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Strong Bases and beyond: The Prominent Contribution of Neutral Push–Pull Organic Molecules towards Superbases in the Gas Phase.
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- International Journal of Molecular Sciences, 2024, v. 25, n. 11, p. 5591, doi. 10.3390/ijms25115591
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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.
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- Molecules, 2022, v. 27, n. 14, p. N.PAG, doi. 10.3390/molecules27144370
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Evolution of Chemical Research in Nice, Côte d′Azur: From Early Laboratories to the 'Institut de Chimie de Nice'.
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- ChemPlusChem, 2022, v. 87, n. 6, p. 1, doi. 10.1002/cplu.202100532
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Front Cover: Evolution of Chemical Research in Nice, Côte d′Azur: From Early Laboratories to the 'Institut de Chimie de Nice'(ChemPlusChem 6/2022).
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- ChemPlusChem, 2022, v. 87, n. 6, p. 1, doi. 10.1002/cplu.202200130
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Metal Triflates as Catalysts in Organic Synthesis: Determination of Their Lewis Acidity by Mass Spectrometry.
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- ChemPlusChem, 2022, v. 87, n. 6, p. 1, doi. 10.1002/cplu.202200037
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Glossary of terms used in physical organic chemistry (IUPAC Recommendations 2021).
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- Pure & Applied Chemistry, 2022, v. 94, n. 4, p. 353, doi. 10.1515/pac-2018-1010
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- Article
Enthalpies of Adduct Formation between Boron Trifluoride and Selected Organic Bases in Solution: Toward an Accurate Theoretical Entry to Lewis Basicity.
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- Molecules, 2021, v. 26, n. 21, p. 6659, doi. 10.3390/molecules26216659
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- Article
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.
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- Symmetry (20738994), 2021, v. 13, n. 9, p. 1554, doi. 10.3390/sym13091554
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Purine tautomeric preferences and bond-length alternation in relation with protonation-deprotonation and alkali metal cationization.
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- Journal of Molecular Modeling, 2020, v. 26, n. 5, p. 1, doi. 10.1007/s00894-020-4343-6
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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 SbCl<sub>5</sub> and BF<sub>3</sub>.
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- ChemPhysChem, 2019, v. 20, n. 19, p. 2566, doi. 10.1002/cphc.201900691
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Bond Strength and Reactivity Scales for Lewis Superacid Adducts: A Comparative Study with In(OTf)<sub>3</sub> and Al(OTf)<sub>3</sub>.
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- ChemPhysChem, 2017, v. 18, n. 6, p. 683, doi. 10.1002/cphc.201601389
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- Article
Dinuclear Copper Intermediates in Copper(I)-Catalyzed Azide-Alkyne Cycloaddition Directly Observed by Electrospray Ionization Mass Spectrometry.
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- Angewandte Chemie, 2015, v. 127, n. 10, p. 3108, doi. 10.1002/ange.201410301
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Dinuclear Copper Intermediates in Copper(I)-Catalyzed Azide-Alkyne Cycloaddition Directly Observed by Electrospray Ionization Mass Spectrometry.
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- Angewandte Chemie International Edition, 2015, v. 54, n. 10, p. 3065, doi. 10.1002/anie.201410301
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Insight into the Mechanisms of the Multicomponent Ugi and Ugi-Smiles Reactions by ESI-MS(/MS) (Eur. J. Org. Chem. 32/2014).
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- European Journal of Organic Chemistry, 2014, v. 2014, n. 32, p. n/a, doi. 10.1002/ejoc.201490090
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Insight into the Mechanisms of the Multicomponent Ugi and Ugi-Smiles Reactions by ESI-MS(/MS).
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- European Journal of Organic Chemistry, 2014, v. 2014, n. 32, p. 7087, doi. 10.1002/ejoc.201403179
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- Article
Catalytic Effect of Cesium Cation Adduct Formation on the Decarboxylation of Carboxylate Ions in the Gas Phase.
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- Chemistry - A European Journal, 2014, v. 20, n. 3, p. 815, doi. 10.1002/chem.201303669
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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. van Eldik ( Chem. Eur. J. 2012, 18, 10969-10982).
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- Chemistry - A European Journal, 2013, v. 19, n. 49, p. 16832, doi. 10.1002/chem.201300147
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Interaction between the Cesium Cation and Cesium Carboxylates: An Extended Cs<sup>+</sup> Basicity Scale.
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- ChemPlusChem, 2013, v. 78, n. 9, p. 1195, doi. 10.1002/cplu.201300181
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Metal triflates and triflimides as Lewis 'superacids': preparation, synthetic application and affinity tests by mass spectrometry Metal triflates and triflimides as Lewis 'superacids': preparation, synthetic application and affinity tests by mass spectrometry
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- Journal of Physical Organic Chemistry, 2013, v. 26, n. 2, p. 87, doi. 10.1002/poc.3019
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Mass spectrometric characterization of metal triflates and triflimides (Lewis superacid catalysts) by electrospray ionization and tandem mass spectrometry.
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- Rapid Communications in Mass Spectrometry: RCM, 2010, v. 24, n. 17, p. 2611, doi. 10.1002/rcm.4680
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Gas-Phase Protonation and Deprotonation of Acrylonitrile Derivatives NCCHCHX (X=CH<sub>3</sub>, NH<sub>2</sub>, PH<sub>2</sub>, SiH<sub>3</sub>).
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- Chemistry - A European Journal, 2006, v. 12, n. 36, p. 9254, doi. 10.1002/chem.200600154
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Bonding energetics in clusters formed by cesium salts: a study by collision-induced dissociation and density functional theory.
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- Rapid Communications in Mass Spectrometry: RCM, 2006, v. 20, n. 13, p. 2057, doi. 10.1002/rcm.2552
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Are nicotinoids protonated on the pyridine or the amino nitrogen in the gas phase?
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- Journal of Physical Organic Chemistry, 2006, v. 19, n. 2, p. 104, doi. 10.1002/poc.1006
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Experimental (FT-ICR) and theoretical (DFT) estimation of the basic site preference for the bidentate molecule 2-(β-aminoethyl)-pyridine: similarity with histamine.
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- Journal of Physical Organic Chemistry, 2005, v. 18, n. 8, p. 856, doi. 10.1002/poc.954
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Computational study of cesium cation-humic substance interactions. A neutral analogue ligand molecules approach.
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- Proceedings of the Estonian Academy of Sciences, Chemistry, 2005, v. 54, n. 2, p. 70, doi. 10.3176/chem.2005.2.03
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Investigations of cluster ions formed between cesium cations and benzoic, salicylic and phthalic acids by electrospray mass spectrometry and density-functional theory calculations. Toward a modeling of the interaction of Cs<sup>+</sup> with humic substances
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- Rapid Communications in Mass Spectrometry: RCM, 2005, v. 19, n. 4, p. 568, doi. 10.1002/rcm.1818
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Determination of benzene, toluene, ethylbenzene and xylenes in air by solid phase micro-extraction/gas chromatography/mass spectrometry.
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- Analytical & Bioanalytical Chemistry, 2004, v. 380, n. 5/6, p. 824, doi. 10.1007/s00216-004-2837-1
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Ab initio study of tautomerism and of basicity center preference in histamine, from gas phase to solution-comparison with experimental data (gas phase, solution, solid state).
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- Journal of Physical Organic Chemistry, 2003, v. 16, n. 10, p. 783, doi. 10.1002/poc.670
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Enhanced Li<sup>+</sup> Binding Energies in Alkylbenzene Derivatives: The Scorpion Effect.
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- Chemistry - A European Journal, 2003, v. 9, n. 18, p. 4330, doi. 10.1002/chem.200304863
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Consequences of proton transfer in guanidine.
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- Journal of Physical Organic Chemistry, 2003, v. 16, n. 2, p. 91, doi. 10.1002/poc.578
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The Gas-Phase Acidity of HCP, CH<sub>3</sub>CP, HCAs, and CH<sub>3</sub>CAs: An Unexpected Enhanced Acidity of the Methyl Group.
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- Chemistry - A European Journal, 2002, v. 8, n. 21, p. 4919, doi. 10.1002/1521-3765(20021104)8:21<4919::AID-CHEM4919>3.0.CO;2-J
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Vinyl- and ethynylsilanes, -germanes and -stannanes. A new case of dissociative proton attachment.
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- Journal of Physical Organic Chemistry, 2002, v. 15, n. 8, p. 509, doi. 10.1002/poc.498
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Thermochemical aspects of proton transfer in the gas phase.
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- Journal of Mass Spectrometry, 2001, v. 36, n. 7, p. 699, doi. 10.1002/jms.202
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PM3 semiempirical calculations of lithium-cation and proton affinities for XYZPO and XYSO.
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- International Journal of Quantum Chemistry, 1996, v. 59, n. 5, p. 409, doi. 10.1002/(SICI)1097-461X(1996)59:5<409::AID-QUA5>3.0.CO;2-1
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Acidity and basicity of thiocarboxamides in the gas phase.
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- Journal of Physical Organic Chemistry, 1994, v. 7, n. 9, p. 511, doi. 10.1002/poc.610070907
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Hydrogen-bonding 8.
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- Journal of Physical Organic Chemistry, 1989, v. 2, n. 7, p. 540, doi. 10.1002/poc.610020706
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Transmission of substituent effects through unsaturated systems. I-relative magnitudes of proton and carbon substituent chemical shifts in ethylenes, butadienes, α-enones and benzenes.
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- Magnetic Resonance in Chemistry, 1977, v. 9, n. 4, p. 181, doi. 10.1002/mrc.1270090402
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