Literature DB >> 17444643

Lone pair-pi and pi-pi interactions play an important role in proton-coupled electron transfer reactions.

Gino A DiLabio1, Erin R Johnson.   

Abstract

Proton-coupled electron transfer (PCET), a class of formal hydrogen atom transfer (HAT) reactions, is of widespread interest because it is implicated in a broad range of chemical and biochemical processes. PCET is typically differentiated from HAT by the fact that it occurs when a proton and electron are transferred between different sets of molecular orbitals. Previous theoretical work predicted that hydrogen bonding between reactants is a necessary but not sufficient condition for H exchanges to take place by PCET. This implies that HAT is the only mechanism for H exchange between two carbon atoms. In this work, we present computational results that show that the H exchange in the tert-butylperoxyl/phenol couple, a prototypical antioxidant exchange reaction, occurs by PCET and that the transfer of the electron can occur via an oxygen lone pair-ring pi overlap. We then show that the H exchange in a model for the tyrosyl/tyrosine couple, which is implicated in ribonucleotide reductase chemistry, occurs via PCET and that one path for the electron transfer is provided by a strong pi-stacking interaction. Finally, we show that a pi-stacking interaction in the benzyl/toluene couple, a system in which there is no H-bonding, can result in this exchange occurring via PCET to some extent. Collectively, these results indicate that PCET reactions are not unique to systems that can engage in H-bonding and that lone pair-pi and pi-pi interactions in these systems may be more important than previously understood.

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Year:  2007        PMID: 17444643     DOI: 10.1021/ja068090g

Source DB:  PubMed          Journal:  J Am Chem Soc        ISSN: 0002-7863            Impact factor:   15.419


  19 in total

Review 1.  Proton-coupled electron transfer.

Authors:  My Hang V Huynh; Thomas J Meyer
Journal:  Chem Rev       Date:  2007-11       Impact factor: 60.622

2.  The DFT local reactivity descriptors of α-tocopherol.

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Journal:  J Mol Model       Date:  2015-03-28       Impact factor: 1.810

3.  A Continuum of Proton-Coupled Electron Transfer Reactivity.

Authors:  Julia W Darcy; Brian Koronkiewicz; Giovanny A Parada; James M Mayer
Journal:  Acc Chem Res       Date:  2018-09-20       Impact factor: 22.384

4.  Do Spin State and Spin Density Affect Hydrogen Atom Transfer Reactivity?

Authors:  Caroline T Saouma; James M Mayer
Journal:  Chem Sci       Date:  2014-01-01       Impact factor: 9.825

5.  Mechanistic study of the structure-activity relationship for the free radical scavenging activity of baicalein.

Authors:  Zoran S Marković; Jasmina M Dimitrić Marković; Dejan Milenković; Nenad Filipović
Journal:  J Mol Model       Date:  2011-01-13       Impact factor: 1.810

6.  Site-specific incorporation of 3-nitrotyrosine as a probe of pKa perturbation of redox-active tyrosines in ribonucleotide reductase.

Authors:  Kenichi Yokoyama; Ulla Uhlin; Joanne Stubbe
Journal:  J Am Chem Soc       Date:  2010-06-23       Impact factor: 15.419

7.  The Third Dimension of a More O'Ferrall-Jencks Diagram for Hydrogen Atom Transfer in the Isoelectronic Hydrogen Exchange Reactions of (PhX)(2)H(•) with X = O, NH, and CH(2).

Authors:  Alessandro Cembran; Makenzie R Provorse; Changwei Wang; Wei Wu; Jiali Gao
Journal:  J Chem Theory Comput       Date:  2012-09-04       Impact factor: 6.006

8.  ENDOR spectroscopy and DFT calculations: evidence for the hydrogen-bond network within α2 in the PCET of E. coli ribonucleotide reductase.

Authors:  Tomislav Argirević; Christoph Riplinger; JoAnne Stubbe; Frank Neese; Marina Bennati
Journal:  J Am Chem Soc       Date:  2012-10-16       Impact factor: 15.419

9.  DFT and MP2 study of low barrier proton transfer in hydrazide schiff base tautomers via water bridges and in the gas.

Authors:  Hossein Tavakol; Hossein Farrokhpour
Journal:  J Mol Model       Date:  2013-05-25       Impact factor: 1.810

10.  Lone pair ... pi interactions between water oxygens and aromatic residues: quantum chemical studies based on high-resolution protein structures and model compounds.

Authors:  Alok Jain; Venkatnarayan Ramanathan; Ramasubbu Sankararamakrishnan
Journal:  Protein Sci       Date:  2009-03       Impact factor: 6.725

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