Charge-tagged N-heterocyclic carbenes

被引:29
|
作者
Corilo, Yuri E. [1 ]
Nachtigall, Fabiane M. [1 ]
Abdelnur, Patricia V. [1 ]
Ebeling, Gunter [2 ]
Dupont, Jairton [2 ]
Eberlin, Marcos N. [1 ]
机构
[1] Univ Estadual Campinas, Inst Chem, ThoMSon Mass Spectrometry Lab, UNICAMP, BR-13083970 Campinas, SP, Brazil
[2] Univ Fed Rio Grande do Sul, Inst Chem, Lab Mol Catalysis, BR-91501970 Porto Alegre, RS, Brazil
基金
巴西圣保罗研究基金会;
关键词
IMIDAZOLIUM IONIC LIQUIDS; ELECTROSPRAY-IONIZATION MASS; GAS-PHASE; MECHANISM; SPECTROMETRY; STABILITY; COMPLEXES; CATIONS; PROBES; SALTS;
D O I
10.1039/c1ra00024a
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The interception, formation and characterization of the first stable, long lived charge-tagged N-heterocyclic carbenes of the general type 4(x+) (x = 1-3) and analogues is reported. Via ESI(+)-MS of solutions of bromine salts of doubly, triply and quadruply charged imidazolium ion IL (3. Br-n, n = 2-4), the isolated 4(x+) as well as charged aggregates [3.Br(n-x)](x+) likely to be participating in the [3.Br(n-x)](x+) reversible arrow 4(x+) + HBr solution equilibrium could be transferred and characterized in the gas phase. Mimicking the solution equilibrium, the gaseous [3.Br(n-x)](x+) were found to dissociate nearly exclusively via HBr loss during thermal activation via collisions to form gaseous 4(x+), which were found to add to acrolein and acetone.
引用
收藏
页码:73 / 78
页数:6
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