Dugan Thomas R, Macleod K Cory, Brennessel William W, Holland Patrick L
Department of Chemistry, University of Rochester, Rochester, NY 14618, , Homepage: http://chem.rochester.edu/~plhgrp/
Eur J Inorg Chem. 2013 Aug 1;2013(22-23). doi: 10.1002/ejic.201300187.
The cooperative binding of N by late transition metals and main-group metals is a promising strategy for N-N bond weakening and activation. We report the use of activated Rieke magnesium for reduction of iron and cobalt complexes supported by bulky β-diketiminate ligands. Binding of N is accompanied by assembly of a linear M-NN-Mg-NN-M (M = Co, Fe) core with N-N bonds that are weakened, as judged by infrared spectroscopy. Both the cobalt and iron complexes require THF solvent, because of Mg-THF binding. The cobalt complex can be isolated as a pure solid, but the iron complex is stable only in solution. These results demonstrate the correlation between the binding mode and N-N weakening in heterobimetallic N complexes.
后过渡金属和主族金属对氮的协同配位是一种很有前景的使N-N键弱化和活化的策略。我们报道了使用活化的里克镁来还原由庞大的β-二酮亚胺配体支撑的铁和钴配合物。通过红外光谱判断,氮的配位伴随着一个线性M-NN-Mg-NN-M(M = Co,Fe)核心的组装,其中N-N键被弱化。由于镁与四氢呋喃(THF)的配位作用,钴和铁的配合物都需要四氢呋喃溶剂。钴配合物可以分离为纯固体,但铁配合物仅在溶液中稳定。这些结果证明了异双金属氮配合物中配位模式与N-N键弱化之间的相关性。