Copyright (c) 2026 Tapashi Ghosh Roy Tapashi

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Bioactive Azamacrocyclic Zinc(II) Complexes: Synthesis and Characterisation
Corresponding Author(s) : Tapashi Ghosh Roy
Asian Journal of Chemistry,
Vol. 38 No. 8 (2026): Vol 38, Issue 8 (2026)
Abstract
Reduction of Me8[14]diene·2HClO4 (L·2HClO4) afforded three isomeric ligands (LA, LB and LC), among which LC underwent cyanoethylation with excess acrylonitrile to form the bis-cyanoethyl derivative (LCX). Reaction of LCX with zinc(II) chloride yielded the six-coordinate complex [Zn(LCX)Cl2], which subsequently underwent axial ligand substitution with KSCN, KNO3, NaNO2, KBr and KI to produce a series of octahedral zinc(II) complexes, [Zn(LCX)(X)2] (X = NCS, NO3, NO2, Br or I). All the Zn(II) synthesised complexes were characterized using various analytical and spectroscopic techniques. Their antibacterial activity was evaluated against four selected bacterial strains and most of the complexes exhibited good antibacterial activity against the tested bacteria.
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- P. Rajakkani, A. Alagarraj and S.A. Gurusamy Thangavelu, Inorg. Chem. Commun., 134, 108989 (2021); https://doi.org/10.1016/j.inoche.2021.108989
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- E. Kimura, Pure Appl. Chem., 65, 355 (1993); https://doi.org/10.1351/pac199365030355
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- W.J. Geary, Coord. Chem. Rev., 7, 81 (1971); https://doi.org/10.1016/S0010-8545(00)80009-0
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H.A. El-Boraey, M.A. El-Salamony and A.A. Hathout, J. Incl. Phenom. Macrocycl. Chem., 86, 153 (2016); https://doi.org/10.1007/s10847-016-0649-5
R. Delgado, V. Félix, L.M.P. Lima and D.W. Price, Dalton Trans., 26, 2734 (2007); https://doi.org/10.1039/B704360K
R.V. Singh and A. Chaudhary, J. Inorg. Biochem., 98, 1712 (2004); https://doi.org/10.1016/j.jinorgbio.2004.07.007
L. Dey, S. Rabi, D. Palit, S.K.S. Hazari, Z.A. Begum, I.M.M. Rahman and T.G. Roy, J. Mol. Struct., 1240, 130579 (2021); https://doi.org/10.1016/j.molstruc.2021.130579
S. Chandra, S. Verma, U. Dev and N. Joshi, J. Coord. Chem., 62, 1327 (2010); https://doi.org/10.1080/00958970802521076
K. Soha, K.M. Rashel, A. Rahman, T. Kamal, T.R. Majumder, S. Rabi, P. Paul, M.M. Hossain, A. Auwal, T. Ul Haque Pronoy, S.R. Kabir, M.H. Rahman, T.G. Roy, N. Roy, J.A. Khanam and F. Islam, Discover Oncol., 17, 1 (2025); https://doi.org/10.1007/s12672-025-04214-3
H.A. El-Boraey and O.A. El-Gammal, Spectrochim. Acta Part A Mol. Biomol. Spectrosc., 138, 553 (2015); https://doi.org/10.1016/j.saa.2014.11.015
D.-Y. Kong, L.-H. Meng, J. Ding, Y.-Y. Xie and X.-Y. Huang, Polyhedron, 19, 217 (2000); https://doi.org/10.1016/S0277-5387(99)00369-1
T.M. Hunter, S.J. Paisey, H.-S. Park, L. Cleghorn, A. Parkin, S. Parsons and P.J. Sadler, J. Inorg. Biochem., 98, 713 (2004); https://doi.org/10.1016/j.jinorgbio.2003.10.018
L. Leone, A. Anemone, A. Carella, E. Botto, D.L. Longo and L. Tei, ChemMedChem, 17, e202200508 (2022); https://doi.org/10.1002/cmdc.202200508
K. Bujno, R. Bilewicz, L. Siegfried and T. Kaden, Electrochim. Acta, 42, 1201 (1997); https://doi.org/10.1016/S0013-4686(96)00286-1
T. Joshi, B. Graham and L. Spiccia, Acc. Chem. Res., 48, 2366 (2015); https://doi.org/10.1021/acs.accounts.5b00142
V. Lozovan, V.C. Kravtsov, I. Bulhac, O. Petuhov, T. Vlase and P.N. Bourosh, J. Mol. Struct., 1321, 140021 (2025); https://doi.org/10.1016/j.molstruc.2024.140021
C. Redshaw, Coord. Chem. Rev., 523, 216147 (2025); https://doi.org/10.1016/j.ccr.2024.216147
E. Kikuta, T. Koike and E. Kimura, J. Inorg. Biochem., 79, 253 (2000); https://doi.org/10.1016/S0162-0134(99)00167-1
A. Azam, M.A. Raza and S.H. Sumrra, Open Chem., 16, 1153 (2018); https://doi.org/10.1515/chem-2018-0118
M. Pellei, F. Del Bello, M. Porchia and C. Santini, Coord. Chem. Rev., 445, 214088 (2021); https://doi.org/10.1016/j.ccr.2021.214088
E. Kimura, Pure Appl. Chem., 65, 355 (1993); https://doi.org/10.1351/pac199365030355
R. Bembi, S.M. Sondhi, A.K. Singh, A.K. Jhanji, T.G. Roy, J.W. Lown and R.G. Ball, Bull. Chem. Soc. Jpn., 62, 3701 (1989); https://doi.org/10.1246/bcsj.62.3701
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W.J. Geary, Coord. Chem. Rev., 7, 81 (1971); https://doi.org/10.1016/S0010-8545(00)80009-0
R. Bembi, M.G.B. Drew, R. Singh and T.G. Roy, Inorg. Chem., 30, 1403 (2002); https://doi.org/10.1021/ic00006a044
N.F. Curtis and Y.M. Curtis, Inorg. Chem., 4, 804 (2002); https://doi.org/10.1021/ic50028a007
E.R. Acuña-Cueva, R. Faure, N.A. Illán-Cabeza, S.B. Jiménez-Pulido, M.N. Moreno-Carretero and M. Quirós-Olozábal, Inorg. Chim. Acta, 342, 209 (2003); https://doi.org/10.1016/S0020-1693(02)01165-9
S. Yasmin, S. Rabi, F.B. Biswas, T.G. Roy, F. Olbrich and D. Rehder, J. Incl. Phenom. Macrocycl. Chem., 87, 239 (2017); https://doi.org/10.1007/s10847-017-0693-9
I. Tabushi, Y. Taniguchi and H. Kato, Tetrahedron Lett., 12, 1049, (1977); https://doi.org/10.1016/S0040-4039(01)92825-4
A. Choudhary and R.V. Singh, Rasayan J. Chem., 1, 15 (2008).
F.B. Biswas, T.G. Roy, M.A. Rahman and T.B. Emran, Asian Pac. J. Trop. Biomed., 4(suppl2), S618 (2014).