<p><strong>Interaction of Indenopyridines with [60]-fullerene: A spectroscopic and computational study</strong></p>
Online Publishing @ NISCAIR
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Title Statement |
<p><strong>Interaction of Indenopyridines with [60]-fullerene: A spectroscopic and computational study</strong></p> |
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Added Entry - Uncontrolled Name |
Chaudhuri, Tandrima ; Dr. Bhupendranath Dutta Smriti Mahavidyalaya, Burdwan University. UGC, India |
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Uncontrolled Index Term |
Indenopyridines; Fullerene Indenopyridines, Fullerene, Isosbestic formation, DFT, electrochemical indices |
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Summary, etc. |
<p><strong>Abstract</strong></p> <p>Heterocyclic polynuclear planar indenopyridines (I1, I3 and I4) revealed superior wrapping of [60]-fullereneand formed stable ground state equilibrium defined via formation of absorption isosbestic and isoemissive as well. All three indenopyridines showed almost similar order of ground state formation constant both in Benesi-Hildebrand and in Stern-Volmer method with[60]-fullerene in toluene medium. DFT based computation warranted the experimental finding in terms of loss of planarity of indenopyridines, FMO features to define electron donor and acceptor, electrochemical indices to affirm the direction of electron swing and finally TD-DFT calculation showed HOMO to (LUMO+2) was most pronounced transition for the strongest binding with I4.</p> |
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Publication, Distribution, Etc. |
Indian Journal of Chemistry -Section A (IJCA) 2020-10-12 16:06:45 |
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Electronic Location and Access |
application/pdf http://op.niscair.res.in/index.php/IJCA/article/view/22798 |
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Data Source Entry |
Indian Journal of Chemistry -Section A (IJCA); ##issue.vol## 58, ##issue.no## 5 (2019): INDIAN JOURNAL OF CHEMISTRY- SECTION A |
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Language Note |
en |
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Nonspecific Relationship Entry |
http://op.niscair.res.in/index.php/IJCA/article/download/22798/465471339 http://op.niscair.res.in/index.php/IJCA/article/download/22798/465471344 http://op.niscair.res.in/index.php/IJCA/article/download/22798/465471601 |
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