Bicycle pedal photoisomerization of 1-phenyl-4-(4-pyridyl)-1,3-butadienes in glassy isopentane at 77 K

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dc.contributor.author Redwood, Christopher E.
dc.contributor.author Kanvah, Sriram
dc.contributor.author Samudrala, Ramakrishna
dc.contributor.author Saltiel, Jack
dc.date.accessioned 2014-03-17T13:00:15Z
dc.date.available 2014-03-17T13:00:15Z
dc.date.issued 2013-07
dc.identifier.citation Redwood, Christopher E.; Kanvah, Sriram; Samudrala, Ramakrishna and Saltiel, Jack, “Bicycle pedal photoisomerization of 1-phenyl-4-(4-pyridyl)-1, 3-butadienes in glassy isopentane at 77 K”, Photochemical & Photobiological Sciences, DOI: 10.1039/C3PP50064K, no. 10, pp. 1754-1760, July. 2013. en_US
dc.identifier.issn 1474-9092
dc.identifier.uri http://dx.doi.org/10.1039/C3PP50064K
dc.identifier.uri https://repository.iitgn.ac.in/handle/123456789/879
dc.description.abstract In glassy isopentane at 77 K, 1-phenyl-4-(4-pyridyl)-cis-1,cis-3-butadiene (cc-PPyB) and 1-phenyl-4-(4-pyridyl)-cis-1,trans-3-butadiene (ct-PPyB) can undergo simultaneous two-bond photoisomerization. Under the same conditions, 1-phenyl-4-(4-pyridyl)-trans-1,cis-3-butadiene (tc-PPyB) gives tt-PPyB, the ultimate photoproduct in all cases. en_US
dc.description.statementofresponsibility by Sriram Kanvah et al.,
dc.format.extent Vol. 12, No. 10, pp. 1754-1760
dc.language.iso en en_US
dc.publisher Royal Society of Chemistry en_US
dc.subject Chemistry en_US
dc.subject Glassy isopentane en_US
dc.subject Photoisomerization en_US
dc.title Bicycle pedal photoisomerization of 1-phenyl-4-(4-pyridyl)-1,3-butadienes in glassy isopentane at 77 K en_US
dc.type Article en_US
dc.relation.journal Photochemical & Photobiological Sciences


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