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Rationalizing hydrogen bond solvation with Kamlet-Taft LSER and molecular torsion balances

Physical chemistry chemical physics : PCCP, 2023-07, Vol.25 (27), p.1788-17814

2023

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Was This Title Generated by ChatGPT? Considerations for Artificial Intelligence Text-Generation Software Programs for Chemists and Chemistry Educators

Journal of chemical education, 2023-04, Vol.100 (4), p.1413-1418

2023

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Quantitative model for rationalizing solvent effect in noncovalent CH-Aryl interactions

Chemical science (Cambridge), 2016-01, Vol.7 (2), p.1401-1407

2016

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Comment on "Neurotoxicity and Outcomes from Developmental Lead Exposure: Persistent or Permanent?"

Environmental health perspectives, 2024-04, Vol.132 (4), p.48001-48001

2024

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Quantifying macrocyclization-induced strain utilizing N -phenylimides as conformational reporters

Chemical communications (Cambridge, England), 2024-04, Vol.60 (30), p.4040-4043

2024

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Determining the Ionization Constants of Organic Acids Using Fluorine Gauche Effects

Journal of organic chemistry, 2020-04, Vol.85 (7), p.4896-4900

2020

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Electrostatic CH−π Interactions Can Override Fluorine Gauche Effects To Exert Conformational Control

Chemistry : a European journal, 2023-01, Vol.29 (6), p.e202203139-n/a

2023

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Using Guiding Questions to Promote Scientific Practices in Undergraduate Chemistry Laboratories

Journal of chemical education, 2021-12, Vol.98 (12), p.3731-3738

2021

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Solvent Modulation of Aromatic Substituent Effects in Molecular Balances Controlled by CH−π Interactions

The journal of physical chemistry. A, Molecules, spectroscopy, kinetics, environment, & general theory, 2018-02, Vol.122 (4), p.909-915

2018

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Quantification of CH⋅⋅⋅π Interactions: Implications on How Substituent Effects Influence Aromatic Interactions

Chemistry : a European journal, 2010-11, Vol.16 (41), p.12357-12362

2010

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Cationic CHπ interactions as a function of solvation

Physical chemistry chemical physics : PCCP, 2016-11, Vol.18 (45), p.30940-30945

2016

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Substituent Effects on Energetics of Peptide-Carboxylate Hydrogen Bonds as Studied by 1H NMR Spectroscopy: Implications for Enzyme Catalysis

Journal of organic chemistry, 2013-12, Vol.78 (23), p.11765-11771

2013

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Relative substituent position on the strength of π–π stacking interactions

Tetrahedron letters, 2010-03, Vol.51 (13), p.1648-1650

2010

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Conformational Equilibria of N,N‑Dimethylsuccinamic Acid and Its Lithium Salt as a Function of Solvent

Organic letters, 2013-02, Vol.15 (4), p.760-763

2013

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Conformational Preferences of N,N -Dimethylsuccinamate as a Function of Alkali and Alkaline Earth Metal Salts: Experimental Studies in DMSO and Water As Determined by 1H NMR Spectroscopy

The journal of physical chemistry. A, Molecules, spectroscopy, kinetics, environment, & general theory, 2014-03, Vol.118 (11), p.1965-1970

2014

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Quantifying macrocyclization-induced strain utilizing -phenylimides as conformational reporters

Chemical communications (Cambridge, England), 2024-04, Vol.6 (3), p.44-443

2024

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Cationic CH π interactions as a function of solvationDedication to Professor John D. Roberts (Caltech) on his 98th birthday.Electronic supplementary information (ESI) available. CCDC 1500195. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/c6cp06800f

2016-11

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Quantitative model for rationalizing solvent effect in noncovalent CH-Aryl interactionsElectronic supplementary information (ESI) available: Correlation plots; proton and carbon NMR spectra of the molecular balances, and the xyz coordinate of the optimized geometries. See DOI: 10.1039/c5sc03550c

2016-01

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Conformational Preferences of cis -1,3-Cyclopentanedicarboxylic Acid and Its Salts by 1 H NMR Spectroscopy: Energetics of Intramolecular Hydrogen Bonds in DMSO

Journal of organic chemistry, 2013-03, Vol.78 (5), p.2005-2011

2013

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Conformational Preferences of cis-1,3-Cyclopentanedicarboxylic Acid and Its Salts by 1H NMR Spectroscopy: Energetics of Intramolecular Hydrogen Bonds in DMSO

Journal of organic chemistry, 2013-03, Vol.78 (5), p.2005-2011

2013

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Quantitative model for rationalizing solvent effect in noncovalent CH–Aryl interactions† †Electronic supplementary information (ESI) available: Correlation plots; proton and carbon NMR spectra of the molecular balances, and the xyz coordinate of the optimized geometries. See DOI: 10.1039/c5sc03550c

Chemical science (Cambridge), 2015-11, Vol.7 (2), p.1401-1407

2015

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Conformational Preferences of N,N -Dimethylsuccinamate as a Function of Alkali and Alkaline Earth Metal Salts: Experimental Studies in DMSO and Water As Determined by 1 H NMR Spectroscopy

The journal of physical chemistry. A, Molecules, spectroscopy, kinetics, environment, & general theory, 2014-03, Vol.118 (11), p.1965-1970

2014

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Rationalizing hydrogen bond solvation with Kamlet-Taft LSER and molecular torsion balances

Was This Title Generated by ChatGPT? Considerations for Artificial Intelligence Text-Generation Software Programs for Chemists and Chemistry Educators

Quantitative model for rationalizing solvent effect in noncovalent CH-Aryl interactions

Comment on "Neurotoxicity and Outcomes from Developmental Lead Exposure: Persistent or Permanent?"

Quantifying macrocyclization-induced strain utilizing N -phenylimides as conformational reporters

Determining the Ionization Constants of Organic Acids Using Fluorine Gauche Effects

Electrostatic CH−π Interactions Can Override Fluorine Gauche Effects To Exert Conformational Control

Using Guiding Questions to Promote Scientific Practices in Undergraduate Chemistry Laboratories

Solvent Modulation of Aromatic Substituent Effects in Molecular Balances Controlled by CH−π Interactions

Taurine-Derived Compounds Produce Anxiolytic Effects in Rats Following Developmental Lead Exposure

Quantification of CH⋅⋅⋅π Interactions: Implications on How Substituent Effects Influence Aromatic Interactions

Assessing the Anxiolytic Properties of Taurine-Derived Compounds in Rats Following Developmental Lead Exposure: A Neurodevelopmental and Behavioral Pharmacological Pilot Study

Cationic CHπ interactions as a function of solvation

Substituent Effects on Energetics of Peptide-Carboxylate Hydrogen Bonds as Studied by 1H NMR Spectroscopy: Implications for Enzyme Catalysis

Relative substituent position on the strength of π–π stacking interactions

Conformational Equilibria of N,N‑Dimethylsuccinamic Acid and Its Lithium Salt as a Function of Solvent

In Vivo Sex-Dependent Effects of Perinatal Pb2+ Exposure on Pilocarpine-Induced Seizure Susceptibility and Taurine Neuropharmacology

Conformational Preferences of N,N -Dimethylsuccinamate as a Function of Alkali and Alkaline Earth Metal Salts: Experimental Studies in DMSO and Water As Determined by 1H NMR Spectroscopy

Quantifying macrocyclization-induced strain utilizing -phenylimides as conformational reporters

Cationic CH π interactions as a function of solvationDedication to Professor John D. Roberts (Caltech) on his 98th birthday.Electronic supplementary information (ESI) available. CCDC 1500195. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/c6cp06800f

Quantitative model for rationalizing solvent effect in noncovalent CH-Aryl interactionsElectronic supplementary information (ESI) available: Correlation plots; proton and carbon NMR spectra of the molecular balances, and the xyz coordinate of the optimized geometries. See DOI: 10.1039/c5sc03550c

Conformational Preferences of cis -1,3-Cyclopentanedicarboxylic Acid and Its Salts by 1 H NMR Spectroscopy: Energetics of Intramolecular Hydrogen Bonds in DMSO

Conformational Preferences of cis-1,3-Cyclopentanedicarboxylic Acid and Its Salts by 1H NMR Spectroscopy: Energetics of Intramolecular Hydrogen Bonds in DMSO

Conformational Preferences of N,N -Dimethylsuccinamate as a Function of Alkali and Alkaline Earth Metal Salts: Experimental Studies in DMSO and Water As Determined by 1 H NMR Spectroscopy

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