Triplet electron transfer is observed in a covalently linked porphyrin-quinone in ethanol at temperatures between 160 and I30 IC. Both, the primary porphyrin triplet state 'P-Q and the radxal pair (+P-Q-)T created by light-induced charge separation, are observed by time-reaclved EPR. The latter is i
The effect of mutual orientation on the triplet state magnetization of covalently linked hybrid porphyrin dimers
β Scribed by A. Regev; T. Galili; H. Levanon; A. Harriman
- Publisher
- Elsevier Science
- Year
- 1986
- Tongue
- English
- Weight
- 629 KB
- Volume
- 131
- Category
- Article
- ISSN
- 0009-2614
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β¦ Synopsis
We report laser excitation-time-resolved EPR spectroscopy on the transient triplet magnetization of covalently Iinked hybrid porphyrin dimers, Zn(-CHz-JnHz, oriented in a uni-axial liquid crystal at 100 K. Three dimers are investigated: for n = 3, the para-para and ortho-ortho, and for n = 6, the ortho-ortho.
Selective singlet excitation of the dlmer components reveals intramolecular singlet energy transfer rates, k,, = 1.5 X log s-t for both the ortho-ortho compounds, and 4.7 x lOa s-l for the para-para compound.
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The cffcct ofdcutcratlon in slowmg the radtationlesc decay of the triplet state of several porphyrin free bxxs is shown to depend critically on the position of deutcration. Deuteration of the N-II positions is one order of magnttude more effective per bond than dcuterdtlon of the rmg pocitions.
In aqueous solutions a-and y-cyclodextrins (CDs) separate the ground state complexes of the porphyrin (P) and viologen (Vi'+) moieties in the zinc porphyrin-tetraviologen supramolecule and modulate dynamics of the connecting polymethylene chains between P and Vi\*+. Effects of the chain dynamics bei
## AhStNCt The recombination kinetics of protonated and perdeuteriated chain-linked ( ( CH2), linker, n = 3, 6, and 10) triplet ketylphenoxyl radical pairs (RP ) have been examined by using the laser flash technique under an external magnetic field. The high values of magnetic isotope effect (MIE)
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