Chiroptical coassemblies between organic carboxylic acids and amino acid derivatives with C3-symmetry

Benzimidazole amino acid derivatives behave as supramolecular hosts to include organic acids via complementary hydrogen bonding whereby supramolecular chirality and chiroptical properties could be manipulated. Organic acids enhanced the chiral assembly that showed tunable circularly polarized lumine...

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Bibliographic Details
Published in:Chinese chemical letters 2023-06, Vol.34 (6), p.107955-322, Article 107955
Main Authors: Xia, Yiran, Hao, Aiyou, Xing, Pengyao
Format: Article
Language:English
Subjects:
Amino acid
Chiroptical property
Coassembly
Organic carboxylic acid
Supramolecular chirality
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Summary:Benzimidazole amino acid derivatives behave as supramolecular hosts to include organic acids via complementary hydrogen bonding whereby supramolecular chirality and chiroptical properties could be manipulated. Organic acids enhanced the chiral assembly that showed tunable circularly polarized luminescence with high dissymmetry g-factors at 10−2 grade. Organic acids enhance the chiral assembly that shows tunable circularly polarized luminescence with high dissymmetry g-factors at 10−2 grade [Display omitted]
ISSN:1001-8417
1878-5964
DOI:10.1016/j.cclet.2022.107955