On the public citation graph
A Highly Active Phosphine–Borane Organocatalyst for the Reduction of CO2 to Methanol Using Hydroboranes
0 signed · 373 inferred · view as graph
Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.
Is this your work? Sign in with ORCID and put your name on the
claims that are yours.
Reference health. See whether every reference in this work resolves to a
known work and none has been retracted — and get a dated CiteStamped
badge you can embed.
What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/anie.200806058openalex-snapshot
Conversion of Carbon Dioxide into Methanol with Silanes over N‐Heterocyclic Carbene Catalysts
inferredcites →https://doi.org/10.1002/anie.200901636openalex-snapshot
Reversible Metal‐Free Carbon Dioxide Binding by Frustrated Lewis Pairs
inferredcites →https://doi.org/10.1002/anie.200905466openalex-snapshot
Non‐Metal‐Mediated Homogeneous Hydrogenation of CO2 to CH3OH
inferredcites →https://doi.org/10.1002/anie.201000431openalex-snapshot
Carbon Dioxide Capture: Prospects for New Materials
inferredcites →https://doi.org/10.1002/anie.201000520openalex-snapshot
Reaction of Singlet Dioxygen with Phosphine–Borane Derivatives: From Transient Phosphine Peroxides to Crystalline Peroxoboronates
inferredcites →https://doi.org/10.1002/anie.201006901openalex-snapshot
Geminal Phosphorus/Aluminum‐Based Frustrated Lewis Pairs: CH versus CC Activation and CO2 Fixation
inferredcites →https://doi.org/10.1002/anie.201107352openalex-snapshot
Borane‐Mediated Carbon Dioxide Reduction at Ruthenium: Formation of C1 and C2 Compounds
inferredcites →https://doi.org/10.1002/anie.201107958openalex-snapshot
Silyl Cation Mediated Conversion of CO2 into Benzoic Acid, Formic Acid, and Methanol
inferredcites →https://doi.org/10.1002/anie.201201282openalex-snapshot
Deoxygenative Reduction of Carbon Dioxide to Methane, Toluene, and Diphenylmethane with [Et2Al]+ as Catalyst
inferredcites →https://doi.org/10.1002/anie.201202320openalex-snapshot
Hydrogenation of Carbon Dioxide to Methanol by Using a Homogeneous Ruthenium–Phosphine Catalyst
inferredcites →https://doi.org/10.1002/anie.201206165openalex-snapshot
Effective Fixation of CO2 by Iridium‐Catalyzed Hydrosilylation
inferredcites →https://doi.org/10.1002/asia.200800388openalex-snapshot
Bridging MCl Bonds with Ambiphilic Phosphine–Borane Ligands
inferredcites →https://doi.org/10.1002/chem.201203226openalex-snapshot
Mild Reduction of Carbon Dioxide to Methane with Tertiary Silanes Catalyzed by Platinum and Palladium Silyl Pincer Complexes
inferredcites →https://doi.org/10.1002/ejic.200800784openalex-snapshot
Coordination Chemistry of Neutral (L n )–Z Amphoteric and Ambiphilic Ligands
inferredcites →https://doi.org/10.1016/0022-328x(91)80257-kopenalex-snapshot
The structure of 2-(diphenylphosphino)phenyllithium: the significance of PLi bonding
inferredcites →https://doi.org/10.1021/ic00062a048openalex-snapshot
Nucleophile promoted degradation of catecholborane: consequences for transition metal-catalyzed hydroborations
inferredcites →https://doi.org/10.1021/ja048911mopenalex-snapshot
Me2AlCH2PMe2: A New, Bifunctional Cocatalyst for the Ni(II)-Catalyzed Oligomerization of PhSiH3
inferredcites →https://doi.org/10.1021/ja0637494openalex-snapshot
On the Versatile and Unusual Coordination Behavior of Ambiphilic Ligands o -R 2 P(Ph)BR‘ 2
inferredcites →https://doi.org/10.1021/ja0647250openalex-snapshot
From Carbon Dioxide to Methane: Homogeneous Reduction of Carbon Dioxide with Hydrosilanes Catalyzed by Zirconium−Borane Complexes
inferredcites →https://doi.org/10.1021/ja103982topenalex-snapshot
An Efficient Nickel Catalyst for the Reduction of Carbon Dioxide with a Borane
inferredcites →https://doi.org/10.1021/ja105320copenalex-snapshot
Tandem Frustrated Lewis Pair/Tris(pentafluorophenyl)borane-Catalyzed Deoxygenative Hydrosilylation of Carbon Dioxide
inferredcites →https://doi.org/10.1021/ja2035514openalex-snapshot
Secondary Coordination Sphere Interactions Facilitate the Insertion Step in an Iridium(III) CO2 Reduction Catalyst
inferredcites →https://doi.org/10.1021/ja208760jopenalex-snapshot
Cascade Catalysis for the Homogeneous Hydrogenation of CO 2 to Methanol
inferredcites →https://doi.org/10.1021/ja208969dopenalex-snapshot
Copper-Mediated Reduction of CO2 with pinB-SiMe2Ph via CO2 Insertion into a Copper–Silicon Bond
inferredcites →https://doi.org/10.1021/ja305318copenalex-snapshot
An Efficient Iridium Catalyst for Reduction of Carbon Dioxide to Methane with Trialkylsilanes
inferredcites →https://doi.org/10.1021/ja9104792openalex-snapshot
Room Temperature Reduction of CO 2 to Methanol by Al-Based Frustrated Lewis Pairs and Ammonia Borane
inferredcites →https://doi.org/10.1021/jo801260fopenalex-snapshot
Chemical Recycling of Carbon Dioxide to Methanol and Dimethyl Ether: From Greenhouse Gas to Renewable, Environmentally Carbon Neutral Fuels and Synthetic Hydrocarbons
inferredcites →https://doi.org/10.1021/om00007a003openalex-snapshot
Hydroboration of Alkynes with Pinacolborane Catalyzed by HZrCp2Cl
inferredcites →https://doi.org/10.1021/om1008428openalex-snapshot
Coordination of Ethylene to a Zwitterionic Rh(III) Half-Sandwich Complex: Influence of Ambiphilic Ligands on Reactivity
inferredcites →https://doi.org/10.1038/nchem.1089openalex-snapshot
Efficient hydrogenation of organic carbonates, carbamates and formates indicates alternative routes to methanol based on CO2 and CO
inferredcites →https://doi.org/10.1039/b700658fopenalex-snapshot
Utilisation of CO2 as a chemical feedstock: opportunities and challenges
inferredcites →https://doi.org/10.1039/c0cs00129eopenalex-snapshot
Transition-metal-catalyzed C–C bond formation through the fixation of carbon dioxide
inferredcites →https://doi.org/10.1039/c1cc14641fopenalex-snapshot
Reactivity of Lewis pairs (R2PCH2AlMe2)2 with carbon dioxide
inferredcites →https://doi.org/10.1039/c2cc30399jopenalex-snapshot
Phosphine-boronates: efficient bifunctional organocatalysts for Michael addition
inferredcites →https://doi.org/10.1039/c2cc35257eopenalex-snapshot
Ambiphilic molecules for trapping reactive intermediates: interrupted Nazarov reaction of allenyl vinyl ketones with Me2PCH2AlMe2
inferredcites →https://doi.org/10.1039/c3cc41838copenalex-snapshot
Highly efficient catalytic hydrosilylation of carbon dioxide by an N-heterocyclic carbene copper catalyst
inferredcites →https://doi.org/10.1039/c3sc50145kopenalex-snapshot
Decamethylscandocinium-hydrido-(perfluorophenyl)borate: fixation and tandem tris(perfluorophenyl)borane catalysed deoxygenative hydrosilation of carbon dioxide
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.2139/ssrn.4749204openalex-extracted
Advancing Co2 Hydrogenation to Formic Acid: Dft Insights into Frustrated Lewis Pair-Functionalized Uio-67 Catalysts
inferred← citeshttps://doi.org/10.1002/9780470682531.pat0839openalex-snapshot
Organoaluminum Compounds and L ewis Pairs
inferred← citeshttps://doi.org/10.1002/9781119951438.eibc2520openalex-snapshot
Small Molecule Activation with Frustrated L ewis P airs
inferred← citeshttps://doi.org/10.1002/9783527824113.ch4openalex-snapshot
Catalytic Homogeneous Hydrogenation of CO 2 to Methanol
inferred← citeshttps://doi.org/10.1002/adsc.201801194openalex-snapshot
Isolable CO 2 Adducts of Polarized Alkenes: High Thermal Stability and Catalytic Activity for CO 2 Chemical Transformation
inferred← citeshttps://doi.org/10.1002/aic.15519openalex-snapshot
Performance of combined use of chlorosilanes and AlCl3 in the carboxylation of toluene with CO2
inferred← citeshttps://doi.org/10.1002/ajoc.202200143openalex-snapshot
Pyridinylidenaminophosphines as Versatile Organocatalysts for CO2 Transformations into Value‐Added Chemicals
inferred← citeshttps://doi.org/10.1002/ange.201309094openalex-snapshot
Selective Hydrosilation of CO2 to a Bis(silylacetal) Using an Anilido Bipyridyl‐Ligated Organoscandium Catalyst
inferred← citeshttps://doi.org/10.1002/ange.201402868openalex-snapshot
Phosphine‐Directed CH Borylation Reactions: Facile and Selective Access to Ambiphilic Phosphine Boronate Esters
inferred← citeshttps://doi.org/10.1002/ange.201407357openalex-snapshot
Carbon Dioxide Reduction to Methylamines under Metal‐Free Conditions
inferred← citeshttps://doi.org/10.1002/ange.201409800openalex-snapshot
Chemie frustrierter Lewis‐Paare: Entwicklung und Perspektiven
inferred← citeshttps://doi.org/10.1002/ange.201500570openalex-snapshot
Cooperative Bond Activation and Catalytic Reduction of Carbon Dioxide at a Group 13 Metal Center
inferred← citeshttps://doi.org/10.1002/ange.201502987openalex-snapshot
Catalytic Asymmetric Synthesis of Phosphine Boronates
inferred← citeshttps://doi.org/10.1002/ange.201503087openalex-snapshot
Facile Protocol for Catalytic Frustrated Lewis Pair Hydrogenation and Reductive Deoxygenation of Ketones and Aldehydes
inferred← citeshttps://doi.org/10.1002/ange.201504072openalex-snapshot
Effective Formylation of Amines with Carbon Dioxide and Diphenylsilane Catalyzed by Chelating bis(tzNHC) Rhodium Complexes
inferred← citeshttps://doi.org/10.1002/ange.201505244openalex-snapshot
Hydrophosphination of CO2 and Subsequent Formate Transfer in the 1,3,2‐Diazaphospholene‐Catalyzed N‐Formylation of Amines
inferred← citeshttps://doi.org/10.1002/ange.201507458openalex-snapshot
Selektive katalytische Synthesen mit Kohlendioxid und Wasserstoff: Katalyse‐Schach an der Nahtstelle zwischen Energie und Chemie
inferred← citeshttps://doi.org/10.1002/ange.201605645openalex-snapshot
Spontaneous Reduction of a Hydroborane To Generate a B−B Single Bond by the Use of a Lewis Pair
inferred← citeshttps://doi.org/10.1002/ange.201608583openalex-snapshot
Direct Mannich‐Type Reactions Promoted by Frustrated Lewis Acid/Brønsted Base Catalysts
inferred← citeshttps://doi.org/10.1002/ange.201609040openalex-snapshot
Metal‐Free Reduction of CO2 to Methoxyborane under Ambient Conditions through Borondiformate Formation
inferred← citeshttps://doi.org/10.1002/ange.201610455openalex-snapshot
N,P‐Heterocyclic Germylene/B(C6F5)3 Adducts: A Lewis Pair with Multi‐reactive Sites
inferred← citeshttps://doi.org/10.1002/ange.201708921openalex-snapshot
Stoichiometric Reactions of CO2 and Indium‐Silylamides and Catalytic Synthesis of Ureas
inferred← citeshttps://doi.org/10.1002/ange.201801800openalex-snapshot
Efficient CO2 Insertion and Reduction Catalyzed by a Terminal Zinc Hydride Complex
inferred← citeshttps://doi.org/10.1002/ange.201810121openalex-snapshot
Katalytische reduktive N‐Alkylierungen unter Verwendung von CO2 und Carbonsäurederivaten: Aktuelle Entwicklungen
inferred← citeshttps://doi.org/10.1002/ange.201812857openalex-snapshot
Accessing Ambiphilic Phosphine Boronates through C−H Borylation by an Unforeseen Cationic Iridium Complex
inferred← citeshttps://doi.org/10.1002/ange.201813064openalex-snapshot
In Situ Generation of an N‐Heterocyclic Carbene Functionalized Metal–Organic Framework by Postsynthetic Ligand Exchange: Efficient and Selective Hydrosilylation of CO2
inferred← citeshttps://doi.org/10.1002/ange.201901171openalex-snapshot
In Situ Formation of Frustrated Lewis Pairs in a Water‐Tolerant Metal‐Organic Framework for the Transformation of CO2
inferred← citeshttps://doi.org/10.1002/ange.202001354openalex-snapshot
Trapping of Difluorocarbene by Frustrated Lewis Pairs
inferred← citeshttps://doi.org/10.1002/ange.202107127openalex-snapshot
Synergistic Catalysis by Brønsted Acid/Carbodicarbene Mimicking Frustrated Lewis Pair‐Like Reactivity
inferred← citeshttps://doi.org/10.1002/ange.202112233openalex-snapshot
Selective Catalytic Frustrated Lewis Pair Hydrogenation of CO 2 in the Presence of Silylhalides
inferred← citeshttps://doi.org/10.1002/ange.202204008openalex-snapshot
Challenges and Prospects in the Catalytic Conversion of Carbon Dioxide to Formaldehyde
inferred← citeshttps://doi.org/10.1002/ange.202207278openalex-snapshot
Homogeneous Hydrogenation of CO2 and CO to Methanol: The Renaissance of Low‐Temperature Catalysis in the Context of the Methanol Economy
inferred← citeshttps://doi.org/10.1002/ange.202208987openalex-snapshot
Design of Frustrated Lewis Pair Catalysts for Direct Hydrogenation of CO2
inferred← citeshttps://doi.org/10.1002/ange.202213615openalex-snapshot
Dynamic B/N Lewis Pairs: Insights into the Structural Variations and Photochromism via Light‐Induced Fluorescence to Phosphorescence Switching
inferred← citeshttps://doi.org/10.1002/ange.202415626openalex-snapshot
Reduction Polymerization of CO 2 with Phenylene Silanes Catalyzed by Single Component B(C 6 F 5 ) 3
inferred← citeshttps://doi.org/10.1002/ange.5038244openalex-snapshot
Photoswitchable Ambiphilicity: Light‐Gated Frustrated Lewis Pair Reactivity and Z‐Type Interaction
inferred← citeshttps://doi.org/10.1002/anie.201309094openalex-snapshot
Selective Hydrosilation of CO2 to a Bis(silylacetal) Using an Anilido Bipyridyl‐Ligated Organoscandium Catalyst
inferred← citeshttps://doi.org/10.1002/anie.201402868openalex-snapshot
Phosphine‐Directed CH Borylation Reactions: Facile and Selective Access to Ambiphilic Phosphine Boronate Esters
inferred← citeshttps://doi.org/10.1002/anie.201407357openalex-snapshot
Carbon Dioxide Reduction to Methylamines under Metal‐Free Conditions
inferred← citeshttps://doi.org/10.1002/anie.201409800openalex-snapshot
Frustrated Lewis Pair Chemistry: Development and Perspectives
inferred← citeshttps://doi.org/10.1002/anie.201500570openalex-snapshot
Cooperative Bond Activation and Catalytic Reduction of Carbon Dioxide at a Group 13 Metal Center
inferred← citeshttps://doi.org/10.1002/anie.201502987openalex-snapshot
Catalytic Asymmetric Synthesis of Phosphine Boronates
inferred← citeshttps://doi.org/10.1002/anie.201503087openalex-snapshot
Facile Protocol for Catalytic Frustrated Lewis Pair Hydrogenation and Reductive Deoxygenation of Ketones and Aldehydes
inferred← citeshttps://doi.org/10.1002/anie.201504072openalex-snapshot
Effective Formylation of Amines with Carbon Dioxide and Diphenylsilane Catalyzed by Chelating bis( tz NHC) Rhodium Complexes
inferred← citeshttps://doi.org/10.1002/anie.201505244openalex-snapshot
Hydrophosphination of CO 2 and Subsequent Formate Transfer in the 1,3,2‐Diazaphospholene‐Catalyzed N ‐Formylation of Amines
inferred← citeshttps://doi.org/10.1002/anie.201507458openalex-snapshot
Selective Catalytic Synthesis Using the Combination of Carbon Dioxide and Hydrogen: Catalytic Chess at the Interface of Energy and Chemistry
inferred← citeshttps://doi.org/10.1002/anie.201605645openalex-snapshot
Spontaneous Reduction of a Hydroborane To Generate a B−B Single Bond by the Use of a Lewis Pair
inferred← citeshttps://doi.org/10.1002/anie.201608583openalex-snapshot
Direct Mannich‐Type Reactions Promoted by Frustrated Lewis Acid/Brønsted Base Catalysts
inferred← citeshttps://doi.org/10.1002/anie.201609040openalex-snapshot
Metal‐Free Reduction of CO2 to Methoxyborane under Ambient Conditions through Borondiformate Formation
inferred← citeshttps://doi.org/10.1002/anie.201610455openalex-snapshot
N,P‐Heterocyclic Germylene/B(C6F5)3 Adducts: A Lewis Pair with Multi‐reactive Sites
inferred← citeshttps://doi.org/10.1002/anie.201708921openalex-snapshot
Stoichiometric Reactions of CO2 and Indium‐Silylamides and Catalytic Synthesis of Ureas
inferred← citeshttps://doi.org/10.1002/anie.201801800openalex-snapshot
Efficient CO2 Insertion and Reduction Catalyzed by a Terminal Zinc Hydride Complex
inferred← citeshttps://doi.org/10.1002/anie.201810121openalex-snapshot
Catalytic Reductive N‐Alkylations Using CO2 and Carboxylic Acid Derivatives: Recent Progress and Developments
inferred← citeshttps://doi.org/10.1002/anie.201812857openalex-snapshot
Accessing Ambiphilic Phosphine Boronates through C−H Borylation by an Unforeseen Cationic Iridium Complex
inferred← citeshttps://doi.org/10.1002/anie.201813064openalex-snapshot
In Situ Generation of an N‐Heterocyclic Carbene Functionalized Metal–Organic Framework by Postsynthetic Ligand Exchange: Efficient and Selective Hydrosilylation of CO2
inferred← citeshttps://doi.org/10.1002/anie.201901171openalex-snapshot
In Situ Formation of Frustrated Lewis Pairs in a Water‐Tolerant Metal‐Organic Framework for the Transformation of CO 2
inferred← citeshttps://doi.org/10.1002/anie.202001354openalex-snapshot
Trapping of Difluorocarbene by Frustrated Lewis Pairs
inferred← citeshttps://doi.org/10.1002/anie.202107127openalex-snapshot
Synergistic Catalysis by Brønsted Acid/Carbodicarbene Mimicking Frustrated Lewis Pair‐Like Reactivity
inferred← citeshttps://doi.org/10.1002/anie.202112233openalex-snapshot
Selective Catalytic Frustrated Lewis Pair Hydrogenation of CO2 in the Presence of Silylhalides
inferred← citeshttps://doi.org/10.1002/anie.202204008openalex-snapshot
Challenges and Prospects in the Catalytic Conversion of Carbon Dioxide to Formaldehyde
inferred← citeshttps://doi.org/10.1002/anie.202207278openalex-snapshot
Homogeneous Hydrogenation of CO2 and CO to Methanol: The Renaissance of Low‐Temperature Catalysis in the Context of the Methanol Economy
inferred← citeshttps://doi.org/10.1002/anie.202208987openalex-snapshot
Design of Frustrated Lewis Pair Catalysts for Direct Hydrogenation of CO 2
inferred← citeshttps://doi.org/10.1002/anie.202213615openalex-snapshot
Dynamic B/N Lewis Pairs: Insights into the Structural Variations and Photochromism via Light‐Induced Fluorescence to Phosphorescence Switching
inferred← citeshttps://doi.org/10.1002/anie.202415626openalex-snapshot
Reduction Polymerization of CO 2 with Phenylene Silanes Catalyzed by Single Component B(C 6 F 5 ) 3
inferred← citeshttps://doi.org/10.1002/anie.5038244openalex-snapshot
Photoswitchable Ambiphilicity: Light‐Gated Frustrated Lewis Pair Reactivity and Z‐Type Interaction
inferred← citeshttps://doi.org/10.1002/cctc.201702019openalex-snapshot
Recent Advances in Catalysis with Transition‐Metal Pincer Compounds
inferred← citeshttps://doi.org/10.1002/cctc.201901255openalex-snapshot
Catalytic CO2 Reduction with Boron‐ and Aluminum Hydrides
inferred← citeshttps://doi.org/10.1002/cctc.202000604openalex-snapshot
Frustrated Lewis Pair Catalyzed Reduction of Carbon Dioxide Using Hydroboranes: New DFT Mechanistic Insights
inferred← citeshttps://doi.org/10.1002/cctc.202201011openalex-snapshot
Metal‐Free Catalytic Hydroboration of Unsaturated Compounds: A Greener Strategy for the Synthesis of Organoboranes
inferred← citeshttps://doi.org/10.1002/ceur.202500360openalex-snapshot
Establishing Indium in Frustrated Lewis Pair Chemistry: From Synthesis to Catalytic Applications
inferred← citeshttps://doi.org/10.1002/chem.201304376openalex-snapshot
Transition‐Metal‐Free Catalytic Reduction of Carbon Dioxide
inferred← citeshttps://doi.org/10.1002/chem.201304845openalex-snapshot
Selective Reduction of CO2 with Silanes over Platinum Nanoparticles Immobilised on a Polymeric Monolithic Support under Ambient Conditions
inferred← citeshttps://doi.org/10.1002/chem.201304870openalex-snapshot
Carbene‐9‐BBN Ring Expansions as a Route to Intramolecular Frustrated Lewis Pairs for CO2 Reduction
inferred← citeshttps://doi.org/10.1002/chem.201400349openalex-snapshot
Metal‐Free Reduction of CO2 with Hydroboranes: Two Efficient Pathways at Play for the Reduction of CO2 to Methanol
inferred← citeshttps://doi.org/10.1002/chem.201501904openalex-snapshot
Activation of Carbon Dioxide by Silyl Triflate‐Based Frustrated Lewis Pairs
inferred← citeshttps://doi.org/10.1002/chem.201504953openalex-snapshot
Hydrogen Sulfide Induced Carbon Dioxide Activation by Metal‐Free Dual Catalysis
inferred← citeshttps://doi.org/10.1002/chem.201603954openalex-snapshot
The Chemistry of a Non‐Interacting Vicinal Frustrated Phosphane/Borane Lewis Pair
inferred← citeshttps://doi.org/10.1002/chem.201700390openalex-snapshot
Frustrated Lewis Pair Mediated Csp3−H Activation
inferred← citeshttps://doi.org/10.1002/chem.201801909openalex-snapshot
Ring‐opening of Epoxides Mediated by Frustrated Lewis Pairs
inferred← citeshttps://doi.org/10.1002/chem.201801932openalex-snapshot
Designing Metal‐Free Frustrated Lewis Pairs Catalyst for the Efficient Dehydrogenation of Ammonia Borane
inferred← citeshttps://doi.org/10.1002/chem.201802603openalex-snapshot
On the Viability of Catalytic Turnover via Al−O/B−H Metathesis: The Reactivity of β‐Diketiminate Aluminium Hydrides towards CO2 and Boranes
inferred← citeshttps://doi.org/10.1002/chem.201901088openalex-snapshot
Activation of SO2 by N/Si+ and N/B Frustrated Lewis Pairs: Experimental and Theoretical Comparison with CO2 Activation
inferred← citeshttps://doi.org/10.1002/chem.201901134openalex-snapshot
A bis‐Pyrazolate Pincer on Reduced Cr Deoxygenates CO2: Selective Capture of the Derived Oxide by CrII
inferred← citeshttps://doi.org/10.1002/chem.201903407openalex-snapshot
Double Phosphinoboration of CO2: A Facile Route to Diphospha‐Ureas
inferred← citeshttps://doi.org/10.1002/chem.201904081openalex-snapshot
An Unprecedented Ga/P Frustrated Lewis Pair: Synthesis, Characterization, and Reactivity
inferred← citeshttps://doi.org/10.1002/chem.201905629openalex-snapshot
Triple Frustrated Lewis Pair‐Type Reactivity on a Single Rare‐Earth Metal Center
inferred← citeshttps://doi.org/10.1002/chem.201905793openalex-snapshot
Evidence for Genuine Bimetallic Frustrated Lewis Pair Activation of Dihydrogen with Gold(I)/Platinum(0) Systems
inferred← citeshttps://doi.org/10.1002/chem.202000842openalex-snapshot
Evidence for Genuine Bimetallic Frustrated Lewis Pair Activation of Dihydrogen with Gold(I)/Platinum(0) Systems
inferred← citeshttps://doi.org/10.1002/chem.202001218openalex-snapshot
Octaboraneyl Complexes of Nickel: Monomers for Redox‐Active Coordination Polymers
inferred← citeshttps://doi.org/10.1002/chem.202103009openalex-snapshot
Pincer‐Supported Gallium Complexes for the Catalytic Hydroboration of Aldehydes, Ketones and Carbon Dioxide
inferred← citeshttps://doi.org/10.1002/chem.202202842openalex-snapshot
Differences in the Reactivity of Geminal Si−O−P and Al−O−P Frustrated Lewis Pairs
inferred← citeshttps://doi.org/10.1002/chem.202203206openalex-snapshot
Three‐ and Five‐Membered Anionic Chains of Pnictogenylboranes
inferred← citeshttps://doi.org/10.1002/chem.202303380openalex-snapshot
Quo Vadis CO2 Activation: Catalytic Reduction of CO2 to Methanol Using Aluminum and Gallium/Carbon‐based Ambiphiles
inferred← citeshttps://doi.org/10.1002/chem.202403449openalex-snapshot
Ce[N(SiMe3)2]3(THF)3‐Catalyzed Hydroboration of CO2, Esters and Epoxides with Pinacolborane: Selective Synthesis of Methanol in Multigram Scale
inferred← citeshttps://doi.org/10.1002/chem.202403942openalex-snapshot
Activation and Fixation of Atmospheric CO 2 through a 1,2,3‐Triazole‐Based Mesoionic Carbene–Borane Adduct
inferred← citeshttps://doi.org/10.1002/cjoc.202000027openalex-snapshot
Frustrated Lewis Pairs: Discovery and Overviews in Catalysis
inferred← citeshttps://doi.org/10.1002/cnma.202500266openalex-snapshot
Metal–Organic Frameworks and Covalent Organic Frameworks as Catalysts and Photocatalysts for the Synthesis of Cyclic Carbonates from CO 2 and Epoxides
inferred← citeshttps://doi.org/10.1002/cplu.202000367openalex-snapshot
An Aminopyridinium Ionic Liquid: A Simple and Effective Bifunctional Organocatalyst for Carbonate Synthesis from Carbon Dioxide and Epoxides
inferred← citeshttps://doi.org/10.1002/cplu.70201openalex-snapshot
Metformin‐Based Bio‐Inspired Organocatalysts for CO 2 Fixation of Terminal/Internal Epoxides
inferred← citeshttps://doi.org/10.1002/cssc.202002087openalex-snapshot
CO 2 Reduction to Methanol in the Liquid Phase: A Review
inferred← citeshttps://doi.org/10.1002/cssc.202002660openalex-snapshot
More Than Just a Reagent: The Rise of Renewable Organohydrides for Catalytic Reduction of Carbon Dioxide
inferred← citeshttps://doi.org/10.1002/ejic.202000437openalex-snapshot
CO2 Capture by 2‐(Methylamino)pyridine Ligated Aluminum Alkyl Complexes
inferred← citeshttps://doi.org/10.1002/ejic.202000449openalex-snapshot
Element‐Ligand Cooperativity with p‐Block Elements
inferred← citeshttps://doi.org/10.1002/ejic.202000723openalex-snapshot
Hydrosilylation and Hydrogermylation of CO2 and CS2 by Al and Ga Functionalized Silanes and Germanes – Cooperative Reactivity with Formation of Silyl Formates and Disilylacetals
inferred← citeshttps://doi.org/10.1002/ejic.202500174openalex-snapshot
Reactivity of an Ortho‐Phenylene‐Bridged Al/P Frustrated Lewis Pair toward Small Molecules
inferred← citeshttps://doi.org/10.1002/ejoc.201601267openalex-snapshot
Reactivity and Structural Diversity in the Reaction of Guanidine 1,5,7‐Triazabicyclo[4.4.0]dec‐5‐ene with CO2, CS2, and Other Heterocumulenes
inferred← citeshttps://doi.org/10.1002/ejoc.201800320openalex-snapshot
Lewis Base Promoted Reduction of CO2 with BH3NH3 into Boryl Formates: CO2 as a Carbon Source in Organic Synthesis Under Mild Conditions
inferred← citeshttps://doi.org/10.1002/er.6970openalex-snapshot
Recent advances in the rational design of 2D MXenes in energy conversion and storage systems
inferred← citeshttps://doi.org/10.1002/er.7043openalex-snapshot
Recent advances in the rational design of 2D MXenes in energy conversion and storage systems
inferred← citeshttps://doi.org/10.1002/ijch.201400121openalex-snapshot
tBu3P/ZnR2 (R=Et, I) Frustrated Lewis Pair Catalysts for Functionalization and Reduction of CO2
inferred← citeshttps://doi.org/10.1002/poc.4250openalex-snapshot
Metal‐free catalytic activation and borylation of the ––H bond of 1‐methyl pyrrole using adamantane‐derived aminoborane frustrated Lewis pairs: A density functional theory study
inferred← citeshttps://doi.org/10.1002/poc.4652openalex-snapshot
Density functional theory study on frustrated Lewis pairs catalyzed C‐H activation of heteroarenes: Mechanism variation tuning by electronic effect
inferred← citeshttps://doi.org/10.1002/qua.26416openalex-snapshot
Molecular electrostatic potential at nuclear position as a new concept in evaluation of the substitution effects of intramolecular B/N frustrated Lewis pairs in H2 splitting and CO2 reduction
inferred← citeshttps://doi.org/10.1002/slct.202301173openalex-snapshot
In Silico Activation of CO 2 , NO 2 , and SO 2 with Light Atom Molecules and Stepwise Conversion of CO 2 into Methanol and Water
inferred← citeshttps://doi.org/10.1007/3418_2015_109openalex-snapshot
Recent Progress in Carbon Dioxide Reduction Using Homogeneous Catalysts
inferred← citeshttps://doi.org/10.1007/430_2026_106openalex-snapshot
Heterobimetallic Frustrated Lewis Pairs Based on Transition and Main Group Metals
inferred← citeshttps://doi.org/10.1007/978-3-319-51807-7_5openalex-snapshot
Stoichiometric Reactivity and Catalytic Applications of Heavier Tetrylene Derivatives
inferred← citeshttps://doi.org/10.1007/978-3-642-44988-8_4openalex-snapshot
Hydrogenation and Related Reductions of Carbon Dioxide with Molecular Catalysts
inferred← citeshttps://doi.org/10.1007/978-981-10-3102-1_10openalex-snapshot
Carbon Dioxide to Energy: Killing Two Birds with One Stone
inferred← citeshttps://doi.org/10.1007/978-981-10-3250-9_4openalex-snapshot
Transformation of CO2 to Methanol with Homogeneous Catalysts
inferred← citeshttps://doi.org/10.1007/978-981-99-2890-3_1openalex-snapshot
Organocatalytic Reductive Functionalization of Carbon Dioxide
inferred← citeshttps://doi.org/10.1007/s10562-020-03135-wopenalex-snapshot
Synthesis of Ionic Liquids as Novel Nanocatalysts for Fixation of Carbon Dioxide with Epoxides by Using a Carbon Dioxide Balloon
inferred← citeshttps://doi.org/10.1007/s11426-015-5405-yopenalex-snapshot
Thermal-reductive transformations of carbon dioxide catalyzed by small molecules using earth-abundant elements
inferred← citeshttps://doi.org/10.1007/s11426-016-0442-5openalex-snapshot
Lewis base-CO2 adducts as organocatalysts for CO2 transformation
inferred← citeshttps://doi.org/10.1007/s11426-023-1804-4openalex-snapshot
Bimolecular reduction of carbon dioxide: double synthons for alkynes trifunctionalization
inferred← citeshttps://doi.org/10.1007/s13369-024-09601-6openalex-snapshot
Biological CO2 Utilization; Current Status, Challenges, and Future Directions for Photosynthetic and Non-photosynthetic Route
inferred← citeshttps://doi.org/10.1016/b978-0-12-818429-5.00003-xopenalex-snapshot
Rivaling transition metal reactivity—an exploration of frustrated Lewis pairs chemistry
inferred← citeshttps://doi.org/10.1016/b978-0-12-820206-7.00129-3openalex-snapshot
Frustrated Lewis Pair Systems
inferred← citeshttps://doi.org/10.1016/b978-0-12-823144-9.00011-xopenalex-snapshot
Frustrated lewis pairs in catalysis
inferred← citeshttps://doi.org/10.1016/b978-0-12-824024-3.00023-3openalex-snapshot
Metal nanoparticles for catalytic hydrogenation reactions
inferred← citeshttps://doi.org/10.1016/b978-0-444-62746-9.00009-8openalex-snapshot
Conversion of Carbon Dioxide to Oxygenated Organics
inferred← citeshttps://doi.org/10.1016/bs.adomc.2021.01.001openalex-snapshot
Bimetallic frustrated Lewis pairs
inferred← citeshttps://doi.org/10.1016/j.cattod.2019.06.040openalex-snapshot
High-performance nano-structured Ni based catalysts for high-temperature CO2CH4 reforming—Greenhouse gases to syngas
inferred← citeshttps://doi.org/10.1016/j.ccr.2015.06.003openalex-snapshot
Boron-mediated activation of carbon dioxide
inferred← citeshttps://doi.org/10.1016/j.ccr.2016.05.005openalex-snapshot
Design principles in frustrated Lewis pair catalysis for the functionalization of carbon dioxide and heterocycles
inferred← citeshttps://doi.org/10.1016/j.cej.2023.145714openalex-snapshot
A robust low coordinate Co(II) catalyst for efficient conversion of CO2 into methanol under mild conditions
inferred← citeshttps://doi.org/10.1016/j.chempr.2017.06.001openalex-snapshot
Electrostatic Catalyst Generated from Diazadiborinine for Carbonyl Reduction
inferred← citeshttps://doi.org/10.1016/j.cogsc.2016.11.004openalex-snapshot
Metal-free reduction of CO2
inferred← citeshttps://doi.org/10.1016/j.cogsc.2017.07.001openalex-snapshot
New routes for CO2 activation and subsequent conversion
inferred← citeshttps://doi.org/10.1016/j.energy.2017.06.065openalex-snapshot
Theoretical evaluation of the organocatalytic behavior of the negatively charged carbon atom in a fused five-member ring in carbon dioxide transformation to methanol
inferred← citeshttps://doi.org/10.1016/j.energy.2017.12.149openalex-snapshot
Understanding the thermodynamic and kinetic performances of the substituted phosphorus ylides as a new class of compounds in carbon dioxide activation
inferred← citeshttps://doi.org/10.1016/j.ica.2018.08.039openalex-snapshot
A multimetal-ligand cooperative approach to CO2 activation
inferred← citeshttps://doi.org/10.1016/j.ijhydene.2016.04.052openalex-snapshot
Reduction of CO2 with KBH4 in solvent-free conditions
inferred← citeshttps://doi.org/10.1016/j.ijhydene.2016.05.050openalex-snapshot
Borohydride salts as high efficiency reducing reagents for carbon dioxide transformation to methanol: Theoretical approach
inferred← citeshttps://doi.org/10.1016/j.ijhydene.2021.02.015openalex-snapshot
Base-assisted transfer hydrogenation of CO2 to formate with ammonia borane in water under mild conditions
inferred← citeshttps://doi.org/10.1016/j.ijhydene.2023.06.187openalex-snapshot
Boron-based hydrogen storage materials towards Power-to-X technology on the path to carbon neutrality
inferred← citeshttps://doi.org/10.1016/j.ijhydene.2024.12.237openalex-snapshot
Boron-based hydrogen storage materials for highly selective conversion to liquid organic hydrogen carriers synthesis focus on formic acid
inferred← citeshttps://doi.org/10.1016/j.ijhydene.2025.152499openalex-snapshot
Unraveling H2 dissociation in CO2 hydrogenation on frustrated Lewis pair-functionalized UiO–67: DFT and nuclear quantum effects
inferred← citeshttps://doi.org/10.1016/j.inoche.2015.10.009openalex-snapshot
Reduction of CO2 to methanol using aluminum ester FLPs
inferred← citeshttps://doi.org/10.1016/j.jcat.2015.09.009openalex-snapshot
Solid poly-N-heterocyclic carbene catalyzed CO2 reduction with hydrosilanes
inferred← citeshttps://doi.org/10.1016/j.jcat.2024.115571openalex-snapshot
Advancing CO2 hydrogenation to formic Acid: DFT insights into Frustrated Lewis Pair−Functionalized UiO−67 catalysts
inferred← citeshttps://doi.org/10.1016/j.jcat.2025.116275openalex-snapshot
Unlocking efficient CO2–to–methanol conversion on frustrated Lewis pair-functionalized UiO–67: A synergistic approach using DFT and SISSO
inferred← citeshttps://doi.org/10.1016/j.jcou.2017.08.015openalex-snapshot
Phosphorus ylides as a new class of compounds in CO2 activation: Thermodynamic and kinetic studies
inferred← citeshttps://doi.org/10.1016/j.jcou.2025.103212openalex-snapshot
Organoboron catalysts: From structural design to functional application in CO2 conversions
inferred← citeshttps://doi.org/10.1016/j.jmgm.2022.108150openalex-snapshot
Exploring the metal-free catalytic reduction of CO2 to methanol with saturated adamantane scaffolds of phosphine-borane frustrated Lewis pair: A DFT study
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2018.11.001openalex-snapshot
The phosphinoboration of 2-diphenylphosphino benzaldehyde and related aldimines
inferred← citeshttps://doi.org/10.1016/j.rser.2013.11.045openalex-snapshot
Conversion of carbon dioxide into methanol – a potential liquid fuel: Fundamental challenges and opportunities (a review)
inferred← citeshttps://doi.org/10.1016/j.rser.2016.01.026openalex-snapshot
Electrochemical conversion of carbon dioxide into renewable fuel chemicals – The role of nanomaterials and the commercialization
inferred← citeshttps://doi.org/10.1021/acs.accounts.7b00514openalex-snapshot
Ambiphilic Molecules: From Organometallic Curiosity to Metal-Free Catalysts
inferred← citeshttps://doi.org/10.1021/acs.energyfuels.5c04900openalex-snapshot
Theoretical Identification of Highly Active Mo 2 B (MBenes) toward CO 2 Capture and Reduction
inferred← citeshttps://doi.org/10.1021/acs.iecr.5b03277openalex-snapshot
Toward the Development and Deployment of Large-Scale Carbon Dioxide Capture and Conversion Processes
inferred← citeshttps://doi.org/10.1021/acs.inorgchem.0c01152openalex-snapshot
Ph2PCH2CH2B(C8H14) and Its Formaldehyde Adduct as Catalysts for the Reduction of CO2 with Hydroboranes
inferred← citeshttps://doi.org/10.1021/acs.inorgchem.0c02012openalex-snapshot
Silica Nanopowder Supported Frustrated Lewis Pairs for CO 2 Capture and Conversion to Formic Acid
inferred← citeshttps://doi.org/10.1021/acs.inorgchem.0c03507openalex-snapshot
Aluminum-Hydride-Catalyzed Hydroboration of Carbon Dioxide
inferred← citeshttps://doi.org/10.1021/acs.inorgchem.1c02654openalex-snapshot
CO 2 Cleavage Reaction Driven by Alkylidyne Complexes of Group 6 Metals and Uranium: A Density Functional Theory Study on Energetics, Reaction Mechanism, and Structural/Bonding Properties
inferred← citeshttps://doi.org/10.1021/acs.inorgchem.2c02754openalex-snapshot
Silicon Carbamates by CO2 Fixation: Brønsted Acid Labile Precursor of a Lewis Superacid
inferred← citeshttps://doi.org/10.1021/acs.inorgchem.4c00500openalex-snapshot
Zinc-Catalyzed Hydroboration of Carbon Dioxide Amplified by Borane-Tethered Heteroscorpionate Bis(Pyrazolyl)methane Ligands
inferred← citeshttps://doi.org/10.1021/acs.inorgchem.5b01102openalex-snapshot
Conversion of Carbon Dioxide to Methanol Using a C–H Activated Bis(imino)pyridine Molybdenum Hydroboration Catalyst
inferred← citeshttps://doi.org/10.1021/acs.inorgchem.5c04011openalex-snapshot
Controlling Selectivity in Carbon Dioxide Hydroboration to Formic Acid and Methanol Levels Regulated by Lewis Acid: A Computational Mechanistic Study
inferred← citeshttps://doi.org/10.1021/acs.inorgchem.6c01255openalex-snapshot
Magnesium-Catalyzed CO 2 Reduction to Formic Acid or Methanol: Solvent or No Solvent Settles the Selectivity
inferred← citeshttps://doi.org/10.1021/acs.joc.1c00302openalex-snapshot
Hydroboration Reaction and Mechanism of Carboxylic Acids using NaNH2(BH3)2, a Hydroboration Reagent with Reducing Capability between NaBH4 and LiAlH4
inferred← citeshttps://doi.org/10.1021/acs.joc.6b00559openalex-snapshot
Theoretical Insights into the Catalytic Mechanism of N-Heterocyclic Olefins in Carboxylative Cyclization of Propargyl Alcohol with CO2
inferred← citeshttps://doi.org/10.1021/acs.jpca.0c00724openalex-snapshot
Evaluation of Influencing Factors in Tetravalent Uranium Complex-Mediated CO2 Functionalization by Density Functional Theory
inferred← citeshttps://doi.org/10.1021/acs.jpca.9b11648openalex-snapshot
Formation of Formic Acid Derivatives through Activation and Hydroboration of CO 2 by Low-Valent Group 14 (Si, Ge, Sn, Pb) Catalysts
inferred← citeshttps://doi.org/10.1021/acs.jpcc.9b04221openalex-snapshot
Transition-Metal Diboride: A New Family of Two-Dimensional Materials Designed for Selective CO2 Electroreduction
inferred← citeshttps://doi.org/10.1021/acs.macromol.0c02258openalex-snapshot
Tailored Triarylborane Polymers as Supported Catalysts and Luminescent Materials
inferred← citeshttps://doi.org/10.1021/acs.organomet.3c00126openalex-snapshot
Pitfalls for POCOP-Type Palladium Pincer Complexes in Catalytic Reduction of CO2 with Catecholborane
inferred← citeshttps://doi.org/10.1021/acs.organomet.5b00250openalex-snapshot
Synthetic Endeavors toward Titanium Based Frustrated Lewis Pairs with Controlled Electronic and Steric Properties
inferred← citeshttps://doi.org/10.1021/acs.organomet.6b00867openalex-snapshot
Dehydrodechlorination of Methylene Chloride, Chloroform, and Chlorodiphenylmethane in the Presence of Ga/N Lewis Pairs
inferred← citeshttps://doi.org/10.1021/acs.organomet.7b00497openalex-snapshot
Selective Ni-Catalyzed Hydroboration of CO2 to the Formaldehyde Level Enabled by New PSiP Ligation
inferred← citeshttps://doi.org/10.1021/acs.organomet.7b00819openalex-snapshot
Frustrated Lewis Pair Behavior of an Open, Noninteracting Phosphane/Borane Pair at a Rigid Organic Framework: Exploring Decisive Factors for FLP Activity
inferred← citeshttps://doi.org/10.1021/acs.organomet.8b00035openalex-snapshot
Metal-Free Carbonylation Route to a Reactive Borataepoxide System
inferred← citeshttps://doi.org/10.1021/acs.organomet.9b00346openalex-snapshot
P–H Functionalized Al/P-Based Frustrated Lewis Pairs in Dipolar Activation and Hydrophosphination: Reactions with CO2 and SO2
inferred← citeshttps://doi.org/10.1021/acs.orglett.5b00167openalex-snapshot
Efficient Synthesis of (P-Chirogenic) o-Boronated Phosphines from sec-Phosphine Boranes
inferred← citeshttps://doi.org/10.1021/acsami.2c06993openalex-snapshot
Visible-Light-Responsive UiO-66(Zr) with Defects Efficiently Promoting Photocatalytic CO 2 Reduction
inferred← citeshttps://doi.org/10.1021/acscatal.3c00020openalex-snapshot
Base- and Additive-Free Carbon Dioxide Hydroboration to Methoxyboranes Catalyzed by Non-Pincer-Type Mn(I) Complexes
inferred← citeshttps://doi.org/10.1021/acscatal.5b00189openalex-snapshot
Hydroboration of Carbon Dioxide Using Ambiphilic Phosphine–Borane Catalysts: On the Role of the Formaldehyde Adduct
inferred← citeshttps://doi.org/10.1021/acscatal.5b00275openalex-snapshot
A Heterobimetallic Mechanism for C–H Borylation Elucidated from Experimental and Computational Data
inferred← citeshttps://doi.org/10.1021/acscatal.5b00428openalex-snapshot
Catalytic Hydroboration of Carbonyl Derivatives, Imines, and Carbon Dioxide
inferred← citeshttps://doi.org/10.1021/acscatal.5b01191openalex-snapshot
Screening Lewis Pair Moieties for Catalytic Hydrogenation of CO 2 in Functionalized UiO-66
inferred← citeshttps://doi.org/10.1021/acscatal.5b01409openalex-snapshot
CO 2 Adducts of Phosphorus Ylides: Highly Active Organocatalysts for Carbon Dioxide Transformation
inferred← citeshttps://doi.org/10.1021/acscatal.5b02354openalex-snapshot
Virtual Issue Posts on Organocatalysis: Design, Applications, and Diversity
inferred← citeshttps://doi.org/10.1021/acscatal.5c06417openalex-snapshot
Designing the Future of Advancing Catalysis: Structural Trends in Metal-Free Systems for CO 2 Conversion
inferred← citeshttps://doi.org/10.1021/acscatal.6b00421openalex-snapshot
Implications of CO2 Activation by Frustrated Lewis Pairs in the Catalytic Hydroboration of CO2: A View Using N/Si+ Frustrated Lewis Pairs
inferred← citeshttps://doi.org/10.1021/acscatal.6b00587openalex-snapshot
BH3 Activation by Phosphorus-Stabilized Geminal Dianions: Synthesis of Ambiphilic Organoborane, DFT Studies, and Catalytic CO2 Reduction into Methanol Derivatives
inferred← citeshttps://doi.org/10.1021/acscatal.6b02101openalex-snapshot
Di(carbene)-Supported Nickel Systems for CO2 Reduction Under Ambient Conditions
inferred← citeshttps://doi.org/10.1021/acscatal.6b02715openalex-snapshot
Utilization of CO2 as a C1 Building Block for Catalytic Methylation Reactions
inferred← citeshttps://doi.org/10.1021/acscatal.6b03306openalex-snapshot
Efficient Reduction of Carbon Dioxide to Methanol Equivalents Catalyzed by Two-Coordinate Amido–Germanium(II) and −Tin(II) Hydride Complexes
inferred← citeshttps://doi.org/10.1021/acscatal.6b03313openalex-snapshot
Tuning Catalytic Activity in the Hydrogenation of Unactivated Olefins with Transition-Metal Oxos as the Lewis Base Component of Frustrated Lewis Pairs
showing the first 200 of 335 · page through all 335
Editorial review for independent work. ICSAC — the Institute for Complexity
Science and Advanced Computing — runs a structured editorial panel for researchers
publishing outside journals, and publishes on CiteStamp rails. Submission is free
and goes through ORCID: icsacinstitute.org/submit.