Intermolecular interactions boost aggregation induced emission in carbazole Schiff base derivatives-Reference-Cited by-同舟云学术

Intermolecular interactions boost aggregation induced emission in carbazole Schiff base derivatives

Published:2017 Issue:1 Volume:15 Page:256-264
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Gan Xiaoping¹²³⁴⁵,Liu Guangjin¹²³⁴⁵,Chu Mingjie¹²³⁴⁵,Xi Wengang⁶⁷⁸⁵,Ren Zili¹²³⁴⁵,Zhang Xiuli¹²³⁴⁵,Tian Yupeng⁶⁷⁸⁵,Zhou Hongping⁶⁷⁸⁵^ORCID

Affiliation:

1. Department of Applied Chemistry

2. School of Science

3. Anhui Agricultural University

4. 230036 Hefei

5. P. R. China

6. College of Chemistry and Chemical Engineering

7. Anhui University and Key Laboratory of Functional Inorganic Materials Chemistry of Anhui Province

8. Hefei

Abstract

The structure–property relationship was discussed and we found that the C–H⋯π interactions and H⋯H interactions played a significant role in AIE performance.

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2017/OB/C6OB02181F

Reference32 articles.

1. Upconversion Luminescent Materials: Advances and Applications

2. Carbazole Compounds as Host Materials for Triplet Emitters in Organic Light-Emitting Diodes: Tuning the HOMO Level without Influencing the Triplet Energy in Small Molecules

3. Simple and Efficient Near-Infrared Organic Chromophores for Light-Emitting Diodes with Single Electroluminescent Emission above 1000 nm

4. Synthesis and fluorescence and electrochemical properties of D–π-A structural isomers of benzofuro[2,3-c]oxazolo[4,5-a]carbazole-type and benzofuro[2,3-c]oxazolo[5,4-a]carbazole-type fluorescent dyes

5. Spectral, electrochemical and structural study of aryl derivatives of trans-stilbenes

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