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Symmetry of Hydrogen Bonds: Application of NMR Method of Isotopic Perturbation and Relevance of Solvatomers

Molecules (Basel, Switzerland), 2023-05, Vol.28 (11), p.4462

Perrin, Charles L

2023

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Are Short, Low-Barrier Hydrogen Bonds Unusually Strong?

Accounts of chemical research, 2010-12, Vol.43 (12), p.1550-1557

Perrin, Charles L

2010

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Symmetry of hydrogen bonds in solution

Pure and applied chemistry, 2009-01, Vol.81 (4), p.571-583

Perrin, Charles L.

2009

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Comment on "The role of electrostatic induction in secondary isotope effects on acidity" by E. A. Halevi, New J. Chem., 2014, 38, 3840

New journal of chemistry, 2015-01, Vol.39 (2), p.1517-1521

Perrin, Charles L

2015

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Linear or Nonlinear Least-Squares Analysis of Kinetic Data?

Journal of chemical education, 2017-06, Vol.94 (6), p.669-672

Perrin, Charles L

2017

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ipso

Journal of organic chemistry, 2021-11, Vol.86 (21), p.14245-14249

Perrin, Charles L

2021

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Malonic Anhydrides, Challenges from a Simple Structure

Journal of organic chemistry, 2022-06, Vol.87 (11), p.7006-7012

Perrin, Charles L.

2022

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Comment on “Topography of the free energy landscape of Claisen–Schmidt condensation: solvent and temperature effects on the rate-controlling step” by N. D. Coutinho, H. G. Machado, V. H. Carvalho-Silva and W. A. da Silva, Phys. Chem. Chem. Phys. , 2021, 23 , 6738

Physical chemistry chemical physics : PCCP, 2021-10, Vol.23 (38), p.22199-22201

Perrin, Charles L.

2021

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Protein-like proton exchange in a synthetic host cavity

Proceedings of the National Academy of Sciences - PNAS, 2015-12, Vol.112 (50), p.15303-15307

2015

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My first publication

Journal of physical organic chemistry, 2022-11, Vol.35 (11), p.n/a

Perrin, Charles L.

2022

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The complete mechanism of an aldol condensation in water

Physical chemistry chemical physics : PCCP, 2022-08, Vol.24 (31), p.18978-18982

2022

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Selectivity and Isotope Effects in Hydronation of a Naked Aryl Anion

Journal of the American Chemical Society, 2014-10, Vol.136 (43), p.15263-15269

2014

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On the Intramolecular Hydrogen Bond in Solution: Car–Parrinello and Path Integral Molecular Dynamics Perspective

Journal of chemical theory and computation, 2011-11, Vol.7 (11), p.3505-3513

2011

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Secondary Deuterium Isotope Effects on the Acidity of Carboxylic Acids and Phenols

Journal of the American Chemical Society, 2007-04, Vol.129 (14), p.4490-4497

2007

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The Complete Mechanism of an Aldol Condensation

Journal of organic chemistry, 2016-07, Vol.81 (13), p.5631-5635

2016

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Cyclohexeno[3,4]cyclodec-1,5-diyne-3-ene: A Convenient Enediyne

Organic letters, 2021-09, Vol.23 (17), p.6911-6915

2021

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Symmetry of Hydrogen Bonds in Two Enols in Solution

Journal of the American Chemical Society, 2019-03, Vol.141 (9), p.4103-4107

2019

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The Logic behind a Physical–Organic Chemist’s Research Topics

Journal of organic chemistry, 2017-01, Vol.82 (2), p.819-838

Perrin, Charles L

2017

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Enthalpic and entropic contributions to the basicity of cycloalkylamines

Chemical science (Cambridge), 2020-08, Vol.11 (32), p.8489-8494

2020

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pH-Free Measurement of Relative Acidities, Including Isotope Effects

Methods in enzymology, 2017, Vol.596, p.331-368

Perrin, Charles L

2017

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Isotopic-Perturbation NMR Study of Hydrogen-Bond Symmetry in Solution: Temperature Dependence and Comparison of OHO and ODO Hydrogen Bonds

Journal of the American Chemical Society, 2019-10, Vol.141 (43), p.17278-17286

2019

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Polynomial coefficients. Application to spin–spin splitting by N equivalent nuclei of spin I > 1/2

Magnetic resonance in chemistry, 2018-09, Vol.56 (9), p.799-802

Perrin, Charles L.

2018

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Polynomial coefficients. Application to spin–spin splitting by N equivalent nuclei of spin I > 1/2

Magnetic resonance in chemistry, 2018-09, Vol.56 (9), p.798-798

Perrin, Charles L.

2018

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Reactivity of nucleophiles toward a p-benzyne derived from an enediyne

Journal of physical organic chemistry, 2013-02, Vol.26 (2), p.206-210

2013

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Nucleophilic Addition of Enolates to 1,4-Dehydrobenzene Diradicals Derived from Enediynes: Synthesis of Functionalized Aromatics

ACS omega, 2022-07, Vol.7 (26), p.22930-22937

2022

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Symmetry of Hydrogen Bonds: Application of NMR Method of Isotopic Perturbation and Relevance of Solvatomers

Are Short, Low-Barrier Hydrogen Bonds Unusually Strong?

Symmetry of hydrogen bonds in solution

Comment on "The role of electrostatic induction in secondary isotope effects on acidity" by E. A. Halevi, New J. Chem., 2014, 38, 3840

Linear or Nonlinear Least-Squares Analysis of Kinetic Data?

ipso

Malonic Anhydrides, Challenges from a Simple Structure

Comment on “Topography of the free energy landscape of Claisen–Schmidt condensation: solvent and temperature effects on the rate-controlling step” by N. D. Coutinho, H. G. Machado, V. H. Carvalho-Silva and W. A. da Silva, Phys. Chem. Chem. Phys. , 2021, 23 , 6738

Protein-like proton exchange in a synthetic host cavity

My first publication

The complete mechanism of an aldol condensation in water

Selectivity and Isotope Effects in Hydronation of a Naked Aryl Anion

On the Intramolecular Hydrogen Bond in Solution: Car–Parrinello and Path Integral Molecular Dynamics Perspective

Secondary Deuterium Isotope Effects on the Acidity of Carboxylic Acids and Phenols

The Complete Mechanism of an Aldol Condensation

Cyclohexeno[3,4]cyclodec-1,5-diyne-3-ene: A Convenient Enediyne

Symmetry of Hydrogen Bonds in Two Enols in Solution

The Logic behind a Physical–Organic Chemist’s Research Topics

Enthalpic and entropic contributions to the basicity of cycloalkylamines

pH-Free Measurement of Relative Acidities, Including Isotope Effects

Isotopic-Perturbation NMR Study of Hydrogen-Bond Symmetry in Solution: Temperature Dependence and Comparison of OHO and ODO Hydrogen Bonds

Polynomial coefficients. Application to spin–spin splitting by N equivalent nuclei of spin I > 1/2

Polynomial coefficients. Application to spin–spin splitting by N equivalent nuclei of spin I > 1/2

Reactivity of nucleophiles toward a p-benzyne derived from an enediyne

Nucleophilic Addition of Enolates to 1,4-Dehydrobenzene Diradicals Derived from Enediynes: Synthesis of Functionalized Aromatics

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