2023
DOI: 10.1002/anie.202301347
|View full text |Cite
|
Sign up to set email alerts
|

A Traceless Chiral Shift Reagent Based on Nonbonding Interactions with Single‐Handed Helical Poly(quinoxaline‐2,3‐diyl)

Abstract: A single-handed poly(quinoxaline-2,3-diyl) (PQX) has been found to serve as a new type of chiral shift reagent (CSR) for determining the enantiomeric ratio by NMR spectroscopy. Even though there is no specific binding site in the PQX, its nonbonding interaction with chiral analytes leads to a significant shift of the NMR chemical shift, allowing quantification of the enantiomeric ratio. The new type of CSR has the advantages of a wide scope of analytes including ethers, haloalkanes, and alkanes, easy tunabilit… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1

Citation Types

0
2
0

Year Published

2023
2023
2025
2025

Publication Types

Select...
3

Relationship

0
3

Authors

Journals

citations
Cited by 3 publications
(2 citation statements)
references
References 77 publications
0
2
0
Order By: Relevance
“…Chiral polymers have gained great attention due to their wide applications in chiral recognition, asymmetric catalysis, and organic optoelectronic materials. As a representative axial chiral moiety, 1,1′-binaphthyl-based enantiomers ( S )- M1h and ( R )- M1h were designed as monomers. The axial chirality embedded in these monomers did not hamper the polymerization, giving the corresponding polymers P1h2a in moderate molecular weight and narrow dispersity (Scheme ).…”
Section: Resultsmentioning
confidence: 99%
“…Chiral polymers have gained great attention due to their wide applications in chiral recognition, asymmetric catalysis, and organic optoelectronic materials. As a representative axial chiral moiety, 1,1′-binaphthyl-based enantiomers ( S )- M1h and ( R )- M1h were designed as monomers. The axial chirality embedded in these monomers did not hamper the polymerization, giving the corresponding polymers P1h2a in moderate molecular weight and narrow dispersity (Scheme ).…”
Section: Resultsmentioning
confidence: 99%
“…Self-assembly has been proved to be a powerful strategy for precisely controlling the arrangement of building blocks and amplifying the g lum . [21][22][23][24][25][26] Chiral nematic liquid crystals (NLCs) as a typical 1D chiral photonic crystals (CPCs) of helical structures have been recognized as powerful platforms to generate CPL. [27] For instance, in our previous work, we achieved tunable CPL with a large |g lum | value up to 0.25 through the coassembly of inorganic nanowires and quantum dots into CPCs via Langmuir-Schaefer technique.…”
Section: Introductionmentioning
confidence: 99%