Photoionization study of L-valine in the gas phase by vacuum ultraviolet synchrotron radiation

被引:5
作者
Zhou, Shaohui
Chu, Genbai
Cao, Lanlan
Shan, Xiaobin
Liu, Fuyi
Han, Ju-Guang
Sheng, Liusi [1 ]
机构
[1] Univ Sci & Technol China, Natl Synchrotron Radiat Lab, Hefei 230029, Anhui, Peoples R China
基金
中国国家自然科学基金;
关键词
photoionization mass spectrometry (PIMS); photoionization efficiency spectrum (PIE); L-vatine; hydrogen migration; formation pathway; AMINO-ACIDS; GLYCINE; ORIGIN;
D O I
10.1255/ejms.1127
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
The photoionization and photodissociation of L-valine are studied by tunable synchrotron vacuum ultraviolet photoionization mass spectrometry at the photon energy of 13 eV. The ionization energy of L-valine and the appearance energies of major fragments are measured by the photoionization efficiency spectrum in the photon energy range of 8-11 eV. Possible formation pathways of the major fragments, NH2CHC(OH)(2)(+) (m/z=75), NH2(CH3)(2)(CH)(2)(+) (m/z=72) and NH2CHCO+ (m/z=57), are discussed in detail with the theoretical calculations at the B3LYP/6-31++G (d, p) level. Hydrogen migration is considered as the key way for the formation of NH2CHC(OH)(2)(+) (m/z= 75) and NH2CHCO+(m/z= 57). Furthermore, other fragments, NH2CHCOOH+(m/z= 74), (CH3)(2)(CH)(2)(+) (m/z= 56), C4H7+ (m/z= 55), NH2CHOH+ (m/z=46), NH2CH2+ (m/z= 30) and m/z= 18, species are also briefly described.
引用
收藏
页码:101 / 112
页数:12
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