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Transition metal complexes bridging

Electron-beam heating, in metal vapor synthesis, 1, 232 Electron-beam vaporization, in metal vapor synthesis, 1, 224 Electron correlation, and computational chemistry, 1, 642 Electron counting, in transition metal complexes bridging ligands, 1, 14 examples, 1, 9 ligand electrons, 1, 5/... [Pg.100]

V. Beck, and D. O Hare, Triple-Decker Transition Metal Complexes Bridged by a Single Carbocyclic Ring, J. Organomet. Chem. 689, 3920-3938 (2004). [Pg.192]

BINUCLEAR TRANSITION METAL COMPLEXES BRIDGED BY METHYLENEBIS(DIPHENYLPHOSPHINE)... [Pg.48]

There are only a few weU-documented examples of catalysis by metal clusters, and not many are to be expected as most metal clusters are fragile and fragment to give metal complexes or aggregate to give metal under reaction conditions (39). However, the metal carbonyl clusters are conceptually important because they form a bridge between catalysts commonly used in solution, ie, transition-metal complexes with single metal atoms, and catalysts commonly used on surfaces, ie, small metal particles or clusters. [Pg.169]

The deoxygenation reaction by means of transition-metal complexes has been extended to oxepins with a tetramethylene bridge across the C2-C3 bond to give products 5.133... [Pg.42]

Transition metal complexes with bridging hydride ligands. L. M. Venazi, Coord. Chem. Rev., 1982, 43, 251-274 (40). [Pg.50]

The finding of preparatively available iminoboranes RB = NR some years ago opened exciting new possibilities not only in B—N chemistry, but also in coordination chemistry. The first examples of iminoborane-transition-metal complexes have now been published. The structurally completely characterized t-BuB = NBu-t adds, like its alkyne analog, to the 03(00)5 fragment as a bridging ligand. When Co2(CO)g and t-BuB = NBu-t are dissolved in pentane at 0°C, warming to RT and evaporation of unreacted iminoborane yields (t-BuBNBu-t)Co2(CO)5 (86%) as a black solid, which can be recrystallized from ether-nitromethane (1 3) ... [Pg.67]

A chiral diphosphine ligand was bound to silica via carbamate links and was used for enantioselective hydrogenation.178 The activity of the neutral catalyst decreased when the loading was increased. It clearly indicates the formation of catalytically inactive chlorine-bridged dimers. At the same time, the cationic diphosphine-Rh catalysts had no tendency to interact with each other (site isolation).179 New cross-linked chiral transition-metal-complexing polymers were used for the chemo- and enantioselective epoxidation of olefins.180... [Pg.261]

Chiorboli C, Indelli MT, Scandola F (2005) Photoinduced Electron/Energy Transfer Across Molecular Bridges in Binuclear Metal Complexes. 257 63-102 Collin J-P, Heitz V, Sauvage J-P (2005) Transition-Metal-Complexed Catenanes and Rotax-anes in Motion Towards Molecular Machines. 262 29-62 Collyer SD, see Davis F (2005) 255 97-124 Commeyras A, see Pascal R (2005) 259 69-122 Correia JDG, see Santos I (2005) 252 45-84 Costanzo G, see Saladino R (2005) 259 29-68 Credi A, see Balzani V (2005) 262 1-27 Crestini C, see Saladino R (2005) 259 29-68... [Pg.202]


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See also in sourсe #XX -- [ Pg.2 , Pg.680 ]




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