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Strong Bases and beyond: The Prominent Contribution of Neutral Push–Pull Organic Molecules towards Superbases in the Gas Phase

International journal of molecular sciences, 2024-06, Vol.25 (11), p.5591

2024

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Nitriles with High Gas-Phase Basicity—Part II Transmission of the Push–Pull Effect through Methylenecyclopropene and Cyclopropenimine Scaffolds Intercalated between Different Electron Donor(s) and the Cyano N-Protonation Site

Molecules (Basel, Switzerland), 2022-07, Vol.27 (14), p.4370

2022

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Push–Pull Effect on the Gas-Phase Basicity of Nitriles: Transmission of the Resonance Effects by Methylenecyclopropene and Cyclopropenimine π-Systems Substituted by Two Identical Strong Electron Donors

Symmetry (Basel), 2021-09, Vol.13 (9), p.1554

2021

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Lewis basicity and affinity scales: data and measurement

1, 2010

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Enhanced Basicity of Push–Pull Nitrogen Bases in the Gas Phase

Chemical reviews, 2016-11, Vol.116 (22), p.13454-13511

2016

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Lewis basicity of alkyl carbonates and other esters. The Gutmann Donor Number (DN), a flawed indicator? Boron trifluoride adduct-formation enthalpy, experimentally or computationally determined, as a reliable alternative

Journal of molecular liquids, 2023-01, Vol.370, p.120997, Article 120997

2023

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Clarification to the article “The New Definitions of the Mole and Kilogram: How and Why These SI Units Took their New Status,” Phys. Teach. 58, 477–479 (2020)

The Physics teacher, 2023-04, Vol.61 (4), p.244-245

2023

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Noble gas cations as Lewis acids: Adduct formation with Lewis bases with high ionization energies

Chemical physics, 2023-07, Vol.571, p.111918, Article 111918

2023

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Evolution of Chemical Research in Nice, Côte d'Azur: From Early Laboratories to the 'Institut de Chimie de Nice'

ChemPlusChem (Weinheim, Germany), 2022-06, Vol.87 (6), p.e202100532-e202100532

2022

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Metal Triflates as Catalysts in Organic Synthesis: Determination of Their Lewis Acidity by Mass Spectrometry

ChemPlusChem (Weinheim, Germany), 2022-06, Vol.87 (6), p.e202200037-n/a

2022

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Directionality of Cation/Molecule Bonding in Lewis Bases Containing the Carbonyl Group

The journal of physical chemistry. A, Molecules, spectroscopy, kinetics, environment, & general theory, 2017-09, Vol.121 (36), p.6810-6822

2017

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Organometallic superacids and hyperacids: Acidity enhancement by internal bonding with a strong electron-pair acceptor group BX2

Chemical physics letters, 2021-01, Vol.763, p.138207, Article 138207

2021

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Energetics and Structures of Adducts of JohnPhos(Au+), PPh3(Au+), and IPr(Au+) with Organic Substrates: A Mass Spectrometry and DFT Study

Organometallics, 2021-06, Vol.40 (11), p.1642-1653

2021

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Insight into the Mechanisms of the Multicomponent Ugi and Ugi-Smiles Reactions by ESI-MS(/MS)

European journal of organic chemistry, 2014-11, Vol.2014 (32), p.7087-7090

2014

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On the Lewis Basicity of Phosphoramides: A Critical Examination of Their Donor Number through Comparison of Enthalpies of Adduct Formation with SbCl5 and BF3

Chemphyschem, 2019-10, Vol.20 (19), p.2566-2576

2019

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Enthalpies of Adduct Formation between Boron Trifluoride and Selected Organic Bases in Solution: Toward an Accurate Theoretical Entry to Lewis Basicity

Molecules (Basel, Switzerland), 2021-11, Vol.26 (21), p.6659

2021

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Assessment of the nature of interactions of cations with cycloheptatriene derivatives using change in the aromaticity: Comparison with electron density and NBO results

Molecular physics, 2020-04, Vol.118 (8), p.e1662507

2020

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Gas-Phase Lithium Cation Basicity: Revisiting the High Basicity Range by Experiment and Theory

Journal of the American Society for Mass Spectrometry, 2014-11, Vol.25 (11), p.1962-1973

2014

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An Excursion into the History of Chromatography: Mikhail Tswett, From Asti, Italy, to Tartu, Estonia

Chromatographia, 2019-02, Vol.82 (2), p.519-521

Gal, Jean-François

2019

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Quality Control of a Functionalized Polymer Catalyst by Energy Dispersive X‑ray Spectrometry (EDX or EDS)

Analytical chemistry (Washington), 2019-02, Vol.91 (3), p.1773-1778

2019

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Change of the favored routes of EI MS fragmentation when proceeding from N¹, N¹-dimethyl-N²-arylformamidines to 1,1,3,3-tetraalkyl-2-arylguanidines: substituent effects

Journal of mass spectrometry., 2010-07, Vol.45 (7), p.762-771

2010

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Effect of the Number of Methyl Groups on the Cation Affinity of Oxygen, Nitrogen, and Phosphorus Sites of Lewis Bases

The journal of physical chemistry. A, Molecules, spectroscopy, kinetics, environment, & general theory, 2016-11, Vol.120 (45), p.9109-9116

2016

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Bond Strength and Reactivity Scales for Lewis Superacid Adducts: A Comparative Study with In(OTf)3 and Al(OTf)3

Chemphyschem, 2017-03, Vol.18 (6), p.683-691

2017

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An Overview of Lewis Basicity and Affinity Scales

Journal of chemical education, 2011-12, Vol.88 (12), p.1651-1657

2011

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Revised and Expanded Scale of Gas-Phase Lithium Cation Basicities. An Experimental and Theoretical Study

The journal of physical chemistry. A, Molecules, spectroscopy, kinetics, environment, & general theory, 2000-03, Vol.104 (12), p.2824-2833

2000

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Strong Bases and beyond: The Prominent Contribution of Neutral Push–Pull Organic Molecules towards Superbases in the Gas Phase

Nitriles with High Gas-Phase Basicity—Part II Transmission of the Push–Pull Effect through Methylenecyclopropene and Cyclopropenimine Scaffolds Intercalated between Different Electron Donor(s) and the Cyano N-Protonation Site

Push–Pull Effect on the Gas-Phase Basicity of Nitriles: Transmission of the Resonance Effects by Methylenecyclopropene and Cyclopropenimine π-Systems Substituted by Two Identical Strong Electron Donors

Lewis basicity and affinity scales: data and measurement

Enhanced Basicity of Push–Pull Nitrogen Bases in the Gas Phase

Lewis basicity of alkyl carbonates and other esters. The Gutmann Donor Number (DN), a flawed indicator? Boron trifluoride adduct-formation enthalpy, experimentally or computationally determined, as a reliable alternative

Clarification to the article “The New Definitions of the Mole and Kilogram: How and Why These SI Units Took their New Status,” Phys. Teach. 58, 477–479 (2020)

Noble gas cations as Lewis acids: Adduct formation with Lewis bases with high ionization energies

Evolution of Chemical Research in Nice, Côte d'Azur: From Early Laboratories to the 'Institut de Chimie de Nice'

Metal Triflates as Catalysts in Organic Synthesis: Determination of Their Lewis Acidity by Mass Spectrometry

Directionality of Cation/Molecule Bonding in Lewis Bases Containing the Carbonyl Group

Organometallic superacids and hyperacids: Acidity enhancement by internal bonding with a strong electron-pair acceptor group BX2

Energetics and Structures of Adducts of JohnPhos(Au+), PPh3(Au+), and IPr(Au+) with Organic Substrates: A Mass Spectrometry and DFT Study

Insight into the Mechanisms of the Multicomponent Ugi and Ugi-Smiles Reactions by ESI-MS(/MS)

On the Lewis Basicity of Phosphoramides: A Critical Examination of Their Donor Number through Comparison of Enthalpies of Adduct Formation with SbCl5 and BF3

Enthalpies of Adduct Formation between Boron Trifluoride and Selected Organic Bases in Solution: Toward an Accurate Theoretical Entry to Lewis Basicity

Assessment of the nature of interactions of cations with cycloheptatriene derivatives using change in the aromaticity: Comparison with electron density and NBO results

Gas-Phase Lithium Cation Basicity: Revisiting the High Basicity Range by Experiment and Theory

An Excursion into the History of Chromatography: Mikhail Tswett, From Asti, Italy, to Tartu, Estonia

Quality Control of a Functionalized Polymer Catalyst by Energy Dispersive X‑ray Spectrometry (EDX or EDS)

Change of the favored routes of EI MS fragmentation when proceeding from N¹, N¹-dimethyl-N²-arylformamidines to 1,1,3,3-tetraalkyl-2-arylguanidines: substituent effects

Effect of the Number of Methyl Groups on the Cation Affinity of Oxygen, Nitrogen, and Phosphorus Sites of Lewis Bases

Bond Strength and Reactivity Scales for Lewis Superacid Adducts: A Comparative Study with In(OTf)3 and Al(OTf)3

An Overview of Lewis Basicity and Affinity Scales

Revised and Expanded Scale of Gas-Phase Lithium Cation Basicities. An Experimental and Theoretical Study

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