Infrared Laser Spectroscopy of Mass-Selected Carbocations

被引:104
作者
Duncan, Michael A. [1 ]
机构
[1] Univ Georgia, Dept Chem, Athens, GA 30602 USA
基金
美国国家科学基金会;
关键词
STABLE CARBONIUM-IONS; FIELD IONIZATION-PHOTOELECTRON; MOLECULAR-ORBITAL THEORY; POLYCYCLIC AROMATIC-HYDROCARBONS; PROTONATED BENZENE DIMER; AB-INITIO CALCULATIONS; TERT-BUTYL CATION; GAS-PHASE; IR-SPECTRA; VIBRATIONAL SPECTROSCOPY;
D O I
10.1021/jp309037d
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Small carbocations are of longstanding interest in mass spectrometry, organic chemistry and astrophysics, but there are few measurements of their spectroscopy in the gas phase. Of existing infrared measurements, few are available across the full range of IR frequencies. In new work described here, a pulsed-discharge supersonicnozzle ion source produces higher densities of carbocations at low temperatures (20-100 K). Mass-selected photodissociation spectroscopy and the method of rare gas "tagging", together with new broadly tunable infrared OPO lasers, produce IR spectra for a variety of small carbocations including C2H3+, C2H5+, C3H3+, C3H5+, the tert-butyl cation, protonated benzene, and protonated naphthalene. Spectra in the frequency range 600-4500 cm(-1) provide new IR data for these ions and evidence for the presence of coexisting isomeric structures (e.g., C3H3+ is present as both cyclopropenyl and propargyl). Protonated naphthalene has bands at 6.2, 7.7, and 8.6 mu m matching prominent features in the interstellar unassigned infrared (UIR) emission spectra.
引用
收藏
页码:11477 / 11491
页数:15
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