State- and conformer-selected beams of aligned and oriented molecules for ultrafast diffraction studies

被引:69
作者
Filsinger, Frank [1 ]
Meijer, Gerard [1 ]
Stapelfeldt, Henrik [2 ,3 ]
Chapman, Henry N. [4 ,5 ]
Kuepper, Jochen [1 ,4 ]
机构
[1] Max Planck Gesell, Fritz Haber Inst, D-14195 Berlin, Germany
[2] Aarhus Univ, Dept Chem, DK-8000 Aarhus C, Denmark
[3] Aarhus Univ, Interdisciplinary Nanosci Ctr iNANO, DK-8000 Aarhus C, Denmark
[4] DESY, Ctr Free Electron Laser Sci, D-22607 Hamburg, Germany
[5] Univ Hamburg, D-22761 Hamburg, Germany
关键词
NONRESONANT DIPOLE FORCE; FREE-ELECTRON LASER; NUCLEIC-ACID BASES; GAS-PHASE; POLAR-MOLECULES; REACTIVE SCATTERING; NEUTRAL PARTICLES; BUILDING-BLOCKS; AMINO-ACID; FIELDS;
D O I
10.1039/c0cp01585g
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
The manipulation of the motion of neutral molecules with electric or magnetic fields has seen tremendous progress over the last decade. Recently, these techniques have been extended to the manipulation of large and complex molecules. In this article we introduce experimental approaches to the manipulation of large molecules, i.e., the deflection, focusing and deceleration using electric fields. We detail how these methods can be exploited to spatially separate quantum states and how to select individual conformers of complex molecules. We briefly describe mixed-field orientation experiments made possible by the quantum-state selection. Moreover, we provide an outlook on ultrafast diffraction experiments using these highly controlled samples.
引用
收藏
页码:2076 / 2087
页数:12
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