Zobrazeno 1 - 10
of 56
pro vyhledávání: '"A. M. R. GALAS"'
Autor:
Antony J. Deeming, Alejandro J. Arce, Silvio Aime, Anita M. R. Galas, Michael B. Hursthouse, Domenico Osella
Publikováno v:
J. Chem. Soc., Dalton Trans.. :1981-1986
Both [Ru3(CO)12] and [Os3(CO)12] react with 3-dimethylaminoprop-1-yne (HCCCH2NMe2) to give fairly low yields of the compounds [M3H(CO)9(Me2NCCCH2)](M = Ru or Os), apparently derived by oxidative addition with cleavage of the terminal C–H bond and a
Autor:
David J. Cole-Hamilton, Michael B. Hursthouse, Anita M. R. Galas, Nigel P.C. Walker, S. David Chappell
Publikováno v:
Polyhedron. 4:121-125
Reaction of [RhCl(PPh3)3] with [o-MeC6H4CH2MgBr] affords high yields of the non-fluxional complex, [Rh(CH2C6H4Me)(PPh3)2] which has been shown crystallographically to contain a 1-3-η-benzyl group bound through the phenyl carbon atom that is not subs
Autor:
Wai-Kwok Wong, Anita M. R. Galas, Geoffrey Wilkinson, Mark Thornton-Pett, Kwok W. Chiu, Michael B. Hursthouse
Publikováno v:
J. Chem. Soc., Dalton Trans.. :1557-1563
The (µ3-acetyl)-nonacarbonyltriferrate(1–) ion, [Fe3(CO)9(µ3-MeCO)]–, reacts with fluoroboric acid to give the neutral clusters Fe3(CO)9(µ3-MeCO)(µ-H)(1), Fe3(CO)10(µ-CMe)(µ-H)(2), and in small yield, Fe3(CO)9(µ3-MeCOH)(3). With methyl flu
Publikováno v:
J. Chem. Soc., Dalton Trans.. :2505-2513
The complexes [Pt(NH3)4][Pt(NH3)4Br2]Y4, Y = HSO4, ClO4, or BF4, and [Pt(NH3)4][Pt(NH3)4I2][HSO4]3[OH]·H2O have been prepared by partial aerial oxidation of Magnus green in 50% H2SO4 in the presence of KBr or KI as appropriate. The complexes are dee
Publikováno v:
J. Chem. Soc., Dalton Trans.. :1867-1871
Reactions of cis- or trans-[RuCl2L4](L = PMe2Ph, PMePh2, or PEt3) with o-MeC6H4CH2MgBr produce [R[graphic omitted]H2)L3] as the only isolable product at temperatures down to –30 °C, presumably by δ-hydrogen-abstraction reactions. For L = PMe3 no
Autor:
Richard A. Jones, Anita M. R. Galas, Michael B. Hursthouse, K. M. Abdul Malik, Geoffrey Wilkinson
Publikováno v:
J. Chem. Soc., Dalton Trans.. :1771-1778
Further chemistry of the triple methylene (–CH2–) bridged compound Ru2(µ-CH2)3(PMe3)6 and its derivatives is described. The compounds [(Me3P)4Ru(µ-CH2)2Ru(µ-CH2)2Ru(PMe3)4][BF4]2, (1), and [Ru2(µ-OH)3(PMe3)6][BF4], (2), have been isolated fro
Autor:
Wai-Kwok Wong, Geoffrey Wilkinson, Anita M. R. Galas, Mark Thornton-Pett, Michael B. Hursthouse
Publikováno v:
J. Chem. Soc., Dalton Trans.. :2496-2500
The iron carbonylate anion [Fe2(CO)8]2– reacts with iodomethane and with chloromethyl methyl ether to give the tri-iron cluster anions [Fe3(CO)9(µ3-CH3CO)]–(1) and [Fe3(CO)9(µ-CO)(µ3-COCH2OCH3)]–(2) respectively. The structures of the cluste
Publikováno v:
J. Chem. Soc., Dalton Trans.. :1879-1885
Cyclic voltammetry shows that [Rh(CO)(PPh3)(η-C5H5)](1) undergoes irreversible one-electron oxidation to the reactive radical cation [Rh(CO)(PPh3)(η-C5H5)]+(2); chemical oxidation of (1), with [Fe(η-C5H5)2][PF6] or [N2C6H4F-p][PF6], or controlled
Publikováno v:
Polyhedron. 1:31-36
The interaction of phenylimidotrichloro bis(trimethylphosphine) with dimethylmagnesium gives the trimethyl compound, Re(NPh)Me3(PMe3)2. Exchange reactions between the trichloro and trimethyl compounds are studied by 1H nuclear magnetic resonance and
Publikováno v:
J. Chem. Soc., Dalton Trans.. :2088-2097
The interaction of t-butyl isocyanide with the following methyl compounds leads to the formation of insertion products in which methyl groups are transferred to the isocyanide ligand: hexamethyltungsten, hexamethylrhenium, tetraneopentylzirconium, bi