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Updated: Nov 2, 2025

Isolating Free Carbenes, their Mixed Dimers and Organic Radicals
Published on: April 19, 2019
Isolation of singlet carbene derived 2-phospha-1,3-butadienes and their sequential one-electron oxidation to radical
Mahendra K Sharma1, Sebastian Blomeyer1, Timo Glodde1
1Molecular Inorganic Chemistry and Catalysis, Inorganic and Structural Chemistry, Center for Molecular Materials, Faculty of Chemistry, Universität Bielefeld Universitätsstrasse 25 Bielefeld D-33615 Germany rghadwal@uni-bielefeld.de.
Abstract:
A synthetic strategy for the 2-phospha-1,3-butadiene derivatives [{(IPr)C(Ph)}P(cAACMe)] (3a) and [{(IPr)C(Ph)}P(cAACCy)] (3b) (IPr = C{(NDipp)CH}2, Dipp = 2,6-iPr2C6H3; cAACMe = C{(NDipp)CMe2CH2CMe2}; cAACCy = C{(NDipp)CMe2CH2C(Cy)}, Cy = cyclohexyl) containing a C[double bond, length as m-dash]C-P[double bond, length as m-dash]C framework has been established. Compounds 3a and 3b have a remarkably small HOMO-LUMO energy gap (3a: 5.09; 3b: 5.05 eV) with a very high-lying HOMO (-4.95 eV for each). Consequently, 3a and 3b readily undergo one-electron oxidation with the mild oxidizing agent GaCl3 to afford radical cations [{(IPr)C(Ph)}P(cAACR)]GaCl4 (R = Me 4a, Cy 4b) as crystalline solids. The main UV-vis absorption band for 4a and 4b is red-shifted with respect to that of 3a and 3b, which is associated with the SOMO related transitions. The EPR spectra of compounds 4a and 4b each exhibit a doublet due to coupling of the unpaired electron with the 31P nucleus. Further one-electron removal from the radical cations 4a and 4b is also feasible with GaCl3, affording the dications [{(IPr)C(Ph)}P(cAACR)](GaCl4)2 (R = Me 5a, Cy 5b) as yellow crystals. The molecular structures of compounds 3-5 have been determined by X-ray diffraction and analyzed by DFT calculations.
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