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Cage effect metal complexes based

The stereochemical situation however, is appreciably more complex in incomplete corrins, such as cob(II)ester (24) and base-off forms of complete corrins. The axial ligand at the corrin-boimd Co(II) center is expected to direct the formation of the Co - C bond. In this way kinetic control can lead with high efficiency to the rare Q -alkyl-Co(III)-corrins [84,128[. In such radical recombination reactions the axial ligand at the a- or -side of the metal center will not only steer the diastereoselectivity of the alkylation but also may contribute to significant altering of the cage effects [122,123[. [Pg.22]

A number of electron acceptors have been identified for reaction (40) that can effectively mediate H2 evolution from water in the presence of Pt-group based redox catalysts. Typical examples are bipyridinium salts such as methyl viologen (MV " "), polypyridine complexes of Rh(III), Co(II) and cage complexes of Co(II). For this reason, the oxidative quenching of various transition metal polypyridine complexes, M(LL)3]" by these electron acceptors have been extensively studied ... [Pg.145]


See other pages where Cage effect metal complexes based is mentioned: [Pg.251]    [Pg.251]    [Pg.78]    [Pg.1197]    [Pg.603]    [Pg.275]    [Pg.12]    [Pg.1656]    [Pg.103]    [Pg.479]    [Pg.88]    [Pg.569]    [Pg.180]    [Pg.111]    [Pg.428]    [Pg.54]    [Pg.251]    [Pg.53]    [Pg.70]    [Pg.261]    [Pg.80]    [Pg.78]    [Pg.699]    [Pg.195]    [Pg.86]    [Pg.486]    [Pg.338]   
See also in sourсe #XX -- [ Pg.94 , Pg.95 , Pg.96 , Pg.97 , Pg.98 , Pg.99 , Pg.100 ]




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Caging effects

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