Benchmark study of molecules with large-amplitude ring-twisting motion: accurate equilibrium structure of succinic anhydride from gas electron diffraction data and coupled-cluster computations

The gas electron diffraction (GED) study of succinic anhydride (dihydro-2,5-furandione) is used as a benchmark example for the reliable determination of the structure of floppy molecules with saturated non-rigid ring. According to results of B3LYP calculations, the molecule has a planar skeleton (C2v total symmetry), whereas the MP2 optimized structure has a non-planar ring with the torsional angle φ(C–C–C–C) of up to 11° (C2 symmetry). It has been revealed that the increase in the quality of ab initio calculations up to CCSD(T) level and the enlargement of basis set up to quadruple-ζ size decrease the non-planarity of the molecular skeleton, which is approximated to be planar in the best-estimated ab initio structure. The semiexperimental equilibrium structure (rese\documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{mathrsfs} \usepackage{upgreek} \setlength{\oddsidemargin}{-69pt} \begin{document}$$r_{\text{e}}^{\text{se}}$$\end{document}) has been determined from the GED data with the application of the so-called dynamic (pseudo-conformer) model describing the large-amplitude ring-twisting motion. Vibrational corrections Δ(ra − re) to the experimental internuclear distances have been calculated from the B3LYP/cc-pVTZ quadratic and cubic force constants. The best-estimated ab initio structure agrees well with the rese\documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{mathrsfs} \usepackage{upgreek} \setlength{\oddsidemargin}{-69pt} \begin{document}$$r_{\text{e}}^{\text{se}}$$\end{document} structure. This fact points to the reliability and a high accuracy of both experimental data and applied theory.