A combined experimental and theoretical study on realizing and using laser controlled torsion of molecules
arXiv:0903.4463 · doi:10.1063/1.3149789
Abstract
It is demonstrated that strong laser pulses can introduce torsional motion in the axially chiral molecule 3,5-diflouro-3',5'-dibromo-biphenyl (DFDBrBPh). A nanosecond laser pulse spatially aligns the stereogenic carbon-carbon (C-C) bond axis allowing a perpendicularly polarized, intense femtosecond pulse to initiate torsional motion accompanied by a rotation about the fixed axis. We monitor the induced motion by femtosecond time-resolved Coulomb explosion imaging. Our theoretical analysis corroborates the experimental findings and on the basis of these results we discuss future applications of laser induced torsion, viz., time-resolved studies of de-racemization and laser controlled molecular junctions based on molecules with torsion.
10 pages, 9 figures, 2 tables; submitted to J. Chem. Phys.;
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Cited by in corpus (10)
- Quantum control of molecular rotation
- Manipulation of Molecules with Electromagnetic Fields
- Control and femtosecond time-resolved imaging of torsion in a chiral molecule
- Ionization of 1D and 3D oriented asymmetric top molecules by intense circularly polarized femtosecond laser pulses
- Motor effect in electron transport through a molecular junction with torsional vibrations
- Topology of surfaces for molecular Stark energy, alignment and orientation generated by combined permanent and induced electric dipole interactions
- Supersymmetry and eigensurface topology of the spherical quantum pendulum
- Directional properties of polar paramagnetic molecules subject to congruent electric, magnetic and optical fields
- Torsional and rotational coupling in non-rigid molecules
- Electron-transport properties of ethyne-bridged diphenyl zinc-porphyrin molecules