Crossover from hydrogen to chemical bonding

Author:

Dereka Bogdan1ORCID,Yu Qi2ORCID,Lewis Nicholas H. C.1ORCID,Carpenter William B.1,Bowman Joel M.2ORCID,Tokmakoff Andrei1ORCID

Affiliation:

1. Department of Chemistry, Institute for Biophysical Dynamics, and James Franck Institute, The University of Chicago, Chicago, IL 60637, USA.

2. Department of Chemistry and Cherry L. Emerson Center for Scientific Computation, Emory University, Atlanta, GA 30322, USA.

Abstract

The nature of short hydrogen bonds Hydrogen bonding (H-bonding) unquestionably plays an important role in chemical and biological systems and is responsible for some of their unusual properties. Strong, short H-bonds constitute a separate class that, owing to their elusive characterization, has remained a point of contention over the past several decades. Using femtosecond two-dimensional infrared spectroscopy in conjunction with quantum chemical calculations, Dereka et al. demonstrate a powerful way to investigate the nature of short H-bonding (see the Perspective by Bonn and Hunger). Their quantitative characterization of multiple coupled motions in the model system of bifluoride anion [F-H-F] in aqueous solution reveals several distinctive features of a crossover from conventional to short, strong H-bonding. Science , this issue p. 160 see also p. 123

Funder

National Science Foundation

U.S. Department of Energy

Army Research Office

Swiss National Science Foundation

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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