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Anion-directed assembly of supramolecular zinc(ii) halides with N,N′-bis-4-methyl-pyridyl oxalamide
Author(s) -
BiingChiau Tzeng,
BoSo Chen,
Shih-Yang Lee,
WeiHsin Liu,
GeneHsiang Lee,
ShieMing Peng
Publication year - 2005
Publication title -
new journal of chemistry
Language(s) - English
Resource type - Journals
eISSN - 1369-9261
pISSN - 1144-0546
DOI - 10.1039/b508293e
Subject(s) - chemistry , supramolecular chemistry , halide , hydrogen bond , zinc , supramolecular polymers , crystallography , supramolecular assembly , amide , ligand (biochemistry) , luminescence , coordination polymer , stereochemistry , polymer chemistry , crystal structure , inorganic chemistry , molecule , organic chemistry , biochemistry , receptor , physics , optoelectronics
We report here the supramolecular structures and solid state luminescence of zinc(II) halides with N,N′-bis-4-methyl-pyridyl oxalamide (L), where the supramolecular assembly formed is dependent on the halide, and led to the formation of one-dimensional coordination polymers for Cl ([ZnCl2(L)]n) and Br ([ZnBr2(L)]n) or a discrete macrocycle for I ([ZnI2(L)]2), respectively. The rectangular structure of iodo compounds with pyridyl amide L shows an interesting nanotube framework built from π⋯π interactions in combination with hydrogen bonding. To our knowledge, these are rare examples of the anion-directed assembly of supramolecular structures. The low energy emission at ca. 500 nm for [ZnI2(L)]2 is assigned to a ligand-to-metal charge-transfer (LMCT) transition.

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