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Nucleophilic Activation of Sulfur Hexafluoride: Metal‐Free, Selective Degradation by Phosphines

Angewandte Chemie International Edition, 2018-04, Vol.57 (18), p.4951-4955

International ed. in English, 2018

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Imidazolin-2-ylidenaminophosphines as Highly Electron-Rich Ligands for Transition-Metal Catalysts

Angewandte Chemie (International ed.), 2015-09, Vol.54 (40), p.11857-11860

International ed. in English, 2015

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Reversible CO2 fixation by N-heterocyclic imines forming water-stable zwitterionic nitrogen-base–CO2 adducts

Green chemistry : an international journal and green chemistry resource : GC, 2019, Vol.21 (3), p.640-648

2019

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Switching the Electron‐Donating Ability of Phosphines through Proton‐Responsive Imidazolin‐2‐ylidenamino Substituents

Chemistry : a European journal, 2019-02, Vol.25 (9), p.2352-2357

2019

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Dialkyl(1,3-diarylimidazolin-2-ylidenamino)phosphines: Strongly Electron-Donating, Buchwald-Type Phosphines

Organometallics, 2018-09, Vol.37 (18), p.3064-3072

2018

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Reversible Carbon Dioxide Binding by Simple Lewis Base Adducts with Electron-Rich Phosphines

Journal of the American Chemical Society, 2016-02, Vol.138 (6), p.1840-1843

2016

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Multistimuli‐Responsive [3]Dioxaphosphaferrocenophanes with Orthogonal Switches

Chemistry : a European journal, 2021-11, Vol.27 (61), p.15066-15073

2021

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Cover Feature: Multistimuli‐Responsive [3]Dioxaphosphaferrocenophanes with Orthogonal Switches (Chem. Eur. J. 61/2021)

Chemistry : a European journal, 2021-11, Vol.27 (61), p.15014-15014

2021

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Tris(imidazolin‐2‐ylidenamino)phosphine: A Crystalline Phosphorus(III) Superbase That Splits Carbon Dioxide

Chemistry : a European journal, 2017-05, Vol.23 (25), p.5929-5933

2017

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Synthesis and characterization of strongly electron-donating bidentate phosphines containing imidazolin-2-ylidenamino substituents and their electron-rich nickel(0), palladium(II) and gold(I) chelate complexes

Journal of organometallic chemistry, 2020-03, Vol.909, p.121097, Article 121097

2020

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Quantifying the efficiency of CO2 capture by Lewis pairs

Chemical science (Cambridge), 2017-04, Vol.8 (4), p.3270-3275

2017

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Reversible CO 2 fixation by N-heterocyclic imines forming water-stable zwitterionic nitrogen-base–CO 2 adducts

Green chemistry : an international journal and green chemistry resource : GC, 2019-02, Vol.21 (3), p.640-648

2019

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Reversible CO fixation by N-heterocyclic imines forming water-stable zwitterionic nitrogen-base-CO adducts

Green chemistry : an international journal and green chemistry resource : GC, 2019-02, Vol.21 (3), p.64-648

2019

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Effective Control of the Electron‐donating Ability of Phosphines by using Phosphazenyl and Phosphoniumylidyl Substituents

Zeitschrift für anorganische und allgemeine Chemie (1950), 2020-07, Vol.646 (13), p.794-799

2020

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Quantifying the efficiency of CO2 capture by Lewis pairsElectronic supplementary information (ESI) available. See DOI: 10.1039/c6sc05607e

2017-03

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Quantifying the efficiency of CO2 capture by Lewis pairs† †Electronic supplementary information (ESI) available. See DOI: 10.1039/c6sc05607e Click here for additional data file

Chemical science (Cambridge), 2017-02, Vol.8 (4), p.3270-3275

2017

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Quantifying the efficiency of CO 2 capture by Lewis pairs

Chemical science (Cambridge), 2017-04, Vol.8 (4), p.3270-3275

2017

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Imidazolin-2-ylidenaminophosphane als sehr elektronenreiche Liganden für Übergangsmetallkatalysatoren

Angewandte Chemie, 2015-09, Vol.127 (40), p.12024-12027

2015

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Nucleophilic Activation of Sulfur Hexafluoride: Metal‐Free, Selective Degradation by Phosphines

Angewandte Chemie, 2018-04, Vol.130 (18), p.5045-5049

2018

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Imidazolin‐2‐ylidenaminophosphane als sehr elektronenreiche Liganden für Übergangsmetallkatalysatoren

Angewandte Chemie, 2015-09, Vol.127 (40), p.12024-12027

2015

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ChemInform Abstract: Imidazolin‐2‐ylidenaminophosphines as Highly Electron‐Rich Ligands for Transition‐Metal Catalysts

ChemInform, 2016-01, Vol.47 (5), p.no-no

2016

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Luteinizing hormone causes MAP kinase-dependent phosphorylation and closure of connexin 43 gap junctions in mouse ovarian follicles: one of two paths to meiotic resumption

Development (Cambridge), 2008-10, Vol.135 (19), p.3229-3238

2008

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Limited life cycle and cost assessment for the bioconversion of lignin‐derived aromatics into adipic acid

Biotechnology and bioengineering, 2020-05, Vol.117 (5), p.1381-1393

2020

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Biotechnology and bioengineering, 2020-05, Vol.117 (5)

2020

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Biotechnology and bioengineering, 2020-05, Vol.117 (5), p.iii-iii

2020

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Nucleophilic Activation of Sulfur Hexafluoride: Metal‐Free, Selective Degradation by Phosphines

Imidazolin-2-ylidenaminophosphines as Highly Electron-Rich Ligands for Transition-Metal Catalysts

Reversible CO2 fixation by N-heterocyclic imines forming water-stable zwitterionic nitrogen-base–CO2 adducts

Switching the Electron‐Donating Ability of Phosphines through Proton‐Responsive Imidazolin‐2‐ylidenamino Substituents

Dialkyl(1,3-diarylimidazolin-2-ylidenamino)phosphines: Strongly Electron-Donating, Buchwald-Type Phosphines

Reversible Carbon Dioxide Binding by Simple Lewis Base Adducts with Electron-Rich Phosphines

Multistimuli‐Responsive [3]Dioxaphosphaferrocenophanes with Orthogonal Switches

Cover Feature: Multistimuli‐Responsive [3]Dioxaphosphaferrocenophanes with Orthogonal Switches (Chem. Eur. J. 61/2021)

Tris(imidazolin‐2‐ylidenamino)phosphine: A Crystalline Phosphorus(III) Superbase That Splits Carbon Dioxide

Synthesis and characterization of strongly electron-donating bidentate phosphines containing imidazolin-2-ylidenamino substituents and their electron-rich nickel(0), palladium(II) and gold(I) chelate complexes

Quantifying the efficiency of CO2 capture by Lewis pairs

Reversible CO 2 fixation by N-heterocyclic imines forming water-stable zwitterionic nitrogen-base–CO 2 adducts

Reversible CO fixation by N-heterocyclic imines forming water-stable zwitterionic nitrogen-base-CO adducts

Effective Control of the Electron‐donating Ability of Phosphines by using Phosphazenyl and Phosphoniumylidyl Substituents

Quantifying the efficiency of CO2 capture by Lewis pairsElectronic supplementary information (ESI) available. See DOI: 10.1039/c6sc05607e

Quantifying the efficiency of CO2 capture by Lewis pairs† †Electronic supplementary information (ESI) available. See DOI: 10.1039/c6sc05607e Click here for additional data file

Quantifying the efficiency of CO 2 capture by Lewis pairs

Imidazolin-2-ylidenaminophosphane als sehr elektronenreiche Liganden für Übergangsmetallkatalysatoren

Nucleophilic Activation of Sulfur Hexafluoride: Metal‐Free, Selective Degradation by Phosphines

Imidazolin‐2‐ylidenaminophosphane als sehr elektronenreiche Liganden für Übergangsmetallkatalysatoren

ChemInform Abstract: Imidazolin‐2‐ylidenaminophosphines as Highly Electron‐Rich Ligands for Transition‐Metal Catalysts

Luteinizing hormone causes MAP kinase-dependent phosphorylation and closure of connexin 43 gap junctions in mouse ovarian follicles: one of two paths to meiotic resumption

Limited life cycle and cost assessment for the bioconversion of lignin‐derived aromatics into adipic acid

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