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Synthesis, Characterization, Spectral and Antimicrobial Studies of Some Trivalent Ln(III) Metal Complexes with Ligands Containing ‘N’ and ‘O’ Donor Atoms
Corresponding Author(s) : Rajesh Kumar Mishra
Asian Journal of Chemistry,
Vol. 27 No. 3 (2015): Vol 27 Issue 3
Abstract
Ten new coloured solid complexes of type [ML2X2], Where M=La(III), Pr(III), Nd(III), Sm(III) & Dy(III), ‘L’ = Ligand i.e., N-(3-methyl-thiocarbamyl-5-oxo-2-pyrazolin-4-ylene-N'-(4'-antipyrine)hydrazine (HATP) and N-(3-methyl-1-thiocarbamyl-5-oxo-2-pyrazolin-4-ylene)-N'-(4'-benzothiazole)hydrazine (HBTP) and ‘X’=H2O have been synthesized and characterized by their elemental analysis, molar conductance values, magnetic susceptibilities, UV, IR and NMR spectral studies. Elemental analysis confirms 1:2 stoichiometry of the synthesized complexes. Spectral studies confirms that the ligand ‘HATP’ and ‘HBTP’ acts as tetradentate and tridentate, respectively and coordinates to central metal ion by ‘N’ and ‘O’ donor atoms. Complexes are ten and eight coordinated. Further the ligands and synthesized complexes have been screened for their antibacterial activity against some Gram-positive and Gram-negative bacteria.
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- K. Dey, S.B. Roy, P.K. Bhattacharya and K.K. Gangopadhyay, J. Indian Chem. Soc., 62, 809 (1985).
- R.C. Sharma and V.K. Varshney, J. Inorg. Biochem., 41, 299 (1991); doi:10.1016/0162-0134(91)80023-B.
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- K. Chetan Modi and B.T. Thaker, Asian J. Chem., 17, 581 (2005).
- S. Prasad, R.K. Agarwal and A. Kumar, J. Iran. Chem. Soc., 8, 825 (2011); doi:10.1007/BF03245913.
- R.K. Agarwal, B. Bhushan and G. Singh, J. Inst. Chemist (India), 65, 131 (1993).
- R.K. Agarwal, R.K. Sarin and H. Agarwal, Bull. Chem. Soc. Ethiop. 9, 23,(1995).
- R.K. Agarwal, H. Agarwal and I. Chakraborti, Synth. React. Inorg. Met. Org. Chem., 25, 679 (1995); doi:10.1080/15533179508218256.
- G. Rajendran and K.G. Usha Devi, Asian J. Chem., 16, 1529 (2004).
- G. Rajendran and K.G. Usha Devi, Asian J. Chem., 19, 223 (2007).
- A.A. Khan and N.K. Sharma, Asian J. Chem., 20, 4969 (2008).
- L. Singh, A. Sharma and S.K. Sindhu, Asian J. Chem., 11, 1445 (1999).
- B.G. Thakur, R.K. Jha and R.K. Chaudhary, Asian J. Chem., 19, 4948 (2007).
- A. Arslantas, M. Isiklar and H. Yuksek, Asian J. Chem., 23, 2701 (2011).
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- A. Kumar, A. Rai and M. Gupta, Asian J. Chem., 23, 2735 (2011).
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- G.D. Christian, Analytical Chemistry, Wiley, India, edn 6 (2007).
- M. Alaudeen and C.P. Prabhakar, Indian J. Chem., 35A, 510 (1996).
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References
K. Dey, S.B. Roy, P.K. Bhattacharya and K.K. Gangopadhyay, J. Indian Chem. Soc., 62, 809 (1985).
R.C. Sharma and V.K. Varshney, J. Inorg. Biochem., 41, 299 (1991); doi:10.1016/0162-0134(91)80023-B.
S. Manap, Master of Sciences Thesis, Kafkas Üniversitesi Fen Bilimleri Enstitúsú, Kars, Turkey (2009).
M. Thankaranjan and K. Nair, J. Coord. Chem., 53, 1156 (1976).
K. Kobayashi, K. Kurihara and K. Hirose, Bull. Chem. Soc. Jpn., 45, 3551 (1972); doi:10.1246/bcsj.45.3551.
D.K. Rastogi, S.K. Sahni, V.B. Rana and S.K. Dua, J. Coord. Chem., 8, 97 (1978); doi:10.1080/00958977808073078.
K. Chetan Modi and B.T. Thaker, Asian J. Chem., 17, 581 (2005).
S. Prasad, R.K. Agarwal and A. Kumar, J. Iran. Chem. Soc., 8, 825 (2011); doi:10.1007/BF03245913.
R.K. Agarwal, B. Bhushan and G. Singh, J. Inst. Chemist (India), 65, 131 (1993).
R.K. Agarwal, R.K. Sarin and H. Agarwal, Bull. Chem. Soc. Ethiop. 9, 23,(1995).
R.K. Agarwal, H. Agarwal and I. Chakraborti, Synth. React. Inorg. Met. Org. Chem., 25, 679 (1995); doi:10.1080/15533179508218256.
G. Rajendran and K.G. Usha Devi, Asian J. Chem., 16, 1529 (2004).
G. Rajendran and K.G. Usha Devi, Asian J. Chem., 19, 223 (2007).
A.A. Khan and N.K. Sharma, Asian J. Chem., 20, 4969 (2008).
L. Singh, A. Sharma and S.K. Sindhu, Asian J. Chem., 11, 1445 (1999).
B.G. Thakur, R.K. Jha and R.K. Chaudhary, Asian J. Chem., 19, 4948 (2007).
A. Arslantas, M. Isiklar and H. Yuksek, Asian J. Chem., 23, 2701 (2011).
A. Arslantas, M. Isiklar and H. Yuksek, Asian J. Chem., 23, 2729 (2011).
A. Kumar, A. Rai and M. Gupta, Asian J. Chem., 23, 2735 (2011).
J.P. Naskar, B. Guhathakurta, L. Lu, M. Zhu and R. Bhattacharya, J. Indian Chem. Soc., 90, 1301 (2013).
R. Harode and T.C. Sharma, J. Indian Chem. Soc., 66, 282 (1989).
A.I. Vogel, A Textbook of Quantitative Inorganic Analysis, Longman Group, London, edn. 5 (1989).
C.H. Collins and P.M. Lyne, Microbiological Methods, Butterworths, London (1970)..
R.C. Maurya and R. Verma, J. Indian Chem. Soc., 75, 29 (1998).
M. Alaudeen and P.K. Radhakrishnan, Synth. React. Inorg. Met. Org. Chem., 20, 673 (1990); doi:10.1080/00945719008048164.
K. Dey and D. Bandopadhyay, Indian J. Chem., 31A, 32 (1992).
Y. Thakur and J. Thakur, J. Proc. Nat. Acad. Sci. India, 47, 11 (1977).
Y. Thakur and B.N. Jha, J. Inorg. Nucl. Chem., 42, 449 (1980); doi:10.1016/0022-1902(80)80022-4
A. Mitchell and D.C. Nonhebel, Tetrahedron, 35, 2013 (1979); doi:10.1016/S0040-4020(01)88971-7.
H.C. Yao, J. Org. Chem., 29, 2959 (2004); doi:10.1021/jo01033a037.
A. Rahman and K.M. Kandeel, Indian J. Chem., 20A, 819 (1991).
G.D. Christian, Analytical Chemistry, Wiley, India, edn 6 (2007).
M. Alaudeen and C.P. Prabhakar, Indian J. Chem., 35A, 510 (1996).
R.K. Agarwal and H. Agarwal, Synth. React. Inorg. Met.-Org. Chem., 31, 263 (2001); doi:10.1081/SIM-100002046.
R.K. Agarwal and S.K. Gupta, Thermochim. Acta, 95, 99 (1985); doi:10.1016/0040-6031(85)80036-8.
J.P. Phillips and L.L. Merritt, J. Am. Chem. Soc., 71, 3984 (1949); doi:10.1021/ja01180a030.
S.N. Bhave, J.P. Bahad, P.M. Sonaparote and A.S. Aswar, J. Indian Chem. Soc., 79, 342 (2002).