Relevant bibliographies by topics / Mesomerism

Contents

  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers

Academic literature on the topic 'Mesomerism'

Author: Grafiati
Published: 4 June 2021
Last updated: 4 March 2023

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Journal articles on the topic "Mesomerism"

1

Wepster, B. M., and P. E. Verkade. "Steric effects on mesomerism. IV. Steric effects on mesomerism in derivatives of ortho-nitro-acetanilide." Recueil des Travaux Chimiques des Pays-Bas 68, no. 1 (2010): 88–110. http://dx.doi.org/10.1002/recl.19490680110.

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Wepster, B. M., and P. E. Verkade. "Steric effects on mesomerism. V.) steric effects on mesomerism in derivatives of para-nitro-acetanilide." Recueil des Travaux Chimiques des Pays-Bas 69, no. 11 (2010): 1393–406. http://dx.doi.org/10.1002/recl.19500691109.

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Zotti, Linda A., and Edmund Leary. "Taming quantum interference in single molecule junctions: induction and resonance are key." Physical Chemistry Chemical Physics 22, no. 10 (2020): 5638–46. http://dx.doi.org/10.1039/c9cp06384f.

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Ritchie, James P. "A look at mesomerism in nitrobenzene." Tetrahedron 44, no. 24 (1988): 7465–78. http://dx.doi.org/10.1016/s0040-4020(01)86241-4.

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Rosenthal, Uwe. "Equilibria and mesomerism/valence tautomerism of group 4 metallocene complexes." Chemical Society Reviews 49, no. 7 (2020): 2119–39. http://dx.doi.org/10.1039/c9cs00637k.

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Priority of equilibrium: reactivity of unusual group 4 metallocene complexes is best explained by the equilibrium and only additionally by the mesomerism/valence tautomerism. The equilibrium predominates the empirically found experimental results.
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Carissan, Yannick, Nicolas Goudard, Denis Hagebaum-Reignier, and Stéphane Humbel. "HuLiS, a program to teach mesomerism and more." Journal of Physics: Conference Series 738 (August 2016): 012015. http://dx.doi.org/10.1088/1742-6596/738/1/012015.

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Lincke, Gerhard. "On quinacridones and their supramolecular mesomerism within the crystal lattice." Dyes and Pigments 52, no. 3 (2002): 169–81. http://dx.doi.org/10.1016/s0143-7208(01)00085-7.

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Wepster, B. M. "Steric effects on mesomerism VIII : Benzoquinuclidine, an aromatic amine without mesomeric interaction between the benzene ring and the amino group." Recueil des Travaux Chimiques des Pays-Bas 71, no. 12 (2010): 1159–70. http://dx.doi.org/10.1002/recl.19520711202.

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Kofod, H., L. E. Sutton, W. A. de Jong, P. E. Verkade, and B. M. Wepster. "Steric effects on mesomerism. VI. Preparation and dipole moment of nitrodurene." Recueil des Travaux Chimiques des Pays-Bas 71, no. 5 (2010): 521–24. http://dx.doi.org/10.1002/recl.19520710514.

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Wepster, B. M. "Steric effects on mesomerism: XIII. Preparation of 2,6-dimethyl-4-nitroaniline." Recueil des Travaux Chimiques des Pays-Bas 73, no. 10 (2010): 809–18. http://dx.doi.org/10.1002/recl.19540731004.

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Dissertations / Theses on the topic "Mesomerism"

1

Lin, Shun-hua. "Resonance raman studies of hemoproteins and model heme complexes." Diss., Georgia Institute of Technology, 1987. http://hdl.handle.net/1853/30311.

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Marley, H. "The synthesis and reactivity of triazolopyrimidine mesomeric betaines." Thesis, Heriot-Watt University, 1988. http://hdl.handle.net/10399/993.

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Thirot, Gérard. "Modelisation des effets de substituants. Approche nouvelle des effets mesomeres." Paris 7, 1998. http://www.theses.fr/1998PA077296.

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Une analyse critique des representations en usage des effets electroniques des substituants met en evidence leurs insuffisances. La variabilite des effets de substituants en fonction du type de reactivite est etudie par analyse de la variance et analyse en composantes principales (acp). On met en evidence 4 types d'effets et 4 types de comportements des substituants (inductif, conjugatif, accepteur resonnant, resonnant donneur). Ces 4 effets sont quantifies en evitant les approximations incorrectes. L'ensemble des facteurs obtenus permet des modelisations precises dans tous les domaines couver
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4

Gholipour, Shilabin Abbas. "Seven-membered ring mesomeric betaines from anti-Hückel aromatics to model compounds of the pyrrolobenzodiazepine alkaloids circumdatin A and B = Siebengliedrige Ringe in mesomeren Betainen /." [S.l.] : [s.n.], 2005. http://deposit.ddb.de/cgi-bin/dokserv?idn=975505645.

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DARI, SAID. "Analyse theorique et experimentale du moment dipolaire de molecules en solution. Application a quelques etudes de conformeres et de mesomeres par une nouvelle methode de calcul." Nantes, 1996. http://www.theses.fr/1996NANT2003.

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Plusieurs aspects fondamentaux de la dipolemetrie en solutions diluees sont etudies, la methode amelioree sur certains points, est ensuite appliquee a quelques molecules organiques. L'analyse des formules de la refraction (rm) et de la polarisation (pm) moleculaires montre que les expressions classiques d'hedestrand ou d'halverstadt et kumler devraient etre remplacees par des expressions plus rigoureuses basees sur l'extrapolation a concentration nulle de rm et pm (et non le carre de l'indice de refraction et la constante dielectrique). La precision des valeurs experimentales du moment dipolai
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Gholipour, Shilabin Abbas [Verfasser]. "Seven-membered ring mesomeric betaines : from anti-Hückel aromatics to model compounds of the pyrrolobenzodiazepine alkaloids circumdatin A and B = Siebengliedrige Ringe in mesomeren Betainen / vorgelegt von Abbas Gholipour Shilabin." 2005. http://d-nb.info/975505645/34.

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Books on the topic "Mesomerism"

1

Garti, Nissim, Raffaele Mezzenga, and P. Somasundaran. Self-assembled supramolecular architectures: Lyotropic liquid crystals. John Wiley & Sons, Inc., 2012.

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Petrovich, Olekhnovich Lev, and Zhdanov I͡U︡ A, eds. Molecular design of tautomeric compounds. D. Reidel Pub. Co., 1988.

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Garti, Nissim, Ponisseril Somasundaran, and Raffaele Mezzenga. Self-Assembled Supramolecular Architectures: Lyotropic Liquid Crystals. Wiley & Sons, Limited, John, 2012.

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Garti, Nissim, Ponisseril Somasundaran, and Raffaele Mezzenga. Self-Assembled Supramolecular Architectures: Lyotropic Liquid Crystals. Wiley & Sons, Incorporated, John, 2012.

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Garti, Nissim, Ponisseril Somasundaran, and Raffaele Mezzenga. Self-Assembled Supramolecular Architectures: Lyotropic Liquid Crystals. Wiley & Sons, Incorporated, John, 2012.

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Garti, Nissim, Ponisseril Somasundaran, and Raffaele Mezzenga. Self-Assembled Supramolecular Architectures: Lyotropic Liquid Crystals. Wiley & Sons, Incorporated, John, 2012.

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7

Antonov, Liudmil. Tautomerism: Concepts and Applications in Science and Technology. Wiley & Sons, Incorporated, John, 2016.

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8

Antonov, Liudmil. Tautomerism: Methods and Theories. Wiley & Sons, Incorporated, John, 2013.

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Antonov, Liudmil. Tautomerism: Concepts and Applications in Science and Technology. Wiley & Sons, Incorporated, John, 2016.

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Antonov, Liudmil. Tautomerism: Concepts and Applications in Science and Technology. Wiley & Sons, Incorporated, John, 2016.

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Book chapters on the topic "Mesomerism"

1

Gooch, Jan W. "Mesomerism." In Encyclopedic Dictionary of Polymers. Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_7330.

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2

Gondesen, Björn. "Mesomerie." In Chemie 2. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-55088-5_13.

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Went, C. "Structure and Physical Properties: Inductive and Mesomeric Effects." In Work Out Organic Chemistry. Macmillan Education UK, 1988. http://dx.doi.org/10.1007/978-1-349-09726-5_1.

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"Mesomerism." In Encyclopedic Dictionary of Polymers. Springer New York, 2007. http://dx.doi.org/10.1007/978-0-387-30160-0_7213.

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"8.5 Mesomerie (Resonanz)." In Chemie, edited by Charles E. Mortimer and Ulrich Müller. Georg Thieme Verlag, 2015. http://dx.doi.org/10.1055/b-0035-126337.

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"8.5 Mesomerie (Resonanz)." In Chemie, edited by Charles E. Mortimer and Ulrich Muller. Georg Thieme Verlag, 2007. http://dx.doi.org/10.1055/b-0034-34443.

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"8.5 Mesomerie (Resonanz)." In Chemie, edited by Charles E. Mortimer and Ulrich Müller. Georg Thieme Verlag, 2010. http://dx.doi.org/10.1055/b-0034-53748.

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8

"12.2 Bindungszustand und Mesomerie." In Organische Chemie, edited by Eberhard Breitmaier and Günther Jung. Georg Thieme Verlag, 2012. http://dx.doi.org/10.1055/b-0034-43863.

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"12.2 Bindungszustand und Mesomerie." In Organische Chemie, edited by Eberhard Breitmaier and Günther Jung. Georg Thieme Verlag, 2009. http://dx.doi.org/10.1055/b-0034-49508.

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10

Ramsden, Christopher A. "Heterocyclic mesomeric betaines: An overview." In Advances in Heterocyclic Chemistry. Elsevier, 2022. http://dx.doi.org/10.1016/bs.aihch.2021.10.001.

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Conference papers on the topic "Mesomerism"

1

Torruellas, W. E., R. Zanoni, G. I. Stegeman, W. H. G. Horsthuis, and G. R. Mohlmann. "Third-order susceptibility dispersion of Mons and Dans side-chain-substituted polymers." In OSA Annual Meeting. Optica Publishing Group, 1990. http://dx.doi.org/10.1364/oam.1990.fd5.

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Third-harmonic generation is used to measure the third-order susceptibility of side- chain-substituted polymers. Both the magnitude and phase ofχ(3)(3ω) are measured for a family of donor-acceptor diphenyl polyene side-chain-substituted polymers. Dimethylaminonitrostilbene (DANS) and methyloxynitrostilbene (MONS) side-chain- substituted polymer thin films are modelled by an inhomogeneously broadened two-level system. In addition to their very good linear and electro-optical properties, this class of organic polymers show χ(3)values comparable to those of fully conjugated backbone polymers. The
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Schnell, Barbara, and Thomas Kappe. "Rearrangement of Heterocycles via-2-oxoketenes: Synthesis and Rearrangement Reactions of Cross-Conjugated Mesomeric Pyridazino[2,3-a]pyrimidine." In The 4th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2000. http://dx.doi.org/10.3390/ecsoc-4-01844.

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