Core-modified octaphyrins: Syntheses and anion-binding properties

dc.contributor.author	Misra, R
dc.contributor.author	Anand, V G
dc.contributor.author	Rath, H
dc.contributor.author	Chandrashekar, T K
dc.date.accessioned	2015-08-08T15:22:46Z
dc.date.available	2015-08-08T15:22:46Z
dc.date.issued	2005
dc.identifier.citation	Journal of Chemical Sciences 117(2):99-103; Mar 2005	en_US
dc.identifier.issn	0253-4134
dc.identifier.uri	http://ir.niist.res.in:8080/jspui/handle/123456789/1942
dc.description.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.	en_US
dc.language.iso	en	en_US
dc.publisher	Indian Academy of Sciences	en_US
dc.subject	Anion binding	en_US
dc.subject	Aromaticity	en_US
dc.subject	34pi electrons	en_US
dc.subject	Octaphyrin	en_US
dc.subject	Oxidative coupling reactions	en_US
dc.title	Core-modified octaphyrins: Syntheses and anion-binding properties	en_US
dc.type	Article	en_US