Abstract
Two new ruthenium complexes, [Ru(L1OMe) 2(NCS)2] and [Ru(L2OMe) 2(NCS)2] (where L1OMe = 2,2′-bipyridine-4,4′-di(methyl ethanoate) and L2 OMe = 2,2′-bipyridine-4,4′-di(methyl propionate)), have been synthesized and characterized using spectroscopic and electrochemical techniques. The [Ru(L2OMe)2(NCS)2] complex has also been characterized by X-ray diffraction studies and reveals a distorted octahedral coordination geometry about the ruthenium center. Cyclic voltammetry studies of both complexes exhibit quasi-reversible Ru(ii/iii) couples and a number of ligand reduction events. The complex with one methylene spacer between the bipyridyl ligand and the methyl ester functional group, [Ru(L1OMe)2(NCS)2], was particularly unstable under reducing conditions. The properties of these complexes are compared with the ethyl ester analogue of the N3 photosensitizer [Ru(L 0OEt)2(NCS)2].
| Original language | English (US) |
|---|---|
| Pages (from-to) | 7396-7401 |
| Number of pages | 6 |
| Journal | Dalton Transactions |
| Issue number | 36 |
| DOIs | |
| State | Published - 2009 |
All Science Journal Classification (ASJC) codes
- Inorganic Chemistry
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