Abstract
Dicyclometalated complexes syn- and anti-[Pt2(L)2(PAnP-H2)](OTf)2(Pt2) are synthesized from reactions of 9,10-bis(diphenylphosphino)anthracene (PAnP) and Pt(L)(OTf)2(L = diphosphines, OTf = CF3SO3). Because of metal perturbation on the electronic structure of the anthracenyl ring, the1B2u-←1Ag transition, which is forbidden in anthracene, is observed in the electronic spectra of Pt2. The complexes display fluorescence arising from the ligand-centered Si excited state. No significant heavy atom effect is observed in the Pt2complexes. To understand the effect of the number of Pt ions on the extent of perturbation, a mononuclear analogue, [Pt(dppe)(PAn-H)] ClO4(PAn = 9-diphenylphosphinoanthracene), is prepared and its spectroscopy studied.
Original language | English |
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Pages (from-to) | 6533-6543 |
Number of pages | 11 |
Journal | Organometallics |
Volume | 26 |
Issue number | 26 |
DOIs | |
Publication status | Published - 17 Dec 2007 |
ASJC Scopus subject areas
- Physical and Theoretical Chemistry
- Organic Chemistry
- Inorganic Chemistry