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Literature DB >> 18600809

Facile heterolytic H2 activation by amines and B(C6F5)3.

Victor Sumerin¹, Felix Schulz, Martin Nieger, Markku Leskelä, Timo Repo, Bernhard Rieger.

Abstract

Entities: Chemical

Year: 2008 PMID： 18600809 DOI： 10.1002/anie.200800935

Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN： 1433-7851 Impact factor: 15.336

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17 in total

1. Stabilizing a different cyclooctatetraene stereoisomer.

Authors: Longfei Li; Ming Lei; Yaoming Xie; Henry F Schaefer; Bo Chen; Roald Hoffmann
Journal: Proc Natl Acad Sci U S A Date: 2017-08-28 Impact factor: 11.205

2. Chemical reactivity of the frustrated Lewis pairs in borophosphines: a theoretical analysis of their Lewis acidity, Lewis basicity and Fukui function.

Authors: Mariano Méndez; Andrés Cedillo
Journal: J Mol Model Date: 2018-08-17 Impact factor: 1.810

3. Carbon dioxide reduction by an Al-O-P frustrated Lewis pair.

Authors: Lucas Wickemeyer; Niklas Aders; Andreas Mix; Beate Neumann; Hans-Georg Stammler; Jorge J Cabrera-Trujillo; Israel Fernández; Norbert W Mitzel
Journal: Chem Sci Date: 2022-06-02 Impact factor: 9.969

4. Superelectrophilic intermediates in nitrogen-directed aromatic borylation.

Authors: Timothy S De Vries; Aleksandrs Prokofjevs; Jeremy N Harvey; Edwin Vedejs
Journal: J Am Chem Soc Date: 2009-10-21 Impact factor: 15.419

5. Main-group elements as transition metals.

Authors: Philip P Power
Journal: Nature Date: 2010-01-14 Impact factor: 49.962

6. A combined "electrochemical-frustrated lewis pair" approach to hydrogen activation: surface catalytic effects at platinum electrodes.

Authors: Elliot J Lawrence; Robin J Blagg; David L Hughes; Andrew E Ashley; Gregory G Wildgoose
Journal: Chemistry Date: 2014-11-07 Impact factor: 5.236

Facile heterolytic H2 activation by amines and B(C6F5)3.

1. Stabilizing a different cyclooctatetraene stereoisomer.

2. Chemical reactivity of the frustrated Lewis pairs in borophosphines: a theoretical analysis of their Lewis acidity, Lewis basicity and Fukui function.

3. Carbon dioxide reduction by an Al-O-P frustrated Lewis pair.

4. Superelectrophilic intermediates in nitrogen-directed aromatic borylation.

5. Main-group elements as transition metals.

6. A combined "electrochemical-frustrated lewis pair" approach to hydrogen activation: surface catalytic effects at platinum electrodes.

7. A Strategy to Control the Reactivation of Frustrated Lewis Pairs from Shelf-Stable Carbene Borane Complexes.

8. Versatile Catalytic Hydrogenation Using A Simple Tin(IV) Lewis Acid.

Review 9. From CO₂ activation to catalytic reduction: a metal-free approach.

10. An electrochemical study of frustrated Lewis pairs: a metal-free route to hydrogen oxidation.

Review 9. From CO2 activation to catalytic reduction: a metal-free approach.

Review 9. From CO₂ activation to catalytic reduction: a metal-free approach.