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Binding sites on the outside of metallo-supramolecular architectures; engineering coordination polymers from discrete architectures

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UNSPECIFIED. (2004) Binding sites on the outside of metallo-supramolecular architectures; engineering coordination polymers from discrete architectures. DALTON TRANSACTIONS (10). pp. 1546-1555. ISSN 1477-9226

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Official URL: http://dx.doi.org/10.1039/b403749a

Abstract

Aggregation of metallo-supramolecular architectures through additional coordination is explored by introducing metal-binding units onto the outside of the supramolecular architectures. This is achieved within the framework of our imine-based approach to supramolecular architecture, by replacing the pyridylimine units with pyrazylketimine units. An advantage of the design is that it retains the ease-of-synthesis which characterises our imine-based approach. Silver(I) complexes of three pyrazylketimine ligand systems are described. The complexes demonstrate that introducing pyrazine donor units does indeed allow higher-order assembly of the distinct supramolecular architectures into engineered coordination polymers. Two distinct types of aggregation are observed. In the first, the donors on the outside of one architecture bind to the metals of another to link the units into a polymeric array. In the second type, the donors on the outside of the architectures bind to separate metal centres which are themselves not part of the architectures, and these separate metal centres link the units to form the macromolecular array. The weaker donor nature of the pyrazine nitrogens ( compared to pyridine) also introduces an additional element into the design; higher coordination numbers are favoured and this can lead to arrays with higher connectivity than those observed in the discrete pyridylimine architectures.

Item Type: Journal Article
Subjects: Q Science > QD Chemistry
Journal or Publication Title: DALTON TRANSACTIONS
Publisher: ROYAL SOC CHEMISTRY
ISSN: 1477-9226
Date: 2004
Number: 10
Number of Pages: 10
Page Range: pp. 1546-1555
Identification Number: 10.1039/b403749a
Publication Status: Published
URI: http://wrap.warwick.ac.uk/id/eprint/8451

Data sourced from Thomson Reuters' Web of Knowledge

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