Zobrazeno 1 - 10
of 41
pro vyhledávání: '"Geoffrey K. Barker"'
Autor:
F. Gordon A. Stone, Geoffrey K. Barker, Thomas Onak, Michael Green, Gowit Siwapanyoyos, Alan J. Welch
Publikováno v:
J. Chem. Soc., Dalton Trans.. :1687-1692
Reaction of [Pt2(µ-cod)(PEt3)4](cod = cyclo-octa-1,5-diene) with 2,3-dicarba-nido-hexaborane(8), 2,3-dimethyl-2,3-dicarba-nido-hexaborane(8), and monocarba-nido-hexaborane(9) affords respectively, [nido-µ4,5-{trans(Et3P)2Pt(H)}-µ5,6-H-2,3-CB5H6],
Autor:
F. Gordon A. Stone, Jean-Marie Bassett, Geoffrey K. Barker, Judith A. K. Howard, Wayne C. Wolsey, Michael Green
Publikováno v:
J. Chem. Soc., Dalton Trans.. :219-227
Ultra-violet irradiation of diethyl ether solutions of [Fe(CNR)5](R = Et or Pri) affords the dinuclear complexes [Fe2(CNR)9]. In contrast, sodium amalgam reduction of trans-[RuCl2(CNPri)4] in the presence of an excess of isopropyl isocyanide affords
Autor:
Michael F. Lappert, Ronald Pearce, Geoffrey K. Barker, William E. Hunter, Jerry L. Atwood, John Holton
Publikováno v:
Journal of the American Chemical Society. 99:6645-6652
Autor:
Paul K. Baker, Michael Green, Ian D. Williams, Daljit S. Gill, Geoffrey K. Barker, A. Guy Orpen, Alan J. Welch
Publikováno v:
J. Chem. Soc., Dalton Trans.. :1321-1331
Reaction of the carbyne complexes [M(CCH2R){P(OMe)3}2(η-C5H5)](M = Mo or W, R = But or Pri) with 2,6-xylyl isocyanide affords the complexes [M{η3-R′NCC(CH2But)CNR′}(CNR′)2(η-C5H5)](R′= 2,6-Me2C6H3), the molybdenum complex being identified
Publikováno v:
J. Chem. Soc., Dalton Trans.. :2063-2069
The reaction (room temperature, diethyl ether) of [Pt2(µ-cod)(PEt3)4](cod = cyclo-octa-1,5-diene) with nido-5,6-C2B8H12 affords [9-H-9,9(Et3P)2-µ10,11-H-7,8,9-C2PtB8H10](1), structurally characterised by X-ray diffraction. Crystals are orthorhombic
Publikováno v:
Canadian Journal of Chemistry. 52:2622-2633
The high yield syntheses of Me2GeHX (X = F, Cl, Br, I) and Me2GeHPs (Ps = CN, N3, NCO, NCS, OAc) are reported. The dimethylgermane derivatives are identified and characterized by various physical methods and by cleavage reactions where appropriate. A
Publikováno v:
J. Chem. Soc., Dalton Trans.. :1839-1847
Reaction of allene or buta-1,3-diene with [Pt(cod)2](cod = cycle-octa-1,5-diene) gives (η-cycle-octa-1,5-diene)(2,3-dimethylenebutane-1,4-diyl)platinum (1) and (η-cycle-octa-1,5-diene)(1,4-trans-divinylbutane-1,4-diyl) platinum (2), respectively. T
Publikováno v:
J. Chem. Soc., Dalton Trans.. :1679-1686
The dihydridocarbaferraborane [FeH2(2,3-Me2-2,3-C2B4H4)2] reacts with [Co(PEt3)4], [Pt2(µ-cod)(PEt3)4](cod = cyclo-octa-1,5-diene), and [Fe(cod)(η-C5H5)] to afford, respectively, the dimetallic species [CoFe( Me4C4B8H8)(PEt3)2], [FePt(Me4C4B8H8)(PE
Publikováno v:
J. Chem. Soc., Chem. Commun.. :627-629
Reaction of [Pt2(µ-cyclo-octa-1,5-diene)(PEt3)4] with 5,6-dicarba-nido-decaborane affords 9-H-9,9-(Et3P)2-µ10,11-H-7,8,9-C2PtB8H10, which on pyrolysis (100 °C) loses H2 and forms 9-H-9,10-(Et3P)2-7,8,9-C2PtB8H9; the structures of these compounds h
Publikováno v:
J. Chem. Soc., Chem. Commun.. :137-139
Reaction (room temperature, toluene) of closo-1-Me-1,2-C2B10H11 with two equivalents of [Co(PEt3)4] affords the title compound, structurally identified by X-ray crystallography.