Polymer-supported Lewis acids and bases: Synthesis and applications. (December 2020)
- Record Type:
- Journal Article
- Title:
- Polymer-supported Lewis acids and bases: Synthesis and applications. (December 2020)
- Main Title:
- Polymer-supported Lewis acids and bases: Synthesis and applications
- Authors:
- Yolsal, Utku
Horton, Thomas A.R.
Wang, Meng
Shaver, Michael P. - Abstract:
- Abstract: In the past decade the synthesis of novel stimuli-responsive materials has been driven by the pursuit of new applications and, more recently, sustainable and reusable systems. Of these materials, those which incorporate main group Lewis acids (LAs) and bases (LBs) into their polymer backbones have shown extraordinary utility as a result of their synthetic diversity, enabling fine tuning of reactivity and ensuing properties tailored to the desired application. Herein, the recent progress made in the synthesis and applications of macromolecular LAs and LBs is being highlighted. Interactions between polymeric LAs and LBs can be exploited to build supramolecular polymeric networks based on both conventional and frustrated Lewis pairs, while using either functionality individually enables the preparation of sensors for anions, cations, explosives and biological molecules. The presence of polymer-supported LAs/LBs in organocatalysis has been extended to controlling polymer morphology, enabled improvements in activity through compartmentalization and the coexistence of classically incompatible functionalities. Finally, the versatility of this field is being demonstrated by highlighting some of the recent advances in CO2 chemisorption systems employing amine-based polymeric LBs for carbon capture and reduction. Graphical abstract: Image, graphical abstract
- Is Part Of:
- Progress in polymer science. Volume 111(2020)
- Journal:
- Progress in polymer science
- Issue:
- Volume 111(2020)
- Issue Display:
- Volume 111, Issue 2020 (2020)
- Year:
- 2020
- Volume:
- 111
- Issue:
- 2020
- Issue Sort Value:
- 2020-0111-2020-0000
- Page Start:
- Page End:
- Publication Date:
- 2020-12
- Subjects:
- Lewis acids and bases -- Functional polymers -- Stimuli-responsive polymers -- Sensors -- Organocatalysis -- CO2 capture
AAM acrylamide -- AIBN azobisisobutyronitrile -- ATR-FTIR attenuated total reflection-Fourier transform infra-red -- BCF trispentafluorophenylborane -- BDTB benzyl benzodithioate -- BET Brunauer–Emmett–Teller -- Boc tert-butoxycarbonyl -- BT benzothiadiazole -- CPDTC 2-cyano-2-propyl dodecyl trithiocarbonate -- CT computed tomography -- CTA chain transfer agent -- DBU 1, 8-diazabicyclo[5.4.0]undec-7-ene -- DCM dichloromethane -- DEAD diethyl azodicarboxylate -- DETA diethylenetriamine -- DMAP 4-dimethylaminopyridine -- DMF dimethylformamide -- DMM dimethoxymethane -- DMP 2-(dodecylthiocarbonothioylthio)-2-methylpropionic -- DMSO dimethyl sulfoxide -- DOX doxorubicin -- DSC differential scanning calorimetry -- DVB divinylbenzene -- EDAC 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide -- EDX energy dispersive X-ray -- FLP frustrated Lewis pairs -- GC gas chromatography -- GMA glycidyl methacrylate -- HOMO highest occupied molecular orbital -- HSAB hard and soft acids and bases -- IDA indicator displacement array -- LA Lewis acid -- LB Lewis base -- LCST lower critical solution temperature -- LPA Lewis pair adduct -- LUMO lowest unoccupied molecular orbital -- MMA methyl methacrylate -- MOFs metal-organic frameworks -- mPEG methoxy-PEG -- NHC N-heterocyclic carbene -- NIPAM N-isopropylacrylamide -- PA photoacoustics -- PAD poly(N-amidino-2, 3-dihydro-1, 4-methyl-1, 2, 3-triazol-ethenylbenzene) -- PAMAM polyamidoamine -- PBA phenylboronic acid -- PDMS polydimethylsiloxane -- PE-g-PAA polyethylene-graft-polyacrylic acid -- PEG polyethylene glycol -- PHEA poly(N-2-hydroxyethyl)aspartamide -- PIM polymers of intrinsic microporosity -- PNs polymeric nanoassemblies -- PNIPAM poly(N-isopropylacrylamide) -- POP porous organic polymer -- PPB arylboronate polyphosphazene derivative -- PPCP polydi(carboxylatophenoxy)phosphazene -- PS polystyrene -- PTh polythiophenes -- PTPE poly(4-undecoxytetraphenylethylene methacrylate) -- QCM quartz crystal microbalance -- RAFT reversible addition-fragmentation chain transfer -- ROMP ring-opening metathesis polymerization -- ROP ring-opening polymerization -- ROS reactive oxygen species -- SCM shell crosslinked micelle -- SDS sodium dodecyl sulfate -- SP SPACeR resins -- TBD triazabicyclodecene -- TBMA tert-butyl methacrylate -- TEA trimethylamine -- TEMP tetrakis(4-ethynyl-phenyl)methane -- TEPA tetraethylenepentamine -- TFA trifluoroacetic acid -- THF tetrahydrofuran -- TMPTA trimethylolpropane triacrylate -- TREN tris(2-aminoethyl)amine -- UCST upper critical solution temperature -- UV ultraviolet -- Vis visible -- WL Wolf and Lamb
Polymers -- Periodicals
Polymerization -- Periodicals
Polymers -- Industrial applications -- Periodicals
Polymères -- Périodiques
Polymérisation -- Périodiques
547.7 - Journal URLs:
- http://www.sciencedirect.com/science/journal/00796700 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.progpolymsci.2020.101313 ↗
- Languages:
- English
- ISSNs:
- 0079-6700
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6873.570000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 14882.xml