Influence of the number and substitution position of phenyl groups on the aggregation-enhanced emission of benzene-cored luminogens-Reference-Cited by-同舟云学术

Influence of the number and substitution position of phenyl groups on the aggregation-enhanced emission of benzene-cored luminogens

Published:2015 Issue:23 Volume:51 Page:4830-4833
ISSN:1359-7345
Container-title:Chemical Communications
language:en
Short-container-title:Chem. Commun.

Author:

Li Lingzhi¹²³⁴⁵,Chen Ming¹²³⁴⁵,Zhang Haoke¹²³⁴⁵,Nie Han⁶⁷⁸⁹⁵,Sun Jing Zhi¹²³⁴⁵,Qin Anjun¹²³⁴⁵,Tang Ben Zhong¹²³⁴⁵

Affiliation:

1. MOE Key Laboratory of Macromolecular Synthesis and Functionalization

2. Department of Polymer Science and Engineering

3. Zhejiang University

4. Hangzhou 310027

5. China

6. Guangdong Innovative Research Team

7. State Key Laboratory of Luminescent Materials and Devices

8. South China University of Technology

9. Guangzhou 510640

Abstract

The influence of the number and substitution position of phenyl groups on the emission of benzene-cored AIEgens is unambiguously revealed.

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,Metals and Alloys,Surfaces, Coatings and Films,General Chemistry,Ceramics and Composites,Electronic, Optical and Magnetic Materials,Catalysis

Link

http://pubs.rsc.org/en/content/articlepdf/2015/CC/C5CC00241A

Reference46 articles.

1. Aggregation-induced emission of 1-methyl-1,2,3,4,5-pentaphenylsilole

2. Cell Membrane Tracker Based on Restriction of Intramolecular Rotation

3. Direct validation of the restriction of intramolecular rotation hypothesis via the synthesis of novel ortho-methyl substituted tetraphenylethenes and their application in cell imaging

4. Molecular luminogens based on restriction of intramolecular motions through host–guest inclusion for cell imaging

5. Aggregation-enhanced emission in fluorophores containing pyridine and triphenylamine terminals: restricted molecular rotation and hydrogen-bond interaction

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