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Title: Effect of positional isomers on the photochromic behaviors of bipyridyltriazolium chloroantimonate hybrids. Author: Shen JJ, Kang XL, Ren QZ, Li GP, Gao YN, Hao PF, Fu YL. Journal: Dalton Trans; 2020 Apr 07; 49(14):4470-4475. PubMed ID: 32186311. Abstract: Two chloroantimonate hybrids with isomeric bipyridyltriazoliums and similar packing patterns, {[2-bpt]2[(SbCl5)Cl2]}n (1) and {[4-bpt]2[(SbCl5)Cl2]}n (2) (2-bpt2+ = protonated 3,5-bis(pyridine-2-yl)-1,2,4-triazole, 4-bpt2+ = protonated 3,5-bis(pyridine-4-yl)-1,2,4-triazole), have been designed and synthesized. Distinct intermolecular electronic interactions and photochromic behaviors are attributed to the remarkable modulation of positional isomeric effect on the electron deficiency of the acceptors and donor-acceptor matching relationship. 1 is the first reported photochromic chloroantimonate hybrid.[Abstract] [Full Text] [Related] [New Search]