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Isolation of Neutral, Mono‐, and Dicationic B 2 P 2 Rings by Diphosphorus Addition to a Boron−Boron Triple Bond
Author(s) -
Brückner Tobias,
Fantuzzi Felipe,
Stennett Tom E.,
Krummenacher Ivo,
Dewhurst Rian D.,
Engels Bernd,
Braunschweig Holger
Publication year - 2021
Publication title -
angewandte chemie international edition
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.831
H-Index - 550
eISSN - 1521-3773
pISSN - 1433-7851
DOI - 10.1002/anie.202102218
Subject(s) - dication , chemistry , boron , singlet state , triple bond , counterion , ring (chemistry) , crystallography , planarity testing , double bond , stereochemistry , ion , medicinal chemistry , photochemistry , excited state , polymer chemistry , atomic physics , organic chemistry , physics
The NHC‐stabilised diboryne (B 2 (SIDep) 2 ; SIDep=1,3‐bis(2,6‐diethylphenyl)imidazolin‐2‐ylidene) undergoes a high‐yielding P−P bond activation with tetraethyldiphosphine at room temperature to form a B 2 P 2 heterocycle via a diphosphoryldiborene by 1,2‐diphosphination. The heterocycle can be oxidised to a radical cation and a dication, respectively, depending on the oxidant used and its counterion. Starting from the planar, neutral 1,3‐bis(alkylidene)‐1,3‐diborata‐2,4‐diphosphoniocyclobutane, each oxidation step leads to decreased B−B distances and loss of planarity by cationisation. X‐ray analyses in conjunction with DFT and CASSCF/NEVPT2 calculations reveal closed‐shell singlet, butterfly‐shaped structures for the NHC‐stabilised dicationic B 2 P 2 rings, with their diradicaloid, planar‐ring isomers lying close in energy.