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Søren Vrønning Hoffmann

The photoelectron spectra of the isomeric 1-and 2-methyltetrazoles; their equilibrium structures and vibrational analysis by ab initio calculations

Publikation: Bidrag til tidsskrift/Konferencebidrag i tidsskrift /Bidrag til avisTidsskriftartikelForskningpeer review

  • Michael H. Palmer, Univ Edinburgh, University of Edinburgh, Sch Chem
  • ,
  • Marcello Coreno, CNR, Istituto di Struttura della Materia (ISM-CNR), Consiglio Nazionale delle Ricerche (CNR), ISM, LD2 Unit
  • ,
  • Monica de Simone, CNR, Consiglio Nazionale delle Ricerche (CNR), Istituto Officina dei Materiali (IOM-CNR), Lab TASC, IOM
  • ,
  • Cesare Grazioli, CNR, Istituto di Struttura della Materia (ISM-CNR), Consiglio Nazionale delle Ricerche (CNR), ISM, LD2 Unit
  • ,
  • Soren Vronning Hoffmann
  • Nykola C. Jones
  • Kirk A. Peterson, Washington State Univ, Washington State University, Dept Chem
  • ,
  • R. Alan Aitken, Univ St Andrews, University of St Andrews, Sch Chem
  • ,
  • Cecile Rouxel, Univ St Andrews, University of St Andrews, Sch Chem

New synchrotron based studies of the photoelectron ionization spectra (PES) for the isomeric 1- and 2-methyltetrazoles (1- and 2-MeTet) show markedly higher resolution than previous reports. The unusual spectral profiles suggest that a considerable overlay of the ionic states occurs for both molecules. Under these circumstances of near degeneracy of two or more ionic states, mutual annihilation of vibrational fine structure occurs for all except the strongest vibrational states; the PES just reflects the resultants rather than full spectra. Theoretical determination of the adiabatic ionization energies (AlEs) proved a challenge; the most successful method was second order Moller-Plesset perturbation theory (MP2). These calculations suggest that the lowest PES bands for both isomers contain ionization both from lone pair sigma-orbitals ((2)A') on the N-atoms (LPN) and pi-orbitals ((2)A ''). The lowest experimental AIEs are as follows: 1-MeTet is 10.315 eV assigned to 1 2 A', while 2-MeTet is 10.543 eV assigned to 1(2)A ''. Franck-Condon analysis shows that the lowest ionization energy regions of both spectra are dominated by IE from the LPN (2)A' manifold, even though the (2)A '' states have a higher absolute intensity. In this example, we have utilized a VUV Rydberg state to assist simplification of the PES; more frequently, the PES assignment is simpler and assists the location of Rydberg states in the VUV. The very slow spectral onset for 2-MeTet demonstrates the importance of vertical ionization energy calculations since maxima are more readily measured than slow onsets. These were performed at the equilibrium structure of the X(1)A' state, using both multi-reference multiroot configuration interaction and the ionization potential variant of the equations-of-motion coupled cluster method, with single and double excitations (EOMIP-CCSD). This enabled the principal ionization bands to be identified over a wider range of energy. Attempts to study the higher ionic states by EOMIP-CCSD showed that several states of each symmetry are close to degenerate for 1-MeTet, in particular. A multi-configuration self-consistent field study confirmed the small separation of ionic states, but state switching during the optimization process largely disabled this method. Published by AIP Publishing.

TidsskriftJournal of Chemical Physics
Antal sider9
StatusUdgivet - 21 jul. 2018

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