A phosphorescence line-narrowing technique involving direct quartet ground state to doublet excited state pumping, is used to resolve completely optical-Zeeman components at field strengths compatible with Q-band EPR spectroscopy. By incorporating this technique, ODMR of the lowest doublet excited s
Optically detected magnetic resonance spectroscopy of rhodium (III) mixed-chelate complexes
✍ Scribed by C.P.M. Giesbergen; C. Terletski; G. Frei; H.U. Güdel; M. Glasbeek
- Publisher
- Elsevier Science
- Year
- 1993
- Tongue
- English
- Weight
- 538 KB
- Volume
- 213
- Category
- Article
- ISSN
- 0009-2614
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✦ Synopsis
An optically detected magnetic resonance study of the lowest excited state of [Rh(thpy) (phpy) (bpy)] +, doped into a single crystal of [Rh(phpy)a(bpy)]PFs, is reported. Here, thpy-=2,2'-thienylpyridine, phpy-=Zphenylpyridine and bpy=2,2'-bipyridine. In emission, the dopant molecule gives rise to two zero-phonon lines, at 519.9 and 517.9 nm, respectively. The two zerophonon lines are characteristic of the two structurally inequivalent forms of the dopant complex in the crystal lattice. From zeroand low-field ODMR data it is concluded that the lowest excited state in each ofthe two complex conformations is a phosphorescent triplet state. The fine structure splittings and the orientation of the fine structure tensor main axes of the triplet states of the two complex conformations are found to be different. It is argued that for both conformations the lowest excited state is a they-localized %t* state.
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