Optical properties of the ion-radical salts of tetracyanquinodimethane in the solid state
β Scribed by R. M. Vlasova; A. I. Gutman; L. D. Rozenshtein; N. F. Kartenko
- Publisher
- John Wiley and Sons
- Year
- 1971
- Tongue
- English
- Weight
- 499 KB
- Volume
- 47
- Category
- Article
- ISSN
- 0370-1972
No coin nor oath required. For personal study only.
β¦ Synopsis
Abstract
Absorption spectra of TCNQ salts with different donors β metals, organic conjugated compounds, dyes in solid stateβare investigated. The study was carried out on thin films obtained by grinding of salt on quartz substrate. For the Cs(TCNQ) salt reflection and absorption spectra were investigated on single crystals. Salt spectra in the solid state differ greatly from the isolated anionβradical spectrum. For simple salts there is a close resemblance between thin film spectra and the spectrum of the () dimer, which proves that in the solid state pair interaction of ionβradicals predominates. Complex salt spectra are characterized by strongly smeared absorption bands, especially in the Qn^+^ (TCNQ) salt. The correlation between absorption spectra and electrical and magnetic properties of the salts is noted. For Cs(TCNQ) single crystals a stronganisotropy of reflection and absorption is found. Both intensity and character of the absorption spectra depend on the polarization direction. The obtained data are correlated with the strong intermolecular interaction along TCNQ molecule stacking directions and the translational symmetry of the crystal. Absorption spectrum changes during destruction of the crystalline structure are found. The absorption spectra of TCNQ derivatives of dyes in solution are the result of superposition of ionβradical bands and the initial dye band. The character of the solid film spectrum is connected with the influence of the steric factor on the intermolecular interaction.
π SIMILAR VOLUMES
The magnetic and optical properties of the two phases of the potassium salt of chloranil are described and discussed in the fratncwork of the hypothesis of alternation of the linear stack oE moIecules.
Absorption spectra of small K-TCNQ particles are interpreted in terms of the Hubbard model for a lincar cluster of four molecules with four electrons. The shift of the electronic excitation band to higher frequency veraus decrease of particle size is attributed to the growth of the on-site Coulomb r
t\_he crys\_tal chemistry of various acridizinium salts (with Br , Cl , I , ClO. , BF. , picrate and oxalate as the counter anions) have been prepar;d and\* the X-ray structures have been determined. Despite the large movement of the acridizinium ions in the [4+41 photodimerization, the majority of
Eu-doped BaY 2 F 8 single crystals have been grown with two different Eu ion concentrations: 0.5%, 1% Eu doping levels. It was found that part of the Eu 3ΓΎ ions added in the melt were reduced during the growth process and the ratio between the Eu 2ΓΎ and Eu 3ΓΎ content in the crystal depends on the du