2019
DOI: 10.1039/c8py01490f
|View full text |Cite
|
Sign up to set email alerts
|

Chiral expression in conjugated helical block copolymers

Abstract: The organizational behaviour of block copolymers consisting of two helical blocks with opposite chiral expression is investigated.

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1

Citation Types

0
1
0

Year Published

2024
2024
2024
2024

Publication Types

Select...
2

Relationship

0
2

Authors

Journals

citations
Cited by 2 publications
(1 citation statement)
references
References 46 publications
0
1
0
Order By: Relevance
“…[1,2] OACPs with controlled helix sense (i.e., chirality) have recently attracted significant interest not only for their synthetic capability in mimicking biological helices but also for achieving novel chirality-relevant properties-circularly polarized luminescence, enantioselective separation and catalysis, and enantioselective recognition and sensing-that are unachievable by achiral analogues. [3][4][5][6][7][8][9][10][11][12][13] Currently, the most straightforward and efficient synthetic methodologies toward artificial OACPs are based on the direct polymerization of conjugated monomers covalently decorated with optically active side moieties, or copolymerization of optically active and silent monomers to form alternating copolymers, [14][15][16][17][18][19][20][21][22][23][24][25] which both require tedious multistep organic syntheses and, hence, are high in cost. Recently, by endowing achiral or prochiral monomers with bulky pendant substituents and introducing chiral catalysts or initiators into the polymerization reaction system, chemists have successfully developed a helix-sense-selective catalytic approach, which can effectively circumvent the disadvantages of direct synthesis.…”
Section: Introductionmentioning
confidence: 99%
“…[1,2] OACPs with controlled helix sense (i.e., chirality) have recently attracted significant interest not only for their synthetic capability in mimicking biological helices but also for achieving novel chirality-relevant properties-circularly polarized luminescence, enantioselective separation and catalysis, and enantioselective recognition and sensing-that are unachievable by achiral analogues. [3][4][5][6][7][8][9][10][11][12][13] Currently, the most straightforward and efficient synthetic methodologies toward artificial OACPs are based on the direct polymerization of conjugated monomers covalently decorated with optically active side moieties, or copolymerization of optically active and silent monomers to form alternating copolymers, [14][15][16][17][18][19][20][21][22][23][24][25] which both require tedious multistep organic syntheses and, hence, are high in cost. Recently, by endowing achiral or prochiral monomers with bulky pendant substituents and introducing chiral catalysts or initiators into the polymerization reaction system, chemists have successfully developed a helix-sense-selective catalytic approach, which can effectively circumvent the disadvantages of direct synthesis.…”
Section: Introductionmentioning
confidence: 99%