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Dimerisation and reactivity of HCCCCFc at ruthenium centres
Authors:Michael I. Bruce  Martyn Jevric  Allan H. White
Affiliation:a School of Chemistry & Physics, University of Adelaide, Adelaide, South Australia 5005, Australia
b Chemistry M313, SBSSC, University of Western Australia, Crawley, Western Australia 6009, Australia
Abstract:In contrast to the simple diynyl complexes formed in reactions between HCtriple bond; length of mdashCCtriple bond; length of mdashCFc and MCl(dppe)Cp∗; (M = Fe, Ru), an analogous reaction with RuCl(PPh3)2Cp∗; in the presence of KPF6 and dbu resulted in dimerisation of the diyne at the Ru centre to afford a mixture of [Ru{η12-C(Ctriple bond; length of mdashCFc)double bond; length as m-dashC(L)CHdouble bond; length as m-dashCCdouble bond; length as m-dashCHFc}(PPh3)Cp∗]PF6 (L = dbu 1, PPh32). Similar reactions with RuCl(PR3)2L gave [Ru{η12-C(Ctriple bond; length of mdashCFc)double bond; length as m-dashC(dbu)CHdouble bond; length as m-dashCCdouble bond; length as m-dashCHFc}(PR3)L]PF6 (L = Cp, R = Ph 3, m-tol 4; L = η5-C9H7, R = Ph 5). The reaction between 3 and I2, followed by crystallization of the paramagnetic product from MeOH, afforded the dicationic [Ru{C(Ctriple bond; length of mdashCFc)C(dbu)CHdouble bond; length as m-dashC(OMe)C(OMe)double bond; length as m-dashCHFc}(PPh3)Cp](I3)26. The molecular structures of 2·2CH2Cl2 and 6.S (S = 2CH2Cl2, C6H6) were determined by single-crystal XRD studies.
Keywords:Ferrocene   Ruthenium   Diyne   Dimerisation   Crystal structure
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