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Christian Laurence

Showing results (1-10 of 18) with videos related to

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The Journal of Organic Chemistry|July 5, 2024
A Collection of Dispersion Induction <i>DI</i>, Electrostatic <i>ES</i>, and Hydrogen Bonding α<sub>1</sub> and β<sub>1</sub> Parameters for 380 Solvents and What They Say on Solvent Effects on Rates, Equilibria, and SpectraChristian Laurence, Julien Legros, Daniela Vuluga
The Journal of Organic Chemistry|May 17, 2022
The p<i>K</i><sub>BHX</sub> Hydrogen-Bond Basicity Scale: From Molecules to AnionsNicolas Galland, Christian Laurence, Jean-Yves Le Questel
The Journal of Physical Chemistry. A|December 22, 2005
B3LYP and MP2 calculations of the enthalpies of hydrogen-bonded complexes of methanol with neutral bases and anions: comparison with experimental dataMawa Koné, Bertrand Illien, Jérôme Graton, et al.
The Journal of Physical Chemistry. A|October 19, 2011
Can quantum-mechanical calculations yield reasonable estimates of hydrogen-bonding acceptor strength? The case of hydrogen-bonded complexes of methanolMawa Koné, Bertrand Illien, Christian Laurence, et al.
The Journal of Organic Chemistry|November 10, 2005
An enthalpic scale of hydrogen-bond basicity. 3. Ammonia, primary, secondary, and tertiary aminesJérôme Graton, Michel Berthelot, François Besseau, et al.
Chemistry (Weinheim an Der Bergstrasse, Germany)|August 12, 2011
The diiodine basicity scale: toward a general halogen-bond basicity scaleChristian Laurence, Jérôme Graton, Michel Berthelot, et al.
The Journal of Organic Chemistry|April 25, 2022
Theoretical, Semiempirical, and Experimental Solvatochromic Comparison Methods for the Construction of the α<sub>1</sub> Scale of Hydrogen-Bond Donation of SolventsChristian Laurence, Sergui Mansour, Daniela Vuluga, et al.
The Journal of Physical Chemistry. B|January 29, 2015
A database of dispersion-induction DI, electrostatic ES, and hydrogen bonding α1 and β1 solvent parameters and some applications to the multiparameter correlation analysis of solvent effectsChristian Laurence, Julien Legros, Agisilaos Chantzis, et al.
The Journal of Organic Chemistry|February 15, 2021
Hydrogen-Bond Acceptance of Solvents: A <sup>19</sup>F Solvatomagnetic β<sub>1</sub> Database to Replace Solvatochromic and Solvatovibrational ScalesChristian Laurence, Sergui Mansour, Daniela Vuluga, et al.
Acta Crystallographica. Section B, Structural Science|August 30, 2003
Halogen-bond geometry: a crystallographic database investigation of dihalogen complexesCarole Ouvrard, Jean-Yves Le Questel, Michel Berthelot, et al.
Pageof 2

Showing results (1-10 of 18) with videos related to

Sort By:
Pageof 2
The Journal of Organic Chemistry|July 5, 2024
A Collection of Dispersion Induction <i>DI</i>, Electrostatic <i>ES</i>, and Hydrogen Bonding α<sub>1</sub> and β<sub>1</sub> Parameters for 380 Solvents and What They Say on Solvent Effects on Rates, Equilibria, and SpectraChristian Laurence, Julien Legros, Daniela Vuluga
The Journal of Organic Chemistry|May 17, 2022
The p<i>K</i><sub>BHX</sub> Hydrogen-Bond Basicity Scale: From Molecules to AnionsNicolas Galland, Christian Laurence, Jean-Yves Le Questel
The Journal of Physical Chemistry. A|December 22, 2005
B3LYP and MP2 calculations of the enthalpies of hydrogen-bonded complexes of methanol with neutral bases and anions: comparison with experimental dataMawa Koné, Bertrand Illien, Jérôme Graton, et al.
The Journal of Physical Chemistry. A|October 19, 2011
Can quantum-mechanical calculations yield reasonable estimates of hydrogen-bonding acceptor strength? The case of hydrogen-bonded complexes of methanolMawa Koné, Bertrand Illien, Christian Laurence, et al.
The Journal of Organic Chemistry|November 10, 2005
An enthalpic scale of hydrogen-bond basicity. 3. Ammonia, primary, secondary, and tertiary aminesJérôme Graton, Michel Berthelot, François Besseau, et al.
Chemistry (Weinheim an Der Bergstrasse, Germany)|August 12, 2011
The diiodine basicity scale: toward a general halogen-bond basicity scaleChristian Laurence, Jérôme Graton, Michel Berthelot, et al.
The Journal of Organic Chemistry|April 25, 2022
Theoretical, Semiempirical, and Experimental Solvatochromic Comparison Methods for the Construction of the α<sub>1</sub> Scale of Hydrogen-Bond Donation of SolventsChristian Laurence, Sergui Mansour, Daniela Vuluga, et al.
The Journal of Physical Chemistry. B|January 29, 2015
A database of dispersion-induction DI, electrostatic ES, and hydrogen bonding α1 and β1 solvent parameters and some applications to the multiparameter correlation analysis of solvent effectsChristian Laurence, Julien Legros, Agisilaos Chantzis, et al.
The Journal of Organic Chemistry|February 15, 2021
Hydrogen-Bond Acceptance of Solvents: A <sup>19</sup>F Solvatomagnetic β<sub>1</sub> Database to Replace Solvatochromic and Solvatovibrational ScalesChristian Laurence, Sergui Mansour, Daniela Vuluga, et al.
Acta Crystallographica. Section B, Structural Science|August 30, 2003
Halogen-bond geometry: a crystallographic database investigation of dihalogen complexesCarole Ouvrard, Jean-Yves Le Questel, Michel Berthelot, et al.
Pageof 2