Al/P‐ and Ga/P‐Based Frustrated Lewis Pairs and Electronically Unsaturated Substrates: Ring Cleavage and Ring Closure, C−C and C−N Bond Formation

2019 ◽  
Vol 25 (39) ◽  
pp. 9315-9325 ◽  
Author(s):  
Damian Pleschka ◽  
Marten Uebing ◽  
Merten Lange ◽  
Alexander Hepp ◽  
Anna‐Lena Wübker ◽  
...  
Keyword(s):  
Bond Formation ◽  
Ring Closure ◽  
Ring Cleavage ◽  
Frustrated Lewis Pairs ◽  
Lewis Pairs

scholarly journals On the concept of frustrated Lewis pairs

2017 ◽  
Vol 375 (2101) ◽  
pp. 20170004 ◽  
Author(s):  
Frédéric-Georges Fontaine ◽  
Douglas W. Stephan
Keyword(s):  
Lewis Acid ◽  
Bond Formation ◽  
Frustrated Lewis Pairs ◽  
Metal Chemistry ◽  
Frustrated Lewis Pair ◽  
Acid And Base ◽  
Definition Of ◽  
Lewis Acid And Base ◽  
Pair Work ◽  
Lewis Pairs

In this concept article, we consider the notion of ‘frustrated Lewis pairs’ (FLPs). While the original use of the term referred to steric inhibition of dative bond formation in a Lewis pair, work in the intervening decade demonstrates the limitation of this simplistic view. Analogies to known transition metal chemistry and the applications in other areas of chemistry are considered. In the light of these findings, we present reflections on the criteria for a definition of the term ‘frustrated Lewis pair’. Segregation of the Lewis acid and base and the kinetic nature of FLP reactivity are discussed. We are led to the conclusion that, while an all-inclusive definition of FLP is challenging, the notion of ‘FLP chemistry’ is more readily recognized. This article is part of the themed issue ‘Frustrated Lewis pair chemistry’.

Formation of Thermally Robust Frustrated Lewis Pairs by Electrocyclic Ring Closure Reactions

2016 ◽  
Vol 128 (18) ◽  
pp. 5616-5620 ◽  
Author(s):  
Guo-Qiang Chen ◽  
Gerald Kehr ◽  
Constantin G. Daniliuc ◽  
Christian Mück-Lichtenfeld ◽  
Gerhard Erker
Keyword(s):  
Ring Closure ◽  
Frustrated Lewis Pairs ◽  
Lewis Pairs

Formation of Thermally Robust Frustrated Lewis Pairs by Electrocyclic Ring Closure Reactions

2016 ◽  
Vol 55 (18) ◽  
pp. 5526-5530 ◽  
Author(s):  
Guo-Qiang Chen ◽  
Gerald Kehr ◽  
Constantin G. Daniliuc ◽  
Christian Mück-Lichtenfeld ◽  
Gerhard Erker
Keyword(s):  
Ring Closure ◽  
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.

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

Oxidative Aromatic C−O Bond Formation: Synthesis of 3-Functionalized Benzo[b]furans by FeCl3-Mediated Ring Closure of α-Aryl Ketones

2009 ◽  
Vol 11 (21) ◽  
pp. 4978-4981 ◽  
Author(s):  
Zhidan Liang ◽  
Weizhe Hou ◽  
Yunfei Du ◽  
Yongliang Zhang ◽  
Yan Pan ◽  
...  
Keyword(s):  
Bond Formation ◽  
Ring Closure ◽  
Aryl Ketones
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