2019
DOI: 10.1039/c9py00495e
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Functional materials generated by allying cyclodextrin-based supramolecular chemistry with living polymerization

Abstract: Cyclodextrin molecules are cyclic oligosaccharides that display a unique structure including an inner side and two faces on their outer sides.

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Cited by 41 publications
(21 citation statements)
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“…Majority of CD-polymer conjugates reported in the literature were prepared via atom transfer radical polymerisation (ATRP) with initiator moieties attached via esterification of cyclodextrin with alpha-halocarboxylic halide. 16 The first reported method used 2-bromoisobutyric anhydride in pyridine with a catalytic amount of 4-(di-methylamino)pyridine to give heptakis[2,3,6-tri-O-(2-bromo-2-methylpropionyl]-β-CD. 65 However, despite a long reaction time, poor yield was achieved.…”
Section: Incorporation Of Initiator Groups For Multiarm Polymersmentioning
confidence: 99%
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“…Majority of CD-polymer conjugates reported in the literature were prepared via atom transfer radical polymerisation (ATRP) with initiator moieties attached via esterification of cyclodextrin with alpha-halocarboxylic halide. 16 The first reported method used 2-bromoisobutyric anhydride in pyridine with a catalytic amount of 4-(di-methylamino)pyridine to give heptakis[2,3,6-tri-O-(2-bromo-2-methylpropionyl]-β-CD. 65 However, despite a long reaction time, poor yield was achieved.…”
Section: Incorporation Of Initiator Groups For Multiarm Polymersmentioning
confidence: 99%
“…Valued for encapsulation properties, cyclodextrin found applications in many fields such as pharmacy, [2][3][4][5] personal care products, 6,7 biomedicine, [8][9][10] food, [11][12][13] molecular recognition 14,15 and supramolecular chemistry. [16][17][18][19][20] Cyclodextrin also proved to be an extremely versatile molecule for polymer science. 16,21,22 It is particularly valued for easy functionalisation, including attachment of initiator moieties as well as unsymmetrical modification.…”
Section: Introductionmentioning
confidence: 99%
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“…Altogether, the results validated the Ad/βCD hostguest tactic for careful fine-tuning of the interaction between lectins and supramolecular glycopolymers ( Figure 7). The alliance between CD supramolecular chemistry and living polymerization has been particularly fruitful at providing fascinating polymer materials [62]. Bercer and coworkers applied one of the most popular of such reactions, reversible addition−fragmentation chain transfer (RAFT), to create triblock glycocopolymers bearing βCD, Ad and mannose residues, combined with PDMA, in different blocks [63].…”
Section: Tailoring Glycopolymer Topology By CD Inclusion-promoted Macmentioning
confidence: 99%
“…Firstly, CD-and CB-based materials, such as nanoaggregates, supramolecular polymers, and hydrogels are mostly explored in aqueous media. 34,35 Secondly, crown ethers (CEs), calixarenes (CAs), and pillararenes (PAs)-based materials are produced in aqueous as well as organic media. [36][37][38] Since the neutral states of the latter macrocycles are insoluble in water, organic solvents have been used to prepare supramolecular polymers and gels from their native states.…”
Section: Bin LImentioning
confidence: 99%