Hydrogen-Bonded π Complexes between Phosphaethyne and Hydrogen Chloride.

The highly labile complexes between phosphaethyne (HCP) and hydrogen chloride (HCl) with 1:1 and 1:2 stoichiometries have been generated in Ar and N 2 matrices at 10 K through laser photolysis of the molecular precursors 1-chlorophosphaethene (CH 2 PCl) and dichloromethylphosphine (CH 3 PCl 2 ), respectively. The IR spectrum of the 1:1 complex suggests the preference of a single "T-shaped" structure in which HCl acts as the hydrogen donor that interacts with the electron-rich C≡P triple bond. In contrast, three isomeric structures for the 1:2 complex bearing a core structure of the "T-shaped" 1:1 complex are present in the matrix. The spectroscopic identification of these rare HCP π-electron complexes is supported by D-isotope labeling and the quantum chemical calculations at the CCSD(T)-F12a/cc-pVTZ-F12 level of theory.