Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/21805
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dc.contributor.authorMallesha, H-
dc.contributor.authorDinesh, N D-
dc.contributor.authorRangappa, K S-
dc.contributor.authorShashikanth, S-
dc.contributor.authorLokanath, N K-
dc.contributor.authorSridhar, M A-
dc.contributor.authorPrasad, J Shashidhara-
dc.date.accessioned2013-10-10T09:44:44Z-
dc.date.available2013-10-10T09:44:44Z-
dc.date.issued2002-01-
dc.identifier.issn0975-0983(Online); 0376-4699(Print)-
dc.identifier.urihttp://hdl.handle.net/123456789/21805-
dc.description196-200en_US
dc.description.abstractPhotoreduction of benzophenone analogues 1 to benzopinacol analogues 2 in 2-propanol and diethyl ether have been studied under various experimental conditions. Two analogues namely 1,2-ethanediol 1,2-bis (3,4-dimethoxyphenyl)-1,2-diphenyl 2a and 1,2-ethanediol, 1,2-bis (l,4-benzodioxin)-1,2 diphenyl 2b have been isolated and structurally characterized by X-ray crystallography. The structures of 2a and 2b indicate that these two are programmed molecular systems with complementary recognition groups that contain information for the self assembly into supramolecular ribbons.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.41B(01) [January 2002]en_US
dc.titlePhotoreduction of benzophenone analogues by alcohol and ether: Self recognition molecular assembliesen_US
dc.typeArticleen_US
Appears in Collections:IJC-B Vol.41B(01) [January 2002]

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