Formation of Strong Boron Lewis Acid Sites on Silica
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[1] M. Conley,et al. A Supported Ziegler-Type Organohafnium Site Metabolizes Polypropylene , 2023, Journal of the American Chemical Society.
[2] J. Dutton,et al. The Effect of Carborane Substituents on the Lewis Acidity of Boranes. , 2023, Inorganic chemistry.
[3] J. Dutton,et al. Bis(1-methyl-ortho-carboranyl)borane. , 2023, Angewandte Chemie.
[4] J. Dutton,et al. Tris(ortho‐carboranyl)borane: An Isolable, Halogen‐Free, Lewis Superacid , 2022, Angewandte Chemie.
[5] Aaron J. Rossini,et al. Formation of a Strong Heterogeneous Aluminum Lewis Acid on Silica. , 2022, Angewandte Chemie.
[6] Hannah E. Starr. A Complex Molecular Symmetry Analysis of Silsesquioxane Catalysts for Inorganic Students , 2022, Journal of Chemical Education.
[7] F. Zaera. Designing Sites in Heterogeneous Catalysis: Are We Reaching Selectivities Competitive With Those of Homogeneous Catalysts? , 2022, Chemical reviews.
[8] Aaron J. Rossini,et al. A Heterogeneous Palladium Catalyst for the Polymerization of Olefins Prepared by Halide Abstraction Using Surface R3Si+ Species. , 2022, Angewandte Chemie.
[9] M. R. Gagné,et al. Probing the Source of Enhanced Activity in Multiborylated Silsesquioxane Catalysts for C–O Bond Reduction , 2022, Organometallics.
[10] L. Greb,et al. What Distinguishes the Strength and the Effect of a Lewis Acid: Analysis of the Gutmann–Beckett Method , 2021, Angewandte Chemie.
[11] A. Lipton,et al. Active Sites in a Heterogeneous Organometallic Catalyst for the Polymerization of Ethylene , 2021, ACS central science.
[12] W. P. McDermott,et al. Controlled Grafting Synthesis of Silica-Supported Boron for Oxidative Dehydrogenation Catalysis , 2021 .
[13] J. Niemantsverdriet,et al. Silica Nanopowder Supported Frustrated Lewis Pairs for CO2 Capture and Conversion to Formic Acid. , 2020, Inorganic chemistry.
[14] David M. Kaphan,et al. Nontraditional Catalyst Supports in Surface Organometallic Chemistry , 2020 .
[15] Michael Spruell,et al. Jason , 2020, Deporting Black Britons.
[16] J. Venegas,et al. Why Boron Nitride is such a Selective Catalyst for the Oxidative Dehydrogenation of Propane. , 2020, Angewandte Chemie.
[17] L. Greb,et al. An Extensive Set of Accurate Fluoride Ion Affinities for p‐Block Element Lewis Acids and Basic Design Principles for Strong Fluoride Ion Acceptors , 2020, Chemphyschem : a European journal of chemical physics and physical chemistry.
[18] L. Kovarik,et al. Precise identification and characterization of catalytically active sites on the surface of γ-alumina. , 2020, Angewandte Chemie.
[19] W. P. McDermott,et al. B-MWW Zeolite: The Case Against Single-Site Catalysis. , 2020, Angewandte Chemie.
[20] Wen‐Cui Li,et al. Supported Boron Oxide Catalysts for Selective and Low-Temperature Oxidative Dehydrogenation of Propane , 2019, ACS Catalysis.
[21] F. Dogan,et al. Modification of rGO by B(C6F5)3 to generated single-site Lewis Acid rGO-O-B(C6F5)2 as co activator of nickel complex, to produce highly disperse rGO-PE nanocomposite , 2019, Applied Catalysis A: General.
[22] J. T. Grant,et al. Probing the Transformation of Boron Nitride Catalysts under Oxidative Dehydrogenation Conditions. , 2018, Journal of the American Chemical Society.
[23] D. B. Culver,et al. Activation of C-F Bonds by Electrophilic Organosilicon Sites Supported on Sulfated Zirconia. , 2018, Angewandte Chemie.
[24] K. Szeto,et al. A Strong Support Effect in Selective Propane Dehydrogenation Catalyzed by Ga(i-Bu)3 Grafted onto γ-Alumina and Silica , 2018, ACS Catalysis.
[25] A. Fedorov,et al. Bridging the Gap between Industrial and Well-Defined Supported Catalysts. , 2018, Angewandte Chemie.
[26] Rebecca L. Melen,et al. Tris(pentafluorophenyl)borane and Beyond: Modern Advances in Borylation Chemistry. , 2017, Inorganic chemistry.
[27] J. T. Grant,et al. Selective oxidative dehydrogenation of propane to propene using boron nitride catalysts , 2016, Science.
[28] Christophe Copéret,et al. Surface Organometallic and Coordination Chemistry toward Single-Site Heterogeneous Catalysts: Strategies, Methods, Structures, and Activities. , 2016, Chemical reviews.
[29] T. Müller,et al. Quantitative Assessment of the Lewis Acidity of Silylium Ions , 2015 .
[30] S. Kerdiles,et al. Functionalization of Silica Nanoparticles and Native Silicon Oxide with Tailored Boron-Molecular Precursors for Efficient and Predictive p-Doping of Silicon , 2015 .
[31] G. Erker,et al. Frustrated Lewis pair chemistry: development and perspectives. , 2015, Angewandte Chemie.
[32] T. Marks,et al. Supported Single-Site Organometallic Catalysts for the Synthesis of High-Performance Polyolefins , 2015, Catalysis Letters.
[33] P. Sautet,et al. Chlorodiethylaluminum supported on silica: A dinuclear aluminum surface species with bridging μ2-Cl-ligand as a highly efficient co-catalyst for the Ni-catalyzed dimerization of ethene , 2014 .
[34] P. Sautet,et al. Triisobutylaluminum: bulkier and yet more reactive towards silica surfaces than triethyl or trimethylaluminum. , 2013, Dalton transactions.
[35] W. Piers,et al. Comparative Lewis Acidity in Fluoroarylboranes: B(o-HC6F4)3, B(p-HC6F4)3, and B(C6F5)3 , 2013 .
[36] D. Curran,et al. Silica gel promotes reductions of aldehydes and ketones by N-heterocyclic carbene boranes. , 2012, Organic letters.
[37] M. Taoufik,et al. On the Fate of Silica-Supported Half-Metallocene Cations: Elucidating a Catalyst’s Deactivation Pathways , 2012 .
[38] P. Sautet,et al. Nature and structure of aluminum surface sites grafted on silica from a combination of high-field aluminum-27 solid-state NMR spectroscopy and first-principles calculations. , 2012, Journal of the American Chemical Society.
[39] Jerry G. Hu,et al. Borane-induced dehydration of silica and the ensuing water-catalyzed grafting of B(C6F5)3 to give a supported, single-site Lewis acid, ≡SiOB(C6F5)2. , 2012, Journal of the American Chemical Society.
[40] P. Sautet,et al. Optimal water coverage on alumina: a key to generate Lewis acid-base pairs that are reactive towards the C-H bond activation of methane. , 2011, Angewandte Chemie.
[41] S. Scott,et al. Evidence for the pairwise disposition of grafting sites on highly dehydroxylated silicas via their reactions with Ga(CH3)3. , 2011, Journal of the American Chemical Society.
[42] C. Santini,et al. A well-defined silica-supported aluminium alkyl through an unprecedented, consecutive two-step protonolysis-alkyl transfer mechanism. , 2011, Chemical communications.
[43] John M. Slattery,et al. Simple Access to the Non-Oxidizing Lewis superacid PhF --> Al(OR(F))3 (R(F) = C(CF3)3). , 2008, Angewandte Chemie.
[44] Philippe Sautet,et al. Molecular understanding of alumina supported single-site catalysts by a combination of experiment and theory. , 2006, Journal of the American Chemical Society.
[45] S. Scott,et al. Formation of Digallium Sites in the Reaction of Trimethylgallium with Silica , 2006 .
[46] H. Kim,et al. Organoborane-Modified Silica Supports for Olefin Polymerization: Soluble Models for Metallocene Catalyst Deactivation , 2002 .
[47] T. Marks,et al. Cocatalysts for metal-catalyzed olefin polymerization: activators, activation processes, and structure-activity relationships. , 2000, Chemical reviews.
[48] R. Duchateau,et al. Silica-Grafted Borato Cocatalysts for Olefin Polymerization Modeled by Silsesquioxane−Borato Complexes , 2000 .
[49] W. Piers,et al. Pentafluorophenylboranes: from obscurity to applications , 1998 .
[50] T. Sodesawa,et al. Surface structure and acidity of alumina-boria catalysts , 1995 .
[51] D. Parks,et al. Bis(pentafluorophenyl)borane: Synthesis, Properties, and Hydroboration Chemistry of a Highly Electrophilic Borane Reagent , 1995 .
[52] Tobin J. Marks,et al. Cationic zirconocene olefin polymerization catalysts based on the organo-Lewis acid tris(pentafluorophenyl)borane. A synthetic, structural, solution dynamic, and polymerization catalytic study , 1994 .
[53] S. Heřmánek. Boron-11 NMR spectra of boranes, main-group heteroboranes, and substituted derivatives. Factors influencing chemical shifts of skeletal atoms , 1992 .
[54] H. Kawashima,et al. An infrared study of hydroboration of lower olefins with diborane on γ-Al2O3 , 1977 .
[55] V. Bermudez. Infrared study of boron trichloride chemisorbed on silica gel , 1971 .
[56] R. Drago,et al. Measurement of the Global Acidity of Solid Acids by 31P MAS NMR of Chemisorbed Triethylphosphine Oxide , 2000 .
[57] T. Marks. Surface-bound metal hydrocarbyls. Organometallic connections between heterogeneous and homogeneous catalysis , 1992 .
[58] T. Marks,et al. Supported Organoactinides. High-Resolution Solid-State 13C NMR Studies of Catalytically Active, Alumina-Bound (Pentamethylcyclopentadienyl)thorium Methyl and Hydride Complexes , 1985 .
[59] B. Morrow,et al. Reactions of silica surfaces with boron halides , 1971 .