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First measurement of the symmetric proton transfer in formic acid dimers

 
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In nature, hydrogen bonds play an important role. The structure of the DNA double helix is determined by double and triple hydrogen bonds. The binding energy of hydrogen bonds with approximately 10 kJ/mol is of medium strength between chemical bonds (~100 kJ/mol) and van-der-Waals interactions (~1 kJ/mol).

Formic acid dimer is the smallest organic prototype with a double hydrogen bond. For the first time we were able to measure the time constant of the proton transfer of formic acid dimer by studying the isotope dimer (DCOOH)2.

Publications:

A. Gutberlet, G.W. Schwaab and M. Havenith

High resolution IR spectroscopy of the carbonyl stretch of (DCOOD)2

submitted


M. Ortlieb, M. Havenith

Proton transfer in (HCOOH)2: An high resolution spectroscopic study of the antisymmetric C-O stretch

J. Phys. Chem. A, accepted (2007) (Roger Miller memorial issue)

 

M. Havenith

Coherent proton tunneling in hydrogen bonds of isolated molecules: carboxylic dimers Hydrogen-Transfer Reactions

Volume 1, 33-53, edited by J.T. Hynes, J.P. Klinman, H.-H. Limbach, R.L. Schowen, Whiley-VCH (2007).

F. Madeja, M. Havenith

High resolution spectroscopy of carboxylic acid in the gas phase: observation of proton transfer in (DCOOH)2

J. Chem. Phys. 117, 7162 (2002).