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Reactions of metalloalkynes VII. Protonation of ruthenium ethyne-1,2-diyl complexes
Authors:Christopher S Griffith  George A Koutsantonis  Brian W Skelton  Allan H White
Institution:

Department of Chemistry, University of Western Australia, 35 Stirling Highway, Crawley, WA 6009, Australia

Abstract:The acid–base chemistry of some ruthenium ethyne-1,2-diyl complexes, {Ru(CO)2(η-C5H4R)}22-C6-point triple bond; length half of m-dashC)] (R=H, Me) has been investigated. Initial protonation of {Ru(CO)2{η-C5H4R}}22-C6-point triple bond; length half of m-dashC)] gave the unexpected complex cation, crystallised as the BF4 salt, {Ru(CO)2(η-C5H4R}}33-C6-point triple bond; length half of m-dashC)]BF4] (R=Me structurally characterised). This synthesis proved to be unreliable but subsequent, careful protonation experiments gave excellent yields of the protonated ethyne-1,2-diyl complexes, {Ru(CO)2{η-C5H4R)}2212-C6-point triple bond; length half of m-dashCH)](BF4) (R=Me structurally characterised) which could be deprotonated in high yield to return the starting ethyne-1,2-diyl complexes.
Keywords:Ruthenium  Ethyne-1  2-diyl  Protonation
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