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Description
| - Komplexy (.mu.3-L1/L2)[Ru(acac)2]3, acac- = 2,4-pentanedionato, L1 = 2,3,8,9,14,15-hexachlorodichinoxalino[2,3-:2',3'-c] fenazin a L2 = 2,3,8,9,14,15-hexamethyldichinoxalino[2,3-:2',3'-c] fenazin, podléhají postupné jednoelektronové oxidaci zahrnující celkově tři elektrony a postupné jednoelektronové redukci se třemi (L2) nebo čtyřmi elektrony (L1). Všechny reversibilně dostupné stavy byly charakterizovány UV-VIS-NIR spektroelektrochemií. Oxidace vede k meziproduktům se smíšenou valencí {(.mu.3-L)[Ru(acac)2]3}+ a {(.mu.3-L)[Ru(acac)2]3}2+, z nichž kombinace RuIIIRuIIRuII vykazují vyšší komproporcionační konstanty Kc než RuIIIRuIIIRuII stavy – na rozdíl od dříve popsaných nesubstituovaných mateřských systémů {(.mu.3-L3)[Ru(acac)2]3}+/2+/, L3 = dichinoxalino[2,3-:2´,3´-c] fenazin. Pro meziprodukty se smíšenou valencí nebyl pozorován v blízké infračervené oblasti žádný zřetelný absorbční pás přenosu náboje. (cs)
- The complexes (.mu.3-L1/L2)[Ru(acac)2]3, acac- = 2,4-pentanedionato, L1 = 2,3,8,9,14,15-hexachlorodiquinoxalino[2,3-a:2’,3’-c]phenazine and L2 = 2,3,8,9,14,15-hexamethyldiquinoxalino[2,3-a:2’,3’-c]phenazine, undergo stepwise one-electron oxidation involving a total of three electrons and stepwise one-electron reduction with three (L2) or four electrons (L1). All reversibly accessible states were characterized by UV–Vis–NIR spectroelectrochemistry. Oxidation leads to mixed-valent intermediates {(.mu.3-L)[Ru(acac)2]3}+ and {(.mu.3-L)[Ru(acac)2]3}2+ of which the RuIIIRuIIRuII combinations exhibit higher comproportionation constants Kc than the RuIIIRuIIIRuII states – in contrast to a previous report for the unsubstituted parent systems {(.mu.3-L3)[Ru(acac)2]3}+/2+, L3 = diquinoxalino[2,3-a:2´,3´-c]phenazine. No conspicuous inter-valence charge transfer absorptions were observed for the mixed-valent intermediates in the visible to near-infrared regions.
- The complexes (.mu.3-L1/L2)[Ru(acac)2]3, acac- = 2,4-pentanedionato, L1 = 2,3,8,9,14,15-hexachlorodiquinoxalino[2,3-a:2’,3’-c]phenazine and L2 = 2,3,8,9,14,15-hexamethyldiquinoxalino[2,3-a:2’,3’-c]phenazine, undergo stepwise one-electron oxidation involving a total of three electrons and stepwise one-electron reduction with three (L2) or four electrons (L1). All reversibly accessible states were characterized by UV–Vis–NIR spectroelectrochemistry. Oxidation leads to mixed-valent intermediates {(.mu.3-L)[Ru(acac)2]3}+ and {(.mu.3-L)[Ru(acac)2]3}2+ of which the RuIIIRuIIRuII combinations exhibit higher comproportionation constants Kc than the RuIIIRuIIIRuII states – in contrast to a previous report for the unsubstituted parent systems {(.mu.3-L3)[Ru(acac)2]3}+/2+, L3 = diquinoxalino[2,3-a:2´,3´-c]phenazine. No conspicuous inter-valence charge transfer absorptions were observed for the mixed-valent intermediates in the visible to near-infrared regions. (en)
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Title
| - Multiple one-electron oxidation and reduction of trinuclear bis(2,4-pentanedionato)ruthenium complexes with substituted diquinoxalino[2,3-a:2´,3´-c]phenazine ligands
- Multiple one-electron oxidation and reduction of trinuclear bis(2,4-pentanedionato)ruthenium complexes with substituted diquinoxalino[2,3-a:2´,3´-c]phenazine ligands (en)
- Vícenásobná jednoelektronová oxidace a redukce tříjaderných bis(1,3-pentanedionato)rutheniových komplexů se substituovanými dichinoxalin[2,3-: 2´,3´-c] fenaziny (cs)
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skos:prefLabel
| - Multiple one-electron oxidation and reduction of trinuclear bis(2,4-pentanedionato)ruthenium complexes with substituted diquinoxalino[2,3-a:2´,3´-c]phenazine ligands
- Multiple one-electron oxidation and reduction of trinuclear bis(2,4-pentanedionato)ruthenium complexes with substituted diquinoxalino[2,3-a:2´,3´-c]phenazine ligands (en)
- Vícenásobná jednoelektronová oxidace a redukce tříjaderných bis(1,3-pentanedionato)rutheniových komplexů se substituovanými dichinoxalin[2,3-: 2´,3´-c] fenaziny (cs)
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skos:notation
| - RIV/61388955:_____/07:00084868!RIV08-MSM-61388955
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http://linked.open.../vavai/riv/strany
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http://linked.open...avai/riv/aktivita
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http://linked.open...avai/riv/aktivity
| - P(1P05OC068), P(LC510), Z(AV0Z40400503)
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http://linked.open...iv/cisloPeriodika
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http://linked.open...vai/riv/dodaniDat
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http://linked.open...aciTvurceVysledku
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http://linked.open.../riv/druhVysledku
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http://linked.open...iv/duvernostUdaju
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http://linked.open...titaPredkladatele
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http://linked.open...dnocenehoVysledku
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http://linked.open...ai/riv/idVysledku
| - RIV/61388955:_____/07:00084868
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http://linked.open...riv/jazykVysledku
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http://linked.open.../riv/klicovaSlova
| - DFT calculation; EPR; radical complexes; electrochemistry (en)
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http://linked.open.../riv/klicoveSlovo
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http://linked.open...odStatuVydavatele
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http://linked.open...ontrolniKodProRIV
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http://linked.open...i/riv/nazevZdroje
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http://linked.open...in/vavai/riv/obor
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http://linked.open...ichTvurcuVysledku
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http://linked.open...cetTvurcuVysledku
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http://linked.open...vavai/riv/projekt
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http://linked.open...UplatneniVysledku
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http://linked.open...v/svazekPeriodika
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http://linked.open...iv/tvurceVysledku
| - Fiedler, Jan
- Kaim, W.
- Lahiri, G. K.
- Sarkar, B.
- Sunoj, R. B.
- Ghumaan, S.
- Patil, M. P.
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http://linked.open...n/vavai/riv/zamer
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issn
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number of pages
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is http://linked.open...avai/riv/vysledek
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