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dc.contributor.authorREDDY, BADDIGAM KIRANen_US
dc.contributor.authorGADEKAR, SANTOSH C.en_US
dc.contributor.authorANAND, V. G.en_US
dc.date.accessioned2020-10-26T06:38:21Z
dc.date.available2020-10-26T06:38:21Z
dc.date.issued2015-05en_US
dc.identifier.citationChemical Communications, 51(39), 8276-8279.en_US
dc.identifier.issn1359-7345en_US
dc.identifier.issn1364-548Xen_US
dc.identifier.urihttp://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/5283-
dc.identifier.urihttps://doi.org/10.1039/C5CC00771Ben_US
dc.description.abstractCocrystallates 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.isoenen_US
dc.publisherRoyal Society of Chemistryen_US
dc.subjectPorphyrinen_US
dc.subjectC-60en_US
dc.subjectTetraphenylporphyrinsen_US
dc.subjectPurificationen_US
dc.subjectCocrystalsen_US
dc.subjectC-70en_US
dc.subject2015en_US
dc.titleNon-covalent composites of antiaromatic isophlorin-fullereneen_US
dc.typeArticleen_US
dc.contributor.departmentDept. of Chemistryen_US
dc.identifier.sourcetitleChemical Communicationsen_US
dc.publication.originofpublisherForeignen_US
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