Boosted molecular mobility during common chemical reactions

Author:

Wang Huan1ORCID,Park Myeonggon12ORCID,Dong Ruoyu1,Kim Junyoung13ORCID,Cho Yoon-Kyoung13ORCID,Tlusty Tsvi12ORCID,Granick Steve14ORCID

Affiliation:

1. Center for Soft and Living Matter, Institute for Basic Science (IBS), Ulsan 44919, South Korea.

2. Department of Physics, Ulsan National Institute of Science and Technology (UNIST), Ulsan 44919, South Korea.

3. Department of Biomedical Engineering, UNIST, Ulsan 44919, South Korea.

4. Department of Chemistry, UNIST, Ulsan 44919, South Korea.

Abstract

Reactions give solvents a kick During a chemical reaction, the reorganization of solvent molecules not directly in contact with reactants and products is normally viewed as a simple diffusion response. Wang et al. studied molecular diffusion in six common reactions—including the copper-catalyzed click reaction and the Diels-Alder reaction—with pulsed-field gradient nuclear magnetic resonance. They observed a boost in mobility relative to Brownian diffusion that was stronger for the catalyzed reactions that were studied. The mobilities for the click reaction were verified with a microfluidic gradient method. They argue that energy release produces transient translational motion of reacting centers that mechanically perturbs solvent molecules. Science , this issue p. 537

Funder

Institute for Basic Science

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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