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Arsine triphenyl-, complexes with

The [NdL4(C104)2]C104 complex has both ionic and bound perchlorate [218]. With L = triphenyl arsine oxide the complex types formed are [215] Ln(NCS)3L3, Ln(N03)3L2 Et0H, Ln(N03)3L3, Ln(NC>3)3L4. Triphenyl arsine oxide complexes appear to be stronger than the phosphine oxide based on the higher dipole moment of arsine. [Pg.295]

Bis-3,4-(trifluoromethyl)-l,2-diselenete 651 is prepared by refluxing selenium with hexafluoro-2-butyne. It reacts with triphenylphosphine and triphenyl-arsine. Triphenylphosphine selenide was isolated, but no other compounds were identified.Ring-opened complexes with nickel, copper, vanadium, molybdenum (652), tungsten, iron, and cobalt are analogous to complexes of the 1,2-dithiete (527) (Section XXXV.2.C.). [Pg.672]

With the ligand dbp similar reactions yielded CoCl(dbp)3 and Co(dbp)4, but no Co(BH4)(dbp)3. Triphenyl-arsine and -stibine and CoCl2 were reduced to black products, probably cobalt metal. From NaBH3CN is afforded a Co(BH3CN)(Ph2-PCH2CH2PPh2) complex, but this does not subsequently yield a dinitrogen complex. [Pg.223]

Chromium hexacarbonyl reacts with Ph2AsCH2AsPh2 yielding a compound of stoichiometry Cr(CO)2(Ph2AsCH2AsPh2) 357) and with triarylphosphines yielding complexes of the type [Cr(CO)2L]2 [L = PPhg, P( i-tolyl)3, and P(p-tolyl)3] (31). The arsine and triphenyl-phosphine compounds have been shown by X-ray analysis to possess the structures (VII) and (VIII), respectively, in which a phenyl group is... [Pg.83]

Grundnes, J., Klaeboe, P. and Plahte, E. (1967) Spectroscopic studies of charge transfer complexes. XV. Triphenyl arsine oxide with iodine and iodine cyanide. Sel. Top. Struct. Chem., 265-275. [Pg.316]


See other pages where Arsine triphenyl-, complexes with is mentioned: [Pg.169]    [Pg.169]    [Pg.352]    [Pg.616]    [Pg.1117]    [Pg.17]    [Pg.139]    [Pg.225]    [Pg.32]    [Pg.5]   


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