Proton-Coupled Electron Transfer in a Hydrogen-Bonded Charge Transfer Complex

被引:10
|
作者
Verma, Sandeep [1 ]
Aute, Sunil [2 ]
Das, Amitava [2 ,3 ]
Ghosh, Hirendra N. [1 ]
机构
[1] Bhabha Atom Res Ctr, Radiat & Photochem Div, Bombay 400085, Maharashtra, India
[2] Natl Chem Lab, CSIR, Pune 411008, Maharashtra, India
[3] Cent Salt & Marine Chem Res Inst, CSIR, Bhavnagar 364002, Gujarat, India
来源
JOURNAL OF PHYSICAL CHEMISTRY B | 2016年 / 120卷 / 41期
关键词
PHENOL RADICAL CATIONS; PICOSECOND TIME-SCALE; FREE-ENERGY; WATER; DYNAMICS; SOLVENT; 2,2-BIPYRIDINE; ACETONITRILE; PHOTOACIDS; GROTTHUSS;
D O I
10.1021/acs.jpcb.6b06032
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
A proton-coupled electron transfer (PCET) reaction in a hydrogen bonded charge-transfer (CT) complex of 4-([2,2'-bipyridin]-4-yl)phenol (bpy-phenol) with a F- ion has been investigated by ultrafast time-resolved transient absorption spectroscopy. The phenolic receptor molecule, bpy-phenol, binds to the F- ion through a hydrogen bond and senses the F- ion-via the Stokes-shifted CT band. Upon photoexcitation, CT from the phenol residue to the bpy residue promotes proton transfer from the phenol radical cation (ArOH center dot+) to the fluoride ion at ultrafast time scales of <150 fs (instrument response function limited) and 3 ps, separately. The fast and slow proton-transfer times are linked to two different types of hydrogen-bonding networks between the phenol residue and fluoride ion. Crystalline water in the fluoride salt hydrates mediates the proton-transfer reaction. This work demonstrates the participation of a hydrogen-bonded water bridge within a PCET reaction in a water restricted environment.
引用
收藏
页码:10780 / 10785
页数:6
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