How to cite this paper
Kale, A., Kohire, R., Sadawarte, G., Phase, R & Jagrut, V. (2024). Efficient synthesis and characterization of new ligand and their transition metal complexes derived from 4-methyl-1,2,3-thiadiazoles-5-carboxylic acid hydrazide.Current Chemistry Letters, 13(3), 531-540.
Refrences
[1] Gomathi, V., & Selvameena, R. (2013) Synthesis, characterisation and biological studies of complexes of 3D transition metals and with Schiff base derived from sulfadiazine and 2-acetylnaphthalene. Int. J. Recent Sci. Res, 4 (1), 94-27.
[2] Shivakumar, K., Shashidhar, Vithal Reddy, P., & Halli, M. B. (2008) Synthesis, spectral characterization and biological activity of benzofuran Schiff bases with Co (II), Ni (II), Cu (II), Zn (II), Cd (II) and Hg (II) complexes. Journal of Coordination Chemistry, 61 (14), 2274-2287.
[3] Hunashal, R. D., & Satyanarayana, D. (2012) One pot synthesis of 3-(substituted phenoxymethyl)-6-phenyl/substituted phenoxymethyl-1, 2, 4-triazolo [3, 4-b][1, 3, 4] thiadiazole derivatives as antimicrobial agents. Int. J. Pharm. Biol. Sci, 3, 183-192.
[4] Tarafder, M. T. H., Ali, M. A., Wee, D. J., Azahari, K., Silong, S., & Crouse, K. A. (2000) Complexes of a tridentate ONS Schiff base. Synthesis and biological properties. Transition Metal Chemistry, 25, 456-460.
[5] Chohan, Z. H., & Sherazi, S. K. (1999) Synthesis and characterisation of some Co (II), Cu (II) and Ni (II) complexes with nicotinoylhydrazine derivatives and the biological role of metals and anions (SO4 2-, NO3−, CzO4 2-and CH3CO− 2) on the antibacterial properties. Synthesis and reactivity in inorganic and metal-organic chemistry, 29 (1), 105-118. https://doi.org/10.1080/009457199093 49437
[6] Jayabalakrishnan, C., & Natarajan, K. (2001) Synthesis, characterization, and biological activities of ruthenium (II) carbonyl complexes containing bifunctional tridentate Schiff bases. Synthesis and Reactivity in Inorganic and Metal-Organic Chemistry, 31 (6), 983-995. https://doi.org/10.1081/ SIM-100105255.
[7] Jeewoth, T., Li Kam Wah, H., Bhowon, M. G., Ghoorohoo, D., & Babooram, K. (2000) Synthesis and anti-bacterial/catalytic properties of Schiff bases and Schiff base metal complexes derived from 2, 3-diaminopyridine. Sythesis and Reactivity in Inorganic and Matel-Organic Chemistry, 30 (6), 1023-1038. https://doi.org/10.1080/ 00945710009351817.
[8] Dharmaraj, N., Viswanathamurthi, P., & Natarajan, K. (2001) Ruthenium (II) complexes containing bidentate Schiff bases and their antifungal activity. Transition Metal Chemistry, 26, 105-109. https://doi.org/10.1023/A:1007132408648
[9] Colins, C.H., Lyne, P.M., (2004) Microhiul Methods, Arnold, a member of the Hodder Headline Group, Microbiological methods, 338.
[10] Naskar, S., Naskar, S., Butcher, R. J., & Chattopadhyay, S. K. (2010) Synthesis, X-ray crystal structures and spectroscopic properties of two Ni (II) complexes of pyridoxal Schiff’s bases with diamines: Importance of steric factor in stabilization of water helices in the lattices of metal complex. Inorganica Chimica Acta, 363 (2), 404-411. https://doi.org/10.1016/j.ica.2009.11.007
[11] Scozzafava, A., Menabuoni, L., Mincione, F., Mincione, G., & Supuran, C. T. (2001) Carbonic anhydrase inhibitors: synthesis of sulfonamides incorporating dtpa tails and of their zinc complexes with powerful topical antiglaucoma properties. Bioorganic & medicinal chemistry letters, 11 (4), 575-582. https://doi.org/10.1016/S0960-894X (00)00722-8
[12] Scozzafava, A., & Supuran, C. T. (2000). Carbonic anhydrase and matrix metalloproteinase inhibitors: sulfonylated amino acid hydroxamates with MMP inhibitory properties act as efficient inhibitors of CA isozymes I, II, and IV, and N-hydroxysulfonamides inhibit both these zinc enzymes. Journal of medicinal Chemistry, 43 (20), 3677-3687. https:// doi.org/10.1021/ jm000027t
[13] Abdel-Rahman, L. H., Abu-Dief, A. M., El-Khatib, R. M., & Abdel-Fatah, S. M. (2016) Some new nano-sized Fe (II), Cd (II) and Zn (II) Schiff base complexes as precursor for metal oxides: Sonochemical synthesis, characterization, DNA interaction, in vitro antimicrobial and anticancer activities. Bioorganic chemistry, 69, 140-152. https://doi.org/10.1016 /j.bioorg.2016.10.009
[14] Chaudhary, A., Bansal, N., Gajraj, A., & Singh, R. V. (2003) Antifertility, antibacterial, antifungal and percent disease incidence aspects of macrocyclic complexes of manganese (II). Journal of inorganic biochemistry, 96 (2-3), 393-400. https://doi.org/10.1016/S0162-0134(03)00157-0
[15] Sivasankaran Nair, M., Suda Kumari, S., & Neelakantan, M. A. (2007) Studies on some novel Schiff-base complexes in solution and solid state. Journal of Coordination Chemistry, 60 (12), 1291-1302. https:// Doi 10.1080/00958970601053776
[16] Romero-Canelon, I., & Sadler, P. J. (2013) Next-generation metal anticancer complexes: multitargeting via redox modulation. Inorganic chemistry, 52 (21), 12276-12291. https://doi.org /10.1021/ic400835n
[17] Zhan, P., Liu, X., Li, Z., Fang, Z., Li, Z., Wang, D. & De Clercq, E. (2009) Novel 1, 2, 3-thiadiazole derivatives as HIV-1 NNRTIs with improved potency: synthesis and preliminary SAR studies. Bioorganic & medicinal chemistry, 17 (16), 5920-5927. https://doi.org/10.1016/j.bmc.2009.07.004
[18] Tripathy, R., Ghose, A., Singh, J., Bacon, E. R., Angeles, T. S., Yang, S. X. & Mallamo, J. P. (2007). 1, 2, 3-Thiadiazole substituted pyrazolones as potent KDR/VEGFR-2 kinase inhibitors. Bioorganic & medicinal chemistry letters, 17 (6), 1793-1798. https://doi.org/10.1016/j.bmcl.2006.12.054
[19] Zuo, X., Mi, N., Fan, Z., Zheng, Q., Zhang, H., Wang, H., & Yang, Z. (2010) Synthesis of 4-methyl-1, 2, 3-thiadiazole derivatives via Ugi reaction and their biological activities. Journal of agricultural and food chemistry, 58 (5), 2755-2762. https://doi.org/10.1021/jf902863z
[20] Wang, S. X., Fang, Z., Fan, Z. J., Wang, D., Li, Y. D., Ji, X. T., & Morzherin, Y. Y. (2013). Synthesis of tetrazole containing 1, 2, 3-thiadiazole derivatives via U-4CR and their anti-TMV activity. Chinese Chemical Letters, 24(10), 889-892. https://doi.org/10.1016/j.cclet.2013.05.026
[21] Dong, W. L., Liu, Z. X., Liu, X. H., Li, Z. M., & Zhao, W. G. (2010) Synthesis and antiviral activity of new acrylamide derivatives containing 1, 2, 3-thiadiazole as inhibitors of hepatitis B virus replication. European journal of medicinal chemistry, 45 (5), 1919-1926. https://doi.org/10.1016/j.ejmech.2010.01.032
[22] Zhang, J. P., Qin, Y. G., Dong, Y. W., Song, D. L., Duan, H. X., & Yang, X. L. (2017) Synthesis and biological activities of (E)-β-farnesene analogues containing 1, 2, 3-thiadiazole. Chinese Chemical Letters, 28 (2), 372-376. https://doi.org/10.1016/j.cclet.2016.10.030
[23] Fan, Z., Shi, Z., Zhang, H., Liu, X., Bao, L., Ma, L., & Mi, N. (2009) Synthesis and biological activity evaluation of 1, 2, 3-thiadiazole derivatives as potential elicitors with highly systemic acquired resistance. Journal of agricultural and food chemistry, 57 (10), 4279-4286. https://doi.org/10.1021/jf8031364
[24] Li, Y. D., Mao, W. T., Fan, Z. J., Li, J. J., Fang, Z., Ji, X. T., & Yu, J. H. (2013) Synthesis and biological evaluation of novel 1, 2, 4-triazole containing 1, 2, 3-thiadiazole derivatives. Chinese Chemical Letters, 24(12), 1134-1136. https://doi.org/10.1016/j.cclet.2013.06.024
[25] Du, Q. S., Shi, Y. X., Li, P. F., Zhao, Z. J., Zhu, W. P., Qian, X. H., ... & Xu, Y. F. (2013) Novel plant activators with thieno[2,3-d]-1,2,3-thiadiazole-6-carboxylate scaffold: Synthesis and bioactivity. Chinese Chemical Letters, 24 (11), 967-969. https://doi.org/10.1016/j.cclet. 2013.07.003
[26] Xu, W. M., Li, S. Z., He, M., Yang, S., Li, X. Y., & Li, P. (2013) Synthesis and bioactivities of novel thioether/sulfone derivatives containing 1, 2, 3-thiadiazole and 1, 3, 4-oxadiazole/thiadiazole moiety. Bioorganic & medicinal chemistry letters, 23 (21), 5821-5824. https://doi.org/10.1016 /j.bmcl.2013.08.107
[27] Zhang, P. Z., Zhou, S. F., Li, T. R., & Jiang, L. (2012) Efficient synthesis and in vitro antifungal activity of 1H-benzimidazol-1-yl acetates/propionates containing 1H-1, 2, 4-triazole moiety. Chinese Chemical Letters, 23 (12), 1381-1384. https://doi.org/10.1016/j.cclet.2012.10.024
[28] CHEN, Q. (2008) Synthesis and herbicidal activities of tetrazolinone derivatives containing oxime ether. Chinese Journal of Organic Chemistry, 28 (09), 1561.
[29] Teng, X., Keys, H., Jeevanandam, A., Porco Jr, J. A., Degterev, A., Yuan, J., & Cuny, G. D. (2007) Structure–activity relationship study of [1, 2, 3] thiadiazole necroptosis inhibitors. Bioorganic & medicinal chemistry letters, 17 (24), 6836-6840. https://doi.org/10.1016/j.bmcl.2007.10.024
[30] Hassan, A. M., Heakal, B. H., Khamis, H., El-Naeem, G., Marzouk. E., Abdelmoaz, M. A.,
and Younis, A. (2021) Design, Synthesis, DFT Studiesand Anticancer Activity of Novel Metal Complexes Containing 1,3,5-triazino[1,2-a]benzimidazole Moiety Using Microwave as an Approach for Green Chemistry. Egypt. J. Chem., 64 (1), 323-340.
[31] Hassan, A. M., Heakal, B. H., Said, A. O., Aboulth, W. M., and Abdelmoaz, M. A. (2020) Comparative Study for Synthesis of Novel Mn (II), Co (II), Ni (II), Cu (II), Zn (II) and Zr (IV) Complexes under Conventional Methods and Microwave Irradiation and Evaluation of their Antimicrobial and Anticancer Activity. Egypt.J.Chem., 63 (7), 2533 – 2550.
[32] Jain, R. K., and Mishra, A. P. (2012) Microwave synthesis, spectral, thermal, and antimicrobial activities of some transition metal complexes involving 5-bromosalicylaldehyde moiety. Current chemistry letters, 1, 163-174. doi: 10.5267/j.ccl.2012.7.003
[33] Villemin, D., Hammadi, M., Hachemi, M., Bar N. (2001) Applications of Microwave in Organic Synthesis: An Improved One-step Synthesis of Metallophthalocyanines and a New Modified Microwave Oven for Dry Reactions, Molecules, 6, 831-844.
[34] (a) Kotalwar S. S., Kale A. D., Kohire R. B. and Jagrut V. B. (2019) Microwave Assisted Synthesis of 1,5-Benzothiazepines Using Greener Reaction Medium. Asian J. Chem, 31 (5), 993-996. (b) Kohire, R. B., Bhale, S. P., Jagrut, V. B., Kale, A. D., & Mirgane, S. R. (2020) SYNTHESIS, CHARACTERIZATION AND ANTIMICROBIAL SCREENING OF ((12E)-4-METHYL-N-((4-OXO-4H-CHROMONE-3-YL) METHYLENE)-1, 2, 3,-THIADIAZOLE-5-CARBOXYLIC ACID HYDRAZIDE AND THEIR TRANSITION METAL COMPLEXES. Journal of Advanced Scientific Research, 11 (3 Sup 7), 141-146.
[35] Al-Jeboori, M. J., Al-Dujaili, A. H., and Al-Janabi, A. E. (2009) Coordination of carbonyl oxygen in the complexes of polymeric N-crotonyl-2-hydroxyphenylazomethine. Transition Metal Chemistry, 34 (1), 109–113.
[36] Livingston, S. E., Mayfield, J. H., and Moorse, D. S. (1975) Thio derivatives of