Multidimensional infrared spectroscopy of water. II. Hydrogen bond switching dynamics

被引:160
作者
Loparo, Joseph J. [1 ]
Roberts, Sean T.
Tokmakoff, Andrei
机构
[1] MIT, Dept Chem, Cambridge, MA 02139 USA
[2] MIT, George R Harrison Spect Lab, Cambridge, MA 02139 USA
关键词
D O I
10.1063/1.2382896
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
We use multidimensional infrared spectroscopy of the OH stretch of HOD in D2O to measure the interconversion of different hydrogen bonding environments. The OH stretching frequency distinguishes hydrogen bonded (HB) and non-hydrogen-bonded (NHB) configurations by their absorption on the low (red) and high (blue) sides of the line shape. Measured asymmetries in the two dimensional infrared OH line shapes are manifestations of the fundamentally different spectral relaxations of HB and NHB. HB oscillators exhibit coherent oscillations within the hydrogen-bonded free energy well before undergoing activated barrier crossing, resulting in the exchange of hydrogen bonded partners. Conversely, NHB oscillators rapidly return to HB frequencies within 150 fs. These results support a picture where NHB configurations are only visited transiently during large fluctuations about a hydrogen bond or during the switching of hydrogen bonding partners. The results are not consistent with the presence of entropically stabilized dangling hydrogen bonds or a conceptual picture of water as a mixture of environments with varying hydrogen bond strength separated by barriers > kT. (c) 2006 American Institute of Physics.
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页数:12
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