Hydrogen-bond lifetime measured by time-resolved 2D-IR spectroscopy: N-methylacetamide in methanol

被引:257
作者
Woutersen, S
Mu, Y
Stock, G
Hamm, P [1 ]
机构
[1] Max Born Inst Nichtlineare Opt & Kurzzeitspektro, D-12489 Berlin, Germany
[2] Univ Frankfurt, Inst Phys & Theoret Chem, D-60439 Frankfurt, Germany
关键词
D O I
10.1016/S0301-0104(01)00224-5
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
2D vibrational spectroscopy is applied to investigate the equilibrium dynamics of hydrogen bonding of N-methyl-acetamide (NMA) dissolved in methanol-d(4). For this particular solute-solvent system, roughly equal populations are found for two conformers of the solute-solvent complex, one of which forms a hydrogen bond from the C=O group of NMA to the surrounding solvent, and one of which does not. Using time-resolved 2D-IR spectroscopy on the amide I band of NMA, the exchange between both conformers is resolved. Equilibration of each conformer is completed after 4.5 ps, while the formation and breaking of the hydrogen bond occurs on a slower, 10-15 ps time scale. This interpretation is supported by classical molecular-dynamics simulations of NMA in methanol. The calculations predict a 64% population of the hydrogen-bonded conformer and an average hydrogen-bond lifetime of approximate to 12 ps. (C) 2001 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:137 / 147
页数:11
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