摘要

The first complete set of homologous alkynyl chalcoether complexes, isolated as the structurally characterized salts [W(eta(2)-(PrEC)-Pr-i equivalent to CPh)(CO)(2)(Tp*)]BF4 (A = O, S, Se, Te; Tp* = hydrotris(dimethylpyrazolyl) borate), result from the reactions of the free alkynes (PrEC)-Pr-i equivalent to CPh with [WI(CO)(3)(Tp*)] in the presence of AgBF4. The neutral complex [W(eta(2)-(PrSeC)-Pr-i equivalent to CPh)Cl(CO)(Tp*)] is obtained from the reaction of [W(eta(2)-(PrSeC)-Pr-i equivalent to CPh)(CO)(2)(Tp*)]BF4 with [(Bu4N)-Bu-n]Cl and co-exists in two forms in solution as a result of slow rotational isomerism of the alkyne. Depending on the choice of solvent, either pure rotamer may be crystallised.

  • 出版日期2017-2-1