Molecular Dyads of Ruthenium(II) or Osmium(II)Bis(terpyridine) Chromophores and Expanded Pyridinium Acceptors: Equilibration between MLCT and Charge-Separated Excited States
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61388955%3A_____%2F13%3A00397875" target="_blank" >RIV/61388955:_____/13:00397875 - isvavai.cz</a>
Result on the web
<a href="http://dx.doi.org/10.1021/ic401639g" target="_blank" >http://dx.doi.org/10.1021/ic401639g</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1021/ic401639g" target="_blank" >10.1021/ic401639g</a>
Alternative languages
Result language
angličtina
Original language name
Molecular Dyads of Ruthenium(II) or Osmium(II)Bis(terpyridine) Chromophores and Expanded Pyridinium Acceptors: Equilibration between MLCT and Charge-Separated Excited States
Original language description
The synthesis, characterization, redox behavior, and photophysical properties (both at room temperature in fluid solution and at 77 K in rigid matrix) of a series of four new molecular dyads (25) containing Ru(II) or Os(II)bis- (terpyridine) subunits aschromophores and various expanded pyridinium subunits as electron acceptors are reported, along with the reference properties of a formerly reported dyad, 1. The molecular dyads 24 have been designed to have their (potentially emissive) triplet metal-to-ligand charge-transfer (MLCT) and charge-separated (CS) states close in energy, so that excited-state equilibration between these levels can take place. Such a situation is not shared by limit cases 1 and 5. For dyad 1, forward photoinduced electron transfer (time constant, 7 ps) and subsequent charge recombination (time constant, 45 ps) are evidenced, while for dyad 5, photoinduced electron transfer is thermodynamically forbidden so that MLCT decays are the only active deactivation proc
Czech name
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Czech description
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Classification
Type
J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)
CEP classification
CF - Physical chemistry and theoretical chemistry
OECD FORD branch
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Result continuities
Project
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Continuities
I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace
Others
Publication year
2013
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Name of the periodical
Inorganic Chemistry
ISSN
0020-1669
e-ISSN
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Volume of the periodical
52
Issue of the periodical within the volume
20
Country of publishing house
US - UNITED STATES
Number of pages
12
Pages from-to
11944-11955
UT code for WoS article
000326065600033
EID of the result in the Scopus database
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