Three dimensional isophlorinoid tetrapodal molecular cage

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DC Field	Value	Language
dc.contributor.author	BASAVARAJAPPA, ASHOKKUMAR	en_US
dc.contributor.author	AMBHORE, MADAN D.	en_US
dc.contributor.author	ANAND, V. G.	en_US
dc.date.accessioned	2021-04-29T11:42:33Z
dc.date.available	2021-04-29T11:42:33Z
dc.date.issued	2021-05	en_US
dc.identifier.citation	Chemical Communications, 57(35), 4299-4302.	en_US
dc.identifier.issn	1359-7345	en_US
dc.identifier.issn	1364-548X	en_US
dc.identifier.uri	http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/5835
dc.identifier.uri	https://doi.org/10.1039/D1CC01002F	en_US
dc.description.abstract	Steric hindrance induced by thiophene molecules in predesigned precursors favors the exclusive formation of a three dimensional (3D) π-conjugated cage and quasi-cage like molecules instead of a porphyrinoid macrocycle. Herein we report the synthesis of a tetrapod 3D fully π-conjugated molecular cage using a simple acid catalysed reaction. The X-Ray crystallography analysis confirmed the tetrapod cage structure and intermediates, which resemble three-fourths or half of the cage structures.	en_US
dc.language.iso	en	en_US
dc.publisher	Royal Society of Chemistry	en_US
dc.subject	Chemistry	en_US
dc.subject	2021-APR-WEEK3	en_US
dc.subject	TOC-APR-2021	en_US
dc.subject	2021	en_US
dc.title	Three dimensional isophlorinoid tetrapodal molecular cage	en_US
dc.type	Article	en_US
dc.contributor.department	Dept. of Chemistry	en_US
dc.identifier.sourcetitle	Chemical Communications	en_US
dc.publication.originofpublisher	Foreign	en_US
Appears in Collections:	JOURNAL ARTICLES

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