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The Journal of Physical Chemistry. A|April 17, 2015
Can a secondary isotope effect be larger than a primary?Charles L Perrin, Kathryn D BurkeJournal of the American Chemical Society|February 18, 2014
Variable-temperature study of hydrogen-bond symmetry in cyclohexene-1,2-dicarboxylate monoanion in chloroform-dCharles L Perrin, Kathryn D BurkeJournal of the American Chemical Society|October 9, 2019
Isotopic-Perturbation NMR Study of Hydrogen-Bond Symmetry in Solution: Temperature Dependence and Comparison of OHO and ODO Hydrogen BondsCharles L Perrin, Annadka Shrinidhi, Kathryn D BurkeAccounts of Chemical Research|October 14, 2010
Are short, low-barrier hydrogen bonds unusually strong?Charles L PerrinThe Journal of Organic Chemistry|January 21, 2017
The Logic behind a Physical-Organic Chemist's Research TopicsCharles L PerrinThe Journal of Organic Chemistry|May 18, 2022
Malonic Anhydrides, Challenges from a Simple StructureCharles L PerrinThe Journal of Organic Chemistry|June 16, 2025
Nonradical Reactions of p-Benzyne DiradicalsCharles L PerrinAccounts of Chemical Research|January 16, 2002
Is there stereoelectronic control in formation and cleavage of tetrahedral intermediates?Charles L PerrinMethods in Enzymology|September 16, 2017
pH-Free Measurement of Relative Acidities, Including Isotope EffectsCharles L PerrinPageof 5