Carl Elena, Stalke Dietmar
Institut für Anorganische Chemie, Georg-August-Universität, Tammannstrasse 4, 37077 Göttingen (Germany).
Chemistry. 2014 Nov 24;20(48):15849-54. doi: 10.1002/chem.201404860. Epub 2014 Oct 3.
Herein, new complexes containing the Ph2PCH2S(NtBu)3 anion are presented, supplying three imido nitrogen atoms and a remote phosphorus atom as potential donor sites to main group and transition-metal cations. The lithiated complex [(tmeda)Li{(NtBu)3SCH2PPh2}] (1) is an excellent starting material in transmetalation reactions. Herein, the transition-metal complexes [M{(NtBu)3SCH2PPh2}2] (M=Mn (2), Ni (3), Zn (4)) were synthesized and structurally characterized. Their isotypical molecules show SN2 chelation and no employment of the adjacent phosphorus atom in coordination. The third pendent imido group is always twisted toward the vacant face of the tetrahedrally coordinated sulfur atom.
本文报道了含有Ph2PCH2S(NtBu)3阴离子的新型配合物,该配合物提供了三个亚氨基氮原子和一个远程磷原子作为主族和过渡金属阳离子的潜在供体位点。锂化配合物[(tmeda)Li{(NtBu)3SCH2PPh2}] (1)是金属转移反应中一种优良的起始原料。在此,合成并对过渡金属配合物[M{(NtBu)3SCH2PPh2}2] (M = Mn (2)、Ni (3)、Zn (4))进行了结构表征。它们的同型分子显示出SN2螯合作用,且配位过程中未使用相邻的磷原子。第三个悬垂亚氨基基团总是朝着四面体配位硫原子的空面扭曲。