The Equilibrium Molecular Structure of Cyclic (Alkyl)(Amino) Carbene Copper(I) Chloride via Gas-Phase Electron Diffraction and Quantum Chemical Calculations

Alexander V Belyakov; Ekaterina P Altova; Anatoliy N Rykov; Pavel Yu Sharanov; Igor F Shishkov; Alexander S Romanov

doi:10.3390/molecules28196897

The Equilibrium Molecular Structure of Cyclic (Alkyl)(Amino) Carbene Copper(I) Chloride via Gas-Phase Electron Diffraction and Quantum Chemical Calculations

Molecules. 2023 Oct 1;28(19):6897. doi: 10.3390/molecules28196897.

Authors

Alexander V Belyakov¹, Ekaterina P Altova², Anatoliy N Rykov², Pavel Yu Sharanov², Igor F Shishkov², Alexander S Romanov³

Affiliations

¹ Saint-Petersburg State Technological Institute, 190013 Saint Petersburg, Russia.
² Department of Chemistry, Moscow State University, 119992 Moscow, Russia.
³ Department of Chemistry, University of Manchester, Oxford Rd., Manchester M13 9PL, UK.

Abstract

Copper-centered carbene-metal-halides (CMHs) with cyclic (alkyl)(amino) carbenes (CAACs) are bright phosphorescent emitters and key precursors in the synthesis of the highly promising class of the materials carbene-metal-amides (CMAs) operating via thermally activated delayed fluorescence (TADF). Aiming to reveal the molecular geometry for CMH phosphors in the absence of the intermolecular contacts, we report here the equilibrium molecular structure of the (CAAC)Cu(I)Cl (1) molecule in the gas-phase. We demonstrate that linear geometry around a copper atom shows no distortions in the ground state. The structure of complex 1 has been determined using the electron diffraction method, supported by quantum chemical calculations with RI-MP2/def2-QZVPP level of theory and compared with the crystal structure determined by X-ray diffraction analysis. Mean vibrational amplitudes, u_ij_,h1, and anharmonic vibrational corrections (r_ij_,e • r_ij_,a) were calculated for experimental temperature T = 20 °C, using quadratic and cubic force constants, respectively. The quantum theory of atoms in molecules (QTAIM) and natural bond order (NBO) analysis of wave function at MN15/def2TZVP level of theory revealed two Cu^…H, three H^…H, and one three-center H^…H^…H bond paths with bond critical points. NBO analysis also revealed three-center, four-electron hyperbonds, (3c4e), [π(N-C) n_π(Cu) ↔ n_π(N) π(N-Cu)], or [N-C: Cu ↔ N: C-Cu] and n_π(Cu) → π(C-N)* hyperconjugation, that is the delocalization of the lone electron pair of Cu atom into the antibonding orbital of C-N bond.

Keywords: carbene–metal–halide; computational; cyclic (alkyl)(amino) carbene; electron diffraction; phosphorescence.

Grants and funding

A.S.R. acknowledges the support from the Royal Society (grant nos. URF\R1\180288 and RGF\EA\181008). The article was made as part of the work entitled “Molecular and supramolecular organization of compounds, hybrid and functional materials” (Number 121031300090-2).