Other version: http://pubs.acs.org/cgi-bin/sample.cgi/jpcafh/2002/106/i31/pdf/jp0201736.pdf
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Titles listResonant Energy Transfer in the Mixed Crystal Series [Rh(bpy)3][NaAlxCr1-x(ox)3]ClO4 (bpy =...
Titles listResonant Energy Transfer in the Mixed Crystal Series [Rh(bpy)3][NaAlxCr1-x(ox)3]ClO4 (bpy =...
Scientific Article
unige:3682 
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Resonant Energy Transfer in the Mixed Crystal Series [Rh(bpy)3][NaAlxCr1-x(ox)3]ClO4 (bpy = 2,2'-bipyridine, ox = Oxalate, x = 0.05-1) |
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| Authors | ||
| Published in | The journal of physical chemistry. A. 2002, vol. 106, no. 31, p. 7099-7105 | |
| Abstract | Efficient resonant energy transfer occurs within the R1 line of the 4A2 → 2E transition of the [Cr(ox)3]3- chromophore in mixed crystal [Rh(bpy)3][NaAl1-xCrx(ox)3]ClO4 (x = 0.05−0.9, ox = oxalate, bpy = 2,2'-bipyridine). This manifests itself in the form of multiline patterns in resonant fluorescence line narrowing (FLN) experiments at 1.5 K. The conditions for such a resonant process to occur are that the inhomogeneous line width of the R1 line is larger than the zero-field splitting of the ground state, which, in turn, is larger than the homogeneous line width of the transition. The number of lines and their relative intensities depend critically upon the [Cr(ox)3]3- concentration and the excitation wavelength within the inhomogeneous distribution. The basic model for resonant energy transfer as presented by von Arx et al. (Phys. Rev B 1996, 54, 15800) is extended to include the effects of diluting the chromophores in an inert host lattice and of nonresonant R2 excitation. In addition, Monte Carlo simulations serve to explain the temporal evolution of the multiline pattern following pulsed excitation. | |
| Identifiers | DOI: 10.1021/jp0201736 | |
| Full text | ||
| Structures | ||
| Research group | Groupe Hauser | |
| Citation (ISO format) | HAZENKAMP-VON ARX, Marianne Elisabeth et al. Resonant Energy Transfer in the Mixed Crystal Series [Rh(bpy)3][NaAlxCr1-x(ox)3]ClO4 (bpy = 2,2'-bipyridine, ox = Oxalate, x = 0.05-1). In: The journal of physical chemistry. A, 2002, vol. 106, n° 31, p. 7099-7105. doi: 10.1021/jp0201736 https://archive-ouverte.unige.ch/unige:3682 |
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