High-resolution photoelectron imaging of cryogenically cooled α- and β-furanyl anions

被引:8
作者
DeVine, Jessalyn A. [1 ]
Weichman, Marissa L. [1 ]
Lyle, Steven J. [1 ]
Neumark, Daniel M. [1 ,2 ]
机构
[1] Univ Calif Berkeley, Dept Chem, Berkeley, CA 94720 USA
[2] Lawrence Berkeley Natl Lab, Div Chem Sci, Berkeley, CA 94720 USA
基金
美国国家科学基金会;
关键词
Photoelectron spectroscopy; Velocity-map imaging; Aromatic heterocycle; Radical; Furan; ANGULAR-DISTRIBUTIONS; ELECTRONIC-STRUCTURE; NEGATIVE-IONS; PYROLYSIS; PHOTODETACHMENT; SPECTROSCOPY; RADICALS; 2,5-DIMETHYLFURAN; DISSOCIATION; CONVERSION;
D O I
10.1016/j.jms.2016.09.002
中图分类号
O64 [物理化学(理论化学)、化学物理学]; O56 [分子物理学、原子物理学];
学科分类号
070203 ; 070304 ; 081704 ; 1406 ;
摘要
Isomer-specific, high-resolution photoelectron spectra of alpha- and beta-furanyl obtained via slow electron velocity-map imaging of cryogenically cooled anions are reported. The spectra yield electron affinities of 1.8546(4) and 1.6566(4) eV for the alpha-and beta-furanyl neutral radicals, respectively. New vibronic structure is resolved and assigned based on density functional theory and Franck-Condon simulations, providing several vibrational frequencies for the ground electronic state of both neutral isomers. Subtle differences in orbital hybridization resulting from varying proximity of the deprotonated carbon to the heteroatom are inferred from photoelectron angular distributions, and the C-beta-H bond dissociation energy is estimated from a combination of experimental and theoretical results to be 119.9(2) kcal mol(-1). (C) 2016 Elsevier Inc. All rights reserved.
引用
收藏
页码:16 / 21
页数:6
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