scholarly journals Room-Temperature Activation of Hydrogen by Semi-immobilized Frustrated Lewis Pairs in Microporous Polymer Networks

2017 ◽  
Vol 139 (10) ◽  
pp. 3615-3618 ◽  
Author(s):  
Matthias Trunk ◽  
Johannes F. Teichert ◽  
Arne Thomas
Keyword(s):  
Room Temperature ◽  
Polymer Networks ◽  
Frustrated Lewis Pairs ◽  
Microporous Polymer ◽  
Temperature Activation ◽  
Lewis Pairs

Room Temperature Synthesis of Heptazine-Based Microporous Polymer Networks as Photocatalysts for Hydrogen Evolution

2013 ◽  
Vol 34 (12) ◽  
pp. 1008-1013 ◽  
Author(s):  
Kamalakannan Kailasam ◽  
Johannes Schmidt ◽  
Hakan Bildirir ◽  
Guigang Zhang ◽  
Siegfried Blechert ◽  
...  
Keyword(s):  
Hydrogen Evolution ◽  
Room Temperature ◽  
Polymer Networks ◽  
Temperature Synthesis ◽  
Room Temperature Synthesis ◽  
Microporous Polymer

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

scholarly journals Recent Observations on the Mechanical Properties of Polymer Networks

1971 ◽  
Vol 44 (5) ◽  
pp. 1256-1272 ◽  
Author(s):  
P. Thirion ◽  
R. Chasset
Keyword(s):  
Crosslink Density ◽  
Room Temperature ◽  
Dynamic Properties ◽  
Polymer Networks ◽  
The Other ◽  
Dilution Ratio ◽  
Chain Entanglement ◽  
Influence Of Temperature ◽  
Terminal Zone ◽  
Crosslinking Agents

Abstract The influence of temperature, elongation, swelling or dilution ratio, crosslink density, nature of the polymers, and crosslinking agents on the dynamic properties, creep and relaxation of polymer networks is surveyed in the terminal region of the spectrum. Whereas the deformation does not change the relaxation kinetics in large ranges of extension, the crosslink density acts as a reduced variable apparently accelerating uniformly the viscoelastic processes beyond the glass transition. The other possible reductions ‘time-temperature’ and ‘time—swelling’ do not necessarily seem related to the variations of free volume. From the viewpoint of the explanation of the relaxation mechanisms in the terminal zone, the fact that the equilibrium of loosely crosslinked elastomers would only virtually be reached after several years at room temperature seem in better agreement with chain entanglement effects, either trapped or not by the permanent network, than with the dissociation of secondary linkages.

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