Non-covalent composites of antiaromatic isophlorin-fullerene

dc.contributor.author	REDDY, BADDIGAM KIRAN	en_US
dc.contributor.author	GADEKAR, SANTOSH C.	en_US
dc.contributor.author	ANAND, V. G.	en_US
dc.date.accessioned	2020-10-26T06:38:21Z
dc.date.available	2020-10-26T06:38:21Z
dc.date.issued	2015-05	en_US
dc.identifier.citation	Chemical Communications, 51(39), 8276-8279.	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/123456789/5283
dc.identifier.uri	https://doi.org/10.1039/C5CC00771B	en_US
dc.description.abstract	Cocrystallates of fullerene C60 and antiaromatic planar tetraoxaisophlorins have been characterized by single crystal X-ray diffraction analysis. The ring-juncture bonds of C60 are found to be at a very close distance to the plane of the antiaromatic isophlorins. NMR measurements and MALDI-TOF mass spectrometry show that this interaction can persist in both solution and gaseous states, which can be attributed to van der Waals dispersion forces.	en_US
dc.language.iso	en	en_US
dc.publisher	Royal Society of Chemistry	en_US
dc.subject	Porphyrin	en_US
dc.subject	C-60	en_US
dc.subject	Tetraphenylporphyrins	en_US
dc.subject	Purification	en_US
dc.subject	Cocrystals	en_US
dc.subject	C-70	en_US
dc.subject	2015	en_US
dc.title	Non-covalent composites of antiaromatic isophlorin-fullerene	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