DIMERIZATION OF THE KETENE CATION RADICAL IN THE GAS-PHASE

被引：5
|
作者：
DASS, C
机构：
[1] Department of Chemistry, University of Nebraska, Lincoln, Nebraska
来源：
RAPID COMMUNICATIONS IN MASS SPECTROMETRY | 1993年 / 7卷 / 01期
关键词：
D O I：
10.1002/rcm.1290070120
中图分类号：
Q5 [生物化学];
学科分类号：
071010 ; 081704 ;
摘要：
The dimerization of the ketene cation radical was investigated by using tandem mass spectrometry. Ketene was ionized by low-energy charge-exchange with CS2+. reagent ions. The high-pressure environment in the ion source permits collisional stabilization of the ion/molecule adduct, which was characterized by obtaining its collisionally activated dissociation (CAD) mass spectrum. Comparison with the CAD spectrum of diketene+. revealed that the structure of the adduct is identical with that of the ionized diketene species. The singly occupied molecular orbital-lowest unoccupied molecular orbital (SOMO-LUMO) interaction was invoked to explain the formation of the ion/molecule adduct.
引用
收藏
页码：95 / 98
页数：4
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