全部 标题 作者
关键词 摘要

OALib Journal期刊
ISSN: 2333-9721
费用:99美元

查看量下载量

相关文章

更多...

Comparative Studies of New Complexes Synthesized by Chemical and Tribochemical Reactions Derived from Malonic Acid Dihydrazide (L; MAD) with Cu2+ and Co2+ Salts

DOI: 10.4236/ojic.2018.81003, PP. 28-42

Keywords: Tribochemical Reactions, MAD Complexes, Spectral and Magnetic Studies, Cu2+ and Co2+ Complexes, Green Chemistry

Full-Text   Cite this paper   Add to My Lib

Abstract:

The reaction of L (MAD) with Cu2+ and Co2+ chlorides affords new metal complexes. The isolated solid complexes were synthesized by two different techniques i.e., chemical and tribochemical methods. Four new complexes were synthesized by direct chemical reactions of MCl2 (M = Co2+ and Cu2+) with MAD in absolute EtOH. The isolated solid complexes were used as starting compounds to synthesize another four new complexes using tribochemical technique by grinding the previous complexes in the solid state with excess KI in agate mortar. The results of the isolated complexes indicate the substitution of the chloride by iodide ions during grinding and extraction of the complexes by a mixture of solvents (EtOH + MeOH). Also, the results suggest that no reduction of Cu2+ or oxidation of Co2+ complexes is observed. The IR spectra of the complexes suggest that L acts in a bidentate manner. Moreover, the results of electronic spectra and magnetic measurements for the chloride and iodide complexes suggest distorted-octahedral and/or tetrahedral for Cu2+ and high-spin octahedral and/or tetrahedral structures around the Co2+ ion, respectively.

References

[1]  Prakash, G., Vinod, K.C.H. and Sangamesh, A.P. (2009) Synthesis, Spectral Characterization, in-Vitrmicrobiological Evaluation and Cytotoxic Activities of Novel Macrocyclicbis-Hydrazone. Medicinal Chemistry, 2, 1-8.
[2]  Kriza, A., Ababel, L.V. and Cioatera, N. (2010) Synthesis and Structural Studies of Complexes of Cu, Co, Ni and Zn with Isonicotinic Acid Hydrazide and Isonicotinic Acid (1-NaphthylMethylene) Hydrazide. Journal of the Serbian Chemical Society, 75, 229-242.
https://doi.org/10.2298/JSC1002229K
[3]  Sondhi, S. Dinodia, M. and Kumar, A. (2006) Synthesis, Anti-Inflammatory and Analgesic Activity Evaluation of some Amidine and Hydrazone Derivatives. Bioorganic & Medicinal Chemistry, 14, 4657-4663.
https://doi.org/10.1016/j.bmc.2006.02.014
[4]  Bredihhin, A., Groth, U.M. and Mäeorg, U. (2007) Formation and Use of a Nitrogen Dianion for Selective Hydrazine Alkylation Provides a Fast and Easy Access to Substituted Hydrazines, Which Are Widely Used As Drugs, Pesticides, and Precursors for a Variety of Compounds in Organic Synthesis. Organic Letters, 9, 1097-1099.
https://doi.org/10.1021/ol070026w
[5]  Tsubrik, O., Sillard, R. and Mäeorg, U. (2006) Excellent Regioselectivity Is Observed in the Addition of Diverse Organometallic Nucleophiles to Unsymmetrical AzoCompounds. Primary/Secondary/Tertiary Alkyl, Aryl and Heteroaryl Substituents Were Introduced This Way in High Yields. Synthesis, 5, 843-846.
[6]  Bredihhin, A. and Mäeorg, U. (2007) Alkylation of Hydrazine Using a Polyanion Strategy Provides a Fast and Convenient Access to Multialkylated Hydrazine Derivatives. Scope and Limitations of the New Method Are Also Investigated. Organic Letters, 9, 4975-4977.
https://doi.org/10.1021/ol702234s
[7]  Kucukguzel, S.G., Mazi, A., Sahin, F., Ozturk, S. and Stables, J. (2003) Synthesis and Biological Activities of Diflunisal Hydrazide-Hydrazones. European Journal of Medicinal Chemistry, 38, 1005-1013.
https://doi.org/10.1016/j.ejmech.2003.08.004
[8]  Narang, R., Narasimhan, B. and Sharma, S. (2012) A Review on Biological Activities and Chemical Synthesis of Hydrazide Derivatives. Current Medicinal Chemistry, 19, 569-612.
https://doi.org/10.2174/092986712798918789
[9]  Susan, M.A., Marc, O., David, P. and Ann, M. (2003) Mechanism of Horseradish Peroxidase Inactivation by Benzhydrazide: A Critical Evaluation of Arylhydrazidesas Peroxidase Inhibitors. Biochemical Journal, 375, 613-621.
https://doi.org/10.1042/bj20021936
[10]  Bredihhin, A., Groth, U.M. and Mäeorg, U. (2007) Formation and Use of a Nitrogen Dianion for Selective Hydrazine Alkylation Provides a Fast and Easy Access to Substituted Hydrazines, Which Are Widely Used as Drugs, Pesticides and Precursors for a Variety of Compounds in Organic Synthesis. Organic Letters, 9, 1097-1099.
https://doi.org/10.1021/ol070026w
[11]  Bredihhin, A. and Mäeorg, U. (2007) Alkylation of Hydrazine using a PolyanionStrategy Provides a Fast and Convenient Access to Multialkylated Hydrazine Derivatives. Scope and Limitations of the New Method Are Also Investigated. Organic Letters, 9, 4975-4977.
https://doi.org/10.1021/ol702234s
[12]  Singh, P., Goel, R.L. and Singh, B.P. (1975) Synthesis, Characterization and Biological Activity of Schiff Bases. Journal of the Indian Chemical Society, 52, 958-959.
[13]  Mahindra, A.M. and Fisher, J.M. (1983) Rabinovitz. Bathocuproine Sulphonate: A Tissue Culture-Compatible Indicator of Copper-Mediated Toxicity. Nature (London), 303, 64-69.
https://doi.org/10.1038/303064a0
[14]  Berkessel, A., Bolte, M.T. and Nemann, L.S. (1996) Synthesis and X-Ray Crystal Structure of the First Mononuclear Nickel(II) Alkane Thiolate Complex with a Mixed (S,N,N,O) Ligand Field. Chemische Berichte, 129, 1183-1189.
https://doi.org/10.1002/cber.19961291007
[15]  Kolodziej, A.F. (1994) The Chemistry of Nickel-Containing Enzymes. Progress in Inorganic Chemistry, 41, 493-495.
[16]  Aggarwal, R.C. and Singh, B. (1976) Synthesis and Structural Studies of Simple and Mixed Acid Dihydrazide Complexes of Oxovanadium (IV). Transition Metal Chemistry, 1, 161-166.
[17]  Ahmed, A.D., Mandal, P.K. and Chaaudhuri, N.R. (1966) Metal Complexes of Malonic Dihydrazide. Journal of Inorganic and Nuclear Chemistry, 28, 2951-2959.
https://doi.org/10.1016/0022-1902(66)80022-2
[18]  Vogel, A.I. (1961) A Text Book of Quantitative Inorganic Chemistry. Longmans, London.
[19]  Lewis, L. and Wilkins, R.G. (1960) Modern Coordination Chemistry. Interscience, New York.
[20]  Geary, W.J. (1971) The Use of Conductivity Measurements in Organic Solvents for the Characterisation of Coordination Compounds. Coordination Chemistry Reviews, 7, 81-122.
https://doi.org/10.1016/S0010-8545(00)80009-0
[21]  Al-Ashqar, S.M. and Mostafa, M.M. (2008) Synthesis of Some Novel CoII and CoIII Complexes by Tribochemical Reactions using KI with Some Derivatives of Thiosemicarbazide Complexes Derived from Girard’s T and P. Spectrochimica Acta, 71, 1321-1326.
https://doi.org/10.1016/j.saa.2008.04.003
[22]  Burger, K., Ruff, I. and Ruff, F. (1965) Some Theoretical and Practical Problems in the Use of Organic Reagents in Chemical Analysis-IV Infrared and Ultraviolet Spectrophotometric Study of the Dimethylglyoxime Complexes of the Transition Metals. Journal of Inorganic and Nuclear Chemistry, 27, 179-190.
https://doi.org/10.1016/0022-1902(65)80208-1
[23]  Lever, A.B.P. (1984) Inorganic Electronic Spectroscopy. Elsevier, Amsterdam.

Full-Text

Contact Us

[email protected]

QQ:3279437679

WhatsApp +8615387084133