Thermal and photoinduced electron transfer in directional bis(terpyridine)ruthenium(II)-(bipyridine)-platinum(II) complexes
- Metalloligands L1 and L2 consisting of directional bis(terpyridine)ruthenium(II) units and bipyridine moieties were constructed by amide formation. From these metalloligands two Ru–Pt heterobimetallic complexes 1 and 2 were derived by a building-block method by means of platination with [PtCl2(dmso)2]. Both bimetallic complexes 1 and 2 feature metal-to-ligand charge transfer (MLCT) absorptions, and emission occurs at room temperature in fluid solution from ³MLCT(Ru) states in all cases. Energy transfer from platinum to ruthenium is observed in 2 but not in 1 (light harvesting). The one-electron-reduced species [1] and [2] were prepared by reduction of 1 and 2 with decamethylcobaltocene. EPR spectra and DFT calculations reveal that the spin density is localized at the tpy–CO/Ru (tpy = terpyridine) site in [1], whereas it is centered at bpy–CO/Pt (bpy = 2,2'-bipyridine) in [2]. Efficient photoinduced electron transfer from triethanolamine to 1 and 2 is feasible by excitation at 500Metalloligands L1 and L2 consisting of directional bis(terpyridine)ruthenium(II) units and bipyridine moieties were constructed by amide formation. From these metalloligands two Ru–Pt heterobimetallic complexes 1 and 2 were derived by a building-block method by means of platination with [PtCl2(dmso)2]. Both bimetallic complexes 1 and 2 feature metal-to-ligand charge transfer (MLCT) absorptions, and emission occurs at room temperature in fluid solution from ³MLCT(Ru) states in all cases. Energy transfer from platinum to ruthenium is observed in 2 but not in 1 (light harvesting). The one-electron-reduced species [1] and [2] were prepared by reduction of 1 and 2 with decamethylcobaltocene. EPR spectra and DFT calculations reveal that the spin density is localized at the tpy–CO/Ru (tpy = terpyridine) site in [1], whereas it is centered at bpy–CO/Pt (bpy = 2,2'-bipyridine) in [2]. Efficient photoinduced electron transfer from triethanolamine to 1 and 2 is feasible by excitation at 500 nm [MLCT(Ru)].…
Autor*innen: | J. Dietrich, A. Wünsche von Leupoldt, Markus Grabolle, Ute Resch-GengerORCiD, K. Heinze |
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Dokumenttyp: | Zeitschriftenartikel |
Veröffentlichungsform: | Verlagsliteratur |
Sprache: | Englisch |
Titel des übergeordneten Werkes (Englisch): | European journal of inorganic chemistry |
Jahr der Erstveröffentlichung: | 2013 |
Verlag: | Wiley-VCH Verl. |
Verlagsort: | Weinheim |
Jahrgang/Band: | 2013 |
Ausgabe/Heft: | 17 |
Erste Seite: | 3009 |
Letzte Seite: | 3019 |
Freie Schlagwörter: | Electron transfer; Luminescence; N ligands; Platinum; Ruthenium |
DOI: | 10.1002/ejic.201201531 |
ISSN: | 1434-1948 |
ISSN: | 1099-0682 |
Verfügbarkeit des Dokuments: | Physisches Exemplar in der Bibliothek der BAM vorhanden ("Hardcopy Access") |
Bibliotheksstandort: | Sonderstandort: Publica-Schrank |
Datum der Freischaltung: | 20.02.2016 |
Referierte Publikation: | Ja |
Datum der Eintragung als referierte Publikation: | 23.10.2013 |