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Yáñez M.
Yanez M.
Yáñez Manuel
Yanez Manuel
Yañez Manuel
Yáñez Manuel
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Yáñez
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http://hub.abes.fr/acs/periodical/jacsat/1984/volume_106/issue_2/101021ja00314a027/authorship/2
http://hub.abes.fr/acs/periodical/jpchax/1989/volume_93/issue_10/101021j100347a014/authorship/3
http://hub.abes.fr/acs/periodical/jacsat/1978/volume_100/issue_22/101021ja00490a024/authorship/2
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http://hub.abes.fr/acs/periodical/jpchax/1990/volume_94/issue_12/101021j100375a011/authorship/3
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http://hub.abes.fr/acs/periodical/jpcafh/2008/volume_112/issue_42/101021jp8051328/authorship/3
http://hub.abes.fr/acs/periodical/jpcafh/2004/volume_108/issue_46/101021jp046624z/authorship/3
http://hub.abes.fr/acs/periodical/jpcafh/2006/volume_110/issue_32/101021jp0628737/authorship/4
http://hub.abes.fr/acs/periodical/jpcafh/2002/volume_106/issue_40/101021jp021160v/authorship/7
http://hub.abes.fr/acs/periodical/jpcafh/2003/volume_107/issue_18/101021jp021619l/authorship/4
http://hub.abes.fr/acs/periodical/jpcafh/2000/volume_104/issue_34/101021jp000674w/authorship/4
http://hub.abes.fr/acs/periodical/jpcafh/2000/volume_104/issue_47/101021jp0023112/authorship/4
http://hub.abes.fr/acs/periodical/jpcafh/2002/volume_106/issue_40/101021jp021159w/authorship/4
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http://hub.abes.fr/acs/periodical/jpcafh/2002/volume_106/issue_40/101021jp026386c/authorship/4
http://hub.abes.fr/acs/periodical/joceah/1984/volume_49/issue_23/101021jo00197a010/authorship/5
http://hub.abes.fr/acs/periodical/jacsat/1988/volume_110/issue_9/101021ja00217a001/authorship/3
http://hub.abes.fr/acs/periodical/jacsat/1984/volume_106/issue_22/101021ja00334a016/authorship/3
http://hub.abes.fr/acs/periodical/jacsat/1979/volume_101/issue_22/101021ja00516a007/authorship/4
http://hub.abes.fr/acs/periodical/jacsat/1979/volume_101/issue_13/101021ja00507a011/authorship/2
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http://hub.abes.fr/acs/periodical/joceah/1995/volume_60/issue_6/101021jo00111a023/authorship/2
http://hub.abes.fr/acs/periodical/jpchax/1992/volume_96/issue_7/101021j100186a045/authorship/3
http://hub.abes.fr/springer/periodical/214/1990/volume_77/issue_1/B8ECE60F1B136116E053120B220A89FA/authorship/4
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Author
of
Relationship between substituent-induced energy and charge effects in proton-transfer equilibria involving heteroaromatic nitrogen systems. The lone pair charge approach
A theoretical study of proton addition to oxirane, aziridine, and 2-azirene
Proton affinities and preferred protonation sites in 3- and 4-substituted pyridines. Prediction from 1s orbital energies
Binding of ammonium ion to azoles in the gas phase. A theoretical study of the N.cntdot.H+.cntdot.N ionic hydrogen bond
Basicity of azoles. Part 6. Calculated intrinsic basicities for methyl-substituted pyrazoles and imidazoles. Comparison to aqueous solution data: N-methylation effect
A theoretical study of hydrogen bonding in malonaldehyde
The .alpha. vs. .beta. protonation of pyrrole and indole
Stabilization of nitrogen-containing three-membered rings by proton and lithium ion association in the gas phase
Enhanced Li+ binding energies of some azines: a molecular orbital study
Experimental and theoretical study of C2H4OAl+ complexes in the gas phase
Electrophilic aromatic nitration in the gas phase
Protonation and proton affinity of anisole. A theoretical study
Gas-phase basicities of .beta.-lactams and azetidines. Cyclization effects. An experimental and theoretical study
Cyclization effects on the gas-phase basicities of esters and ethers. An experimental and MO study
Thermochemistry of the Reactions F+(3P, 1D) + PH3 in the Gas Phase
Ab Initio Study of the Structural, Energetic, Bonding, and IR Spectroscopic Properties ofComplexes with Dihydrogen Bonds
Low Energy Dissociation Processes of Ionized Cyclohexene: A Theoretical Insight,
Synthesis, X-ray Structure, and Properties of 2-(1‘-Pyridin-2‘-one)Benzimidazole
Gas-Phase Structure of Protonated Histidine and Histidine Methyl Ester: CombinedExperimental Mass Spectrometry and Theoretical ab Initio Study
Hydrogen Bond vs Proton Transfer in HZSM5 Zeolite. A Theoretical Study
Experimental and Theoretical Investigation of the Reactions between Glucose and Cu+ inthe Gas Phase
Gas-Phase Chemistry of Ethyl and Vinyl Amines, Phosphines, and Arsines: A DFT Studyof the Structure and Stability of Their Cu+ Complexes
Gas-Phase Deprotonation of Uracil−Cu2+ and Thiouracil−Cu2+ Complexes
Gas-Phase Reactions between Urea and Ca2+: The Importance of Coulomb Explosions
An ab Initio Study of 15N−11B Spin−Spin Coupling Constants for Borazine and SelectedDerivatives
Selenourea−Ca2+ Reactions in Gas Phase. Similarities and Dissimilarities with Urea andThiourea
Ni+ Reactions with Aminoacrylonitrile, A Species of Potential Astrochemical Relevance
Competition between X···H···Y Intramolecular Hydrogen Bonds and X····Y (X = O, S, andY = Se, Te) Chalcogen−Chalcogen Interactions
Two-Bond 19F−15N Spin−Spin Coupling Constants (2hJF-N) across F−H···N HydrogenBonds
Two-Bond 13C−15N Spin−Spin Coupling Constants (2hJC-N) Across C−H−N HydrogenBonds
One-Bond (1dJH-H) and Three-Bond (3dJX-M) Spin−Spin Coupling Constants AcrossX−H···H−M Dihydrogen Bonds
Resonance-Assisted Hydrogen Bonds: A Critical Examination. Structure and Stability ofthe Enols of β-Diketones and β-Enaminones
Are the Thiouracils Sulfur Bases in the Gas-phase?
Theoretical Survey of the Potential Energy Surface of Ethylenediamine + Cu+ Reactions
Gas-Phase Basicity of 2,7-Dimethyl-[1,2,4]-Triazepine Thio Derivatives
A Theoretical Study of the Reaction between N+(3P) and Formaldehyde and RelatedProcesses in the Gas Phase
Two-Bond 15N−19F Spin−Spin Coupling Constants (2hJN-F) across N−H+...F HydrogenBonds
A theoretical study of the structure and charge distribution of some alkynylcarbenium ions
Study of the gas-phase basicity of 1-methylazaindole, 7-methyl-7H-pyrrolo[2,3-b]pyridine, and related compounds
Experimental and theoretical study of lithium(1+) affinities of methyldiazoles
Bent Bonds in Benzocyclopropenes and Their Fluorinated Derivatives
Protonation energies and tautomerism of azoles. Basis set effects
Enhanced aluminum(1+) binding energies of some azoles: a theoretical study of azole-X+ (X = Na, K, Al) complexes
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