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Valence-state distribution in the ruthenium o-quinonoid systems [Ru(trpy)(Cl)(L-1)](+) and [Ru(trpy)(Cl)(L-2)](+) (L-1 = o-iminobenzoquinone, L-2 = o-diiminobenzoquinone; trpy=2,2 ': 6 ',2 ''-terpyridine)

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Title Valence-state distribution in the ruthenium o-quinonoid systems [Ru(trpy)(Cl)(L-1)](+) and [Ru(trpy)(Cl)(L-2)](+) (L-1 = o-iminobenzoquinone, L-2 = o-diiminobenzoquinone; trpy=2,2 ': 6 ',2 ''-terpyridine)
 
Creator MAJI, S
PATRA, S
CHAKRABORTY, S
JANARDANAN, D
MOBIN, SM
SUNOJ, RB
LAHIRI, GK
 
Subject density-functional theory
transition-metal complexes
ray crystal-structure
bridging ligand
spectroelectrochemical properties
terpyridine complexes
electronic-structure
redox series
electrochemical properties
semiquinone ligands
ruthenium
quinonoid ligands
valence-state distributions
density functional calculations
spectroelectrochemistry
 
Description Valence-state distributions in the ruthenium quinonoid (L) frameworks of [Ru(trpy)(Cl)(L-1))ClO4 (1-ClO4) and [Ru(trpy)-(CI) (L-2)]ClO4 (2-ClO4) (L-1 = o-iminobenzoquinone, L-2 = o-diiminobenzoquinone, and trpy = 2,2':6',2"-terpyridine) have been examined by structural, spectroelectrochemical, and density functional studies. The structural data, in corroboration with the DFT-calculated bond lengths, suggest that the primary valence formulation of 1(+) and 21 is a spin-coupled singlet configuration of [Ru-III(trpy)(Cl)(L-Sq)](+) with a minority contribution from diamagnetic [Ru-II(trpy)(Cl)(L-Q)](+). Consequently, the closely spaced successive two oxidation processes of 1(+) and 2(+) can be assigned to Ru-III -> Ru-IV and L-Sq -> L-Q, which involve the HOMO and HOMO-3 levels, respectively. The one-electron-oxidized species 1(2+) and 2(2+) display sharp EPR signals with g values of 2.011 and 2.014 at 77 K, respectively. The free radical EPR signal (g approximate to 2.0) of the one-electron-reduced species I or 2 signifies the preferential involvement of the ruthenium-based orbitals in the first reduction process to yield [Ru-II(trpy)(Cl)(L-Sq)], although the LUMO is calculated to be a mixture of d pi(Ru) (approximate to 24 %) and pi * (L) (approximate to 70 %). The subsequent second (1(-)/2(-)) and third (1(2-)/2(2-)) reduction steps in each case are associated simply with the terpyridyl-based orbitals (>= 90 %). The lowest energy charge-transfer transitions of 1(+) and 2(+) at 556 and 509 nm are predicted to be HOMO -> LUMO+1 and HOMO-1 -> LUMO+1 transitions, respectively. In the successive oxidations 1(+)/2(+) -> 1(2+)/2(2+) -> 1(3+)/2(3+) the lowest energy charge-transfer transitions undergo a blue shift with a substantial reduction in intensity. The lowest energy charge-transfer transitions, however, are red shifted with a reduction in intensity on going from (1(+)/2(+)) to 1/2. The origin of the transitions in the 1(2+)/2(2+) and 1/2 systems is predicted by TDDFT analysis. ((c) Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2007)
 
Publisher WILEY-V C H VERLAG GMBH
 
Date 2011-09-01T23:12:35Z
2011-12-26T12:59:50Z
2011-12-27T05:52:47Z
2011-09-01T23:12:35Z
2011-12-26T12:59:50Z
2011-12-27T05:52:47Z
2007
 
Type Article
 
Identifier EUROPEAN JOURNAL OF INORGANIC CHEMISTRY, (2), 314-323
1434-1948
http://dx.doi.org/10.1002/ejic.200600830
http://dspace.library.iitb.ac.in/xmlui/handle/10054/12889
http://hdl.handle.net/10054/12889
 
Language en