Precursors for the Development of π‐Conjugated Low‐Coordinate Phosphorus Compounds

Abstract

The synthesis of a novel monomeric precursor and its butadiyne-bridged dimeric form for the preparation of novel πconjugated organophosphorus compounds is presented. The precursors are synthesized from commercially available starting materials, and based on a Dmp (2,6-dimesitylphenyl) group for kinetic stabilization of the P-functionality, a bromo substituent for the introduction of the phosphorus center, and an acetylene unit at the para position of the Dmp moiety. Such acetylenic units are synthetically versatile, and can be explored for the construction of larger phosphorus-containing π-conjugates. The precursors are utilized to prepare Dmp-stabilized C,C-dibromophosphaalkenes, and butadiyne-bridged dimeric species thereof. The effect of the low-coordinate phosphorus centers and the extent of π-conjugation on the spectroscopic and electronic properties is evaluated by NMR and UV/Vis spectroscopy, as well as cyclic voltammetry. In addition to the phosphaalkenes, the successful syntheses of two new diphosphenes are presented, indicating a broad applicability of the precursor.