Colour-tuneable solid-state fluorescence of crystalline powders formed from push–pull substituted 2,5-diphenyl-stilbenes-Reference-Cited by-同舟云学术

Colour-tuneable solid-state fluorescence of crystalline powders formed from push–pull substituted 2,5-diphenyl-stilbenes

Published:2022 Issue:54 Volume:12 Page:34797-34807
ISSN:2046-2069
Container-title:RSC Advances
language:en
Short-container-title:RSC Adv.

Author:

Pauk Karel¹,Luňák Stanislav²,Růžička Aleš³^ORCID,Marková Aneta²,Teichmanová Kateřina¹,Mausová Anna¹,Kratochvíl Matouš²,Smolka Rastislav²,Mikysek Tomáš⁴,Weiter Martin²,Imramovský Aleš¹,Vala Martin²^ORCID

Affiliation:

1. Institute of Organic Chemistry and Technology, Faculty of Chemical Technology, University of Pardubice, Studentská 95, Pardubice CZ-530 09, Czech Republic

2. Materials Research Centre, Faculty of Chemistry, Brno University of Technology, Purkyňova 464/118, Brno CZ-612 00, Czech Republic

3. Department of General and Inorganic Chemistry, Faculty of Chemical Technology, University of Pardubice, Studentská 573, Pardubice CZ-532 10, Czech Republic

4. Department of Analytical Chemistry, Faculty of Chemical Technology, University of Pardubice, Studentská 573, Pardubice CZ-532 10, Czech Republic

Abstract

Polycrystalline powders of push–pull substituted stilbenes with various acceptors emit from blue to infrared. Exciton localization on a monomer (in J-like packing) or a stacked dimer (for H-aggregates) avoid exciton migration to the quenching sites.

Funder

Grantová Agentura České Republiky

Ministerstvo Školství, Mládeže a Tělovýchovy

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemical Engineering,General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2022/RA/D2RA05593G

Reference51 articles.

1. Aggregation-Induced Emission: Together We Shine, United We Soar!

2. Self-Assembled α-Cyanostilbenes for Advanced Functional Materials