Abstract
AbstractThe reaction oftrans‐[M(N2)2(dppe)2] (M=Mo,1Mo, M=W,1W) with B(C6F5)3(2) provides the adducts [(dppe)2M=N=N‐B(C6F5)3] (3) which can be regarded as M/B transition‐metal frustrated Lewis pair (TMFLP) templates activating dinitrogen. Easy borylation and silylation of the activated dinitrogen ligands in complexes3with a hydroborane and hydrosilane occur by splitting of the B−H and Si−H bonds between the N2moiety and the perfluoroaryl borane. This reactivity of3is reminiscent of conventional frustrated Lewis pair chemistry and constitutes an unprecedented approach for the functionalization of dinitrogen.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have