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

Journal Article · · Dalton Transactions
DOI:https://doi.org/10.1039/d0dt01216e· OSTI ID:1801394
ORCiD logo [1]; ORCiD logo [2];  [3];  [4];  [5]; ORCiD logo [1]
  1. Université catholique de Louvain (UCLouvain); Institut de la Matière Condensée et des Nanosciences (IMCN); Molecular Chemistry; Materials and Catalysis (MOST); 1348 Louvain-la-Neuve
  2. Laboratoire de Chimie Organique; Université libre de Bruxelles (ULB); 1050 Brussels; Belgium; Department of Chemistry
  3. Department of Chemistry; University of North Carolina at Chapel Hill; Chapel Hill; USA
  4. Département de Chimie Moléculaire; Univ. Grenoble-Alpes (UGA); 38058 Grenoble; France
  5. Spectroscopy; Quantum Chemistry and Atmospheric Remote Sensing (CP 160/09); Université libre de Bruxelles; B-1050 Brussels; Belgium

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+.

Research Organization:
University of North Carolina, Chapel Hill, NC (United States)
Sponsoring Organization:
USDOE Office of Science (SC)
DOE Contract Number:
SC0001011
OSTI ID:
1801394
Journal Information:
Dalton Transactions, Vol. 49, Issue 24; ISSN 1477-9226
Publisher:
Royal Society of Chemistry
Country of Publication:
United States
Language:
English

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