Doubly-linked 1D coordination polymers derived from 2 : 2 metallamacrocyclic Ni(II) complexes with bipodal acylthiourea and exo-biaentate N-donor bridging ligands: Toward potentially selective chemical sensors?
Date
2005, 2005
Authors
Hallale O.
Bourne S.A.
Koch K.R.
Hallale O.
Bourne S.A.
Koch K.R.
Journal Title
Journal ISSN
Volume Title
Publisher
Abstract
The square planar 2 : 2 metallamacrocyclic Ni(II) complex of 3,3,3′,3′-tetraethyl-1,1′-isophthaloylbis(thiourea) readily forms coordination polymers by axial coordination of various exo-bidentate N-donor linkers: pyrazine, 4,4′-bipyridine, 1,2-bis(4-pyridyl)ethane and 1,2-di(4-pyridyl)ethylene. Steric constraints, together with coordination limited to the axial directions, result in the self-assembly of double-linked ID ladder structures. One compound in particular, with the bridging ligand 1,2-di(4-pyridyl)ethylene, is found to exist as a quasi-polymer, realising only one-third of its potential linkages. On exposure to various solvents, this compound appears to undergo complete polymerisation, both rapidly and fully reversibly with an associated colour change, making it a potential chemical sensor. © The Royal Society of Chemistry and the Centre National de la Recherche Scientifique 2005.
The square planar 2 : 2 metallamacrocyclic Ni(II) complex of 3,3,3′,3′-tetraethyl-1,1′-isophthaloylbis(thiourea) readily forms coordination polymers by axial coordination of various exo-bidentate N-donor linkers: pyrazine, 4,4′-bipyridine, 1,2-bis(4-pyridyl)ethane and 1,2-di(4-pyridyl)ethylene. Steric constraints, together with coordination limited to the axial directions, result in the self-assembly of double-linked ID ladder structures. One compound in particular, with the bridging ligand 1,2-di(4-pyridyl)ethylene, is found to exist as a quasi-polymer, realising only one-third of its potential linkages. On exposure to various solvents, this compound appears to undergo complete polymerisation, both rapidly and fully reversibly with an associated colour change, making it a potential chemical sensor. © The Royal Society of Chemistry and the Centre National de la Recherche Scientifique 2005.
The square planar 2 : 2 metallamacrocyclic Ni(II) complex of 3,3,3′,3′-tetraethyl-1,1′-isophthaloylbis(thiourea) readily forms coordination polymers by axial coordination of various exo-bidentate N-donor linkers: pyrazine, 4,4′-bipyridine, 1,2-bis(4-pyridyl)ethane and 1,2-di(4-pyridyl)ethylene. Steric constraints, together with coordination limited to the axial directions, result in the self-assembly of double-linked ID ladder structures. One compound in particular, with the bridging ligand 1,2-di(4-pyridyl)ethylene, is found to exist as a quasi-polymer, realising only one-third of its potential linkages. On exposure to various solvents, this compound appears to undergo complete polymerisation, both rapidly and fully reversibly with an associated colour change, making it a potential chemical sensor. © The Royal Society of Chemistry and the Centre National de la Recherche Scientifique 2005.
Description
Keywords
acylthiourea; ethane; ethylene derivative; ligand; nickel complex; polymer; pyrazine; solvent; thiourea derivative; unclassified drug; article; chemical binding; chemical reaction; chemical sensor; chemical structure; metal binding; polymerization; priority journal; reaction analysis; sensor; stereochemistry, acylthiourea, ethane, ethylene derivative, ligand, nickel complex, polymer, pyrazine, solvent, thiourea derivative, unclassified drug, article, chemical binding, chemical reaction, chemical sensor, chemical structure, metal binding, polymerization, priority journal, reaction analysis, sensor, stereochemistry
Citation
New Journal of Chemistry
29
11
New Journal of Chemistry
29
11
29
11
New Journal of Chemistry
29
11