Intramolecular Scrambling of Aryl Groups in Organopalladium Complexes [ArPd(PPh3)2]+: From Solution to the Gas Phase, Back Again, and In-Between

被引:28
作者
Agrawal, Divya [1 ]
Zins, Emilie-Laure [1 ]
Schroeder, Detlef [1 ]
机构
[1] Acad Sci Czech Republic, Inst Organ Chem & Biochem, Prague 16610 6, Czech Republic
基金
欧洲研究理事会;
关键词
electrospray ionization; intramolecular scrambling; palladium catalysts; phosphine ligands; solution chemistry; ELECTROSPRAY MASS-SPECTROMETRY; CROSS-COUPLING REACTIONS; FORMING REDUCTIVE ELIMINATION; TRANSITION-METAL-COMPLEXES; H BOND ACTIVATION; CATALYZED C-N; COORDINATED PHOSPHINES; ORGANOMETALLIC CHEMISTRY; PALLADIUM(II) ACETATE; OXIDATIVE ADDITION;
D O I
10.1002/asia.201000086
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Gas-phase experiments are used to probe the intramolecular scrambling of aryl groups between palladium and phosphorus in organopalladium complexes, [ArPd(PPh3)(2)](+), generated by means of electrospray ionization (ESI). To this aim, ESI mass spectrometry, including tandem mass spectrometric experiments, were carried out on deuterated, non-deuterated, and substituted [ArPd(PPh3)(2)](+) complexes. The fragment ions obtained from the deuterated parent ions clearly show the occurrence of intramolecular scrambling between the aryl group bound to palladium and the phenyl groups of the phosphine in the gas phase. Fragmentation pathways, supported by a statistical model, are proposed to explain these migrations and the implications for the condensed-phase chemistry are probed experimentally by using ESI mass spectrometry.
引用
收藏
页码:1667 / 1676
页数:10
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