -O of the deprotonated phenolic group, -O of another deprotonated -OH group formed due to enolization, and -N of the azomethine group. Table 8 shows that the L2 acts as a tridentate ligand similar to L1 and the -OH groups of the resacetophenone moiety do not participate in coordination. Table 9 gives the data for L3 which enolizes and acts as a tridentate ligand coordinating through the -O of the deprotonated phenolic group, -S of the -SH group after deprotonation, and -N of the azomethine group. Thus it is found to remain in the "thione" form and not in the "thiol" form [65, 66] in the solid state. Table 10 gives details on L4 acting as a bidentate ligand with -O and -N donors. Table 11 shows the details of L5 acting as a tetradentate bound through three -O's and one -N and L6, not a Schiff base but used directly for complexation, binds through carbonyl -O atom and -O of phenolic group as is shown in Table 12.

They were used to make complexes with Cu(II), Ni(II), Co(II), Fe(III), Mn(II), Cr(III), and VO(II) metal ions. Generally all the metal complexes were synthesized in alcoholic solutions at room temperature or by reflux at pH 5.5 or 8.5. These were characterized by the usual analytical and spectroscopic methods. All the complexes formed with the respective ligands have been shown to coordinate with the denticity mentioned above and the shift of the coordinating atoms is also shown in Tables 7-12, thus confirming the formation of stable metal chelates with the new Schiff bases and DHA, L6. The physical data, elemental analyses are also given in Tables 1-6 for all the complexes synthesized. These data for all the complexes also show a loss of a few molecules during the analysis of CHN, probably due to the lower decomposition temperature, while the IR spectra show all the expected structural peaks. Some of the complexes have one, two, or four coordinated water molecules which were analysed by TGA analyses. The variable temperature data of these complexes from room temperature to decomposition of the complex and the loss in weight of the material taken confirm the percentage of coordinated water which is present in the complex composition predicted.

The chemistry of ligands upon binding to different metal atoms leads to the formation of expected four and/or six coordinate complexes and the salient features are discussed below based on the collected electronic and magnetic data. The data are presented in Tables 13-19 and Figures 1-8 for different metal ions.

3.1. VO(II) Complexes. All the OXOVANADIUM complexes are highly coloured, fine amorphous powders. They are stable to air, moisture and insoluble in water and other common organic polar and nonpolar solvents. They all decompose above 300[degrees]C (except complex of L1 at 285[degrees]C). V complex with L4 showed loss of weight starting at 52[degrees]C (0.0006 gm) and decomposed at 300[degrees]C (0.0090 gm), complex with L3 at 50[degrees]C (0.0004 gm) and decomposed at 310[degrees]C (0.0088 gm), complex with L5 at 50[degrees]C (0.0008 gm) and decomposed at 305[degrees]C (0.0096 gm), and complex with L6 at 50[degrees]C (0.0009 gm) and decomposed at 305[degrees]C (0.0099 gm) in the thermal analysis, thus confirming one or two molecules of water coordination in the complexes as per the composition predicted.

All the VO(II) complexes are paramagnetic as shown in Table 13; Figures 1 and 2. The values of L6, L3, and L5 based complexes are in agreement with the expected spin-only value of 1.73 BM at RT. However, the complexes with L1 and L2 have shown lower values 1.5-1.6 BM maybe due to low symmetry expected at 1.73 BM when the orbital angular contribution is almost quenched [67] and may occur due to the presence of exchange coupled antiferromagnetism [68]. Several reports indicate such behavior [69-71]. Hence, they are assigned binuclear structures.

Electronic spectra show three bands below 30,000 [cm.sup.-1] at RT in diffuse reflectance mull data as given in Table 13 corresponding to octahedral symmetry (Oh) with tetragonal distortion. The bands, transitions, molecular structure, and the predicted geometry are given in Table 13. A few complexes may also show a vibrational structure with a spacing of 700 [cm.sup.-1] at the 2B2 ^ 2E transition band, corresponding to the V=O stretching frequency in the excited state, which is not clearly observed.

3.2. Cr(III) Complexes. All the Cr(III) complexes are coloured solids and they are stable to air and moisture. They are insoluble in water and in most of the common organic solvents like methanol, ethanol, benzene, acetone, and so forth. Hence, conductivity could not be measured due to the insolubility. Cr complex with L4 at lower pH showed loss of weight starting at 110[degrees]C (0.0005 gm) and decomposed at 270[degrees]C (0.0091 gm), complex with L4 at higher pH at 52[degrees]C (0.0005 gm) and decomposed at 310[degrees]C (0.0091 gm), and complex with L3 at 52[degrees]C (0.0005 gm) and decomposed at 265[degrees]C (0.0091 gm) in the thermal analysis. Thus, confirming one or two molecules of water coordination in the complexes as per the composition predicted.

The Cr(III) complexes are synthesized with L3, L4, L5, and L6 and are characterized [72, 73] as havng Oh geometry as shown in Table 14; Figure 3. The magnetic moments of L6 and L4 (prepared at pH 8.5) at RT are close to the expected spin-only value for Oh complexes of Cr(III) [72-75]. The other complexes show lower values and so may be due to metal-metal interactions with binuclear bridge structures. All the electronic spectra for several greenish Cr(III) complexes fit with very large number of such complexes studied and surveyed. However in the present case, the highest energy band is found to be obscured due to the dark colour of all the complexes.

3.3. Mn(II) Complexes. The Mn(II) complex of L1 is a fine powder, light-yellow in colour and decomposed at 280[degrees] C without melting. The Mn(II) complex of L2 is a dark-brown powder decomposed at 286[degrees]C. Both the compounds are very stable in air and moisture and are insoluble in water and in common organic solvents like methanol, ethanol, chloroform, benzene, and so forth. Mn complex with L1 at lower pH showed loss of weight starting at 56[degrees]C (0.0014 gm) and decomposed at 280[degrees]C (0.0205 gm) in the thermal analysis, thus confirming a molecule of water coordination in the complex as per the composition predicted.

As can be seen from Table 15; Figure 4, Mn(II) complex of L1 shows subnormal magnetic moment which may be due to metal-metal interactions or due to spin-exchange or superexchange in the solid state [76,77]. The Mn(II) complex of L2 is 5.92 BM expected region for high-spin Oh Mn(II) complexes [72,73]. The electronic spectra are consistent with the Oh symmetry in both the cases.

3.4. Fe(III) Complexes. All the complexes are dark coloured and fine amorphous powders. All decomposed above 300[degrees]C are very stable to air, moisture and insoluble in most of the common organic solvents like acetone, methanol, ethanol, and so forth. They are soluble to some extent in solvents like 1-4 dioxane, dimethylformamide, and dimethyl sulfoxide. Their conductivity could not be measured owing to their insoluble nature. Fe complex with L2 showed loss of weight starting at 68[degrees]C (0.0012 gm) and decomposed at 305[degrees]C (0.0057 gm) and complex with L3 at 66[degrees]C (0.0018 gm) and decomposed at 300[degrees]C (0.0055 gm) in the thermal analysis. Thus, confirming two molecules of water coordination in the complexes as per the composition predicted.

All the Fe(III) complexes formed with L1-L3 ligands have subnormal magnetic moments which may be due to the fact that metal-metal interactions or superexchange is anticipated [76, 78, 79], as all the complexes may be binuclear in nature as shown in Table 16; Figure 5. The electronic spectra have very weak transitions and could not be concluded decisively and, however, are close to Oh symmetry with some tetragonal distortion.

3.5. Co Complexes. All Co(II) complexes are coloured, fine amorphous powders and decompose above 260[degrees]C without melting. They are all very stable to air, moisture and insoluble in most of the common organic solvents and to a small extent in 1-4 dioxane, dimethylformamide, and dimethyl sulfoxide. The conductivity of the compounds could not be determined owing to their insoluble nature. Co complex with L1 showed loss of weight starting at 52[degrees]C (0.0020 gm) and decomposed at 260[degrees]C (0.0555 gm) and complexwith L3 at 54[degrees]C (0.0007 gm) and decomposed at 295[degrees]C (0.0089 gm) in the thermal analysis, thus confirming two molecules of water coordination in the complexes as per the composition predicted.

The observed magnetic moments of all the three Co(II) complexes formed with L1-L3 ligands are slightly lower than the expected 4.7-5.2BM for high-spin octahedral Co(II) complexes as given in Table 17; Figure 6. The lower moments maybe due to the metal-metal interactions [80].

In the Oh Co(II) complexes 4T1g and Eg are the spin-free and spin-paired ground states. Broad band in lower energies and a multiple band in slightly higher energy in admixtures with spin-forbidden transition to doublet state are expected [72]. The asymmetric visible band is typical of Oh Co(II) complexes, the shoulder on the high energy side being assigned to spin-forbidden transitions [74].

3.6. Ni(II) Complexes. Ni(II) complexes are bright-red, green, and dark-brown in colour. These are insoluble in water and sparingly soluble in common organic solvents and also in 1-4 dioxane, dimethylformamide, and dimethyl sulfoxide. The conductivity could not be measured owing to very low solubility of the complexes. Ni complex with L1 at lower pH showed loss of weight starting at 68[degrees]C (0.0010 gm) and decomposed at 265[degrees]C (0.0053 gm) in the thermal analysis, thus confirming a molecule of water coordination in the complex as per the composition predicted.

The L1 complex at pH 5.5-70 and the L3 complexes are diamagnetic [81] and the other two with L1 at pH 8.5 and L2 have magnetic moment around 2.91-3.40 BM as expected for six-coordinated spin-free Ni(II) complexes as seen in Table 18; Figure 7. In regular Oh complexes of Ni(II) consideration of spin-orbit coupling and contribution from the 3A2g and the next higher 3T2g states give a somewhat higher magnetic moment than the spin-only moment of 2.83 BM [72, 82, 83].

The electronic spectra of the diamagnetic complex with L1 at pH 5.5-70 show two bands assigned to strong charge-transfer d-[pi.sup.*] transition [84] and the lower energy band to 1A1g [right arrow] 1A2g transition [74, 84-87] as expected for square-planar complexes. The other two complexes show three intense bands expected for regular octahedral geometry.

3.7. Cu(II) Complexes. All the complexes are coloured, fine amorphous powders and decompose above 250[degrees]C without melting. They are all very stable to air, moisture and are insoluble in most of the common organic solvents, except to a small extent in 1-4 dioxane, dimethylformamide, and dimethyl sulfoxide. The conductivity could not be measured owing to their insoluble nature and their stoichiometry is deduced from the analytical data and geometry from the diffuse reflectance data in conjunction with magnetic moments. Cu complex with L1 at higher pH showed loss of weight starting at 73[degrees]C (0.0010 gm) and decomposed at 280[degrees]C (0.0300 gm) in the thermal analysis, thus confirming a molecule of water coordination in the complex as per the composition predicted.

The subnormal magnetic moments of Cu L1 at lower pH and Cu L3 indicate some metal-metal interactions in the solid state. The dimeric nature of the complexes predicted with O and -S as bridges supports this [88, 89]. All the data in the references cited show that magnetic moments of square-planar Cu(II) complexes lie in the range of 1.7-1.9 BM. While slightly higher values of the other two complexes suggest presence of one unpaired electron with spin-orbit coupling [90]. Thus, all of the Cu(II) complexes are assigned [72] square-planar geometry as shown in Table 19; Figure 8. Two of them indicate metal-metal interactions due to slightly lower magnetic moments; one of them shows a loss of weight corresponding to one molecule of water from the TGA at variable temperature and one another with the chloride estimation.

3.8. Physiological Activity. The effect of the metal complex on fungal growth is measured by poisoning the nutrient (a solid like an agar-agar or a liquid medium) with a fungi toxicant. Then, it is allowed to grow as a test fungus.

3.9. For the Organism Rhizoctonia Solani

(i) L1 has shown 30% inhibition at 1000 ppm, 17% at 500 ppm, and nil effect at 250 ppm (Table 20). Hence, all the newly synthesized complexes were tested for activity at 1000 ppm (observe carefully Figure 9). It was found that the VO(II) complex is 100% effective, Mn(II) 95%, Fe(III) 62%, Co(II) nil effect, Ni(II) 45% and Cu(II) nil effect. Thus, the activity order may be evaluated as VO > Mn > Fe > Ni > L1 > Co = Cu.

(ii) L2 shows the following trend VO > Mn > Ni > Cu > L2 > Co.

(iii) quite unexpectedly, L3 upon complexation completely subsides the activity. This may be due to the presence of two free -OH groups and one free N[H.sub.2] group in the ligand, the structure of which is comparable to the antidotes used for the expulsion of food poisoning in hospitals.

(iv) L4 trend shows VO > Cr > L4.

(v) L5, L6 show VO > Cr.

Thus the complexes with L1, L2, and L4 are as effective as the commercially used Dithane M-45 (Table 20). The VO complexes with L1 and L2 are dimeric in nature and probably in solution dissociate to monomeric units due to the V=O group unlike the other dimeric complexes synthesized. The -O of V=O might bind in such a way that the activity order is tremendously increased and the growth of fungus is completely inhibited making it 100% effective. And probably the ligands are bound to metal atoms by rearrangement caused by enolization, thus making them more viable for dissociation, unlike the first deceptive appearance they give as if they are coordinately more saturated.

In the Case of Acrocylindrium oryzae, a nominal activity for the L4-L6 Cr(III) complexes and maximum activity for all VO(II) complexes were observed. Hence, screening of VO(II) complex of L1 was done at lower concentrations and compared with the commercially used fungicide Dithane M-45 (observe carefully Figure 10). From the average of four replications in each case, the dry-weight of the fungal mycelium was recorded in milligrams and was shown in Table 20. It was observed that L1-L3 has totally inhibited the growth at 1000, 500, and 250 ppm. Nominal growth of the organism on the disc of the inoculums was observed to be about 2-5 mg. but L4 showed nominal activity at 1000 ppm with decreased activity at lower concentrations. So the activity order for all these is given as follows. L1 > VO > Ni > Mn > Fe > Co > Cu and L2 > Ni > VO > Mn > Fe > Cu > Co. Cr(III) complexes of L3-L6 were found less toxic than VO(II) complexes. The activity of these was found to be marginal when compared to that of the commercial Dithane M-45. Interestingly, it was found that the VO(II) complex at 250 ppm is more effective compared to Dithane M-45 at 500 ppm and maybe more useful. It is interesting to note from the above data that L1 and L2 are very toxic to this organism compared to Rhizoctonia solani and also VO(II) complexes show more activity.

After 48 hrs of inoculation of the bacterium Xanthomonas oryzae, percentage inhibition growth was calculated from each plate and average readings from fine replicas are shown in Table 20. It was observed that neither the ligands nor the complexes could control the growth of this bacterium fully. None of the complexes showed considerable percentage inhibition at the 1000 ppm concentration and, hence, they were not screened at lower concentrations. The saturated bactericide, Branidiol, was also found to be effective only to the extent of 50% but its effect so persists in the system that the growth is arrested at that stage and never continues. The order of activity of complexes of L1 is as follows: VO > Mn > Fe > L1 > Ni > Co > Cu and that in the complexes of L2 is Ni > Mn > VO > Co > Fe > Cu > L2. L3 and all its complexes have shown nil activity on this bacterium. L4-L6 and their Cr(III), VO(II) complexes were screened and the order of activity in them was as follows: VO > Cr > L4 > L5 > L6. Thus it was observed that the complexation increases the activity of ligand, but it was less than the standard bactericide, Bronidiol.

4. Conclusions

Synthesis of Schiff bases L1-L5 and L6 and their use as ligands for coordination with VO(II), Cr(III), Mn(II), Fe(III), Co(II), Ni(II), and Cu(II) form a major study. All the prepared complexes were analyzed by C, H, N, Cl, and metal analyses. They were assigned molecular structures and geometries using information obtained from IR, UV-Vis, magnetic susceptibility, and TGA analysis. The physiological activity studies with ligands L1-L4 along with some results of metal complexes with L1-L6 ligands are tabulated, suggesting them to be toxic to the organisms studied and, hence, maybe useful as fungicides and bactericides. The VO(II) complexes are found to be more active compared to the activity of the commercial standard.

http://dx.doi.org/10.1155/2014/736538

Conflict of Interests

The authors declare that there is no conflict of interests regarding the publication of this paper.

Acknowledgment

The author, T. Mangamamba, would like to thank All India Coordinated Rice Improvement Project (ACRIP), Rajendranagar, Hyderabad, for allowing her to use their facility for the study of physiological activity.

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T. Mangamamba, (1) M. C. Ganorkar, (1) and G. Swarnabala (2,3)

(1) Agarwal Siksha Samiti, Charminar, Hyderabad 500 002, India

(2) Shadan PG Institute, Khairatabad, Hyderabad 500 001, India

(3) Centre for Materials for Electronics Technology (C-MET), IDA Phase III, Cherlapally (HCL PO), Hyderabad 500 051, India Correspondence should be addressed to G. Swarnabala; swarnabalaganti@gmail.com

Received 22 February 2014; Revised 8 May 2014; Accepted 9 May 2014; Published 18 September 2014

Academic Editor: Alfonso Castineiras

TABLE 1: Elemental composition and physical data of BHFH ligand
and its complexes.

S.              Complex              Mpt       Colour
number                            [degrees]C

1               BHFH-L1              210       White
          ([C.sub.12][H.sub.8]
          [N.sub.2][O.sub.3])

2         [[Cu(BHFH)].sub.2]-        308        Grey
               pH 5.5-70
          [Cu.sub.2][C.sub.24]
          [H.sub.16][N.sub.4]
               [O.sub.6]

3        [Cu(BHFH)[H.sub.2]O]-       280       Green
                 pH 8.5
         Cu[C.sub.12][H.sub.10]
           [N.sub.2][O.sub.4]

4        [Ni(BHFH)[H.sub.2]O]-       265        Red
               pH 5.5-70
         Ni[C1.sub.2][H.sub.10]
           [N.sub.2][O.sub.4]

5         [Ni[(BHFH).sub.2]]-        280       Green
                 pH 8.5
         Ni[C.sub.24][H.sub.16]
           [N.sub.4][O.sub.6]

6        [[Co(BHFH)([H.sub.2]O)      260        Pink
               Cl].sub.2]
          [Co.sub.2][C.sub.24]
          [H.sub.20][N.sub.4]
          [O.sub.8][Cl.sub.2]

7        [[Fe(BHFH)[Cl.sub.2]].      320        Red
                 sub.2]
          [Fe.sub.2][C.sub.24]
          [H.sub.16][N.sub.4]
          [O.sub.8][Cl.sub.4]

8        [[Mn(BHFH)([H.sub.2]O)      280       Yellow
               Cl].sub.2]
          [Mn.sub.2][C.sub.24]
          [H.sub.20][N.sub.4]
          [O.sub.8][Cl.sub.2]

9         [[VO(BHFH)Cl].sub.2]       285        Grey
          [V.sub.2][C.sub.24]
          [H.sub.16][N.sub.4]
          [O.sub.8][Cl.sub.2]

S.          C        H         N         M        Cl
number

                         Observed (calculated) %

1         63.00     4.50     12.56      --        --
         (63.18)   (4.38)   (12.27)

2         50.02     2.90     10.00     20.95      --
         (50.10)   (2.78)   (9.73)    (22.09)

3         47.20     3.45     9.50      20.00      --
         (47.44)   (3.29)   (9.22)    (20.94)

4         50.00     3.50     9.20      20.00      --
         (50.25)   (3.49)   (9.76)    (20.47)

5         56.00     4.00     11.00     11.50      --
         (56.17)   (3.90)   (10.92)   (11.45)

6         42.55     3.30     8.51      17.50     10.50
         (42.70)   (3.26)   (8.29)    (17.46)   (10.52)

7         40.50     2.80     7.92      16.00     20.00
         (40.58)   (2.82)   (7.89)    (15.74)   (20.01)

8         44.50     2.98     8.12      17.00     10.00
         (44.65)   (3.10)   (8.68)    (16.90)   (11.01)

9         44.00     3.00     8.50      15.00     10.74
         (44.14)   (3.06)   (8.57)    (15.60)   (10.87)

S.        Mol            Remarks
number   Wt gm

1        228.13        Loss of 2H

2        575.35        Loss of 8H

3        303.55        Loss of 8H

4        286.83    Loss of [H.sub.2]O

5        512.70        Loss of 6H

6        675.12        Loss of 8H

7        709.70        Loss of 4H

8        645.00   Loss of 1.5[H.sub.2]O

9        653.14        Loss of 8H

TABLE 2: Elemental composition and physical data of BHEH ligand
and its complexes.

S. number         Complex          Mpt [degrees]C   Colour

1           BHEH-L2 ([C.sub.15]         215         Yellow
            [H.sub.13] [N.sub.2]
                 [O.sub.4])

2               [Cu(BHEH)Cl]            305         Green
                Cu[C1.sub.5]
            [H.sub.13] [N.sub.2]
                [O.sub.4]Cl

3               [Ni(BHEH)2]             270          Red
                Ni[C.sub.30]
            [H.sub.26] [N.sub.4]
                 [O.sub.8]

4               [Co(BHEH)2]             260         Brown
                Co[C.sub.30]
            [H.sub.28] [N.sub.4]
                 [O.sub.8]

5            [Fe(BHEH)(H2O)Cl]2         305         Black
                 [Fe.sub.2]
                 [C.sub.30]
            [H.sub.30] [N.sub.4]
                 [O.sub.10]
                 [Cl.sub.2]

6               [Mn(BHEH)2]             285         Brown
                Mn[C.sub.30]
            [H.sub.26] [N.sub.4]
                 [O.sub.8]

7           [[VO(BHEH)Cl].sub.2]        300          Grey
            [V.sub.2] [C.sub.30]
            [H.sub.26] [N.sub.4]
                 [O.sub.10]
                 [Cl.sub.2]

S. number         C              H             N

            Observed (calculated) %

1           63.00 (63.18)   5.00 (4.91)   9.89 (9.82)

2           47.05 (47.36)   3.50 (3.42)   7.50 (7.37)

3           57.00 (57.26)   4.20 (4.14)   8.77 (8.91)

4           57.50 (57.61)   4.35 (4.48)   9.01 (8.96)

5           45.55 (45.64)   4.35 (3.80)   7.23 (7.10)

6           58.00 (58.02)   3.93 (3.87)   9.00 (9.02)

7           44.20 (44.28)   3.29 (3.34)   7.25 (738)

S. number         M             Cl

            Observed (calculated) %

1                --             --

2           16.00 (16.72)   9.50 (9.35)

3            9.50 (9.34)        --

4           10.00 (9.43)        --

5           14.52 (14.16)   9.50 (9.00)

6           10.00 (8.78)        --

7           12.86 (13.43)   9.20 (9.46)

S. number   Mol Wt gm        Remarks

1            285.16         Loss of H

2            380.10        Loss of 4H

3            628.70         Loss of 2H

4            630.93            --

5            788.70         Loss of 2H

6            620.50        Loss of 4H

7            758.88     Loss of 2C and 2H

TABLE 3: Elemental composition and physical data of HAEP ligand and
its complexes.

S. number              Complex              Mpt [degrees]C   Colour

1                HAEP-L3 ([C.sub.9]              193         Brown
                [H.sub.11] [N.sub.2]
                     [O.sub.2]S)

2                    [Cu(HAEP)]2                 310         Brown
                     [Cu.sub.2]
                     [C.sub.18]
                [H.sub.18] [N.sub.6]
                 [O.sub.4] [S.sub.2]

3                    [Ni(HAEP)2]                 305         Brown
                     [Ni.sub.2]
                     [C.sub.18]
                [H.sub.18] [N.sub.6]
                 [O.sub.4] [S.sub.2]

4                    [[Co(HAEP)                  295         Brown
            [([H.sub.2]O).sub.2]].sub.2]
                     [Co.sub.2]
                     [C.sub.18]
                [H.sub.26] [N.sub.4]
                 [O.sub.8] [S.sub.2]

5                    [[Fe(HAEP)                  300         Green
               ([H.sub.2]O)Cl].sub.2]
                     [Fe.sub.2]
                     [Cl.sub.6]
                [H.sub.22] [N.sub.4]
                [O.sub.6] [Cl.sub.2]
                      [S.sub.2]

6                    [[Cr(HAEP)                  265         Green
               ([H.sub.2]O)Cl].sub.2]
                     [Cr.sub.2]
                     [C1.sub.8]
                [H.sub.22] [N.sub.4]
                [O.sub.6] [Cl.sub.2]
                      [S.sub.2]

7                    [[VO(HAEP)                  310          Grey
                ([H.sub.2]O).sub.2]]
                     V[C.sub.9]
                [H.sub.13] [N.sub.2]
                     [O.sub.5] S

S. number         C              H              N

            Observed (calculated) %

1           52.00 (52.18)   5.40 (5.31)   13.30 (13.52)

2           40.00 (40.21)   3.50 (3.35)   15.50 (15.64)

3           39.00 (39.31)   3.50 (3.28)   15.30 (15.29)

4           35.70 (35.89)   4.30 (4.32)    9.30 (9.30)

5           30.50 (30.88)   3.51 (3.54)    8.91 (9.01)

6           35.00 (35.23)   4.21 (3.59)    9.00 (9.13)

7           34.50 (34.62)   3.20 (4.17)    8.99 (8.97)

S. number         M              Cl

            Observed (calculated) %

1                --              --

2           24.00 (23.6)         --

3           21.00 (21.36)        --

4           20.00 (19.58)        --

5           18.00 (17.97)   11.00 (11.42)

6           15.50 (16.96)   10.25 (11.58)

7           15.74 (16.33)

S. number   Mol Wt gm                 Remarks

1            207.16          Loss of N[H.sub.2] and 2H

2            537.22         Loss of 2N[H.sub.2] and 2OH

3            549.52             Loss of N[H.sub.2]

4            601.86          Loss of N[H.sub.2] and 4H

5            621.70     Loss of 2N, 2C; add 0.5 [H.sub.2]O

6            613.12             Loss of N[H.sub.2]

7            312.00             Loss of N[H.sub.2]

TABLE 4: Elemental composition and physical data of BFH ligand
and its complexes.

S. number         Complex          MPt [degrees]C   Colour

1            BFH-L4 ([C.sub.12]         182         Yellow
            [H.sub.10] [N.sub.2]
                 [O.sub.2])

2                [[Cr(BFH)              270         Brown
                ([H.sub.2]O)
             [Cl.sub.2]].sub.2]
                 [Cr.sub.2]
                 [C.sub.24]
            [H.sub.20] [N.sub.4]
            [O.sub.6] [Cl.sub.4]
                 pH 5.5-7.0

3            [Cr [(BFH).sub.2]          310          Red
               ([H.sub.2]O)]
                 [Cl.sub.2]
                Cr[C.sub.24]
            [H.sub.20] [N.sub.4]
             [O.sub.5]Cl pH 8.5

4            [VO [(BFH).sub.2]          300          Red
               ([H.sub.2]O)]
                V[C.sub.24]
            [H.sub.18] [N.sub.4]
                 [O.sub.6]

S. number         C              H              N

            Observed (calculated) %

1           6750 (67.63)    5.00 (4.69)   13.00 (13.14)

2           42.00 (42.42)   3.25 (2.95)    8.10 (8.25)

3           55.00 (55.38)   3.50 (3.85)   10.50 (10.77)

4           58.50 (58.42)   4.00 (4.06)   10.90 (11.36)

S. number         M              Cl

            Observed (calculated) %

1                --              --

2           13.50 (15.32)   19.52 (20.91)

3           10.00 (10.00)   12.52 (13.65)

4           10.00 (10.33)        --

S. number   Mol Wt gm          Remarks

1            213.13           Loss of H

2            679.00     Loss of 1.5 [H.sub.2]O

3            520.00     Loss of 2.5 [H.sub.2]O

4            492.94       Loss of [H.sub.2]O

TABLE 5: Elemental composition and physical data of BHDH ligand and
its complexes.

S. number         Complex          MPt [degrees]C   Colour

1           BHDH-L5 ([C1.sub.5]         240         Yellow
            [H.sub.14] [N.sub.2]
                 [O.sub.5])

2           [[Cr(BHDH)Cl].sub.2]        300         Green
                 [Cr.sub.2]
                 [C.sub.30]
            [H.sub.24] [N.sub.4]
                 [O.sub.10]
                 [Cl.sub.2]

3                [VO(BHDH)              305         Green
               ([H.sub.2]O)]
                V[C.sub.15]
            [H.sub.14] [N.sub.2]
                 [O.sub.7]

S. number         C              H             N

            Observed (calculated) %

1           60.00 (60.02)   5.00 (4.66)   9.40 (9.33)

2           47.00 (47.06)   3.00 (3.14)   7.52 (7.32)

3           40.55 (40.63)   3.90 (3.91)   7.30 (729)

S. number         M             Cl

            Observed (calculated) %

1                --             --

2           10.00 (13.59)   9.25 (9.28)

3           13.12 (13.27)       --

S. number   Mo. Wt gm                 Remarks

1            300.16                 Loss of 2H

2            765.00                 Loss of 2H

3            383.94     Loss of 2H, 2C; add [H.sub.2]O, 4H

TABLE 6: Elemental composition and physical data of DHA
ligand and its complexes.

S. number   Complex                     MPt          Colour
                                        [degrees]C

1           DHA-L6 [C.sub.8][H.sub.8]   109          Colorless
              [O.sub.4]
2           [Cr[(DHA).sub.3]]           285          Green
              Cr[C.sub.24][H.sub.24]
              [O.sub.12]
3           [VO[(DHA).sub.2]            305          Green
              ([H.sub.2]O)]
              V[C.sub.16][H.sub.18]
              [O.sub.10]

S. number   C               H             M
                    Observed (calculated) %

1           57.00 (57.17)   5.00 (4.76)   --

2           55.00 (55.41)   4.25 (4.61)   10.00 (10.00)

3           45.50 (45.61)   --            11.75 (12.10)

S. number   Mol Wt gm   Remarks

1           168.08      -

2           520.26      Loss
                        of two
                        [H.sub.2]O
3           420.94      --

TABLE 7: Characteristic IR data for the L1-BHFH (tridentate
-O, -O, and -N) and its participation in complex formation
with metal ions.

S. number          Complex               Coord       IR [cm.sup.-1]
                                       water (e)      (s = sharp;
                                                       b = broad;
                                                      d = doublet;
                                                       w = weak;
                                                       vw = very
                                                         weak)

                                                        vO-H and

                                                        vN-H (e)

1              BHFH-Ll (c-d-e)            --            3260 (a)
2             [[Cu(BHFH)].sub.2]          --             Absent
3            [Cu(BHFH)[H.sub.2]0]    3420-3220(b)        Absent

4            [Ni(BHFH)[H.sub.2]0]    3500-3400(b)        Absent
5                [Ni(BHFH)2]              --            3210 (s)
6           [[Co(BHFH)([H.sub.2]0)   3500-3400 (b)      3210 (s)
                  C1].sub.2]
7           [[Fe(BHFH)[Cl.sub.2]].        --            3220 (s)
                    sub.2]
8            [[Mn(BHFH)([H.sub.2]    3500-3400 (b)      3220 (s)
                 O)Cl].sub.2]
9            [[VO(BHFH)Cl].sub.2]         --            3175 (s)

S. number     IR [cm.sup.-1] (s = sharp;
              b = broad; d = doublet; w =
                  weak; vw = very weak)

            vC=O (e)        vC=N (e)

1           1640 (s)        1610 (s)
2            Absent         1590 (d)
3            Absent         1590 (s)

4            Absent    1620 (s), 1590 (s)
5            Absent         1610 (d)
6            Absent    1615 (s) 1580 (s)

7            Absent    1615 (s), 1585 (s)

8            Absent    1610 (s), 1575 (s)

9            Absent    1610 (s), 1585 (s)

S. number   IR [cm.sup.-1] M-O, M-N, or M-Cl (e)
            (s = sharp;
             b = broad;
            d = doublet;
             w = weak;
             vw = very
               weak)

                vC=0
            phenolic (e)

1            1220 (s)b              --
2             1250 (s)         490, 475, 430
3               1190        830 (s), 485, 430,
                                    410
4             1255 (s)       830 (s), 580, 560
5             1250 (s)            450,370
6             1255 (s)      870 (s), 550, 440,
                                    360
7             1250 (s)         550, 440, 360

8             1245 (s)       845-835 (d), 440,
                                 390, 350
9             1250 (s)      970 (V=0) (f), 550,
                                 420, 370

(a) Overlap of hydrogen bonded O-H and N-H; (b) Stretching
frequency; (c) No change in vN=N at 1075 [cm.sup.-1],
Shyamal and Kale [88]; (d) No change in symmetric and
asymmetric frequencies of furfural ring vC-O-C at 1020 (s);
895 (s) [cm.sup.-1] indicates noninvolvement of O of
furfural ring in complexation; (e) The enolization of the
hydrazide residue and the subsequent deprotonation of both
the hydroxyl groups or cleavage of hydrogen bond forming
M-O bonds confirmed by vC-O phenolic shift, doublet for
two vC=N groups (one azomethine participating in complex
formation and one formed due to enolization of ligand),
absence of vC=0, and new bands for vN-H, vC=N, M-O, and
M-N vibrations; Nakamoto [91], Ueno and Martell [92, 93];
(f) Selbin [94].

TABLE 8: Characteristic IR data for the L2-BHEH
(tridentate -O, -O, and -N) and its participation in
complex formation with metal ions.

S. number         Complex           IR [cm.sup.-1] (s = sharp;
                                   b = broad; d = doublet; w =
                                      weak; vw = very weak)

                                   Coord water      vO-H (c)

1               BHEH-L2 (g)             --        3330 (b) (a)
2               [Cu(BHEH)Cl]            --          3460 (b)
3            [Ni[(BHEH).sub.2]]         --          3600 (b)
4            [Co[(BHEH).sub.2]]         --          3450 (b)
5                [[Fe(BHEH)        3500-3450(b)        --
              ([H.sub.2]O)Cl].
                   sub.2]
6            [[Mn(BHEH).sub.2]]         --          3460 (b)
7           [[VO(BHEH)Cl].sub.2]        --          3500 (w)

S. number      IR [cm.sup.-1] (s = sharp; b =
                broad; d = doublet; w = weak;
                      vw = very weak)

              vN-H (c)     vC=O (d)   vC=N (d)

1           3260 (b) (b)   1650 (s)   1610 (s)
2             3340(b)      1600 (s)   1585 (s)
3             3340 (b)     1620 (s)   1600 (s)
4             3280 (s)     1620 (s)   1600 (s)
5             3340(b)      1605 (s)   1580 (s)

6             3280 (s)     1620 (d)   1600 (s)
7             3260 (b)     1600 (s)   1590 (s)

S. number    IR [cm.sup.-1] (s = sharp;
            b = broad; d = doublet; w =
               weak; vw = very weak)

                vC=O        M-O or M-N or
            phenolic (e)        M-Clf

1             1240 (s)           --
2             1255 (s)      690, 510, 270
3             1255 (s)        500, 380
4             1255 (s)         650-400
5             1255 (s)      840 (s), 620,
                              580, 490

6             1255 (s)         650-400
7             1260 (s)     970 (V=O), 570,
                              520, 340

(a) Intramolecular hydrogen bonding; (b) Hydrogen
bonding; (c) Shift indicates cleavage of intramolecular
H bonds after complex formation; (d) Involvement of O
of carbonyl group and N of azomethine group in complex
formation, Watt and Dowes [95]; Truter and Rutherford
[96]; Cotton and Wilkinson [97]; (e) Davison and
Christie [98]; Kubo et al. [99]; indicates
deprotonation of phenolic OH and binding to M; (f)
Nakamoto [91,100] and Selbin [94]; (g) No change in
vN-N at 1040 (w) [cm.sup.-1].

TABLE 9: Characteristic IR data for the L3-HAEP
(tridentate -O, -N, and -S) and its participation
in complex formation with metal ions.

S. number        Complex          Coord water    IR [cm.sup.-1]
                                                  (s = sharp;
                                                   b = broad;
                                                  d = doublet;
                                                   w = weak;
                                                   vw = very
                                                     weak)

                                                    vO-E (a)

1                HAEP-L3              --            3400(b)
2           [[Cu(HAEP)].sub.2]        --          3440 (s) (c)
3           [Ni[(HAEP).sub.2]]        --            3460 (s)
4               [[Co(HAEP)          3560(b)         3480(b)
              [([H.sub.2]0).
              sub.2]].sub.2]
5               [[Fe(HAEP)          3560(b)         3480(b)
             ([H.sub.2]O)Cl].
                  sub.2]
6               [[Cr(HAEP)       3500-3450 (b)      3480(b)
               ([H.sub.2]0)
               Cl].sub.2]Z
7               [[V0(HAEP)          3560(b)         3460 (s)
              ([H.sub.2]0).
                 sub.2]]

S. number   IR [cm.sup.-1] (s = sharp; b = broad; d = doublet;
                       w = weak; vw = very weak)

             vN-[H.sub.2] (b)      vC=N (d)          vC=0
                                                 phenolic (c)

1           3320 (s), 3280 (s)     1630 (s)        1270 (s)
2           3320 (s), 3280 (s)   1640,1610 (s)     1295 (s)
3             3320-3280 (s)      1640,1610 (s)     1295 (s)
4           3320 (b), 3280 (b)   1610-1620 (b)     1280 (s)

5           3320 (s), 3280 (s)   1640,1620 (d)     1295 (s)

6           3320 (s), 3280 (s)   1605,1595 (d)     1280 (s)

7           3320 (s), 3280 (s)     1600-1610       1290 (s)

S. number   IR [cm.sup.-1] (s = sharp; b = broad;
            d = doublet; w = weak; vw = very weak)

            vC=S **      M-O, M-N, and M-S **

1           1280 (s)              --
2           1225 (s)        850, 500, 400
3           1220 (w)         850, 600-400
4           1220 (w)   850, 570, 470, 410, 400

5           1220 (w)      850, 575, 480, 400

6           1010 (w)      850, 520, 440, 295

7              --      970 (V=0), 850, 310, 300

** Ligand exists in "thione" form and not "thiol" form
in the solid state as the expected vS-H band at 2570
(s) [cm.sup.-1] for "thiol" form is not observed and
vC=S is present, Pradhan and Rao [65]; Saha and Deepak
[66] and other references therein; Suzuki [101];
Pradhan and Rao [102]; (a) Overlap of two hydroxyl
groups of resacetophenone moiety and hydrogen bonding
to some extent; (b) Symmetric and asymmetric
frequencies of N[H.sub.2] group not participated in
complexation; (c) New sharp band of free -OH indicates
deprotonation and coordination; (d) New vC=N group due
to enolization and shift in original vC=N group of
azomethine.

TABLE 10: Characteristic IR data for the L4-BFH (bidentate
-O, -N) and its participation in complex formation with
metal ions.

S.              Complex           IR [cm.sup.1] (s = sharp;
number                            b = broad; d = doublet;
                                  w = weak; vw = very weak)

                                   Coord water        vN-H

1              BFH-L4 (b)              --         3240 (s) (a)
2        [[Cr(BFH)([H.sub.2]O)      3550-3450      Absent (c)
           [Cl.sub.2]].sub.2]
3           [Cr[(BFH).sub.2]        3550-3450      Absent (c)
            ([H.sub.2]O)Cl]
4        [VO[(BFH).sub.2](ThO)]   3550-3450 (b)    Absent (c)

S.              Complex           IR [cm.sup.1] (s = sharp;
number                            b = broad; d = doublet;
                                  w = weak; vw = very weak)

                                    vC=O          vC=N (d)

1              BFH-L4 (b)         1650 (s)        1620 (s)
2        [[Cr(BFH)([H.sub.2]O)       --      1610 (s), 1590 (s)
           [Cl.sub.2]].sub.2]
3           [Cr[(BFH).sub.2]         --      1610 (s) 1590 (s)
            ([H.sub.2]O)Cl]
4        [VO[(BFH).sub.2](ThO)]      --        1600-1610 (s)

S.              Complex           IR [cm.sup.1] (s = sharp;
number                            b = broad; d = doublet;
                                  w = weak; vw = very weak)

                                      M-O, M-N, M-Cl (e)

1              BFH-L4 (b)                     --
2        [[Cr(BFH)([H.sub.2]O)    830, 570, 400 (s), 300 (vw)
           [Cl.sub.2]].sub.2]
3           [Cr[(BFH).sub.2]      840, 575, 395 (s), 300 (vw)
            ([H.sub.2]O)Cl]
4        [VO[(BFH).sub.2](ThO)]    970 (V=O), 810, 440, 350

(a) Hydrazone moiety; (b) No shift in symmetric and asymmetric
stretching frequencies of furfural ring oxygen at 1020 (s),
895 (s) [cm.sup.-1] and N-N at 1040 (w) indicates no involvement
in complex formation; (c) Absence of vN-H band suggests
enolization of the ligand which is confirmed by disappearance
of strong vC=O band; dShift indicates participation of -N of
azomethine group in coordination; eNakamoto [91,100] and Selbin 94].

TABLE 11: Characteristic IR data for the L5-BHDH (tetradentate -O, -O,
-N, and -O) and its participation in complex formation with metal
ions.

S.              Complex           IR [cm.sup.1] (s = sharp;
number                            b = broad; d = doublet; w = weak;
                                  vw = very weak)

                                   Coord water          vO-H

1             BHDH-L5 (c)              --         3350-3400 (b) (a)
2         [[Cr(BHDH)Cl].sub.2]         --            Absent (b)
3        [VO(BHDH)([H.sub.2]O)]   3500-3450 (b)      Absent (b)

S.              Complex           IR [cm.sup.1] (s = sharp;
number                            b = broad; d = doublet; w = weak;
                                  vw = very weak)

                                    vN-H       vC=O       vC=N

1             BHDH-L5 (c)         3280 (s)   1655 (s)   1600 (s)
2         [[Cr(BHDH)Cl].sub.2]    3280 (s)   1635 (s)   1580 (s)
3        [VO(BHDH)([H.sub.2]O)]   3280 (s)   1610 (s)   1575 (s)

S.              Complex           IR [cm.sup.1] (s = sharp;
number                            b = broad; d = doublet; w = weak;
                                  vw = very weak)

                                      vC-O         M-O, M-N, or M-Cl
                                    phenolic

1             BHDH-L5 (c)           1260 (s)              --
2         [[Cr(BHDH)Cl].sub.2]    1300-1310 (d)      550 (w), 435,
                                                     310, 295 (w)
3        [VO(BHDH)([H.sub.2]O)]     1270 (s)      970 (V=O), 820 (s),
                                                  520, 470, 440, 340

(a) Inter and intramolecular hydrogen bonding; (b) The breakage of
hydrogen bonding and the deprotonation of both the hydroxyl groups
(phenolic), that is, hydrazide -OH and pyrone -OH and their M-O
coordination; (c) No shift of lactone vC=O at 1710 (s) [cm.sup.-1];
and vC-O-C at 1010 (s) [cm.sup.-1] suggests noninvolvement in
complex formation; shift of hydrazide, phenolic vC-O and vC=N
indicate participation in complexation.

TABLE 12: Characteristic IR data for the ligand DHA (bidentate
-O, -O) and its participation in complex formation with metal
ions.

S.            Complex        IR [cm.sup.1] (s = sharp; b = broad;
number                       d = doublet; w = weak; vw = very weak)

                              Coord water        vO-H         vC=O
                                                            (lactone)

1           DHA-L6 (b)            --         3030 (s) (a)   1710 (s)
2        [Cr[(DHA).sub.3]]        --          Absent (c)    1740 (s)
3        [VO[(DHA).sub.2]    3500-3400 (b)    Absent (c)    1740 (s)
           ([H.sub.2]O)]

S.            Complex        IR [cm.sup.1] (s = sharp; b = broad;
number                       d = doublet; w = weak; vw = very weak)

                               vC=O       vC-O          M-O
                                        phenolic

1           DHA-L6 (b)       1655 (s)   1265 (s)         --
2        [Cr[(DHA).sub.3]]   1635 (s)   1280 (s)      480, 440
3        [VO[(DHA).sub.2]    1640 (s)   1290 (s)   910 (V=O) (d),
           ([H.sub.2]O)]                           850, 480, 440

(a) Intramolecular hydrogen bonded; (b) No shift in vC-O-C
indicates noninvolvement in complex formation, Mahesh and Gupta
[103]; (c) Cleavage of hydrogen bonding due to complexation,
(d) Selbin [94].

TABLE 13: Electronic spectra and magnetic moment data for
VO(II) complexes with L1-L6 ligands predicted molecular
formula, structure, and geometry.

S.       Molecular formula-electronic spectra
number   (b) bands, transitions (a), predicted
         structure (a rough M-L sketch given),
         and geometry (a)

1             [[VO(BHFH)Cl].sub.2]         28,006
          M-M complex with Cl bridges,     18,270
           V=O and two L1 with -O, -O,     13,330
               and -N coordination

2             [[VO(BHEH)Cl].sub.2]         25,000
          M-M complex with Cl bridges,     14,920
           V=O and two L2 with -O, -O,     13,000
               and -N coordination

3        [VO(HAEP)[([H.sub.2]O).sub.2]]    25,000
         Distorted Oh complex, V=O, two    22,200
          -O[H.sub.2], and L3 with -N,     13,560
             -O, and -S coordination
             on the equatorial plane                 2B2-2A1
                                                     2B2-2B1
                                                     2B2-2E
                                                     Correspond to
                                                     Oh symmetry
                                                     with tetragonal
                                                     distortion.

4         [VO[(BFH).sub.2]([H.sub.2]O)]    25,000-
           Distorted Oh complex, V=O,      22,200
          -O[H.sub.2], and two L4 with     16,100
               -N, -O coordination

5            [VO(BHDH)([H.sub.2]O)]        25,800
           Distorted Oh complex, V=O,      15,380
          -O[H.sub.2], and L5 with -N,     13,150
           -O, -O, and -O coordination
             on the equatorial plane

6            [VO(DHA)2([H.sub.2]O)]        30,000
           Distorted Oh complex, V=O,      25,500
          -O[H.sub.2], and two L6 with     18,180
             -O, -O coordination on
              the equatorial plane

S.       Molecular formula-electronic spectra
number   (b) bands, transitions (a), predicted
         structure (a rough M-L sketch given),
         and geometry (a)

1             [[VO(BHFH)Cl].sub.2]         [FORMULA NOT
          M-M complex with Cl bridges,     REPRODUCIBLE
           V=O and two L1 with -O, -O,     IN ASCII]
               and -N coordination

2             [[VO(BHEH)Cl].sub.2]         [FORMULA NOT
          M-M complex with Cl bridges,     REPRODUCIBLE
           V=O and two L2 with -O, -O,     IN ASCII]
               and -N coordination

3        [VO(HAEP)[([H.sub.2]O).sub.2]]    [FORMULA NOT
         Distorted Oh complex, V=O, two    REPRODUCIBLE
          -O[H.sub.2], and L3 with -N,     IN ASCII]
             -O, and -S coordination
             on the equatorial plane

4         [VO[(BFH).sub.2]([H.sub.2]O)]    [FORMULA NOT
           Distorted Oh complex, V=O,      REPRODUCIBLE
          -O[H.sub.2], and two L4 with     IN ASCII]
               -N, -O coordination

5            [VO(BHDH)([H.sub.2]O)]        [FORMULA NOT
           Distorted Oh complex, V=O,      REPRODUCIBLE
          -O[H.sub.2], and L5 with -N,     IN ASCII]
           -O, -O, and -O coordination
             on the equatorial plane

6            [VO(DHA)2([H.sub.2]O)]        [FORMULA NOT
           Distorted Oh complex, V=O,      REPRODUCIBLE
          -O[H.sub.2], and two L6 with     IN ASCII]
             -O, -O coordination on
              the equatorial plane

S.       Molecular formula-electronic      [[mu].sub.eff]
number   spectra (b) bands, transitions          BM
         (a), predicted structure (a
         rough M-L sketch given),
                and geometry (a)

1             [[VO(BHFH)Cl].sub.2]              1.54
          M-M complex with Cl bridges,          M-M
           V=O and two L1 with -O, -O,
               and -N coordination

2             [[VO(BHEH)Cl].sub.2]              1.63
          M-M complex with Cl bridges,          M-M
           V=O and two L2 with -O, -O,
               and -N coordination

3        [VO(HAEP)[([H.sub.2]O).sub.2]]         1.72
         Distorted Oh complex, V=O, two
          -O[H.sub.2], and L3 with -N,
             -O, and -S coordination
             on the equatorial plane

4         [VO[(BFH).sub.2]([H.sub.2]O)]
           Distorted Oh complex, V=O,           1.74
          -O[H.sub.2], and two L4 with
               -N, -O coordination

5            [VO(BHDH)([H.sub.2]O)]             1.71
           Distorted Oh complex, V=O,
          -O[H.sub.2], and L5 with -N,
           -O, -O, and -O coordination
             on the equatorial plane

6            [VO(DHA)2([H.sub.2]O)]             1.72
           Distorted Oh complex, V=O,
          -O[H.sub.2], and two L6 with
             -O, -O coordination on
              the equatorial plane

(a) Lever [73]; Rana et al. [104]; (b) Recorded for solid compounds
(mull-diffuse reflectance) at room temperature--Figures 1 and 2.

Table 14: Predicted molecular formula, structure and
geometry from electronic spectra and magnetic moment
data for Cr(III) complexes with L3-L6 ligands.

S.       Molecular formula-electronic
number   spectra (b) bands, transitions (a),
         predicted structure (a rough M-L
         sketch given), and geometry (a)

1              [[Cr(HAEP         27,930
             ([H.sub.2]O)        17,390
         Cl].sub.2] Distorted
          Oh complex with Cl
             bridges, two
         -O[H.sub.2], and two
          L3 with -O, -N, and
          -S coordination on
            the  equatorial
                 plane

2        [[Cr(BFH)([H.sub.2]O)   27,878
          [Cl.sub.2]].sub.2]     17,420
         Distorted Oh complex
         with Cl bridges, two
         -Cl, two -O[H.sub.2],
          and two L3 with -O,             4A2g-4T1g(F)
          -N coordination on               4A2g-4T2g
         the equatorial plane

3          [Cr[(BFH).sub.2]      26,670      Charge
            ([H.sub.2]O)Cl]      17,500     transfer
         Distorted Oh complex              transition
         with -O[H.sub.2], Cl,             4A2g-4T1g
          and two L3 with -O,                (P) is
          -N coordination on                obscured
         the equatorial plane                due to
                                          dark colour

                                           Octahedral
                                            symmetry
                                           high-spin
                                            complex

4        [[Cr(BHDH)Cl].sub.2]    28,980
         Distorted Oh complex
          with Cl bridges and    17,390
          two L5 with -O, -N,
              -O, and -O
            coordination on
         the equatorial plane

5          [Cr[(DHA).sub.3]]     26,670
         Distorted Oh complex    18,200
          with three L6 with
          -O, -O coordination

S.       Molecular             [[mu].sub.
number   formula-electronic     eff] BM
         spectra (b) bands,
         transitions (a),
         predicted structure
         (a rough M-L sketch
         given), and
         geometry (a)

1        [FORMULA NOT           3.49 M-M
         REPRODUCIBLE
         IN ASCII]

2        [FORMULA NOT           3.55 M-M
         REPRODUCIBLE
         IN ASCII]

3        [FORMULA NOT             3.88
         REPRODUCIBLE
         IN ASCII]

4        [FORMULA NOT           3.74 M-M
         REPRODUCIBLE
         IN ASCII]

5
         [FORMULA NOT             3.89
         REPRODUCIBLE
         IN ASCII]

(a) Lever [73]; (b) Recorded for solid compounds (mull-diffuse
reflectance) at room temperature--Figure 3.

Table 15: Predicted molecular formula, structure,
and geometry from electronic spectra and magnetic
moment data for Mn(II) complexes with L1-L2 ligands.

S.       Molecular formula-electronic spectra (b)
number   bands, transitions (a), predicted structure
         (a rough M-L sketch given), and geometry (a)

1              [[Mn(BHFH          27,030
         ([H.sub.2]O)Cl].sub.2]   21,270
          Distorted Oh complex    19,610
          with Cl bridges, two    18,180   6A1g-4Eg,
          -O[H.sub.2], and two             4A1g (G)
         L1 with -O, -O, and -N            6A1g x
          coordination on the              4T2g (G)
            equatorial plane               6A1g x
                                           T1g (G)

2        [Mn[(BHEH).sub.2[] Oh             Oh
          complex with two L2     26,670   high-spin
          with -O, -O, and -N     17,240   geometry
              coordination                 is
                                           predicted

S.       Molecular            [[mu].sub.eff]
number   formula-electronic         BM
         spectra (b)
         bands, transitions
         (a), predicted
         structure (a rough
         M-L sketch given),
         and geometry (a)

1        [FORMULA NOT            5.44 M-M
         REPRODUCIBLE
         IN ASCII]

2        [FORMULA NOT              5.92
         REPRODUCIBLE
         IN ASCII]

(a) Pappalardo [105]; (b) recorded for solid compounds
(mull-diffuse reflectance) at room temperature--Figure 4.

Table 16: Predicted molecular formula, structure,
and geometry from electronic spectra and magnetic
moment data for Fe(III) complexes
with L1-L3.

S.       Molecular formula-electronic
number   spectra (b) bands, transitions
         (a), predicted structure (a rough
         M-L sketch given), and geometry (a)

1        [[Fe(BHFH)Cl].sub.2] Distorted      23,260
           Oh complex with Cl bridges,       21,740
          two -Cl, and two L1 with -O,       19,040
           -O, and -N coordination on        17,540
              the equatorial plane

2           [[Fe(BHEH)(H2O)Cl].sub.2]        26,670
          Distorted Oh complex with Cl       22,220
          bridges, two -O[H.sub.2], and      18,520
           two L2 with -O, -O, and -N        17,390
               coordination on the           15,600
                equatorial plane

3                  [[Fe(HAEP)               Extremely
             ([H.sub.2]O)Cl].sub.2]           weak
            Distorted Oh complex with      transitions
           S bridges, two -O[H.sub.2],
            two -Cl, and two L3 with
              -O, -N, and -S (used
                  in bridging)
               coordination on the
                equatorial plane

S.       Molecular             [[mu].sub.eff]
number   formula-electronic          BM
         spectra (b) bands,
         transitions (a),
         predicted structure
         (a rough M-L sketch
         given), and
         geometry (a)

1        [FORMULA NOT             5.70 M-M
         REPRODUCIBLE
         IN ASCII]

2        [FORMULA NOT             5.73 M-M
         REPRODUCIBLE
         IN ASCII]

3        [FORMULA NOT             5.88 M-M
         REPRODUCIBLE
         IN ASCII]

(a) Oh geometry with metal-metal interactions;
(b) Recorded for solid compounds (mull-diffuse
reflectance) at room temperature--Figure 5.

Table 17: Predicted molecular formula, structure,
and geometry from electronic spectra and magnetic
moment data for Co(II) complexes with L1-L3 ligands.

S.       Molecular formula-electronic
number   spectra (b) bands, transitions (a),
         predicted structure (a rough M-L
         sketch given), and geometry (a)

1            [[Co(BHFH)        31,250
            ([H.sub.2]O)       20,000
             Cl].sub.2]        18,520
            Distorted Oh       15,400
           complex with Cl
            bridges, two
          -O[H.sub.2], and
           two L1 with -O,
             -O, and -N
           coordination on
           the equatorial
                plane

2        [Co[(BHEH).sub.2]]    19,750   4T1g (F)-4T1g (P)
           Oh complex with     18,450   4T1g (F)-4T2g (F)
         two L2 with -O, -O,   15,700   broad bands
         and -N coordination   8,430    Multiple bands in
          on the equatorial             admixture with
                plane                   spin-forbidden
                                        transition to
                                        doublet state

3            [[Co(HAEP)        27,030
             [([H.sub.2]       17,700
          O).sub.2]].sub.2]    15,630
            Distorted Oh       8,330
           complex with S
            bridges, two
          -O[H.sub.2], two
           -Cl, and two L3
            with -O, -N,
           and-S (used in
              bridging)
           coordination on
           the equatorial
                plane

S.       Molecular             [[mu].sub.
number   formula-electronic     eff] BM
         spectra (b) bands,
         transitions (a),
         predicted structure
         (a rough M-L sketch
         given), and
         geometry (a)

1        [FORMULA NOT           4.58 M-M
         REPRODUCIBLE
         IN ASCII]

2        [FORMULA NOT             3.92
         REPRODUCIBLE
         IN ASCII]

3        [FORMULA NOT           4.53 M-M
         REPRODUCIBLE
         IN ASCII]

(a) Lever [73]; the asymmetric visible band is typical of
Oh Co(II) complexes and the shoulder on the high energy
side being assigned to spin-forbidden transitions, Drago
[74]; (b) Recorded for solid compounds (mull-diffuse
reflectance) at room temperature--Figure 6.

TABLE 18: Predicted molecular formula, structure, and geometry
from electronic spectra and magnetic moment data for Ni(II)
complexes with L1-L3 ligands.

S.       Molecular formula-electronic spectra (b)
number   bands, transitions (a), predicted structure
         (a rough M-L sketch given), and geometry (a)

1        [Ni(BHFH)[H.sub.2]O]     26,130
            Square-planar         18,100
            complex with -
          O[H.sub.2] and L1
         with -O, -O, and -N
         coordination on the
           equatorial plane

2         [Ni[(BHFH).sub.2]]      26,300
          Regular Oh complex      15,000
          with two L1 with -    9,520 (w)
            O, -O, and -N
             coordination

3         [Ni[(BHEH).sub.2]]    26,670 (s)
          Regular Oh complex      20,000
          with two L1 with -      13,100
            O, -O, and -N       8,200 (w)
             coordination

4         [Ni[(HAEP).sub.2]]      27,030
          Distorted square-       16,600
         planar complex with
         S bridges and two L3
           with -O, -N, -S
          (used in bridging)
         coordination on the
           equatorial plane

S.       Molecular formula-electronic spectra        [[mu].sub.eff]
number   (b) bands, transitions (a),                       BM
         predicted structure (a rough M-L
         sketch given), and geometry (a)

1        Charge-transfer band d-pi*   [FORMULA NOT        Dia
                 transition           REPRODUCIBLE
                1A1g x 1A2g            IN ASCII]
           Square-planar geometry

2               3A2g-3T1g(P)          [FORMULA NOT        3.24
                3A2g-3T1g(G)          REPRODUCIBLE
                 3A2g-3T2g             IN ASCII]
            Regular Oh geometry
           Strong charge-transfer

3          band-d-pi* transition      [FORMULA NOT        2.91
                3A2g-3T1g(P)          REPRODUCIBLE
            3A2g-2T1g, 3T1g (F)        IN ASCII]
                 3A2g-3T2g
            Regular Oh geometry

4        Charge-transfer band d-pi*   [FORMULA NOT      Dia M-M
                 transition           REPRODUCIBLE
                 1A1g-1A2g             IN ASCII]
         Diamagnetic tetragonal or
         square planar complex with
           high intensity band in
          14000-18000 [cm.sup.-1]

(a) Holm et al. [77]; Shaw and Dudek [106]; Drago [74]; (b)
Recorded for solid compounds (mull-diffuse reflectance) at
room temperature--Figure 7.

TABLE 19: Predicted molecular formula, structure, and
geometry from electronic and magnetic moment data for
Cu(II) complexes with L1-L3 ligands.

S. number   Molecular formula-electronic spectra
            (b) bands, transitions (a),
            predicted structure (a rough M-L
            sketch given), and geometry (a)

1            [[Cu(BHFH)].sub.2]     28,570 (sm)
                 Distorted          14,300 (b)
               square-planar
              complex with M-M
             complex with -O of
             L1 bridges and L1
            with the rest of -O,
              -N coordination

2           [Cu(BHFH)[H.sub.2]O]
                 Distorted
               square-planar
                complex with
             -O[H.sub.2] and L1     27,030 (s)
            with -O, -O, and -N     18,180 (b)
                coordination

3               [Cu(BHEH)Cl]       26,650 17,540
                 Distorted
               square-planar
            complex with -Cl and
            L1 with -O, -O, and
              -N coordination

4            [[Cu(HAEP)].sub.2]       25,640
                 Distorted            15,380
               square-planar          13,330
               complex with S
             bridges and two L3
            with -O, -N, and -S
             (used in bridging)
            coordination on the
              equatorial plane

S. number   Molecular formula-electronic        [[mu].sub.eff]
            spectra (b) bands, transitions            BM
            (a), predicted structure (a
            rough M-L sketch given),
            and geometry (a)

1           Strong              [FORMULA NOT       1.50 M-M
            charge-transfer     REPRODUCIBLE
            band d-pi*            IN ASCII]
            transition
            2B2g-Eg
            2B2g-2A1g
            2B2g-2B1g
            Normally Cu(II)
            show broad bands
2           around              [FORMULA NOT         2.04
            16670-1110          REPRODUCIBLE
            [cm.sup.-1].          IN ASCII]
            The observed
            spectra resemble
            Cu(II)-SB
            complexes whose
            geometry is
3           considered square   [FORMULA NOT         1.91
            planar              REPRODUCIBLE
                                  IN ASCII]

4                               [FORMULA NOT       1.40 M-M
                                REPRODUCIBLE
                                  IN ASCII]

(a) Lever [73]; Sutton [107]; Satyanarayana and Mohapathra
[108]; Sacconi and Ciampolini [109]; Muzundar and Bhattacharya
[110]; Sheela [111]; (b) Recorded for solid compounds (mull-
diffuse reflectance) at room temperature--Figure 8.

TABLE 20: Evaluation of fungicidal property of Schiff bases and metal
complexes in vitro.

S.                      Chemical                   Rhizoctonia solani
number                   complex                   (PDA medium),
                                                   average %
                                                   inhibition of growth
                                                   after 72hrs;
                                                   poisoned food
                                                   technique
                                                   concentration in ppm

                                                   1000    500    250

1                         BLANK                     -       -      -
2                     DITHANE-M-45                 100     100    80
3                        L1-BHFH                    30    16.66    -
4                  [[Cu(BHFH)].sub.2]               -      --     --
5           [[Co(BHFH)([H.sub.2]O)Cl].sub.2]        -      --     --
6                  [[Ni(BHFH)].sub.2]              45.5    15      -
7             [[Fe(BHFH)[Cl.sub.2]].sub.2]         62.2   34.4    10
8           [[Mn(BHFH)([H.sub.2]O)Cl].sub.2]       95.2   67.2    40
9                 [[VO(BHFH)Cl].sub.2]             100    69.66   50
10                       L2-BHEH                    20     6.6     -
11                    [Cu(BHEH)Cl]                  25    21.1    10
12                 [Co[(BHEH).sub.2]]               -      --     --
13                 [Ni[(BHEH).sub.2]]               27     --     --
14          [[Fe(BHEH)([H.sub.2]O)Cl)].sub.2]       35     20      -
15                 [Mn[(BHEH).sub.2]]               82     50     50
16                [[VO(BHEH)Cl].sub.2]             100     45     40
17                       L3-HAEP                    50     20      -
18                 [[Cu(HAEP)].sub.2]               -      --     --
19       [[Co(HAEP)[([H.sub.2]O).sub.2]].sub.2]     -      --     --
20                 [Ni[(HAEP).sub.2]]               -      --     --
21          [[Fe(HAEP)([H.sub.2]O)Cl].sub.2]        -      --     --
22          [[Cr(HAEP)([H.sub.2]O)Cl].sub.2]        -      --     --
23           [VO(HAEP)[([H.sub.2]O).sub.2]]         -      --     --
24                       L4-BFH                     32     20      -
25                [[Cr(BFH)([H.sub.2]O)             -      --     --
                   [Cl.sub.2]].sub.2]
26                    [VO(BFHMThO)]                 98    69.66   50
27                [[Cr(BHDH)Cl].sub.2]             15.5   5.12     5
28               [VO(BHDH)([H.sub.2]O)]            32.2    15      -
29                  [Cr[(DHA).sub.3]]              28.5    --     --
30            [VO[(DHA).sub.2]([H.sub.2]O)]         50     30     15

S.       Acrocylindrium oryzae   Xanthomonas oryzae
number   (PA liquid) average %   (Hayward's medium)
         inhibition ofgrowth     average % inhibition
         after 48 hrs; liquid    of growth after 8
         broth method            days; inhibition zone
         concentration in ppm    technique
                                 concentration in ppm

         1000   500   250        1000   500   250

1        246    245   246         -      -     -
2        nil    200   240         55    50    48
3        nil    nil    2          12    --    --
4        190    200   240         5     --    --
5        170    150   240         8     --    --
6         5     28    130        11.2   --    --
7         55    100   220        22.3   --    --
8         25    76    130         23    --    --
9        nil    nil   12          20    --    --
10       nil    nil    2          3     --    --
11       150    200   245         8     --    --
12       175    190   225        16.7   --    --
13       nil    nil   nil         30    --    --
14       100    155   200         15    --    --
15        96    100   150         19    --    --
16       nil    nil   50          20    --    --
17        5      5     5          10    --    --
18       245    --    --          --    --    --
19       240    --    --          --    --    --
20       185    --    --          --    --    --
21       200    --    --          --    --    --
22       242    --    --          --    --    --
23       245    --    --          2     --    --
24        70    100   240         20    --    --
25       150    200   240         22    --    --

26       125    150   200         25    --    --
27       190    --    --          15    --    --
28       150    198   240         20    --    --
29       200    240   245         15    --    --
30       170    200   238         18    --    --

- indicates negative effect; -- indicates that the
compound is not screened.
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Title Annotation:Research Article
Author:Mangamamba, T.; Ganorkar, M.C.; Swarnabala, G.
Publication:International Journal of Inorganic Chemistry
Article Type:Report
Date:Jan 1, 2014
Words:14799
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