Chirality detection of surface desorption products using photoelectron circular dichroism

被引:4
作者
Westphal, Georg [1 ]
Wega, Johannes [1 ]
Dissanayake, Rasika E. A. [2 ]
Schaefer, Tim [1 ,3 ]
机构
[1] Georg August Univ Gottingen, Inst Phys Chem, Tammannstr 6, D-37077 Gottingen, Germany
[2] Natl Inst Fundamental Studies, Plant & Environm Sci Lab, Hantana Rd, Kandy, Sri Lanka
[3] Max Planck Inst Biophys Chem, Fassberg 11, D-37077 Gottingen, Germany
基金
美国国家科学基金会;
关键词
MULTIPHOTON IONIZATION; ENANTIOSELECTIVE ADSORPTION; MOLECULES; ENERGETICS; KINETICS; AUTOCATALYSIS; DEPENDENCE; ASYMMETRY; CHEMISTRY;
D O I
10.1063/5.0014917
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
Chirality detection of gas-phase molecules at low concentrations is challenging as the molecular number density is usually too low to perform conventional circular dichroism absorption experiments. In recent years, new spectroscopic methods have been developed to detect chirality in the gas phase. In particular, the angular distribution of photoelectrons after multiphoton laser ionization of chiral molecules using circularly polarized light is highly sensitive to the enantiomeric form of the ionized molecule [multiphoton photoelectron circular dichroism (MP-PECD)]. In this paper, we employ the MP-PECD as an analytic tool for chirality detection of the bicyclic monoterpene fenchone desorbing from a Ag(111) crystal. We record velocity-resolved kinetics of fenchone desorption on Ag(111) using pulsed molecular beams with ion imaging techniques. In addition, we measure temperature-programmed desorption spectra of the same system. Both experiments indicate weak physisorption of fenchone on Ag(111). We combine both experimental techniques with enantiomer-specific detection by recording MP-PECD of desorbing molecules using photoelectron imaging spectroscopy. We can clearly assign the enantiomeric form of the desorption product fenchone in sub-monolayer concentration. The experiment demonstrates the combination of MP-PECD with surface science experiments, paving the way for enantiomer-specific detection of surface reaction products on heterogeneous catalysts for asymmetric synthesis.
引用
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页数:9
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