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Iron complexes arsines

C1bHi5As, Arsine, triphenyl-iron complex, 26 61 C H 5OjP, Triphenyl phosphite ruthenium complex, 26 178 CuHijP, Phosphine, triphenyl-cobalt complex, 26 190—197 cobalt-gold-ruthenium, 26 327 gold complex, 26 90, 325, 326 gold-manganese complex, 26 229 iridium complexes, 26 117-120, 122-125, 201, 202... [Pg.416]

The iron compound readily sublimes and yields well-formed, black lustrous crystals. The cobalt complex will also readily sublime, but dependent upon the temperature at which the crystals are formed, they can be either black or brown in color. The crystal structures of both the cobalt and iron complexes have been determined.3 The nickel complex sublimes only in small amounts with difficulty. All three complexes are unstable to air and water, and the nickel complex readily undergoes thermal decomposition above 100°C. All three compounds will also readily form complexes with a variety of donor ligands such as tertiary arsines or phosphines. The nickel compound usually forms 2 1 adducts such as [(C6HS )3P]2Ni(NO)I, while the iron and cobalt complexes often undergo disproportionation.5... [Pg.89]

The enantiomerically pure secondary arsine-iron complex 2 has been used for assym-metric synthesis of a tertiary arsine (equation 61) . ... [Pg.824]

AsBrFgS7, Arsenate(l —)hexafluoro-, cyclo-heptasulfur(l +), bromo-, 27 336 AsC,gH,3, Arsine, triphenyl-, iron complex, 28 171... [Pg.387]

C 7H,40, l,4-pentadien-3-one, 1,5-diphenyl-, palladium complex, 28 110 CjgHtjAs, Arsine, tri]riienyl-, iron complex, 26 61... [Pg.395]

Although trialkyl- and triarylbismuthines are much weaker donors than the corresponding phosphoms, arsenic, and antimony compounds, they have nevertheless been employed to a considerable extent as ligands in transition metal complexes. The metals coordinated to the bismuth in these complexes include chromium (72—77), cobalt (78,79), iridium (80), iron (77,81,82), manganese (83,84), molybdenum (72,75—77,85—89), nickel (75,79,90,91), niobium (92), rhodium (93,94), silver (95—97), tungsten (72,75—77,87,89), uranium (98), and vanadium (99). The coordination compounds formed from tertiary bismuthines are less stable than those formed from tertiary phosphines, arsines, or stibines. [Pg.131]

AsFe04C 2H]5, Iron, tetracarbonyl-(triphenylarsine)-, 26 61 As2C Hu, Arsine, 1,2-phenylenebis-(dimethyl)-gold complex, 26 89 As4Au2F,( C,2H1 , Gold(I), bis[ 1,2-... [Pg.411]

Anionic iron bis(dithiolene) complexes have been reported to catalyze the autoxidation of phosphine, arsine, and cumene (92). No evidence for formation of molecular oxygen complexes has been found. The catalytic activity has been proposed to be a consequence of the redox activity of the complex. On this... [Pg.289]

There are several examples of iron(I) complexes in which the +1 oxidation state is stabilized by coordination of carbon monoxide or arsine ligands. In an early paper217 Hieber and Lagally... [Pg.1197]

Diiron enneacarbonyl, synthesis 46 Triiron dodecacarbonyl, synthesis 46 Tricarbonyl(cyclooctatetraene)iron, synthesis 47 Iron carbonyl complexes of triphenylphosphine, triphenyl-arsine, and triphenylstibine, synthesis 48 cis-Dinitrobis(ethylenediamine)cobalt(III) nitrite and nitrate, synthesis 60... [Pg.14]


See other pages where Iron complexes arsines is mentioned: [Pg.1234]    [Pg.283]    [Pg.357]    [Pg.357]    [Pg.380]    [Pg.283]    [Pg.1234]    [Pg.341]    [Pg.352]    [Pg.4688]    [Pg.380]    [Pg.3]    [Pg.225]    [Pg.148]    [Pg.149]    [Pg.347]    [Pg.287]    [Pg.60]    [Pg.199]    [Pg.818]    [Pg.325]    [Pg.205]    [Pg.249]    [Pg.239]    [Pg.226]    [Pg.579]    [Pg.1150]    [Pg.1155]    [Pg.1197]    [Pg.247]   
See also in sourсe #XX -- [ Pg.1197 ]

See also in sourсe #XX -- [ Pg.4 , Pg.1197 ]




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Arsine complexes

Arsine triphenyl-, iron complex

Iron complexes arsine oxide

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