Works matching Lewis
Results: 5000
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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- Article
The role of the Lewis acid−base properties in the supramolecular association of 1,2,5-chalcogenadiazoles.
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- Canadian Journal of Chemistry, 2013, v. 91, n. 5, p. 338, doi. 10.1139/cjc-2012-0323
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- Article
Fluorinated 9-borafluorenes vs. conventional perfluoroaryl boranes — Comparative Lewis acidity.
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- Canadian Journal of Chemistry, 2005, v. 83, n. 12, p. 2098, doi. 10.1139/V05-240
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- Article
A Heterogeneous Metal‐Free Catalyst for Hydrogenation: Lewis Acid–Base Pairs Integrated into a Carbon Lattice.
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- Angewandte Chemie, 2018, v. 130, n. 42, p. 13996, doi. 10.1002/ange.201803977
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- Article
Acid-Base Pairs in Lewis Acidic Zeolites Promote Direct Aldol Reactions by Soft Enolization.
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- Angewandte Chemie International Edition, 2015, v. 54, n. 34, p. 9835, doi. 10.1002/anie.201502939
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- Article
The Field of Main Group Lewis Acids and Lewis Superacids: Important Basics and Recent Developments.
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- Chemistry - A European Journal, 2024, v. 30, n. 1, p. 1, doi. 10.1002/chem.202302457
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How to Deal with Charge in the Ranking of Lewis Acidity: Critical Evaluation of an Extensive Set of Cationic Lewis Acids.
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- Angewandte Chemie, 2024, v. 136, n. 22, p. 1, doi. 10.1002/ange.202403356
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- Article
Frustrated Lewis Pairs Comprising Nitrogen Lewis Acids for Si–H Bond Activation.
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- Angewandte Chemie, 2020, v. 132, n. 52, p. 23682, doi. 10.1002/ange.202008798
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- Article
Asymmetric Hydrogenation of Ketones and Enones with Chiral Lewis Base Derived Frustrated Lewis Pairs.
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- Angewandte Chemie, 2020, v. 132, n. 11, p. 4528, doi. 10.1002/ange.201914568
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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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- Article
Non-Covalent Interactions of the Lewis Acids Cu–X, Ag–X, and Au–X (X = F and Cl) with Nine Simple Lewis Bases B: A Systematic Investigation of Coinage–Metal Bonds by Ab Initio Calculations.
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- Inorganics, 2021, v. 9, n. 2, p. 13, doi. 10.3390/inorganics9020013
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- Article
Recent Advances in Group 14 and 15 Lewis Acids for Frustrated Lewis Pair Chemistry.
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- Chemistry - An Asian Journal, 2022, v. 17, n. 10, p. 1, doi. 10.1002/asia.202200148
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- Article
Front Cover: Bifunctional Gyroidal MOFs: Highly Efficient Lewis Base and Lewis Acid Catalysts (Chem. Asian J. 20/2019).
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- Chemistry - An Asian Journal, 2019, v. 14, n. 20, p. 3449, doi. 10.1002/asia.201901038
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- Article
Bifunctional Gyroidal MOFs: Highly Efficient Lewis Base and Lewis Acid Catalysts.
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- Chemistry - An Asian Journal, 2019, v. 14, n. 20, p. 3682, doi. 10.1002/asia.201900853
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Reactivity of an NHC-Stabilized Silylene towards Lewis Acids and Lewis Bases.
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- European Journal of Inorganic Chemistry, 2016, v. 2016, n. 25, p. 4123, doi. 10.1002/ejic.201600779
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Chemical reactivity of the frustrated Lewis pairs in borophosphines: a theoretical analysis of their Lewis acidity, Lewis basicity and Fukui function.
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- Journal of Molecular Modeling, 2018, v. 24, n. 9, p. 1, doi. 10.1007/s00894-018-3776-7
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Hydrogen Bond and Other Lewis Acid–Lewis Base Interactions as Preliminary Stages of Chemical Reactions.
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- Molecules, 2020, v. 25, n. 20, p. 4668, doi. 10.3390/molecules25204668
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Lewis Acidic Boranes, Lewis Bases, and Equilibrium Constants: A Reliable Scaffold for a Quantitative Lewis Acidity/Basicity Scale.
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- Chemistry - A European Journal, 2021, v. 27, n. 12, p. 4070, doi. 10.1002/chem.202003916
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- Article
Computational Elucidation of a Role That Brønsted Acidification of the Lewis Acid-Bound Water Might Play in the Hydrogenation of Carbonyl Compounds with H<sub>2</sub> in Lewis Basic Solvents.
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- Chemistry - A European Journal, 2017, v. 23, n. 48, p. 11489, doi. 10.1002/chem.201700937
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Reactivity-Tuning in Frustrated Lewis Pairs: Nucleophilicity and Lewis Basicity of Sterically Hindered Phosphines.
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- Chemistry - A European Journal, 2017, v. 23, n. 31, p. 7422, doi. 10.1002/chem.201701080
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Understanding the Role of Dispersion in Frustrated Lewis Pairs and Classical Lewis Adducts: A Domain-Based Local Pair Natural Orbital Coupled Cluster Study.
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- Chemistry - A European Journal, 2017, v. 23, n. 4, p. 865, doi. 10.1002/chem.201604127
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Dual Lewis Acid/Lewis Base Catalyzed Acylcyanation of Aldehydes: A Mechanistic Study.
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- Chemistry - A European Journal, 2016, v. 22, n. 11, p. 3821, doi. 10.1002/chem.201503782
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- Article
Endohedral Functionalized Cage as a Tool to Create Frustrated Lewis Pairs.
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- Angewandte Chemie, 2018, v. 130, n. 43, p. 14408, doi. 10.1002/ange.201808291
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- Article
Applications of Selenonium Cations as Lewis Acids in Organocatalytic Reactions.
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- Angewandte Chemie, 2018, v. 130, n. 39, p. 13051, doi. 10.1002/ange.201806965
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N-Methylacridinium Salts: Carbon Lewis Acids in Frustrated Lewis Pairs for σ-Bond Activation and Catalytic Reductions.
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- Angewandte Chemie, 2014, v. 126, n. 42, p. 11488, doi. 10.1002/ange.201406122
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- Article
Structural Flexibility is a Decisive Factor in FLP Dihydrogen Cleavage with Tetrahedral Lewis Acids: A Silane Case Study.
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- Chemistry - A European Journal, 2024, v. 30, n. 46, p. 1, doi. 10.1002/chem.202401912
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- Article
Front Cover: Bismuth Cations: Fluoride Ion Abstraction, Isocyanide Coordination, and Impact of Steric Bulk on Lewis Acidity (Chem. Eur. J. 30/2023).
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- Chemistry - A European Journal, 2023, v. 29, n. 30, p. 1, doi. 10.1002/chem.202301353
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Bismuth Cations: Fluoride Ion Abstraction, Isocyanide Coordination, and Impact of Steric Bulk on Lewis Acidity.
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- Chemistry - A European Journal, 2023, v. 29, n. 30, p. 1, doi. 10.1002/chem.202204012
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Gold Teflates Revisited: From the Lewis Superacid [Au(OTeF<sub>5</sub>)<sub>3</sub>] to the Anion [Au(OTeF<sub>5</sub>)<sub>4</sub>]<sup>−</sup>.
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- Chemistry - A European Journal, 2023, v. 29, n. 20, p. 1, doi. 10.1002/chem.202203634
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Dihydrogen Activation with a Neutral, Intermolecular Silicon(IV)‐Amine Frustrated Lewis Pair.
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- Chemistry - A European Journal, 2022, v. 28, n. 60, p. 1, doi. 10.1002/chem.202202273
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What Distinguishes the Strength and the Effect of a Lewis Acid: Analysis of the Gutmann–Beckett Method.
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- Angewandte Chemie, 2022, v. 134, n. 4, p. 1, doi. 10.1002/ange.202114550
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A Highly Lewis Acidic Strontium ansa‐Arene Complex for Lewis Acid Catalysis and Isobutylene Polymerization.
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- Angewandte Chemie, 2020, v. 132, n. 49, p. 22207, doi. 10.1002/ange.202010019
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- Article
Controlled Generation of 9‐Boratriptycene by Lewis Adduct Dissociation: Accessing a Non‐Planar Triarylborane.
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- Angewandte Chemie, 2020, v. 132, n. 30, p. 12502, doi. 10.1002/ange.202003119
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Pushing the Lewis Acidity Boundaries of Boron Compounds With Non‐Planar Triarylboranes Derived from Triptycenes.
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- Angewandte Chemie, 2019, v. 131, n. 47, p. 17045, doi. 10.1002/ange.201910908
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- Article
Aggregation Behavior of a Six‐Membered Cyclic Frustrated Phosphane/Borane Lewis Pair: Formation of a Supramolecular Cyclooctameric Macrocyclic Ring System.
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- Angewandte Chemie, 2019, v. 131, n. 3, p. 892, doi. 10.1002/ange.201811873
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- Article
Hydrogenation of CO<sub>2</sub> to Formate with H<sub>2</sub>: Transition Metal Free Catalyst Based on a Lewis Pair.
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- Angewandte Chemie, 2019, v. 131, n. 3, p. 732, doi. 10.1002/ange.201809634
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- Article
CO<sub>2</sub>‐Cross‐Linked Frustrated Lewis Networks as Gas‐Regulated Dynamic Covalent Materials.
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- Angewandte Chemie, 2019, v. 131, n. 1, p. 270, doi. 10.1002/ange.201812365
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- Article
Hetero-Diels–Alder reactions involving Fe(CO)<sub>3</sub>-coordinated dienal and formyltrimethylenemethane catalyzed by Lewis acids — A theoretical study<sup>1</sup>.
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- Canadian Journal of Chemistry, 2009, v. 87, n. 7, p. 1074, doi. 10.1139/V09-046
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A new fluorous soluble Lewis acidic borane system.
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- Canadian Journal of Chemistry, 2004, v. 82, n. 4, p. 533, doi. 10.1139/v04-018
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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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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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- Article
Frustrated Lewis Pair Catalysis: It Takes Two to Make a Thing Go Right.
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- Chinese Journal of Chemistry, 2021, v. 39, n. 5, p. 1344, doi. 10.1002/cjoc.202000570
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A Lewis Base–Silyl Lewis Acid Cooperative Catalyst for the Iodochlorination of Tetrasubstituted Alkenes.
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- Asian Journal of Organic Chemistry, 2023, v. 12, n. 8, p. 1, doi. 10.1002/ajoc.202300228
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Synergy, Compatibility, and Innovation: Merging Lewis Acids with Stereoselective Enamine Catalysis.
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- Chemistry - An Asian Journal, 2014, v. 9, n. 4, p. 984, doi. 10.1002/asia.201301549
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- Article
Multifunctional Phosphorus‐Containing Lewis Acid and Base Passivation Enabling Efficient and Moisture‐Stable Perovskite Solar Cells.
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- Advanced Functional Materials, 2020, v. 30, n. 15, p. 1, doi. 10.1002/adfm.201910710
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Frustrated Lewis Pair Chemistry with Magnesium Lewis Acids.
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- European Journal of Inorganic Chemistry, 2017, v. 2017, n. 36, p. 4187, doi. 10.1002/ejic.201700787
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- Article
Structure and Stability of Hydrogen Compounds of Group 13/15 Elements Stabilized with Lewis Acids and Bases.
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- Russian Journal of General Chemistry, 2023, v. 93, n. 4, p. 900, doi. 10.1134/S1070363223040175
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- Article
Rational Optimization of Lewis‐Acid Catalysts for the Direct Amination of Alcohols, Part 1 – Activity Descriptors for Metal Triflates and Triflimides.
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- European Journal of Organic Chemistry, 2020, v. 2020, n. 22, p. 3219, doi. 10.1002/ejoc.202000229
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- Article
Lewis Acidities of Indol-3-ylmethylium Ions and Intrinsic Barriers of Their Reactions with Phosphines and Pyridines.
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- European Journal of Organic Chemistry, 2016, v. 2016, n. 23, p. 4050, doi. 10.1002/ejoc.201600572
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- Article
Frustrated Lewis pairs: Design and reactivity.
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- Journal of Chemical Sciences, 2015, v. 127, n. 2, p. 241, doi. 10.1007/s12039-015-0783-4
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- Article