Valence and Ionic Lowest-Lying Electronic States of Isobutyl Formate Studied by High-Resolution Vacuum Ultraviolet Photoabsorption, Photoelectron Spectroscopy, and Ab Initio Calculations - Publication - Bridge of Knowledge

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Valence and Ionic Lowest-Lying Electronic States of Isobutyl Formate Studied by High-Resolution Vacuum Ultraviolet Photoabsorption, Photoelectron Spectroscopy, and Ab Initio Calculations

Abstract

The highest resolution vacuum ultraviolet photoabsorption spectrum of isobutyl formate, C5H10O2, yet reported is presented over the energy range 4.5−10.7 eV (275.5−118.0 nm) revealing several new spectral features. Valence and Rydberg transitions and their associated vibronic series observed in the photoabsorption spectrum have been assigned in accordance with new ab initio calculations of the vertical excitation energies and oscillator strengths. Calculations have also been carried out to determine the ionization energies and fine structure of the lowest ionic state of isobutyl formate and are compared with a newly recorded photoelectron spectrum (from 9.0 to 27.0 eV). The value of the first ionization energy was determined to be 10.508 eV (adiabatic) and 10.837 eV (vertical). New vibrational structure is observed in the first photoelectron band, predominantly resulting from C−O and CO stretches of the molecule. The photoabsorption cross sections have been used to calculate the photolysis lifetime of isobutyl formate in the upper stratosphere (20−50 km), indicating that the hydroxyl radical processes will be the main loss process for isobutyl formate.

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Category:
Articles
Type:
artykuł w czasopiśmie wyróżnionym w JCR
Published in:
JOURNAL OF PHYSICAL CHEMISTRY A no. 119, pages 8647 - 8656,
ISSN: 1089-5639
Language:
English
Publication year:
2015
Bibliographic description:
Śmiałek-Telega M., Łabuda M., Guthmuller J., Hoffmam S., Jones N., Macdonald M., Zuin L., Mason N., Limao-Vieira P.: Valence and Ionic Lowest-Lying Electronic States of Isobutyl Formate Studied by High-Resolution Vacuum Ultraviolet Photoabsorption, Photoelectron Spectroscopy, and Ab Initio Calculations// JOURNAL OF PHYSICAL CHEMISTRY A. -Vol. 119, nr. 32 (2015), s.8647-8656
DOI:
Digital Object Identifier (open in new tab) 10.1021/acs.jpca.5b06053
Verified by:
Gdańsk University of Technology

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