SELECTIVE REACTIONS (HYDROLYSIS OR DEBENZOTRIAZOLATION) OF BIS(BENZOTRIAZOL-1-YL)METHYLIMINE BY METAL(II) SALTS

Citation
S. Thambidurai et Sk. Ramalingam, SELECTIVE REACTIONS (HYDROLYSIS OR DEBENZOTRIAZOLATION) OF BIS(BENZOTRIAZOL-1-YL)METHYLIMINE BY METAL(II) SALTS, Polyhedron, 16(3), 1997, pp. 423-425
Citations number
7
Categorie Soggetti
Chemistry Inorganic & Nuclear",Crystallography
Journal title
ISSN journal
02775387
Volume
16
Issue
3
Year of publication
1997
Pages
423 - 425
Database
ISI
SICI code
0277-5387(1997)16:3<423:SR(ODO>2.0.ZU;2-4
Abstract
The reactions of bis(benzotriazol-1-yl)methylimine (BBTMI) with acetat es and chlorides of Cu-II, Ni-II, Co-II, Zn-II, Cd-II and Mn-II were s tudied in ethanol. While the metal acetates induced debenzotriazolatio n to form 1-cyanobenzotriazole and benzotriazole, the chlorides induce d hydrolysis of BBTMI to form 1,1'bis(benzotriazol-1-yl)carbonyl. Thes e intermediates subsequently formed the mixed ligand complexes [1-cyan obenzotriazolediacetato M(II)] and [benzotriazolatochloro M(II)] respe ctively. The chemo-selectivity of the reactions could be attributed to a facile cleavage of one of the M-O bonds of the bidentately bound ac etates and to the acidic nature in the case of the chloride solution. Copyright (C) 1996 Elsevier Science Ltd