Accessing the triplet manifold of naphthalene benzimidazole–phenanthroline in rhenium(i ) bichromophores
Author(s) -
Kaylee A. Wells,
James E. Yarnell,
Sara Sheykhi,
Jonathan R. Palmer,
Daniel T. Yonemoto,
Rosalynd Ruby-Michelle Joyce,
Sofia Garakyaraghi,
Felix N. Castellano
Publication year - 2021
Publication title -
dalton transactions
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.98
H-Index - 184
eISSN - 1477-9234
pISSN - 1477-9226
DOI - 10.1039/d1dt02329b
Subject(s) - benzimidazole , rhenium , naphthalene , phenanthroline , chemistry , manifold (fluid mechanics) , organic chemistry , engineering , mechanical engineering
The steady-state and ultrafast to supra-nanosecond excited state dynamics of fac -[Re(NBI-phen)(CO) 3 (L)](PF 6 ) (NBI-phen = 16H-benzo[4',5']isoquinolino[2',1':1,2]imidazo[4,5- f ][1,10]phenanthrolin-16-one) as well as their respective models of the general molecular formula [Re(phen)(CO) 3 (L)](PF 6 ) (L = PPh 3 and CH 3 CN) has been investigated using transient absorption and time-gated photoluminescence spectroscopy. The NBI-phen containing molecules exhibited enhanced visible light absorption with respect to their models and a rapid formation (<6 ns) of the triplet ligand-centred (LC) excited state of the organic ligand, NBI-phen. These triplet states exhibit an extended excited state lifetime that enable the energized molecules to readily engage in triplet-triplet annihilation photochemistry.
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