Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/21645
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dc.contributor.authorKundu, Sandip Kumar-
dc.contributor.authorGupta, Twishasri Das-
dc.contributor.authorDas, Suven-
dc.contributor.authorPramanik, Animesh-
dc.date.accessioned2013-10-07T10:10:57Z-
dc.date.available2013-10-07T10:10:57Z-
dc.date.issued2003-07-
dc.identifier.issn0975-0983(Online); 0376-4699(Print)-
dc.identifier.urihttp://hdl.handle.net/123456789/21645-
dc.description1716-1722en_US
dc.description.abstractIn Bergman cyclization the antisymmetric combination (n1-n2) of the hybrid orbitals at the radical sites in 1,4-dehydrobenzene is preferentially stabilized via through-bond interactions. The resultant splitting between the frontier orbitals is crucial in making Bergman cyclization a thermally symmetry allowed process. 1,4-Pentadiyne and 1,6-heptadiyne have been used as model systems to explore theoretically the role of orbital symmetry in Bergman cyclization.en_US
dc.language.isoen_USen_US
dc.publisherNISCAIR-CSIR, Indiaen_US
dc.rights CC Attribution-Noncommercial-No Derivative Works 2.5 Indiaen_US
dc.sourceIJC-B Vol.42B(07) [July 2003]en_US
dc.titleThe role of orbital symmetry in Bergman cyclizationen_US
dc.typeArticleen_US
Appears in Collections:IJC-B Vol.42B(07) [July 2003]

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