Ring-opening of cyclopropanes by “frustrated Lewis pairs”

2010 ◽  
Vol 46 (47) ◽  
pp. 8947 ◽  
Author(s):  
Jason G. M. Morton ◽  
Meghan A. Dureen ◽  
Douglas W. Stephan
Keyword(s):  
Ring Opening ◽  
Frustrated Lewis Pairs ◽  
Lewis Pairs

Frustrated Lewis Pairs and Ring-Opening of THF, Dioxane, and Thioxane†

2010 ◽  
Vol 29 (21) ◽  
pp. 5310-5319 ◽  
Author(s):  
Birgit Birkmann ◽  
Tanja Voss ◽  
Stephen J. Geier ◽  
Matthias Ullrich ◽  
Gerald Kehr ◽  
...  
Keyword(s):  
Ring Opening ◽  
Frustrated Lewis Pairs ◽  
Lewis Pairs

scholarly journals Ring-opening of Epoxides Mediated by Frustrated Lewis Pairs

2018 ◽  
Vol 24 (48) ◽  
pp. 12669-12677 ◽  
Author(s):  
Tetiana Krachko ◽  
Emmanuel Nicolas ◽  
Andreas W. Ehlers ◽  
Martin Nieger ◽  
J. Chris Slootweg
Keyword(s):  
Ring Opening ◽  
Frustrated Lewis Pairs ◽  
Ring Opening Of Epoxides ◽  
Lewis Pairs

scholarly journals Bifunctional Fluorophosphonium Triflates as Intramolecular Frustrated Lewis Pairs: Reversible CO 2 Sequestration and Binding of Carbonyls, Nitriles and Acetylenes

2021 ◽  
Author(s):  
Chun‐Xiang Guo ◽  
Kai Schwedtmann ◽  
Jannis Fidelius ◽  
Felix Hennersdorf ◽  
Arne Dickschat ◽  
...  
Keyword(s):  
Frustrated Lewis Pairs ◽  
Lewis Pairs

Bis(perchlorocatecholato)silane and Heteroleptic Bidonors: Hidden Frustrated Lewis Pairs by Ring Strain

2021 ◽  
Author(s):  
Deborah Hartmann ◽  
Sven Braner ◽  
Lutz Greb
Keyword(s):  
Ammonia Borane ◽  
Frustrated Lewis Pairs ◽  
Ring Strain ◽  
Frustrated Lewis Pair ◽  
Lewis Pairs

Bis(perchlorocatecholato)silane and bidentate N,N- or N,P-heteroleptic donors form hexacoordinated complexes. Depending on the ring strain and hemilability in the adducts, Frustrated Lewis pair reactivity with aldehydes and catalytic ammonia borane...

scholarly journals Supramolecular Systems Containing B–N Frustrated Lewis Pairs of Tris(pentafluorophenyl)borane and Triphenylamine Derivatives

2021 ◽  
Vol 03 (02) ◽  
pp. 174-183
Author(s):  
P. Chidchob ◽  
S. A. H. Jansen ◽  
S. C. J. Meskers ◽  
E. Weyandt ◽  
N. P. van Leest ◽  
...  
Keyword(s):  
Materials Science ◽  
Supramolecular Polymers ◽  
Frustrated Lewis Pairs ◽  
Paramagnetic Resonance ◽  
Donor And Acceptor ◽  
Donor Acceptor ◽  
Noncovalent Polymers ◽  
Electron Paramagnetic ◽  
Supramolecular Polymerization ◽  
Lewis Pairs

The introduction of a chemical additive to supramolecular polymers holds high potential in the development of new structures and functions. In this regard, various donor- and acceptor-based molecules have been applied in the design of these noncovalent polymers. However, the incorporation of boron–nitrogen frustrated Lewis pairs in such architectures is still rare despite their many intriguing properties in catalysis and materials science. The limited choices of suitable boron derivatives represent one of the main limitations for the advancement in this direction. Here, we examine the use of the commercially available tris(pentafluorophenyl)borane with various triphenylamine derivatives to create supramolecular B–N charge transfer systems. Our results highlight the importance of a proper balance between the donor/acceptor strength and the driving force for supramolecular polymerization to achieve stable, long-range ordered B–N systems. Detailed analyses using electron paramagnetic resonance and optical spectroscopy suggest that tris(pentafluorophenyl)borane displays complex behavior with the amide-based triphenylamine supramolecular polymers and may interact in dimers or larger chiral aggregates, depending on the specific structure of the triphenylamines.

Aromaticity can enhance the reactivity of P-donor/borole frustrated Lewis pairs

2019 ◽  
Vol 55 (5) ◽  
pp. 675-678 ◽  
Author(s):  
Jorge Juan Cabrera-Trujillo ◽  
Israel Fernández
Keyword(s):  
Frustrated Lewis Pairs ◽  
Key Factor ◽  
Novel Concept ◽  
Lewis Pairs

Herein we introduce a novel concept in FLP chemistry: aromaticity as the key factor enhancing the reactivity of FLPs.

Rationalizing the Reactivity of Frustrated Lewis Pairs: Thermodynamics of H2Activation and the Role of Acid−Base Properties

2009 ◽  
Vol 131 (30) ◽  
pp. 10701-10710 ◽  
Author(s):  
Tibor András Rokob ◽  
Andrea Hamza ◽  
Imre Pápai
Keyword(s):  
Frustrated Lewis Pairs ◽  
Acid Base ◽  
Base Properties ◽  
Lewis Pairs

Development of silica-supported frustrated Lewis pairs: highly active transition metal-free catalysts for the Z-selective reduction of alkynes

2016 ◽  
Vol 6 (3) ◽  
pp. 882-889 ◽  
Author(s):  
Kai C. Szeto ◽  
Wissam Sahyoun ◽  
Nicolas Merle ◽  
Jessica Llop Castelbou ◽  
Nicolas Popoff ◽  
...  
Keyword(s):  
Transition Metal ◽  
Lewis Acid ◽  
Selective Reduction ◽  
Frustrated Lewis Pairs ◽  
Acid Base ◽  
Metal Free ◽  
Highly Active ◽  
Active Transition ◽  
Lewis Pairs

Supported Lewis acid/base systems based have been prepared and characterized.

Frustrated Lewis Pairs constructed on 2D Amorphous Carbon Nitride for High‐Selective Photocatalytic CO 2 Reduction to CH 4

Solar RRL ◽  
2021 ◽  
Author(s):  
Lina Du ◽  
Bo Gao ◽  
Qingyong Tian ◽  
Xiaoli Zheng ◽  
Wei Liu ◽  
...  
Keyword(s):  
Amorphous Carbon ◽  
Carbon Nitride ◽  
Frustrated Lewis Pairs ◽  
Amorphous Carbon Nitride ◽  
Lewis Pairs
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