Dynamics and Coordination of a P₂N₂ Ligand – from Twisted Conformation to Chelation

Abstract

Based on their general spacial flexibility, their Lewis and Brønsted basicity, and ability to mimic second sphere effects the 1,5‐diaza‐3,7‐diphosphacyclooctane ligand family and their complexes have re‐gained substantial scientific interest. It was now possible to structurally analyze a recently reported member of this family with p‐tolyl and t‐butyl substituents on P and N, respectively, (P2p‐tolN2tBu). Notably, the ligand crystallizes with a ‘twisted’ backbone. This compound is the very first of its kind to have been unambiguously characterized with regard to its chemical and molecular structure as being in this conformation. A temperature‐dependent NMR study provides insight into the molecular dynamics of two isomers in solution, which are most likely also both twisted, as judged by the observed limited reactivity. Despite the in principle unfavorable conformation of the free ligand, it was successfully chelated to tungsten and molybdenum centers in mononuclear carbonyl complexes. The ligand, a derivative thereof and four new complexes were comprehensively characterized and analyzed in comparison. This includes single crystal XRD molecular structures of P2p‐tolN2tBu and all four complexes. P2p‐tolN2tBu, regardless of its twisted conformation, is able to coordinate to metal centers given that enough energy (heat) for a conformational change is provided.