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Titanium complexes clusters

Use of D2 yielded CD4, and methane was formed from reaction of the complex with just H2. The water produced in the reaction hydrolyzes the titanium complex to an inactive cluster Cp6Ti608 containing bridging oxide ligands. [Pg.374]

Chiralsil-val, 6 96-97 Chiral smectic C liquid crystals, 15 106-107 Chiral stationary phases, 6 79-82 Chiral supramolecular clusters, 24 61 Chiral synthons, 11 5 Chiral titanium complexes, 25 98—99 Chirobiotic phases, for chiral separations, 6 90-91... [Pg.174]

Supported metal complexes and clusters with well-defined structures offer the advantages of catalysts that are selective and structures that can be understood in depth. Such catalysts can be synthesized precisely with organometallic precursors, as illustrated in this review. Synthetic methods are illustrated with examples, including silica-supported chromium and titanium complexes for alkene polymerization rhodium carbonyls bonded predominantly at crystallographically specific sites in a zeolite and metal clusters, including Ir4, Rhg, OsjC, and bimetallics. [Pg.237]

In crystals of more complex formula, such as titanium dioxide, TiC>2, a Schottky defect will consist of two anion vacancies and one cation vacancy. This is because it is necessary to counterbalance the loss of one Ti4+ ion from the crystal by the absence of two O2- ions in order to maintain composition and electroneutrality. This ratio of two anion vacancies per one cation vacancy will hold in all ionic compounds of formula MX2. In crystals like A1203, two Al3+ vacancies must be balanced by three O2- vacancies. Thus, in crystals with a formula M2X3, a Schottky defect will consist of two vacancies on the cation sublattice and three vacancies on the anion sublattice. These vacancies are not considered to be clustered together but are distributed... [Pg.26]

The films, ca. 50 nm thick, comprised small (2-4 nm) nanocrystals of anatase Ti02, possibly in an amorphous matrix, and were uniform, adherent, and pore free. In contrast, only a small amount of irregular deposit was formed on bare Si. The role of the sulphonate endgroups was believed to promote nucleation of the nanocrystals and/or facilitate attachment of TiOi clusters in solution to the substrate. Hydrolysis of TiCU proceeds through various titanium hydroxy and chloro-hydroxy complex cations. The anionic sulphonate groups could thus promote attachment and nucleation of these cationic complexes. [Pg.276]

Binding energy, pentacarbonyliron, 6, 3 Binuclear complexes bis-Cp titanium halides, 4, 522 with Ni-M and Ni-C cr-bonds heterometallic clusters, 8, 115 homometallic clusters, 8, 111 Binuclear dicarbonyl(cyclopentadienyl)hydridoiron complexes, with rand C5 ligands, 6, 178 Binuclear iridium hydrides, characteristics, 7, 410 Binuclear monoindenyl complexes, with Ti(IV), 4, 397 Binuclear nickel(I) carbonyl complexes, characteristics, 8, 13 Binuclear osmium compounds, with hydrocarbon bridges without M-M bonds, 6, 619... [Pg.62]

Imidazolium ligands, in Rh complexes, 7, 126 Imidazolium salts iridium binding, 7, 349 in silver(I) carbene synthesis, 2, 206 Imidazol-2-ylidene carbenes, with tungsten carbonyls, 5, 678 (Imidazol-2-ylidene)gold(I) complexes, preparation, 2, 289 Imidazopyridine, in trinuclear Ru and Os clusters, 6, 727 Imidazo[l,2-a]-pyridines, iodo-substituted, in Grignard reagent preparation, 9, 37—38 Imido alkyl complexes, with tantalum, 5, 118—120 Imido-amido half-sandwich compounds, with tantalum, 5,183 /13-Imido clusters, with trinuclear Ru clusters, 6, 733 Imido complexes with bis-Gp Ti, 4, 579 with monoalkyl Ti(IV), 4, 336 with mono-Gp Ti(IV), 4, 419 with Ru half-sandwiches, 6, 519—520 with tantalum, 5, 110 with titanium(IV) dialkyls, 4, 352 with titanocenes, 4, 566 with tungsten... [Pg.125]


See other pages where Titanium complexes clusters is mentioned: [Pg.181]    [Pg.175]    [Pg.276]    [Pg.136]    [Pg.155]    [Pg.331]    [Pg.716]    [Pg.506]    [Pg.362]    [Pg.2346]    [Pg.159]    [Pg.150]    [Pg.534]    [Pg.184]    [Pg.355]    [Pg.31]    [Pg.2902]    [Pg.156]    [Pg.212]    [Pg.72]    [Pg.164]    [Pg.92]    [Pg.134]    [Pg.24]    [Pg.242]    [Pg.283]    [Pg.46]    [Pg.51]    [Pg.90]    [Pg.136]   
See also in sourсe #XX -- [ Pg.160 , Pg.169 , Pg.170 ]




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