The interplay of intersystem crossing and internal conversion in quadrupolar tetraarylpyrrolo[3,2-<i>b</i>]pyrroles-Reference-Cited by-同舟云学术

The interplay of intersystem crossing and internal conversion in quadrupolar tetraarylpyrrolo[3,2-b]pyrroles

Published:2024 Issue: Volume: Page:
ISSN:2050-7526
Container-title:Journal of Materials Chemistry C
language:en
Short-container-title:J. Mater. Chem. C

Author:

Górski Krzysztof¹^ORCID,Kusy Damian¹^ORCID,Ozaki Shuhei²³,Banasiewicz Marzena⁴^ORCID,Valiev Rashid⁵,Sahoo Smruti Ranjan⁶,Kamada Kenji²³^ORCID,Baryshnikov Glib⁶⁷^ORCID,Gryko Daniel T.¹^ORCID

Affiliation:

1. Institute of Organic Chemistry, Polish Academy of Sciences, Kasprzaka 44/52, 01-224 Warsaw, Poland

2. NMRI, National Institute of Advanced Industrial Science and Technology (AIST), Ikeda, Osaka 563-8577, Japan

3. Department of Chemistry, Graduate School of Science and Technology, Kwansei Gakuin University, Sanda 669-1337, Japan

4. Institute of Physics, Polish Academy of Sciences, Al. Lotników 32/46, 02-668 Warsaw, Poland

5. Department of Chemistry, University of Helsinki, FI-00014 Helsinki, Finland

6. Laboratory of Organic Electronics, Department of Science and Technology, Linköping University, SE-60174 Norrköping, Sweden

7. Department of Chemistry and Nanomaterials Science, Bohdan Khmelnytsky National University, 18031 Cherkasy, Ukraine

Abstract

In centrosymmetric, quadrupolar dyes the weak donor–acceptor conjugation results in negligible emission and weak two-photon absorption.

Funder

Vetenskapsrådet

Fundacja na rzecz Nauki Polskiej

Japan Society for the Promotion of Science

Narodowe Centrum Nauki

Olle Engkvists Stiftelse

Ministry of Education and Science of Ukraine

Academy of Finland

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2024/TC/D3TC03851C

Reference49 articles.

1. Photoproducts and triplet reactivity of 4′-nitro- and 2′,4′-dinitro-substituted 4-hydroxystilbenes

2. Making Nitronaphthalene Fluoresce

3. How To Make Nitroaromatic Compounds Glow: Next‐Generation Large X‐Shaped, Centrosymmetric Diketopyrrolopyrroles

4. Synthesis, photophysics and molecular structures of luminescent 2,5-bis(phenylethynyl)thiophenes (BPETs)

5. Tuning Electron‐Withdrawing Strength on Phenothiazine Derivatives: Achieving 100 % Photoluminescence Quantum Yield by NO 2 Substitution