Ambient-Temperature Synthesis of 2-Phosphathioethynolate, PCS-, and the Ligand Properties of ECX- (E = N, P; X = O, S)

作者：Jupp Andrew R; Geeson Michael B; McGrady John E; Goicoechea Jose M

来源：European Journal of Inorganic Chemistry, 2016, 2016(5): 639-648.

DOI：10.1002/ejic.201501075

• Coordination modes
• Ligand effects
• P ligands
• Cyanates
• Thiocyanates

A synthesis of the 2-phosphathioethynolate anion, PCS-, under ambient conditions is reported. The coordination chemistry of PCO-, PCS- and their nitrogen-containing congeners is also explored. Photolysis of a solution of W(CO)(6) in the presence of PCO- [or a simple ligand displacement reaction using W(CO)(5)(MeCN)] affords [W(CO)(5)(PCO)](-) (1). The cyanate and thiocyanate analogues, [W(CO) 5(NCO)](-) (2) and [W(CO)(5)- (NCS)](-) (3), are also synthesised using a similar methodology, allowing for an in-depth study of the bonding properties of this family of related ligands. Our studies reveal that, in the coordination sphere of tungsten(0), the PCO- anion preferentially binds through the phosphorus atom in a strongly bent fashion, while NCO- and NCS- coordinate linearly through the nitrogen atom. Reactions between PCS- and W(CO)(5)-( MeCN) similarly afford [W(CO)(5)(PCS)](-); however, due to the ambidentate nature of the anion, a mixture of both the phosphorus- and sulfur-bonded complexes (4a and 4b, respectively) is obtained. It was possible to establish that, as with PCO-, the PCS- ion also coordinates to the metal centre in a bent fashion.

• 出版日期2016-2