Zobrazeno 1 - 10
of 176
pro vyhledávání: '"Brian T. Heaton"'
Publikováno v:
Dalton Transactions. 44:16611-16613
Experimental results (recent IR, DFT calculations and modern multinuclear NMR measurements on Rh-containing clusters, together with earlier VT multinuclear NMR measurements) show that the use of the Ligand Polyhedral Model (LPM) to provide a general
Autor:
Vadim I. Ponomarenko, Brian T. Heaton, Ivan S. Podkorytov, Jonathan A. Iggo, Sergey P. Tunik, Stanislav I. Selivanov
Publikováno v:
Inorganica Chimica Acta. 363:549-554
Addition of excess CF 3 CO 2 H (HTFA) to [Rh 2 Pt 2 (CO) 7 (PPh 3 ) 3 ], I , under nitrogen results in the formation of a salt ( X 2+ Y 2− ) , which contains only the second example of a di-cationic carbonyl hydride tetra-nuclear cluster , [H 2 Rh
Publikováno v:
Magnetic Resonance in Chemistry. 46:S100-S106
The fragmentation and redistribution reactions of [Rh4(CO)12−x{P(OPh)3}x] (x = 1–4) with carbon monoxide have been studied using high-resolution, high-pressure NMR spectroscopy. Under the conditions of efficient gas mixing in a high-pressure NMR
Autor:
Jeyagowry T. Sampanthar, Stefano Zacchini, Chacko Jacob, Brian T. Heaton, Jonathan A. Iggo, Kerry J. Bradd
Publikováno v:
Dalton Trans.. :685-690
The progressive addition of anhydrous pyridine, (py), to a solution of [Rh(4)(CO)(12)] in CH(2)Cl(2) under CO, even at low temperature, results in immediate disproportionation to give cis-[Rh(CO)(2)py(2)][Rh(5)(CO)(15)]; further addition of pyridine
Publikováno v:
Inorganica Chimica Acta. 359:3557-3564
Both Rh4(CO)12 and Rh6(CO)16 exhibit CO-fluxionality and modern, variable temperature, NMR methods allow the unambiguous assignment of the three terminal CO resonances and, for Rh4(CO)12, show that the mechanism of CO-fluxionality, which has been con
Publikováno v:
Journal of Molecular Catalysis A: Chemical. :149-155
The promotional effect of low concentrations of water on the catalytic activity in the Co-catalysed methoxycarbonylation of oct-1-ene to straight and branched chain C 9 methylesters has been demonstrated. Under rigorously anhydrous conditions, only m
Autor:
Brian T. Heaton, Alexander Steiner, Giorgos Athanasellis, Jamie F. Bickley, John Markopoulos, Efstathios Gavrielatos, Olga Igglessi-Markopoulou
Publikováno v:
Inorganica Chimica Acta. 351:21-26
Progressive displacement of acac from [Pd(acac)2] occurs on reaction with different tetramic acids (HL � /Hata, Habta) to give [Pd(acac)(h 2 -L)] and [Pd(h 2 -L)2] but, when HL� /Haceta, only [Pd(acac)(h 2 -L)] is formed, even when the ratio of P
Autor:
Mark R. J. Elsegood, Robin Whyman, Robert P. Tooze, Stefano Zacchini, Brian T. Heaton, William Clegg, Jonathan A. Iggo, Graham R. Eastham
Publikováno v:
Journal of the Chemical Society, Dalton Transactions. :3300-3308
The sequence of reaction steps and the role of each reactant, required for the transformation of the Pd(0) precursor [Pd(dtbpx)(dba)] [dtbpx = 1,2-(CH2PBut2)2C6H4; dba = trans,trans-(PhCHCH)2CO], 1, into [Pd(dtbpx)H(MeOH)]+, 2a, the active Pd(II)-hyd
Publikováno v:
Zeitschrift für Naturforschung B. 57:610-614
Tetrabutylammonium carbonyltribromoplatinate(II) [(C4H9)4N][PtBr3(CO)] crystallises in the monoclinic system in the space group P21/n with a = 1487.84(13), b = 897.41(8), c = 1849.6(2) pm, β = 106.558(2)° and four formula units per unit cell. The [
Autor:
Mark R. J. Elsegood, Robin Whyman, Stefano Zacchini, William Clegg, Jonathan A. Iggo, Robert P. Tooze, Graham Ronald Eastham, Brian T. Heaton
Publikováno v:
Organometallics. 21:1832-1840
A detailed spectroscopic study has allowed the solution structure and dynamic properties of all the intermediates in the Pd-catalyzed methoxycarbonylation of ethene to be established. [Pd(L−L)H(solv)]+ 1 (L−L = 1,2-(CH2PBut2)2C6H4; solv = MeOH, 1