Tuning the excited-state deactivation pathways of dinuclear ruthenium(ii) 2,2′-bipyridine complexes through bridging ligand design-Reference-Cited by-同舟云学术

Tuning the excited-state deactivation pathways of dinuclear ruthenium(ii) 2,2′-bipyridine complexes through bridging ligand design

Published:2020 Issue:24 Volume:49 Page:8096-8106
ISSN:1477-9226
Container-title:Dalton Transactions
language:en
Short-container-title:Dalton Trans.

Author:

Cerfontaine Simon¹²³⁴⁵^ORCID,Troian-Gautier Ludovic⁶⁷⁸⁹¹⁰^ORCID,Wehlin Sara A. M.¹⁰¹¹¹²¹³,Loiseau Frédérique¹⁴¹⁵¹⁶¹⁷,Cauët Emilie¹⁸¹⁹²⁰²¹⁹,Elias Benjamin¹²³⁴⁵^ORCID

Affiliation:

1. Université catholique de Louvain (UCLouvain)

2. Institut de la Matière Condensée et des Nanosciences (IMCN)

3. Molecular Chemistry

4. Materials and Catalysis (MOST)

5. 1348 Louvain-la-Neuve

6. Laboratoire de Chimie Organique

7. Université libre de Bruxelles (ULB)

8. 1050 Brussels

9. Belgium

10. Department of Chemistry

11. University of North Carolina at Chapel Hill

12. Chapel Hill

13. USA

14. Département de Chimie Moléculaire

15. Univ. Grenoble-Alpes (UGA)

16. 38058 Grenoble

17. France

18. Spectroscopy

19. Quantum Chemistry and Atmospheric Remote Sensing (CP 160/09)

20. Université libre de Bruxelles

21. B-1050 Brussels

Abstract

A detailed photophysical study of binuclear complexes was performed using steady-state and time-resolved photoluminescence measurements at variable temperature. The results were compared with the prototypical [Ru(bpy)₃]²⁺.

Funder

Fonds De La Recherche Scientifique - FNRS

Université Catholique de Louvain

U.S. Department of Energy

Publisher

Royal Society of Chemistry (RSC)

Subject

Inorganic Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2020/DT/D0DT01216E

Reference91 articles.

1. CHARGE TRANSFER LUMINESCENCE OF A RUTHENIUM(II) CHELATE