期刊
JOURNAL OF PHYSICAL CHEMISTRY A
卷 120, 期 27, 页码 5389-5398出版社
AMER CHEMICAL SOC
DOI: 10.1021/acs.jpca.6b02410
关键词
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资金
- Italian Ministry for Education, Univ. and Research, MIUR [RBFR132WSM_003, RBSI14U3VF]
- Ministry of Science and Technology, Taiwan [NSC 102-2113-M-002-009-MY3]
- Grants-in-Aid for Scientific Research [26248006] Funding Source: KAKEN
Molecular orientation is a fundamental requisite in the study of stereodirected dynamics of collisional and photoinitiated processes. In this past decade, variable hexapolar electric filters have been developed and employed for the rotational-state selection and the alignment of molecules of increasing complexity, for which the main difficulties are their mass, their low symmetry, and the very dense rotational manifold. In this work, for the first time, a complex molecule such as 2-bromobutane, an asymmetric top containing a heavy atom (the bromine), was successfully oriented by a weak homogeneous field placed downstream from the hexapolar filter. Efficiency of the orientation was characterized experimentally, by combining time-of flight measurements and a slice-ion-imaging detection technique. The application is described to the photodissociation dynamics of the oriented 2-bromobutane, which was carried out at a laser wavelength of 234 nm, corresponding to the breaking of the C-Br bond. The Br photofragment is produced in both the ground Br (P-2(3/2)) and the excited Br (P-2(1/2)) electronic states, and both channels are studied by the slice imaging technique, revealing new features in the velocity and angular distributions with respect to previous investigations on nonoriented molecules.
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