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Literature DB >> 19552435

Chiral recognition based on enantioselectively aggregation-induced emission.

Abstract

Novel chiral AIE compounds bearing a tartaric acid group were synthesized. They selectively aggregated with one enantiomer of a number of chiral amines, such that one enantiomer led to strong fluorescence and another enantiomer showed no or only weak fluorescence. This was used for the quantitative analysis of enantiomeric composition.

Entities: Chemical

Year: 2009 PMID： 19552435 DOI： 10.1021/jo900527e

Source DB: PubMed Journal: J Org Chem ISSN： 0022-3263 Impact factor: 4.354

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Cited

7 in total

1. Synthesis of Tripeptide Derivatives with Three Stereogenic Centers and Chiral Recognition Probed by Tetraaza Macrocyclic Chiral Solvating Agents Derived from d-Phenylalanine and (1 S,2 S)-(+)-1,2-Diaminocyclohexane via ¹H NMR Spectroscopy.

Authors: Lei Feng; Guangpeng Gao; Hongmei Zhao; Li Zheng; Yu Wang; Pericles Stavropoulos; Lin Ai; Jiaxin Zhang
Journal: J Org Chem Date: 2018-10-30 Impact factor: 4.354

2. Gated photochromic molecules with AIEgen: turn-on the photochromism with an oxidation reagent.

Authors: Leyu Wang; Tao Yu; Zongliang Xie; Eethamukkala Ubba; Tianya Zhan; Zhiyong Yang; Yi Zhang; Zhenguo Chi
Journal: RSC Adv Date: 2018-05-22 Impact factor: 4.036

3. The HOF structures of nitrotetraphenylethene derivatives provide new insights into the nature of AIE and a way to design mechanoluminescent materials.

Authors: Tao Yu; Depei Ou; Zhiyong Yang; Qiuyi Huang; Zhu Mao; Junru Chen; Yi Zhang; Siwei Liu; Jiarui Xu; Martin R Bryce; Zhenguo Chi
Journal: Chem Sci Date: 2016-09-02 Impact factor: 9.825

4. Combined aggregation induced emission (AIE), photochromism and photoresponsive wettability in simple dichloro-substituted triphenylethylene derivatives.

Authors: Depei Ou; Tao Yu; Zhiyong Yang; Tiangang Luan; Zhu Mao; Yi Zhang; Siwei Liu; Jiarui Xu; Zhenguo Chi; Martin R Bryce
Journal: Chem Sci Date: 2016-04-26 Impact factor: 9.825

Chiral recognition based on enantioselectively aggregation-induced emission.

1. Synthesis of Tripeptide Derivatives with Three Stereogenic Centers and Chiral Recognition Probed by Tetraaza Macrocyclic Chiral Solvating Agents Derived from d-Phenylalanine and (1 S,2 S)-(+)-1,2-Diaminocyclohexane via ¹H NMR Spectroscopy.

2. Gated photochromic molecules with AIEgen: turn-on the photochromism with an oxidation reagent.

3. The HOF structures of nitrotetraphenylethene derivatives provide new insights into the nature of AIE and a way to design mechanoluminescent materials.

4. Combined aggregation induced emission (AIE), photochromism and photoresponsive wettability in simple dichloro-substituted triphenylethylene derivatives.

5. Chiral recognition and enantiomer excess determination based on emission wavelength change of AIEgen rotor.

Review 6. Chiral assembly of organic luminogens with aggregation-induced emission.

7. A colour-tunable chiral AIEgen: reversible coordination, enantiomer discrimination and morphology visualization.

Chiral recognition based on enantioselectively aggregation-induced emission.

1. Synthesis of Tripeptide Derivatives with Three Stereogenic Centers and Chiral Recognition Probed by Tetraaza Macrocyclic Chiral Solvating Agents Derived from d-Phenylalanine and (1 S,2 S)-(+)-1,2-Diaminocyclohexane via 1H NMR Spectroscopy.

2. Gated photochromic molecules with AIEgen: turn-on the photochromism with an oxidation reagent.

3. The HOF structures of nitrotetraphenylethene derivatives provide new insights into the nature of AIE and a way to design mechanoluminescent materials.

4. Combined aggregation induced emission (AIE), photochromism and photoresponsive wettability in simple dichloro-substituted triphenylethylene derivatives.

5. Chiral recognition and enantiomer excess determination based on emission wavelength change of AIEgen rotor.

Review 6. Chiral assembly of organic luminogens with aggregation-induced emission.

7. A colour-tunable chiral AIEgen: reversible coordination, enantiomer discrimination and morphology visualization.

1. Synthesis of Tripeptide Derivatives with Three Stereogenic Centers and Chiral Recognition Probed by Tetraaza Macrocyclic Chiral Solvating Agents Derived from d-Phenylalanine and (1 S,2 S)-(+)-1,2-Diaminocyclohexane via ¹H NMR Spectroscopy.