DSpace logo

Please use this identifier to cite or link to this item: http://dspace.bits-pilani.ac.in:8080/jspui/handle/123456789/18778
Full metadata record
DC FieldValueLanguage
dc.contributor.authorJames, Robert G.-
dc.contributor.authorMoyes, Richard B.-
dc.date.accessioned2025-04-24T10:17:40Z-
dc.date.available2025-04-24T10:17:40Z-
dc.date.issued1978-
dc.identifier.urihttp://dspace.bits-pilani.ac.in:8080/jspui/handle/123456789/18778-
dc.description.abstractThe hydrogenation and exchange reactions of benzene with molecular deuterium catalysed by evaporated films of twelve transition elements (Sc, Ti, V, Cr, Mn, Fe, Co, Ni, Ta, W, Re and Ir) have been examined in the region of room temperature. Copper, silver and gold were found to be inactive. Concentrations of surface sites were measured by deuterium chemisorption at 77 or 273 K and were used to calculate specific activities. The patterns of activity for exchange and for hydrogenation show a remarkable parallelism across the first and third transition series; this pattern is mirrored by changes in the electrical conductivities of the bulk metals, and this implies a relation with the electronic structures of the metals. An inverse relation is found between the specific rates and the calculated densities of states at the Fermi level. New information concerning the mechanisms of reaction is reported.en_US
dc.language.isoenen_US
dc.publisherJournal of the Chemical Society : Faraday Transaction - I. The Chemical Society, London. 1978, 74 (07)en_US
dc.subjectChemistryen_US
dc.subjectBenzene–deuterium exchangeen_US
dc.subjectHydrogenation of benzeneen_US
dc.subjectJournal of the Chemical Society : Faraday Transaction - Ien_US
dc.titlePatterns of activity in the benzene–deuterium exchange reaction and the hydrogenation of benzene catalysed by evaporated metal filmsen_US
dc.typeArticleen_US
Appears in Collections:Journal Articles (before-1995)

Files in This Item:
File Description SizeFormat 
1666-1675.pdf
  Restricted Access
647.7 kBAdobe PDFView/Open Request a copy


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.