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Updated: Aug 11, 2025

Preparation and Reactivity of a Triphosphenium Bromide Salt: A Convenient and Stable Source of PhosphorusI
Published on: November 22, 2016
ortho-Phenylene-bridged phosphorus/silicon Lewis pairs
Lucas Wickemeyer1, Jan Schwabedissen1, Pia C Trapp1
1Lehrstuhl für Anorganische Chemie und Strukturchemie, Centrum für Molekulare Materialien CM2, Fakultät für Chemie, Universität Bielefeld, Universitätsstraße 25, 33615 Bielefeld, Germany. mitzel@uni-bielefeld.de.
Abstract:
A series of five ortho-phenylene-bridged phosphorus-silicon Lewis pairs was synthesized, with phosphorus bearing isopropyl groups while the substituents at the silicon atom vary (-CH3, -Cl, -F). Possible interactions between Lewis acid and base were investigated both experimentally (NMR, XRD) and theoretically to determine the influence of the different substituents. Calculated ortho-interaction energies (OIEs) show a stabilizing interactions between the acidic and basic units which were also found for the meta- and para-interaction energies (MIEs and PIEs, respectively), indicating stabilization resulting not from direct acid-base interaction but from electronic interactions through the ring. Further spectroscopic (NMR, XRD) and theoretical (NBO, QTAIM, SAPT) investigations confirmed the absence of direct interactions between silicon and phoshorus.
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