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Iron, Ruthenium, and Osmium Carbonyl Complexes

SbMe ] exhibit axial-equatorial isomerism in solution. The tendency to give the less-common equatorial isomer follows the orders Ru Os Fe, Sb As P, Ph Me and P(OCH..) CMe PMe, [Pg.215]

Elimination of HI from these products gives the n -thiophosphinito- [Pg.215]

S -bridging the iron-iron bond of a Fe (CO), moiety and P-bonded [Pg.215]

Among the nitrogen donor ligand complexes that have been [Pg.217]

Ph2pCH2CH(Me)PPh2 to give [CpRu(chelate)H] products. [Pg.218]


Iron, Ruthenium, and Osmium Carbonyl Complexes.— The rates of carbonyl substitution in [Fe(CO)2L2l radicals (L = phosphine) by a variety of pyridines have been studied electrochemically. [Pg.215]


See other pages where Iron, Ruthenium, and Osmium Carbonyl Complexes is mentioned: [Pg.215]    [Pg.542]   


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Carbonyl complexes iron and ruthenium

Carbonyl complexes, osmium

Carbonylation Iron carbonyl

Iron and ruthenium

Iron carbonyl complexes

Iron complexes carbonylation

Iron-ruthenium

Osmium complexes

Osmium complexes carbonylation

Osmium ruthenium

Ruthenium carbonyl

Ruthenium carbonyl complexes

Ruthenium carbonylations

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