Department of Chemistry, 6128 Burke Laboratories, Dartmouth College, Hanover, New Hampshire 03755, USA.
Dalton Trans. 2011 Jan 7;40(1):47-55. doi: 10.1039/c0dt01006e. Epub 2010 Nov 17.
A family of group 6 transition metal complexes M(C(5)R(5))(CO)(2)(CF) [M = Cr, Mo, W; R = H, Me] with terminal fluoromethylidyne ligands have been synthesized through the reduction of the corresponding trifluoromethyl precursors with potassium graphite or magnesium graphite. They have been characterized spectroscopically and in some cases crystallographically, although the structures show disorder between the CO and CF ligands. The M[triple bond]CF subunit reacts as a triple bond to form cluster complexes containing μ(3)-CF ligands on reaction with Co(2)(CO)(8). Computational (DFT/NBO/NRT) studies on M(C(5)H(5))(CO)(2)(CF) [M = Cr, Mo, W] and the corresponding cationic fragments M(CO)(2)(XY)(+) illustrate significant differences in the metal-ligand bonding between CF and its isoelectronic analogue NO, as well as with its hydrocarbon analogue CH.
一个 6 族过渡金属配合物家族 M(C(5)R(5))(CO)(2)(CF) [M = Cr, Mo, W; R = H, Me],具有终端氟甲叉配体,通过用钾石墨或镁石墨还原相应的三氟甲基前体而合成。它们已经通过光谱学和在某些情况下晶体学进行了表征,尽管结构显示 CO 和 CF 配体之间存在无序。M[三重键]CF 亚基反应为三重键,与 Co(2)(CO)(8)反应形成含有 μ(3)-CF 配体的簇配合物。对 M(C(5)H(5))(CO)(2)(CF) [M = Cr, Mo, W] 和相应的阳离子片段 M(CO)(2)(XY)(+)的计算(DFT/NBO/NRT)研究表明,CF 与其等电子类似物 NO 以及与其烃类似物 CH 之间的金属-配体键存在显著差异。