Works matching DE "HYPERCONJUGATION"
Results: 92
What Determines the Lewis Acidity of a Bismuthane? Towards Bi‐Based FLPs.
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- Chemistry - A European Journal, 2024, v. 30, n. 57, p. 1, doi. 10.1002/chem.202402154
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Electrostatic CH−π Interactions Can Override Fluorine Gauche Effects To Exert Conformational Control.
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- Chemistry - A European Journal, 2023, v. 29, n. 6, p. 1, doi. 10.1002/chem.202203139
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Synthesis and reactivity of 3-(2,2-dimethylhydrazono)-5-R-cyclopentane-1,1,2,2-tetracarbonitriles.
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- Russian Journal of General Chemistry, 2015, v. 85, n. 10, p. 2285, doi. 10.1134/S1070363215100114
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On the Harmonic Oscillator Model of Electron Delocalization (HOMED) Index and its Application to Heteroatomic Π-Electron Systems.
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- Symmetry (20738994), 2010, v. 2, n. 3, p. 1485, doi. 10.3390/sym2031485
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Conformational stability and rotational energy barrier of RC-CR dimers: hyperconjugation versus steric effect.
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- Journal of the Iranian Chemical Society, 2012, v. 9, n. 2, p. 205, doi. 10.1007/s13738-011-0042-7
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Eclipsed Acetaldehyde as a Precursor for Producing Vinyl Alcohol.
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- International Journal of Molecular Sciences, 2012, v. 13, n. 11, p. 15360, doi. 10.3390/ijms131115360
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Charge-Scaling Effect in Ionic Liquids from the Charge-Density Analysis of N, N′-Dimethylimidazolium Methylsulfate.
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- Angewandte Chemie, 2014, v. 126, n. 12, p. 3207, doi. 10.1002/ange.201308760
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The Homopolyatomic Sulfur Cation [S 20 ] 2+.
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- Inorganics, 2025, v. 13, n. 1, p. 23, doi. 10.3390/inorganics13010023
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<sup>13</sup>C-<sup>13</sup>C spin-spin coupling constants in structural studies: XLIV. Carbonyl-containing oximes.
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- Russian Journal of Organic Chemistry, 2009, v. 45, n. 4, p. 481, doi. 10.1134/S1070428009040010
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Effect of Ligand Chirality and Hyperconjugation on the Thermodynamic Stability of a Tris(aquated) Gd<sup>III</sup> Complex: Synthesis, Characterization, and T<sub>1</sub>‐Weighted Phantom MR Image Study.
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- European Journal of Inorganic Chemistry, 2019, v. 2019, n. 20, p. 2518, doi. 10.1002/ejic.201900043
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An outstanding heat-resistant hydroxyl boron-silicone oil with hyperconjugation action in backbone.
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- Journal of Thermal Analysis & Calorimetry, 2018, v. 132, n. 3, p. 1825, doi. 10.1007/s10973-018-7065-6
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Structural formulas and explanation in organic chemistry.
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- Foundations of Chemistry, 2008, v. 10, n. 2, p. 117, doi. 10.1007/s10698-007-9033-2
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Interheteromolecular Hyperconjugation Boosts (De)hydrogenation for Reversible H<sub>2</sub> Storage.
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- ChemSusChem, 2023, v. 16, n. 1, p. 1, doi. 10.1002/cssc.202201512
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Blue shifts of the C&bond;H stretching vibrations in hydrogen-bonded and protonated trimethylamine. Effect of hyperconjugation on bond properties.
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- Journal of Computational Chemistry, 2008, v. 29, n. 9, p. 1490, doi. 10.1002/jcc.20910
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Influence of stereoelectronic effects on the <sup>1</sup>J<sub>C─F</sub> spin–spin coupling constant in fluorinated heterocyclic compounds.
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- Magnetic Resonance in Chemistry, 2019, v. 57, n. 7, p. 373, doi. 10.1002/mrc.4854
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The nature of resonance and hyperconjugation for cyclic β-silyl substituted carbocations: NBO, NRT, EDA, and NMR studies.
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- Research on Chemical Intermediates, 2013, v. 39, n. 5, p. 2011, doi. 10.1007/s11164-012-0733-4
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Synthesis and conformational features of sym N,N′,N″-triarylguanidines.
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- Journal of Chemical Sciences, 2010, v. 122, n. 2, p. 157, doi. 10.1007/s12039-010-0017-8
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The Effects of Hybridization and Hyperconjugation in the Intramolecular Blue-shifted H-Bonds N-H…O.
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- Chemistry Letters, 2008, v. 37, n. 6, p. 1, doi. 10.1246/cl.2008.596
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Two-coordinate Group 13 Element (Al, Ga) Centered Cations Formed by Silyl Group Migration: Synthesis and Characterization.
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- Chemistry Letters, 2007, v. 36, n. 8, p. 984, doi. 10.1246/cl.2007.984
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Control of Excited‐State Conformations in B,N‐Acenes.
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- Angewandte Chemie, 2019, v. 131, n. 13, p. 4303, doi. 10.1002/ange.201814104
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The Comparability of Pt to Pt‐Ru in Catalyzing the Hydrogen Oxidation Reaction for Alkaline Polymer Electrolyte Fuel Cells Operated at 80 °C.
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- Angewandte Chemie, 2019, v. 131, n. 5, p. 1456, doi. 10.1002/ange.201812662
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Exceptionally Long C−C Single Bonds in Diamino‐o‐carborane as Induced by Negative Hyperconjugation.
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- Angewandte Chemie, 2019, v. 131, n. 5, p. 1411, doi. 10.1002/ange.201812555
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Donor-σ-Acceptor Motifs: Thermally Activated Delayed Fluorescence Emitters with Dual Upconversion.
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- Angewandte Chemie, 2017, v. 129, n. 52, p. 16763, doi. 10.1002/ange.201708876
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Hyperconjugation Is the Source of Helicity in Perfluorinated n-Alkanes.
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- Angewandte Chemie, 2017, v. 129, n. 27, p. 7975, doi. 10.1002/ange.201704112
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A Phosphine-Coordinated Boron-Centered Gomberg-Type Radical.
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- Angewandte Chemie, 2015, v. 127, n. 32, p. 9330, doi. 10.1002/ange.201504502
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Probing Hyperconjugative Aromaticity of Monosubstituted Cyclopentadienes.
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- Asian Journal of Organic Chemistry, 2019, v. 8, n. 1, p. 123, doi. 10.1002/ajoc.201800680
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Geometrical Dependence of the Highest Occupied Molecular Orbital in Bicyclic Systems: π-Facial Stereoselectivity of Bicyclic and Tricyclic Olefins.
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- Asian Journal of Organic Chemistry, 2015, v. 4, n. 7, p. 659, doi. 10.1002/ajoc.201500054
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The nature of the electronic factor governing diastereofacial selectivity in remotely substituted (X) 2-adamantyl cations: 5-X versus 4-X substitution.
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- Journal of Physical Organic Chemistry, 2007, v. 20, n. 10, p. 791, doi. 10.1002/poc.1247
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The anionic chain process mechanism for reactions of perchlorofluoroethanes with nucleophiles in solution: a theoretical study.
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- Journal of Physical Organic Chemistry, 2007, v. 20, n. 1, p. 65, doi. 10.1002/poc.1128
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EFFECT OF META SUBSTITUTION OF METHYL GROUP ON 2-HYDROXYPYRIDINE: SPECTROSCOPIC INVESTIGATION.
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- Lithuanian Journal of Physics, 2020, v. 60, n. 1, p. 35, doi. 10.3952/physics.v60i1.4162
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Low-Frequency CH Stretch Vibrations of Free Alkoxide Ions.
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- Angewandte Chemie International Edition, 2017, v. 56, n. 1, p. 217, doi. 10.1002/anie.201609437
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Highly Efficient Catalytic Formation of ( Z)-1,4-But-2-ene Diols Using Water as a Nucleophile.
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- Angewandte Chemie International Edition, 2016, v. 55, n. 37, p. 11037, doi. 10.1002/anie.201603638
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Theoretical study of H bonds of HArF and HF with isoelectronic systems N<sub>2</sub>, CO, and BF.
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- Canadian Journal of Chemistry, 2010, v. 88, n. 4, p. 352, doi. 10.1139/V10-004
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Variation of the ease of α-sulfonyl carbanion formation with the orientation of different β-substituents: Experimental evidence for the generality of negative hyperconjugation as an important substituent effect.
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- Canadian Journal of Chemistry, 2003, v. 81, n. 6, p. 638, doi. 10.1139/v03-015
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An ab initio study of conformations and sigmatropic shifts in triazene and its mono-, di-, and trimethyl derivatives.
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- Canadian Journal of Chemistry, 2002, v. 80, n. 5, p. 447, doi. 10.1139/v02-049
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Theoretical study on dithieno[3,2- b:2′,3′- d]phosphole derivatives: high-efficiency blue-emitting materials with ambipolar semiconductor behavior.
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- Theoretical Chemistry Accounts: Theory, Computation, & Modeling, 2010, v. 127, n. 4, p. 419, doi. 10.1007/s00214-010-0730-x
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Car-Parrinello molecular dynamics simulations and EPR property calculations on aqueous ubisemiquinone radical anion.
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- Theoretical Chemistry Accounts: Theory, Computation, & Modeling, 2008, v. 119, n. 5/6, p. 477, doi. 10.1007/s00214-007-0408-1
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Extremely localized molecular orbitals: theory and applications.
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- Theoretical Chemistry Accounts: Theory, Computation, & Modeling, 2007, v. 117, n. 5/6, p. 685, doi. 10.1007/s00214-006-0200-7
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Isomerization reactions of RSNO (R=H, C<sub> n </sub>H<sub>2 n+1</sub> n≤ 4).
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- Theoretical Chemistry Accounts: Theory, Computation, & Modeling, 2007, v. 117, n. 1, p. 145, doi. 10.1007/s00214-006-0164-7
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Computational Review of Conformers 2-Choroacetaldehyd.
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- International Journal of New Chemistry, 2021, v. 8, n. 3, p. 345, doi. 10.22034/ijnc.2020.127669.1119
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Hyperconjugation and Hydrogen Bonding Interactions Effect with the Nonlinear Optical Features of 4-Chlorophenoxy Acetonitrile: An Experimental and DFT Methodology.
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- Polycyclic Aromatic Compounds, 2024, v. 44, n. 5, p. 2887, doi. 10.1080/10406638.2023.2225677
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Induktiver Effekt und Hyperkonjugation bei Radikalkettenreaktionen: Neue Lerngelegenheit zur Erarbeitung von Schlüsselkonzepten der Organischen Chemie.
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- Chemkon - Chemie Konkret, 2023, v. 30, n. 7, p. 300, doi. 10.1002/ckon.202100090
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Konzepte verstehen anhand vergleichender qualitativer Kinetik‐Messungen bei S<sub>N</sub>1‐Reaktionen: Die Wirkung von Mesomerie und Hyperkonjugation im Vergleich.
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- Chemkon - Chemie Konkret, 2021, v. 28, n. 2, p. 74, doi. 10.1002/ckon.202000050
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Chalcogen Bonding with Diaryl Ditellurides: Evidence from Solid State and Solution Studies.
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- Chemistry - A European Journal, 2022, v. 28, n. 25, p. 1, doi. 10.1002/chem.202200395
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The Combination of Cross‐Hyperconjugation and σ‐Conjugation in 2,5‐Oligosilanyl Substituted Siloles.
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- Chemistry - A European Journal, 2020, v. 26, n. 71, p. 17252, doi. 10.1002/chem.202003150
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Understanding the Conformational Behavior of Fluorinated Piperidines: The Origin of the Axial‐F Preference.
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- Chemistry - A European Journal, 2020, v. 26, n. 28, p. 6141, doi. 10.1002/chem.202001355
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Dismantling the Hyperconjugation of π‐Conjugated Phosphorus Heterocycles.
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- Chemistry - A European Journal, 2019, v. 25, n. 38, p. 9035, doi. 10.1002/chem.201900225
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Agostic Interactions in Early Transition‐Metal Complexes: Roles of Hyperconjugation, Dispersion, and Steric Effect.
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- Chemistry - A European Journal, 2019, v. 25, n. 26, p. 6591, doi. 10.1002/chem.201900436
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Hyperconjugation in hydrocarbons: Not just a "mild sort of conjugation".
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- Pure & Applied Chemistry, 2013, v. 85, n. 5, p. 921, doi. 10.1351/PAC-CON-13-01-03
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Predicting an Antiaromatic Benzene Ring in the Ground State Caused by Hyperconjugation.
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- Chemistry - An Asian Journal, 2019, v. 14, n. 23, p. 4309, doi. 10.1002/asia.201901261
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