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Time-Resolved Photodetachment Anisotropy: Gas-Phase Rotational and Vibrational Dynamics of the Fluorescein Anion.

作者信息

Horke Daniel A, Chatterley Adam S, Bull James N, Verlet Jan R R

机构信息

†Center for Free-Electron Laser Science, DESY, Notkestrasse 85, 22607 Hamburg, Germany.

‡Ultrafast X-ray Science Laboratory, Cyclotron Road, Berkeley, California 94720, United States.

出版信息

J Phys Chem Lett. 2015 Jan 2;6(1):189-94. doi: 10.1021/jz5022526. Epub 2014 Dec 24.

Abstract

The photoelectron signal of the singly deprotonated fluorescein anion is found to be highly dependent on the relative polarization between pump and probe pulses, and time-resolved photodetachment anisotropy (TR-PA) is developed as a probe of the rotational dynamics of the chromophore. The total photoelectron signal shows both rotational and vibrational wavepacket dynamics, and we demonstrate how TR-PA can readily disentangle these dynamical processes. TR-PA in fluorescein presents specific opportunities for its development as a probe for rotational dynamics in large biomolecules as fluorescein derivatives are commonly incorporated in complex biomolecules and have been used extensively in time-resolved fluorescence anisotropy measurements, to which TR-PA is a gas-phase analogue.

摘要

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