Influence des solvants sur la transition n → π - II. — Cétones saturées. Nouvelle méthode rigoureuse de calcul
J. Chim. Phys., 65 (1968) 1259-1265
Published online: 2017-05-28
Articles citing this article
The Citing articles tool gives a list of articles citing the current article.
The citing articles come from EDP Sciences database, as well as other publishers participating in CrossRef Cited-by Linking Program. You can set up your personal account to receive an email alert each time this article is cited by a new article (see the menu on the right-hand side of the abstract page).
Cited article:
This article has been cited by the following article(s):
Handbook of Solvents
Handbook of Solvents 511 (2019)https://doi.org/10.1016/B978-1-927885-38-3.50011-5
https://doi.org/10.1002/9781119044307.bref
Quantum Modeling of Complex Molecular Systems
Vincenzo Barone, Enrico Benassi and Ivan CarnimeoChallenges and Advances in Computational Chemistry and Physics, Quantum Modeling of Complex Molecular Systems 21 447 (2015)
https://doi.org/10.1007/978-3-319-21626-3_17
Handbook of Solvents
JAVIER CATALANHandbook of Solvents 581 (2014)
https://doi.org/10.1016/B978-1-895198-64-5.50016-7
A solvatochromic study of N-[4-(9-acridinylamino)-3-methoxyphenyl]methanesulfonamide hydrochloride: An experimental and theoretical approach
Katarzyna NowakSpectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy 130 208 (2014)
https://doi.org/10.1016/j.saa.2014.03.004
On the solvatochromism of the n ↔π* electronic transitions in ketones
Javier Catalán and Juan Pablo CatalánPhysical Chemistry Chemical Physics 13 (9) 4072 (2011)
https://doi.org/10.1039/c0cp02282a
https://doi.org/10.1002/9783527632220.refs
Characterization of solvent mixtures: preferential solvation of chemical probes in binary solvent mixtures of polar hydrogen-bond acceptor solvents with polychlorinated co-solvents
P. M. Mancini, A. Terenzani, C. Adam, A. del C. Pérez and L. R. VotteroJournal of Physical Organic Chemistry 12 (9) 713 (1999)
https://doi.org/10.1002/(SICI)1099-1395(199909)12:9<713::AID-POC182>3.0.CO;2-0
Extending the Solvent Acidiy Scale to Highly Acidic Organic Solvents: The Unique Photophysical Behaviour of 3,6-Diethyltetrazine
Javier Catalán and Cristina DíazEuropean Journal of Organic Chemistry 1999 (4) 885 (1999)
https://doi.org/10.1002/(SICI)1099-0690(199904)1999:4<885::AID-EJOC885>3.0.CO;2-W
Characterization of solvent mixtures. Part 8 — preferential solvation of chemical probes in binary solvent systems of a polar aprotic hydrogen-bond acceptor solvent with acetonitrile or nitromethane. Solvent effects on aromatic nucleophilic substitution reactions
P. M. E. Mancini, A. Terenzani, C. Adam, A. Pérez and L. R. VotteroJournal of Physical Organic Chemistry 12 (3) 207 (1999)
https://doi.org/10.1002/(SICI)1099-1395(199903)12:3<207::AID-POC113>3.0.CO;2-W
A Generalized Solvent Acidity Scale: The Solvatochromism of o‐tert‐Butylstilbazolium Betaine Dye and Its Homomorph o,o′‐Di‐tert‐butylstilbazolium Betaine Dye
Javier Catalán and Cristina DíazLiebigs Annalen 1997 (9) 1941 (1997)
https://doi.org/10.1002/jlac.199719970921
Solvent effects on aromatic nucleophilic substitution reactions. Part 7. Determination of the empirical polarity parameterET(30) for dipolar hydrogen bond acceptor-co-solvent (chloroform or dichloromethane) mixtures. Kinetics of the reactions of halonitrobenzenes with aliphatic amines
P. M. E. Mancini, A. Terenzani, C. Adam and L. R. VotteroJournal of Physical Organic Chemistry 10 (11) 849 (1997)
https://doi.org/10.1002/(SICI)1099-1395(199711)10:11<849::AID-PCA936>3.0.CO;2-3
Solvent effects on aromatic nucleophilic substitutions. Part 6. Kinetics of the reaction of 1‐chloro‐2, 4‐dinitrobenzene with piperidine in binary solvent mixtures
P. M. E. Mancini, A. Terenzani, M. G. Gasparri and L. R. VotteroJournal of Physical Organic Chemistry 9 (7) 459 (1996)
https://doi.org/10.1002/(SICI)1099-1395(199607)9:7<459::AID-POC806>3.0.CO;2-#
Determination of the empirical polarity parameter ET(30) for binary solvent mixtures
P. M. E. Mancini, A. Terenzani, M. G. Gasparri and L. R. VotteroJournal of Physical Organic Chemistry 8 (9) 617 (1995)
https://doi.org/10.1002/poc.610080908
Über Pyridinium‐N‐phenolat‐Betaine und ihre Verwendung zur Charakterisierung der Polarität von Lösungsmitteln, X. Erweiterung, Korrektur und Neudefinition der ET‐Lösungsmittelpolaritätsskala mit Hilfe eines lipophilen penta‐tert‐butyl‐substituierten Pyridinium‐N‐phenolat‐Betainfarbstoffes
Christian Reichardt and Erwin Harbusch‐GörnertLiebigs Annalen der Chemie 1983 (5) 721 (1983)
https://doi.org/10.1002/jlac.198319830502
Empirische Parameter der Lösungsmittelpolarität als lineare „Freie Enthalpie”-Beziehungen
Christian ReichardtAngewandte Chemie 91 (2) 119 (1979)
https://doi.org/10.1002/ange.19790910206
Empirical Parameters of Solvent Polarity as Linear Free‐Energy Relationships
Christian ReichardtAngewandte Chemie International Edition in English 18 (2) 98 (1979)
https://doi.org/10.1002/anie.197900981
Effet de Solvant en Résonance Magnétique Nucléaire du Carbone‐13. V. Autoassociation des Cétones Aliphatiques et Alicycliques Saturées
Bernard Tiffon and Jacques‐Emile DuboisOrganic Magnetic Resonance 12 (1) 24 (1979)
https://doi.org/10.1002/mrc.1270120106
Advances in Linear Free Energy Relationships
I. A. Koppel and V. A. PalmAdvances in Linear Free Energy Relationships 203 (1972)
https://doi.org/10.1007/978-1-4615-8660-9_5
Evolution en fonction dn solvant de la modulation de la banded'absorption n→ π* des cétones saturées
A. Cossé-Babbi and J.E. DuboisSpectrochimica Acta Part A: Molecular Spectroscopy 28 (3) 539 (1972)
https://doi.org/10.1016/0584-8539(72)80241-1
Zur theorie der α-ketosäuren
G. Fischer, G. Oehme and A. SchellenbergerTetrahedron 27 (22) 5683 (1971)
https://doi.org/10.1016/S0040-4020(01)91733-8