Electronic and nuclear contributions to the third-order optical susceptibility of the C60-TTF dyads
β Scribed by I. Fuks-Janczarek; B. Sahraoui; I.V. Kityk; J. Berdowski
- Publisher
- Elsevier Science
- Year
- 2004
- Tongue
- English
- Weight
- 263 KB
- Volume
- 236
- Category
- Article
- ISSN
- 0030-4018
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β¦ Synopsis
We have measured the third-order susceptibility v h3i ijkl of a C 60 -TTF compounds in tetrahydrofuran (THF) solutions using the degenerate four wave mixing technique at k ΒΌ 532 nm in the picosecond regime. To know the physical nature of the optical non-linearities, we separate the electronic and nuclear contributions in v h3i . From these measurements we have deduced the values of the second-order hyperpolarisabilities c. For the calculation of the susceptibility values, CS 2 has been used a reference material (having v h3i ΒΌ 1:24 Γ 10 Γ20 m 2 V Γ2 ) in a standard commonly used procedure taking into account the linear absorption of the sample. As the absorption of the studied compounds is very weak at k ΒΌ 532. This paper presents a theoretical analysis of the second-order hyperpolarisabilities c t of fullerenes modified, too. Theoretical calculations of the c were carried out at the restricted Hartree-Fock level (RHF) using AM1 and PM3 semiempirical SCF-MO methods within the HyperChem 7.0 program.
π SIMILAR VOLUMES
The bis-linking of a tetrathiafulvalene (ITF) to C60 is carried out by [4+2] Diels-Alder cycloaddition of C60 to the 2,3-dimethylene-TTF 2, this transient diene being generated by crown-6 mediated dibromine reductive elimination of the 2,3-bis(bromomethyl)'FYF 3. The C60-TTF target cycloadduct la is
The dynamic nonlinear susceptibility Z {3~ (co) was investigated in ct-[bisethylenedithiotetrathiofulvalene ] triiodide, a-[BEDT-TTF] 213, by four-wave mixing with femtosecond time resolution, ct-[ BEDTΒ°TTF] 213 undergoes a metal-insulator phase transition at 135 K. This organic conductor has a larg