2017 Craig Lecture

Date & time

4–5pm 21 March 2017

Location

Building #35 Lecture Theatre

Speakers

Professor Peter R. Schreiner, Institute of Organic Chemistry, Justus-Liebig University

Contacts

 Mr Gavin Perri
 6125 2391

Tunneling Control of Chemical Reactions

Chemical reactivity is traditionally understood[2] in terms of kinetic versus thermodynamic control,[3] wherein the driving force is the lowest activation barrier among the possible reaction paths or the lowest free energy of the final products, respectively. Here we expose quantum mechanical tunneling as a third driving force that can overwrite traditional kinetic control and govern reactivity based on nonclassical penetration of the potential energy barriers connecting the reactants and products. These findings are exemplified with the first experimental isolation and full spectroscopic and theoretical characterization of the elusive hydroxycarbenes (R–C–OH)[4] that undergo facile [1,2]hydrogen tunneling to the corresponding aldehydes under barriers of nearly 30.0 kcal mol–1 with half-lives of around 1–2 h even at 10 K, despite of the presence of paths with substantially lower barriers. We will demonstrate that this is a general phenomenon,[5] as exemplified by other OH-tunneling examples such as the rotational isomerization of a variety of carbocylic acids.[6] Such tunneling processes do not merely represent corrections to the reaction rate, they are the reaction rate, i.e., they completely control the reaction outome.[1a] They can also override common notions such as the Curtin-Hammett principle.[7]

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[1] a) P. R. Schreiner, H. P. Reisenauer, D. Ley, D. Gerbig, C.-H. Wu, W. D. Allen, Science 2011, 332, 1300; b) D. Ley, D. Gerbig, P. R. Schreiner, Org. Biomol. Chem. 2012, 19, 3769; c) D. Gerbig, P. R. Schreiner, Tunneling in the reactions of Carbenes and Oxacarbenes, John Wiley & Sons, Inc., Hoboken, 2014.
[2] a) H. Eyring, J. Chem. Phys. 1935, 3, 107; b) M. G. Evans, M. Polanyi, Trans. Faraday Soc. 1935, 31, 875.
[3] a) R. B. Woodward, H. Baer, J. Am. Chem. Soc. 1944, 66, 645; b) A. G. Catchpole, E. D. Hughes, C. K. Ingold, J. Chem. Soc. 1944, 11, 8.
[4] a) D. Gerbig, H. P. Reisenauer, C.-H. Wu, D. Ley, W. D. Allen, P. R. Schreiner, J. Am. Chem. Soc. 2010, 132, 7273; b) D. Gerbig, D. Ley, H. P. Reisenauer, P. R. Schreiner, Beilstein J. Org. Chem. 2010, 6, 1061; c) P. R. Schreiner, H. P. Reisenauer, F. C. Pickard IV, A. C. Simmonett, W. D. Allen, E. Mátyus, A. G. Császár, Nature 2008, 453, 906; d) P. R. Schreiner, H. P. Reisenauer, Angew. Chem. Int. Ed. 2008, 47, 7071.
[5] a) D. Ley, D. Gerbig, P. R. Schreiner, Chem. Sci. 2013, 4, 677; b) D. Ley, D. Gerbig, J. P. Wagner, H. P. Reisenauer, P. R. Schreiner, J. Am. Chem. Soc. 2011, 133, 13614; c) D. Gerbig, D. Ley, P. R. Schreiner, Org. Lett. 2011, 13, 3526.
[6] a) S. Amiri, H. P. Reisenauer, P. R. Schreiner, J. Am. Chem. Soc. 2010, 132, 15902; b) D. Gerbig, P. R. Schreiner, J. Phys. Chem. B 2014, 119, 693.
[7] A. Mardyukov, H. Quanz, P. R. Schreiner, Nature Chem. 2017, 9, 71.

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