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Please use this identifier to cite or link to this item: http://dspace.bits-pilani.ac.in:8080/jspui/handle/123456789/20710
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dc.contributor.authorOkura, Ichiro-
dc.contributor.authorKim-Thuan, Nguyen-
dc.date.accessioned2026-02-09T06:43:01Z-
dc.date.available2026-02-09T06:43:01Z-
dc.date.issued1981-
dc.identifier.urihttp://dspace.bits-pilani.ac.in:8080/jspui/handle/123456789/20710-
dc.description.abstractHighly active photoinduced systems for methyl viologen reduction have been developed by using ruthenium complexes with long lifetimes in the photoexcited state. The order of activities is as follows: Ru(dime-phen)2+3 > Ru(Cl-phen)2+3 > Ru(phen)2+3 > Ru(bpy)2+3. By kinetic studies the rate constants for quenching the excited ruthenium complexes by methyl viologen have been determined. When hydrogenase was added to the systems containing ruthenium complex, methyl viologen and reducing agent, hydrogen evolution was observed in every system. A higher activity for hydrogen evolution was observed for the system having a higher activity for methyl viologen reduction.en_US
dc.language.isoenen_US
dc.publisherJournal of the Chemical Society : Faraday Transaction - I. The Chemical Society, London. 1981, 77 (06)en_US
dc.subjectChemistryen_US
dc.subjectKinetic Studiesen_US
dc.subjectRuthenium complexesen_US
dc.subjectJournal of the Chemical Society : Faraday Transaction - Ien_US
dc.titleKinetic Studies of Photoinduced Methyl Viologen Reduction with Ruthenium Complexes and Hydrogen Evolution from Water by Hydrogenaseen_US
dc.typeThesisen_US
Appears in Collections:Journal Articles (before-1995)

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