Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/40879
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dc.contributor.authorLaatsch, Hartmut-
dc.contributor.authorSchmidt, Andreas Johann-
dc.contributor.authorKral, Andreas-
dc.contributor.authorHeine, Niklas-
dc.contributor.authorHaucke, Gunter-
dc.date.accessioned2017-03-23T04:54:32Z-
dc.date.available2017-03-23T04:54:32Z-
dc.date.issued1997-06-
dc.identifier.issn0975-0975(Online); 0376-4710(Print)-
dc.identifier.urihttp://nopr.niscair.res.in/handle/123456789/40879-
dc.description476-484en_US
dc.description.abstractThe deep blue-violet bis-o-quinonemethide 3 cyclizes thermally in a [4s+4a]cycloaddition reaction, yielding the colourless [3,2- b]furofurane 1a. The latter is re-opened by irradiation with UV light back to the methide in its Z,Z- configuration 2a. By metallation of 1a, the highly photoreactive acetylene 8a is obtained which again forms a methide under irradiation, but now in its E,E-configuration 3. The properties of this unique new photochromic system and related furofurans and alkyneshave been investigated.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-A Vol.36A(06) [June 1997]en_US
dc.titleSynthesis and properties of photochromic furofuransen_US
dc.typeArticleen_US
Appears in Collections:IJC-A Vol.36A(06) [June 1997]

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