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Phosphorus, arsenic, and antimony donor ligands

Phosphorus, arsenic, and antimony donor ligands. A general synthesis has been reported for trialkyl phosphite complexes of noble metals, including [RuLeJ, [RuXLsl, and [RuHLs]+ [L = P(OMe)3 or P(OEt)3 X = Cl or Br]. The complexes were isolated as their tetraphenylborate salts from reaction of the phosphite with methanolic solutions of suitable labile olefin [Pg.361]


C. A. McAuliffe and W. Levason, Phosphine, Arsine and Stibine Complexes of the Transition Elements, Elsevier, Amsterdam, 1979, 546 pp. A review with over 2700 references. See also C. A. McAuliffe (ed,), Transition-Metal Complexes of Phosphorus, Arsenic and Antimony Donor Ligands, Macmillan, London, 1972,... [Pg.494]

S.2.4.2.4. Complexes of Mercury(l) with Phosphorus-, Arsenic-and Antimony-Donor Ligands. [Pg.520]

Platinum(II) Complexes with Phosphorus-, Arsenic-, and Antimony-donor Ligands 706... [Pg.673]

COMPLEXES OF GOLD(I) WITH PHOSPHORUS, ARSENIC AND ANTIMONY DONOR LIGANDS... [Pg.881]

Transition-metal complexes of Phosphorus, Arsenic, and Antimony Donor Ligands , ed. C. A. McAuliffe. McMillan, London, 1973. [Pg.328]

Although trialkyl- and triarylbismuthines are much weaker donors than the corresponding phosphorus, 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]

Complexes with Ligands Containing Phosphorus, Arsenic and Antimony as Donor Atoms 106... [Pg.2]

The most common nickel(O) complexes are those containing phosphorus, arsenic and antimony as donor atoms. Besides the Malatesta and Cenini book/1 which specifically deals with metal(O) complexes, nickel(O) complexes have been summarized in books and review articles which report complexes with phosphine, arsine and stibine ligands.31-37 Actually the nickel(O) complexes with these ligands amount to hundreds and the number of new complexes which are synthesized is increasing very rapidly, making nickel(0) phosphine chemistry a very extensive topic. [Pg.8]

Chiswell, B. Chemistry of multidentate ligands containing heavy Group VA donors. Transition Metal Complexes of Phosphorus, Arsenic and Antimony Ligands. McAuliffe, C. A., Ed., Macmillan London, Chapter 4, 1973, 269-307. [Pg.390]

S. D. Robinson Transition metal complexes containing phosphorus, arsenic, antimony and bismuth donor ligands. [Pg.382]

Ligands containing phosphorus, arsenic, or antimony as the donor atom do not cause disproportionation of iron carbonyls, and fairly stable, simple substitution products are obtained. The direct reaction, carried out either thermally or photochemicaUy, with any of the three iron carbonyls, has yielded the complexes [Fe(CO)4L], with L = P(C6Hs)3 12, 35, 214, 215, 125a), P[N(CHj)2]3 71), pentaphenylphosphole 216,21, As(C6Hs)j 12,... [Pg.224]


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Antimony arsenates

Antimony ligands

Arsenic Antimonial

Arsenic donor ligands

Arsenic-donors

Arsenic-phosphorus

Donor ligand

Donor phosphorus

Phosphorus and Arsenic

Phosphorus and arsenic donor ligands

Phosphorus and arsenic ligands

Phosphorus, donor ligands

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