| Literature DB >> 27654835 |
Jakub Hyvl1, Wesley Y Yoshida1, Arnold L Rheingold2, Russell P Hughes3, Matthew F Cain1.
Abstract
The trapping of a phosphinidene (R-P) in an NCN pincer is presented. Stabilized phosphinidene 1 was characterized by 31 P{1 H}, 1 H, and 13 C{1 H} NMR spectroscopy, exhibiting an averaged C2v symmetry in solution between -60 and 60 °C. In the solid state, the phosphinidene is coordinated by one adjacent N atom featuring a formal P-N bond (1.757(2) Å) to give a five-membered ring with some aromatic character, confirmed by DFT calculations (B3LYP-D3/6-311G**++) to be the ground-state structure. Equilibration of the two N ligands occurs rapidly in solution via a "bell-clapper"-type process through an associative symmetric transition state calculated to lie 4.0 kcal mol-1 above the ground state.Entities:
Keywords: NCN ligands; VT NMR spectroscopy; azaphospholes; phosphinidenes; pincer ligands
Year: 2016 PMID: 27654835 DOI: 10.1002/chem.201604415
Source DB: PubMed Journal: Chemistry ISSN: 0947-6539 Impact factor: 5.236