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Title:

Hydrogen Bond Dynamics Probed with Ultrafast Infrared Heterodyne-Detected Multidimensional Vibrational Stimulated Echoes

Author(s):
Asbury, John B.; Steinel, Tobias; Stromberg, C.; Gaffney, K. J.; Piletic, I. R.; Goun, Alexi; Fayer, M. D.
Abstract:
Hydrogen bond dynamics are explicated with exceptional detail using multidimensional IR vibrational echo correlation spectroscopy with full phase information. Probing the hydroxyl stretch of methanol-OD oligomers in CCl4, the dynamics of the evolving hydrogen bonded network are measured with ultrashort (<50 fs) pulses. The data along with detailed model calcns. demonstrate that vibrational relaxation leads to selective hydrogen bond breaking on the red side of the spectrum (strongest hydrogen bonds) and the prodn. of singly hydrogen bonded photoproducts. [on SciFinder(R)]
Keywords:
Hydrogen bond Molecular vibration Photon echo Vibrational relaxation (hydrogen bond breaking dynamics following vibrational relaxation in methanol-OD oligomers probed with ultrafast IR heterodyne-detected multidimensional vibrational stimulated echoes) Bond cleavage (hydrogen hydrogen bond breaking dynamics following vibrational relaxation in methanol-OD oligomers probed with ultrafast IR heterodyne-detected multidimensional vibrational stimulated echoes) hydrogen bond dynamics methanol IR heter...     »
Congress title:
CAN 140:189227 73-3 Optical, Electron, and Mass Spectroscopy and Other Related Properties Department of Chemistry, Stanford University, Stanford, CA, USA. Journal 0031-9007 1455-13-6 (Methanol-d) Role: CPS (Chemical process), PEP (Physical, engineering or chemical process), PRP (Properties), PYP (Physical process), PROC (Process) (hydrogen bond breaking dynamics following vibrational relaxation in methanol-OD oligomers probed with ultrafast IR heterodyne-detected multidimensional vibrational sti...     »
Journal title:
Phys. Rev. Lett.
Year:
2003
Journal volume:
91
Journal issue:
23
Pages contribution:
237402/1-237402/4
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