Issue 6, 1996

New supramolecular architectures based on polyfunctional organotin tetrazoles: synthesis and characterisation of phenylene-bridged bis(organotin tetrazoles)

Abstract

Seven bis(organostannyltetrazoles), R3SnN4C–X–CN4SnR3(R = Et, Bu or Pri; X = 1,2-, 1,3- or 1,4-C6H4), have been synthesised by a cycloaddition reaction involving SnR3N3 and NC–X–CN. All of the products formed incorporate a trans-N2SnC3 stereochemistry about tin, though the co-ordination mode of the tetrazole has been found to vary in the combinations of ligating nitrogen atoms used. The crystal structure of 1,3-(2-Bu3SnN4C)2C6H4·2MeOH showed that the preferred co-ordination site for tin on the tetrazole is the less-hindered N2 position. The crystal structures of 1,2-(2-Et3SnN4C)2C6H4 and 1,2-(2-Bu3SnN4C)2C6H4, respectively showed that these compounds are either two- or three-dimensional supramolecular arrays, the arrangements of which are dictated by the organic groups on tin.

Article information

Article type
Paper

J. Chem. Soc., Dalton Trans., 1996, 835-845

New supramolecular architectures based on polyfunctional organotin tetrazoles: synthesis and characterisation of phenylene-bridged bis(organotin tetrazoles)

M. Hill, M. F. Mahon, J. McGinley and K. C. Molloy, J. Chem. Soc., Dalton Trans., 1996, 835 DOI: 10.1039/DT9960000835

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