P4 functionalization by hydrides: direct synthesis of P-H bonds

Chem Commun (Camb). 2016 Apr 14;52(29):5179-82. doi: 10.1039/c6cc01683a. Epub 2016 Mar 21.

Abstract

A direct method for white phosphorus functionalization by hydride sources is presented. Excess BH4(-) in n-butylamine produces HP4(-) as the major P-containing species. Reaction with LiBEt3H forms the borane-stabilized phosphanide Li(PH2)(BEt3)2, which may be used to synthesize various phosphines. Triethylborane may be replaced by BH3, resulting in the formation of LiPH2(BH3)2.

Publication types

  • Research Support, Non-U.S. Gov't