Please use this identifier to cite or link to this item: http://localhost:8080/xmlui/handle/123456789/1942
Title: Core-modified octaphyrins: Syntheses and anion-binding properties
Authors: Misra, R
Anand, V G
Rath, H
Chandrashekar, T K
Keywords: Anion binding
Aromaticity
34pi electrons
Octaphyrin
Oxidative coupling reactions
Issue Date: 2005
Publisher: Indian Academy of Sciences
Citation: Journal of Chemical Sciences 117(2):99-103; Mar 2005
Abstract: In this paper, a brief review of the syntheses, characterization and anion-binding properties of core-modified octaphyrins is presented. It has been shown that the core-modified octaphyrins, exhibit aromaticity both in solution and in solid state, confirming the validity of the (4n + 2) Huckel rule for larger pi-electron systems. Solid-state binding characteristics of TFA anions of two core-modified octaphyrins are also described.
URI: http://ir.niist.res.in:8080/jspui/handle/123456789/1942
ISSN: 0253-4134
Appears in Collections:2005

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