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Dynamic cis-trans bridge isomerism in the cyclidene family of dioxygen carriers: A bicyclic cyclidene with a trans bridge orientation

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UNSPECIFIED (1997) Dynamic cis-trans bridge isomerism in the cyclidene family of dioxygen carriers: A bicyclic cyclidene with a trans bridge orientation. INORGANIC CHEMISTRY, 36 (13). pp. 2754-2759. ISSN 0020-1669

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Abstract

A new type of isomerism has been detected in the cyclidene family of lacunar dioxygen carriers, providing an additional Structural variable for the central of their oxygen affinity. In those rare complexes that do not have methyl substituents on the primary macrocycle, NMR and X-ray crystallographic data indicate that, in addition to their usual cis orientation, the bridges can also adopt a trans orientation. In the crystal structure of [Co(C8MeHH[16]cyclidene)](PF6)(2) . 3CH(3)OH, the bridge has this trails orientation with one end in the ''lid-on'' configuration while the other end is ''lid-off'. The trans orientation of the bridge is identified as the principal cause of the decreased dioxygen affinity of such unsubstituted cyclidenes.

Item Type: Journal Article
Subjects: Q Science > QD Chemistry
Journal or Publication Title: INORGANIC CHEMISTRY
Publisher: AMER CHEMICAL SOC
ISSN: 0020-1669
Date: 18 June 1997
Volume: 36
Number: 13
Number of Pages: 6
Page Range: pp. 2754-2759
Publication Status: Published
URI: http://wrap.warwick.ac.uk/id/eprint/17683

Data sourced from Thomson Reuters' Web of Knowledge

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