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The pKBHX Database: Toward a Better Understanding of Hydrogen-Bond Basicity for Medicinal Chemists

Journal of medicinal chemistry, 2009-07, Vol.52 (14), p.4073-4086

2009

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Solvent polarity scales: determination of new ET(30) values for 84 organic solvents

Journal of physical organic chemistry, 2014-06, Vol.27 (6), p.512-518

2014

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The Diiodine Basicity Scale: Toward a General Halogen-Bond Basicity Scale

Chemistry : a European journal, 2011-09, Vol.17 (37), p.10431-10444

2011

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Solvatomagnetic Comparison Method: A Proper Quantification of Solvent Hydrogen-Bond Basicity

The journal of physical chemistry. B, 2014-07, Vol.118 (27), p.7594-7608

2014

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Influence of the Structure of Polyfluorinated Alcohols on Brønsted Acidity/Hydrogen-Bond Donor Ability and Consequences on the Promoter Effect

Journal of organic chemistry, 2011-02, Vol.76 (4), p.1126-1133

2011

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Solvatochromic Shifts in UV–Vis Absorption Spectra: The Challenging Case of 4‑Nitropyridine N‑Oxide

Journal of chemical theory and computation, 2016-04, Vol.12 (4), p.1919-1929

2016

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Lewis basicity and affinity scales: data and measurement

1, 2010

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Halogen-bond geometry: a crystallographic database investigation of dihalogen complexes

Acta crystallographica. Section B, Structural science, 2003-08, Vol.59 (4), p.512-526

2003

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The pK BHX Hydrogen-Bond Basicity Scale: From Molecules to Anions

Journal of organic chemistry, 2022-06, Vol.87 (11), p.7264-7273

2022

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The p K BHX Hydrogen-Bond Basicity Scale: From Molecules to Anions

Journal of organic chemistry, 2022-06, Vol.87 (11), p.7264-7273

2022

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Theoretical, Semiempirical, and Experimental Solvatochromic Comparison Methods for the Construction of the α 1 Scale of Hydrogen-Bond Donation of Solvents

Journal of organic chemistry, 2022-05, Vol.87 (9), p.6273-6287

2022

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Hydrogen-Bond Acceptance of Solvents: a 19 F Solvatomagnetic  1 Database to Replace Solvatochromic and Solvatovibrational Scales

Journal of organic chemistry, 2021-03, Vol.86 (5), p.4143-4158

2021

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Hydrogen-Bond Acceptance of Solvents: A 19 F Solvatomagnetic β 1 Database to Replace Solvatochromic and Solvatovibrational Scales

Journal of organic chemistry, 2021-03, Vol.86 (5), p.4143-4158

2021

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Measurement of the hydrogen bond acceptance of ionic liquids and green solvents by the F solvatomagnetic comparison method

Green chemistry : an international journal and green chemistry resource : GC, 2021-03, Vol.23 (4), p.1816-1822

2021

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Measurement of the hydrogen bond acceptance of ionic liquids and green solvents by the 19 F solvatomagnetic comparison method

Green chemistry : an international journal and green chemistry resource : GC, 2021-03, Vol.23 (4), p.1816-1822

2021

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Measurement of the hydrogen bond acceptance of ionic liquids and green solvents by the 19F solvatomagnetic comparison method

Green chemistry : an international journal and green chemistry resource : GC, 2021-01, Vol.23 (4), p.1816-1822

2021

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A Database of Dispersion-Induction DI, Electrostatic ES, and Hydrogen Bonding α 1 and β 1 Solvent Parameters and Some Applications to the Multiparameter Correlation Analysis of Solvent Effects

The journal of physical chemistry. B, 2015-02, Vol.119 (7), p.3174-3184

2015

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The pK(BHX) database: toward a better understanding of hydrogen-bond basicity for medicinal chemists

Journal of medicinal chemistry, 2009-07, Vol.52 (14), p.4073-4086

2009

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Theoretical, Semiempirical, and Experimental Solvatochromic Comparison Methods for the Construction of the α1 Scale of Hydrogen-Bond Donation of Solvents

Journal of organic chemistry, 2022-05, Vol.87 (9), p.6273-6287

2022

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Correlation analysis of solvent effects on solvolysis rates: What can the empirical parameters of solvents actually say?

Journal of physical organic chemistry, 2020-09, Vol.33 (9), p.n/a

2020

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Determination of a Solvent Hydrogen-Bond Acidity Scale by Means of the Solvatochromism of Pyridiniurn-N-phenolate Betaine Dye 30 and PCM-TD-DFT Calculations

The journal of physical chemistry. B, 2014-05, Vol.118 (17), p.4605-4614

2014

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Solvent polarity scales: determination of new E T (30) values for 84 organic solvents

Journal of physical organic chemistry, 2014-06, Vol.27 (6), p.512-518

2014

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Site of Protonation of Nicotine and Nornicotine in the Gas Phase: Pyridine or Pyrrolidine Nitrogen?

Journal of the American Chemical Society, 2002-09, Vol.124 (35), p.10552-10562

2002

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Hydrogen-Bond Acceptance of Solvents: A 19F Solvatomagnetic β1 Database to Replace Solvatochromic and Solvatovibrational Scales

Journal of organic chemistry, 2021-03, Vol.86 (5), p.4143-4158

2021

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Comment on the Article "Gutmann Donor and Acceptor Numbers for Ionic Liquids" by M. Schmeisser, P. Illner, R. Puchta, A. Zahl, and R. vanEldik (Chem. Eur. J. 2012, 18, 10969-10982)

Chemistry : a European journal, 2013-12, Vol.19 (49), p.16832

2013

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The pKBHX Database: Toward a Better Understanding of Hydrogen-Bond Basicity for Medicinal Chemists

Solvent polarity scales: determination of new ET(30) values for 84 organic solvents

The Diiodine Basicity Scale: Toward a General Halogen-Bond Basicity Scale

Solvatomagnetic Comparison Method: A Proper Quantification of Solvent Hydrogen-Bond Basicity

Influence of the Structure of Polyfluorinated Alcohols on Brønsted Acidity/Hydrogen-Bond Donor Ability and Consequences on the Promoter Effect

Solvatochromic Shifts in UV–Vis Absorption Spectra: The Challenging Case of 4‑Nitropyridine N‑Oxide

Lewis basicity and affinity scales: data and measurement

Halogen-bond geometry: a crystallographic database investigation of dihalogen complexes

The pK BHX Hydrogen-Bond Basicity Scale: From Molecules to Anions

The p K BHX Hydrogen-Bond Basicity Scale: From Molecules to Anions

Theoretical, Semiempirical, and Experimental Solvatochromic Comparison Methods for the Construction of the α 1 Scale of Hydrogen-Bond Donation of Solvents

Hydrogen-Bond Acceptance of Solvents: a 19 F Solvatomagnetic  1 Database to Replace Solvatochromic and Solvatovibrational Scales

Hydrogen-Bond Acceptance of Solvents: A 19 F Solvatomagnetic β 1 Database to Replace Solvatochromic and Solvatovibrational Scales

Measurement of the hydrogen bond acceptance of ionic liquids and green solvents by the F solvatomagnetic comparison method

Measurement of the hydrogen bond acceptance of ionic liquids and green solvents by the 19 F solvatomagnetic comparison method

Measurement of the hydrogen bond acceptance of ionic liquids and green solvents by the 19F solvatomagnetic comparison method

A Database of Dispersion-Induction DI, Electrostatic ES, and Hydrogen Bonding α 1 and β 1 Solvent Parameters and Some Applications to the Multiparameter Correlation Analysis of Solvent Effects

The pK(BHX) database: toward a better understanding of hydrogen-bond basicity for medicinal chemists

Theoretical, Semiempirical, and Experimental Solvatochromic Comparison Methods for the Construction of the α1 Scale of Hydrogen-Bond Donation of Solvents

Correlation analysis of solvent effects on solvolysis rates: What can the empirical parameters of solvents actually say?

Determination of a Solvent Hydrogen-Bond Acidity Scale by Means of the Solvatochromism of Pyridiniurn-N-phenolate Betaine Dye 30 and PCM-TD-DFT Calculations

Solvent polarity scales: determination of new E T (30) values for 84 organic solvents

Site of Protonation of Nicotine and Nornicotine in the Gas Phase: Pyridine or Pyrrolidine Nitrogen?

Hydrogen-Bond Acceptance of Solvents: A 19F Solvatomagnetic β1 Database to Replace Solvatochromic and Solvatovibrational Scales

Comment on the Article "Gutmann Donor and Acceptor Numbers for Ionic Liquids" by M. Schmeisser, P. Illner, R. Puchta, A. Zahl, and R. vanEldik (Chem. Eur. J. 2012, 18, 10969-10982)

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