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Osmium carbonyls reactions

This proton transfer reaction is not fast, and it is suggested that this may be a more complicated reaction than was anticipated, perhaps occurring by initial addition of OH or OR to the metal followed by H2O or ROH expulsion. In support of this is the isolation of a complex Os(CO)-(CNC6H4CH3)(PPh3)2(H)OR from an analogous reaction sequence. (This is the only reference yet to any osmium carbonyl-isocyanide chemistry.)... [Pg.62]

Methylbenzene halogen complex of, 3 122 iodine monochloridecomplese, 3 109 Methylchlorosilanes hydrolysis, 42 149-150, 157 pyrolysis products of, 7 356-363 Methylcobalamin, 19 151, 152 Methyl-coenzyme M reductase, 32 323-325 EPR spectra, 32 323, 325 F43 and, 32 323-324 function, 32 324-325 Methyl-CoM reductase, 32 329 Methyl cyanide, osmium carbonyl complexes, reaction, 30 198-201 Methylcyclophosphazene salts, 21 70 synthesis, 21 109... [Pg.184]

In many cases the reaction of osmium carbonyls and acetylenes does not stop at the first stages as in [56], [57], or [57]. Instead, two or more acetylene molecules are incorporated, and in some cases acetylene trimerization to benzenes takes place (182, 371, 379). Incorporation of two acetylene molecules can lead to metallacyclo-pentadiene clusters like [55] (126,168,171,182,184, 223, 371), or to metallacyclo-hexadienone clusters hke [59] (126, 223). And the complex [90], another intermediate, is related to [55] by an intramolecular oxidative addition reaction (168,169). [Pg.33]

Osmium-Carbonyl-Hydride Clusters and Related Ruthenium Complexes. Our investigation of these species began with a study of the species (/i2-H)(H)Os3(CO)n, prepared from Os3(CO)i2 via the unsaturated species (M2-H)20s3(CO)io (33) (see Reaction 1). [Pg.49]

Scheme 9. Preparation of osmium carbonyl/hydride/phosphine or arsine synthetic intermediates via the reactions of coordinated ligands. Scheme 9. Preparation of osmium carbonyl/hydride/phosphine or arsine synthetic intermediates via the reactions of coordinated ligands.
Not only N, but also C atoms can take part as donor centers in azacymantrene 760 (E = N, R = H) and azaferrocene 763 (R = H). In this respect, the formation of a trinuclear osmium-carbonyl adduct 768 is representative, which takes place in the reaction of the indicated azacenes with acetonitrile complex of triosmium decarbonyl [482] ... [Pg.241]


See other pages where Osmium carbonyls reactions is mentioned: [Pg.277]    [Pg.69]    [Pg.277]    [Pg.278]    [Pg.278]    [Pg.297]    [Pg.319]    [Pg.31]    [Pg.60]    [Pg.218]    [Pg.80]    [Pg.295]    [Pg.15]    [Pg.18]    [Pg.19]    [Pg.25]    [Pg.34]    [Pg.204]    [Pg.181]    [Pg.184]    [Pg.193]    [Pg.198]    [Pg.201]    [Pg.1251]    [Pg.258]    [Pg.108]    [Pg.110]    [Pg.22]   
See also in sourсe #XX -- [ Pg.711 , Pg.720 , Pg.723 ]

See also in sourсe #XX -- [ Pg.818 , Pg.819 , Pg.828 , Pg.831 ]

See also in sourсe #XX -- [ Pg.900 , Pg.901 , Pg.910 , Pg.912 ]




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Osmium carbonyl clusters reaction with base

Osmium carbonyl clusters reactions

Osmium reaction

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