Theoretical Design of Strong Neutral Radical–Boron Adducts: Trisubstituted Boranes as Potential Radical Scavengers-Reference-Cited by-同舟云学术

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Theoretical Design of Strong Neutral Radical–Boron Adducts: Trisubstituted Boranes as Potential Radical Scavengers

Published:2013-07-03 Issue:12 Volume:14 Page:2759-2763
ISSN:1439-4235
Container-title:ChemPhysChem
language:en
Short-container-title:ChemPhysChem

Author:

Braïda Benoît¹²,Derat Etienne²³,Chaquin Patrick¹²

Affiliation:

1. UPMC Univ Paris 06, UMR 7616, Laboratoire de Chimie Théorique, case courrier 137, 4, place Jussieu, 75005 Paris (France)

2. Centre National de la Recherche Scientifique (CNRS), UMR 7616, Laboratoire de Chimie Théorique, F‐75005 Paris (France)

3. UPMC Univ Paris 06, UMR 7201, Institut Parisien de Chimie Moléculaire, case courrier 229, 4, place Jussieu, 75005 Paris (France)

Publisher

Wiley

Subject

Physical and Theoretical Chemistry,Atomic and Molecular Physics, and Optics

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/cphc.201300361

Reference47 articles.

1.

2. Organoboranes as a Source of Radicals

3. Radical Chain Reactions: Organoborane Initiators

4.

5. Complexes of Borane and N-Heterocyclic Carbenes: A New Class of Radical Hydrogen Atom Donor

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3. Boron-Boron One-Electron Sigma Bonds versus B-X-B Bridged Structures;Chemistry - A European Journal;2016-08-17

4. Are Boryl Radicals from Amine-Boranes and Phosphine-Boranes the Most Stable Radicals?;ChemPhysChem;2014-05-28

5. Confirmed by X-ray Crystallography: The B⋅B One-Electron σ Bond;Angewandte Chemie International Edition;2014-03-25

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