AB INITIO STUDY OF THE NP $(N=3-5)$ AND $4S-3D$ RYDBERG COMPLEXES OF ACETYLENE

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1996

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Ohio State University

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Large scale internally-contracted MRCI calculations have been performed on the singlet states arising from the np (n=3-5) and 4s-3d Rydberg complexes of acetylene. Term energies are predicted with an accuracy of about 0.05 eV, leading to a reliable energy scale helpful for the interpretation of MPI $spectra^{a}$. The Rydberg-valence and 4s-3d mixings are quantified from the analysis of the wave functions, and the corresponding anisotropy of the ionic core along the Rydberg series is discussed. Quantum defect values are reported. The calculations also investigate the region of the potential energy surfaces where the whole np series is crossed by doubly excited singlet valence states, namely by the $C^{t}$ $^{1}A_{g}$ $state^{b}$. This region corresponds to intermediate geometries between those of the llinear ground state and of the trans bent $C^{0}$ state, i.e. around $R_{CC} = 1.4$ \AA and $HCC = 140^{\circ}$. The predissociative features of both the $C_{t}$ and the np Rydberg states are explained from the high degree of Rydberg valence mixing in this region.

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$^{a}$ J. H. Fillion, A. Campos, J. Pedersen, N. Shafizadeh and D. Gauyacq, to be published. $^{b}$ J. Li\'{e}vin, J. Mol. Spectrosc. 156, 123 (1992)
Author Institution: Laboratoire de Chimie Physique Mol\'{e}culaire, Universit\'{e} Libre de Bruxelles

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