Toward control of electron transfer in donor-acceptor molecules by bond-specific infrared excitation

被引:171
作者
Delor, Milan [1 ]
Scattergood, Paul A. [1 ]
Sazanovich, Igor V. [1 ,2 ]
Parker, Anthony W. [2 ]
Greetham, Gregory M. [2 ]
Meijer, Anthony J. H. M. [1 ]
Towrie, Michael [2 ]
Weinstein, Julia A. [1 ]
机构
[1] Univ Sheffield, Dept Chem, Sheffield S3 7HF, S Yorkshire, England
[2] Sci & Technol Facil Council, Rutherford Appleton Lab, Cent Laser Facil, Chilton OX11 0QX, Oxon, England
基金
英国科学技术设施理事会; 英国工程与自然科学研究理事会;
关键词
CHARGE-TRANSFER; EXCITED-STATE; COHERENT CONTROL; BASIS-SETS; DYNAMICS; COMPLEXES; CHEMISTRY; PHOTODISSOCIATION; SPECTROSCOPY; MODELS;
D O I
10.1126/science.1259995
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Electron transfer (ET) from donor to acceptor is often mediated by nuclear-electronic (vibronic) interactions in molecular bridges. Using an ultrafast electronic-vibrational-vibrational pulse-sequence, we demonstrate how the outcome of light-induced ET can be radically altered by mode-specific infrared (IR) excitation of vibrations that are coupled to the ET pathway. Picosecond narrow-band IR excitation of high-frequency bridge vibrations in an electronically excited covalent trans-acetylide platinum(II) donor-bridge-acceptor system in solution alters both the dynamics and the yields of competing ET pathways, completely switching a charge separation pathway off. These results offer a step toward quantum control of chemical reactivity by IR excitation.
引用
收藏
页码:1492 / 1495
页数:4
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