Works matching DE "LEWIS pairs (Chemistry)"
Results: 561
The Capacity of the R[OE(C<sub>6</sub>F<sub>5</sub>)<sub>2</sub>]<sub>2</sub> (E = B, Al; R = C<sub>2</sub>H<sub>4</sub>, p-C<sub>6</sub>H<sub>4</sub>, m-C<sub>6</sub>H<sub>4</sub>) Complexes with Pyrazine and 3,3′-Bipyridine Towards Activation of Hydrogen Molecules
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- Russian Journal of General Chemistry, 2024, v. 94, n. 12, p. 3296, doi. 10.1134/S107036322412020X
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Mesoionic N‐Heterocyclic Olefins as Initiators for the Lewis Pair Polymerization of Epoxides.
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- Macromolecular Rapid Communications, 2024, v. 45, n. 12, p. 1, doi. 10.1002/marc.202300716
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Metal-Free Catalytic Hydrogenation of Imines with Recyclable [2.2]Paracyclophane-Derived Frustrated Lewis Pairs Catalysts.
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- Advanced Synthesis & Catalysis, 2014, v. 356, n. 8, p. 1747, doi. 10.1002/adsc.201301007
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Exploring an intermolecular Ge/B frustrated Lewis pair from a multicentre Zintl Lewis base.
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- Theoretical Chemistry Accounts: Theory, Computation, & Modeling, 2023, v. 142, n. 2, p. 1, doi. 10.1007/s00214-023-02961-6
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Can a decrease in anti-aromaticity increase the dihydrogen activation ability of a frustrated phosphorous/borane Lewis pair?: a DFT study.
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- Theoretical Chemistry Accounts: Theory, Computation, & Modeling, 2020, v. 139, n. 12, p. 1, doi. 10.1007/s00214-020-02698-6
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The acid strength of the HClO<sub>4</sub>/<italic>n</italic>(AlF<sub>3</sub>) and HClO<sub>4</sub>/<italic>n</italic>(SbF<sub>5</sub>) (<italic>n </italic>= 1-3) Lewis-Brønsted superacids containing the excess of the Lewis acid component.
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- Theoretical Chemistry Accounts: Theory, Computation, & Modeling, 2018, v. 137, n. 4, p. 1, doi. 10.1007/s00214-018-2235-y
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On the thermodynamic stability of the intermolecular association between Lewis acids and Lewis bases: a DFT study.
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- Theoretical Chemistry Accounts: Theory, Computation, & Modeling, 2016, v. 135, n. 3, p. 1, doi. 10.1007/s00214-016-1829-5
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Enhancing polyol/sugar cascade oxidation to formic acid with defect rich MnO<sub>2</sub> catalysts.
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- Nature Communications, 2023, v. 14, n. 1, p. 1, doi. 10.1038/s41467-023-40306-w
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High-density frustrated Lewis pairs based on Lamellar Nb<sub>2</sub>O<sub>5</sub> for photocatalytic non-oxidative methane coupling.
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- Nature Communications, 2023, v. 14, n. 1, p. 1, doi. 10.1038/s41467-023-37663-x
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Borane‐Catalyzed Hydrogenation of Tertiary Amides Activated by Oxalyl Chloride: DFT Mechanistic Insights.
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- European Journal of Organic Chemistry, 2019, v. 2019, n. 28, p. 4609, doi. 10.1002/ejoc.201900827
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Mechanisms in Frustrated Lewis Pair‐Catalyzed Reactions.
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- European Journal of Organic Chemistry, 2019, v. 2019, n. 2/3, p. 283, doi. 10.1002/ejoc.201800944
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Efficient Synthesis of Multifunctional Chelating Agents Based on Tetraazacycloalkanes.
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- European Journal of Organic Chemistry, 2018, v. 2018, n. 34, p. 4762, doi. 10.1002/ejoc.201800801
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Air‐Stable CpCo<sup>I</sup>–Phosphite–Fumarate Precatalyst in Cyclization Reactions: Comparing Different Methods of Energy Supply.
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- European Journal of Organic Chemistry, 2018, v. 2018, n. 24, p. 3193, doi. 10.1002/ejoc.201800196
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Lewis Base Catalyzed Intramolecular Reduction of Salicylaldehydes by Pinacol‐Derived Chlorohydrosilane.
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- European Journal of Organic Chemistry, 2018, v. 2018, n. 23, p. 2910, doi. 10.1002/ejoc.201800544
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Facile Modulation of FLP Properties: A Phosphinylvinyl Grignard Reagent and Ga/P- and In/P<sub>2</sub>-Based Frustrated Lewis Pairs.
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- Angewandte Chemie International Edition, 2017, v. 56, n. 11, p. 3094, doi. 10.1002/anie.201612485
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Reductive Dehydrogenation of a Stannane via Multiple Sn−H Activation by Frustrated Lewis Pairs.
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- Angewandte Chemie International Edition, 2017, v. 56, n. 8, p. 2198, doi. 10.1002/anie.201610254
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N,P-Heterocyclic Germylene/B(C<sub>6</sub>F<sub>5</sub>)<sub>3</sub> Adducts: A Lewis Pair with Multi-reactive Sites.
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- Angewandte Chemie International Edition, 2017, v. 56, n. 5, p. 1365, doi. 10.1002/anie.201610455
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Diverse Activation Modes in the Hydroboration of Aldehydes and Ketones with Germanium, Tin, and Lead Lewis Pairs.
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- Angewandte Chemie International Edition, 2017, v. 56, n. 1, p. 333, doi. 10.1002/anie.201609155
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Versatile Catalytic Hydrogenation Using A Simple Tin(IV) Lewis Acid.
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- Angewandte Chemie International Edition, 2016, v. 55, n. 47, p. 14738, doi. 10.1002/anie.201606639
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A Frustrated and Confused Lewis Pair.
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- Angewandte Chemie International Edition, 2016, v. 55, n. 46, p. 14335, doi. 10.1002/anie.201608968
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Reversible Dihydrogen Activation by Reduced Aryl Boranes as Main-Group Ambiphiles.
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- Angewandte Chemie International Edition, 2016, v. 55, n. 45, p. 14067, doi. 10.1002/anie.201608324
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Atom-Efficient Synthesis of Alkynylfluoroborates Using BF<sub>3</sub>-Based Frustrated Lewis Pairs.
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- Angewandte Chemie International Edition, 2016, v. 55, n. 45, p. 14146, doi. 10.1002/anie.201608520
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Frustrated Lewis Pair Catalyzed Dehydrogenative Oxidation of Indolines and Other Heterocycles.
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- Angewandte Chemie International Edition, 2016, v. 55, n. 40, p. 12219, doi. 10.1002/anie.201606426
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Unraveling the Catalytic Synergy between Ti<sup>3+</sup> and Al<sup>3+</sup> Sites on a Chlorinated Al<sub>2</sub>O<sub>3</sub>: A Tandem Approach to Branched Polyethylene.
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- Angewandte Chemie International Edition, 2016, v. 55, n. 37, p. 11203, doi. 10.1002/anie.201604136
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Contrasting Frustrated Lewis Pair Reactivity with Selenium- and Boron-Based Lewis Acids.
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- Angewandte Chemie International Edition, 2016, v. 55, n. 37, p. 11292, doi. 10.1002/anie.201605239
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Formation of Thermally Robust Frustrated Lewis Pairs by Electrocyclic Ring Closure Reactions.
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- Angewandte Chemie International Edition, 2016, v. 55, n. 18, p. 5526, doi. 10.1002/anie.201510994
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Frustrated Lewis Pair-Catalyzed Cycloisomerization of 1,5-Enynes via a 5- endo-dig Cyclization/Protodeborylation Sequence.
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- Angewandte Chemie International Edition, 2016, v. 55, n. 13, p. 4336, doi. 10.1002/anie.201511921
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A P−H Functionalized Al/P Frustrated Lewis Pair: Substrate Activation and Selective Hydrogen Transfer.
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- Angewandte Chemie International Edition, 2016, v. 55, n. 9, p. 3212, doi. 10.1002/anie.201511048
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B(C<sub>6</sub>F<sub>5</sub>)<sub>3</sub>: A Lewis Acid that Brings the Light to the Solid State.
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- Angewandte Chemie International Edition, 2016, v. 55, n. 3, p. 1196, doi. 10.1002/anie.201508461
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Polyboramines for Hydrogen Release: Polymers Containing Lewis Pairs in their Backbone.
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- Angewandte Chemie International Edition, 2015, v. 54, n. 52, p. 15744, doi. 10.1002/ange.201508395
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A Neutral Silicon/Phosphorus Frustrated Lewis Pair.
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- Angewandte Chemie International Edition, 2015, v. 54, n. 45, p. 13416, doi. 10.1002/anie.201504171
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Formation of Frustrated Lewis Pairs in Pt<sub> x</sub>-Loaded Zeolite NaY.
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- Angewandte Chemie International Edition, 2015, v. 54, n. 44, p. 13080, doi. 10.1002/anie.201506790
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A Strategy to Control the Reactivation of Frustrated Lewis Pairs from Shelf-Stable Carbene Borane Complexes.
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- Angewandte Chemie International Edition, 2015, v. 54, n. 40, p. 11666, doi. 10.1002/anie.201505974
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Cover Picture: A Strategy to Control the Reactivation of Frustrated Lewis Pairs from Shelf-Stable Carbene Borane Complexes (Angew. Chem. Int. Ed. 40/2015).
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- Angewandte Chemie International Edition, 2015, v. 54, n. 40, p. 11583, doi. 10.1002/anie.201507437
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Facile Protocol for Catalytic Frustrated Lewis Pair Hydrogenation and Reductive Deoxygenation of Ketones and Aldehydes.
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- Angewandte Chemie International Edition, 2015, v. 54, n. 29, p. 8511, doi. 10.1002/anie.201503087
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Catalytic Asymmetric Synthesis of Phosphine Boronates.
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- Angewandte Chemie International Edition, 2015, v. 54, n. 27, p. 7867, doi. 10.1002/anie.201502987
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Inside Cover: Catalytic Asymmetric Synthesis of Phosphine Boronates (Angew. Chem. Int. Ed. 27/2015).
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- Angewandte Chemie International Edition, 2015, v. 54, n. 27, p. 7720, doi. 10.1002/anie.201505253
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Elusive Silane-Alane Complex [SiH⋅⋅⋅Al]: Isolation, Characterization, and Multifaceted Frustrated Lewis Pair Type Catalysis.
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- Angewandte Chemie International Edition, 2015, v. 54, n. 23, p. 6842, doi. 10.1002/anie.201502400
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Frustrated Lewis Pair Chemistry: Development and Perspectives.
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- Angewandte Chemie International Edition, 2015, v. 54, n. 22, p. 6400, doi. 10.1002/anie.201409800
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Activation of Molecular Hydrogen by a Singlet Carbene through Quantum Mechanical Tunneling.
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- Angewandte Chemie International Edition, 2015, v. 54, n. 15, p. 4603, doi. 10.1002/anie.201410501
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Cooperative Lewis Pairs Based on Late Transition Metals: Activation of Small Molecules by Platinum(0) and B(C<sub>6</sub>F<sub>5</sub>)<sub>3</sub>.
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- Angewandte Chemie International Edition, 2015, v. 54, n. 7, p. 2223, doi. 10.1002/anie.201409872
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Graphical Abstract: Angew. Chem. Int. Ed. 6/2015.
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- Angewandte Chemie International Edition, 2015, v. 54, n. 6, p. 1683, doi. 10.1002/anie.201590004
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Back Cover: Intramolecular Frustrated Lewis Pair with the Smallest Boryl Site: Reversible H<sub>2</sub> Addition and Kinetic Analysis (Angew. Chem. Int. Ed. 6/2015).
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- Angewandte Chemie International Edition, 2015, v. 54, n. 6, p. 1976, doi. 10.1002/anie.201412312
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Intramolecular Frustrated Lewis Pair with the Smallest Boryl Site: Reversible H<sub>2</sub> Addition and Kinetic Analysis.
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- Angewandte Chemie International Edition, 2015, v. 54, n. 6, p. 1749, doi. 10.1002/anie.201410141
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Inside Back Cover: The Reactivities of Iminoboranes with Carbenes: BN Isosteres of Carbene-Alkyne Adducts (Angew. Chem. Int. Ed. 5/2015).
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- Angewandte Chemie International Edition, 2015, v. 54, n. 5, p. 1677, doi. 10.1002/anie.201411644
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The Reactivities of Iminoboranes with Carbenes: BN Isosteres of Carbene-Alkyne Adducts.
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- Angewandte Chemie International Edition, 2015, v. 54, n. 5, p. 1662, doi. 10.1002/anie.201409699
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Frustrated Lewis Pair Activation of an N-Sulfinylamine: A Source of Sulfur Monoxide.
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- Angewandte Chemie International Edition, 2015, v. 54, n. 3, p. 809, doi. 10.1002/anie.201409969
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Thermal Decomposition of the Complex [tBu<sub>3</sub>PH][HB(C<sub>6</sub>F<sub>5</sub>)<sub>3</sub>].
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- Russian Journal of General Chemistry, 2024, v. 94, p. S36, doi. 10.1134/S1070363224140056
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Ru/Beta Zeolite Catalysts for Levulinic Acid Hydrogenation: The Importance of Catalyst Synthesis Methodology.
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- Catalysts (2073-4344), 2025, v. 15, n. 1, p. 80, doi. 10.3390/catal15010080
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Two-Dimensional Zeolitic Imidazolate Framework ZIF-L: A Promising Catalyst for Polymerization.
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- Catalysts (2073-4344), 2022, v. 12, n. 5, p. 521, doi. 10.3390/catal12050521
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