Nickel complexes antimony ligands

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. 

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. 

Adducts of the l,2-dithiole-3-thione with silver nitrate and copper dichloride have been described, and for various l,2-dithiole-3-thiones, adducts containing iron, cobalt, nickel, and copper have been studied in more detail. The ligands (L) used are either unsubstituted l,2-dithiole-3-thione or its methyl- or aryl-substituted derivatives. If X represents a halogen atom, the following types of coordination compounds have been characterized CuXLj and CuXLa, FeXjLj, CoXaL, and NiX Lj. Complexes of titanium(III), tin(IV), antimony(III) and (V), and bismuth(III) have also been studied. ... 

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