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Methyldiphenylphosphine is the
organophosphine Organophosphines are organophosphorus compounds with the formula PR''n''H3โˆ’''n'', where R is an organic substituent. These compounds can be classified according to the value of ''n'': primary phosphines (''n'' = 1), secondary phosphine ...
with the formula CH3(C6H5)2P, often abbreviated PMePh2. It is a colorless, viscous liquid. It is a member of series (CH3)3-n(C6H5)2P that also includes n = 0, n = 1, and n = 3 that are often employed as
ligand In coordination chemistry, a ligand is an ion or molecule ( functional group) that binds to a central metal atom to form a coordination complex. The bonding with the metal generally involves formal donation of one or more of the ligand's elec ...
s in metal phosphine complexes. Methyldiphenylphosphine is prepared by reaction of
chlorodiphenylphosphine Chlorodiphenylphosphine is an organophosphorus compound with the formula (C6H5)2PCl, abbreviated Ph2PCl. It is a colourless oily liquid with a pungent odor that is often described as being garlic-like and detectable even in the ppb range. It is u ...
with methyl Grignard reagent: :Cl(C6H5)2P + CH3MgBr โ†’ CH3(C6H5)2P + MgBrCl Selected derivatives: *The phosphine oxide OPMePh2, prepared by treatment with hydrogen peroxide. *The coordination complex MoH4(PMePh2)4, prepared by treatment of MoCl4(PMePh2)2 with
sodium borohydride Sodium borohydride, also known as sodium tetrahydridoborate and sodium tetrahydroborate, is an inorganic compound with the formula Na BH4. This white solid, usually encountered as an aqueous basic solution, is a reducing agent that finds applica ...
in the presence of excess ligand. *The coordination complex CoCl2(PMePh2)2, prepared by treating
cobalt(II) chloride Cobalt(II) chloride is an inorganic compound of cobalt and chlorine, with the formula . The compound forms several hydrates ยท''n'', for ''n'' = 1, 2, 6, and 9. Claims of the formation of tri- and tetrahydrates have not been confirmed.M. T. Saug ...
with the phosphine. *The phosphine-borane H3BPMePh2 prepared by treating the phosphine with borane.{{cite book , doi=10.1002/9780470132463.ch29, chapter=Methyldiphenylphosphine-Borane and Dimethylphenylphosphine-Borane, series =Inorganic Syntheses, year=1974, last1=Mathur, first1=M. A., last2=Myers, first2=W. H., last3=Sisler, first3=H. H., last4=Ryschkewitsch, first4=G. E., title=Inorganic Syntheses, pages=128โ€“133, volume=15, isbn=9780470132463


References

Tertiary phosphines Phenyl compounds