Structure, optical and electro-physical properties of tetramerized anion-radical salt (N-Xy-Qn)(TCNQ).

The (N-Xy-Qn)(TCNQ) anion-radical salt characterized by tetramerized stacks of the TCNQ acceptor molecules has been synthesized and characterized using vibrational spectroscopy and electrical resistivity measurements. The bond lengths analysis based on the crystal structure data, indicates that the TCNQ molecules are non-uniformly charged with -0.83 e localized on the inner B molecules and -0.

Synthesis and study of -substituted methylthio derivatives of cobalt bis(dicarbollide).

The -methylthio derivatives of cobalt bis(dicarbollide) were synthesized by reaction of anhydrous CoCl with -carborane [7-MeS-7,8-CBH] and isolated as a mixture of -[1,1'-(MeS)-3,3'-Co(1,2-CBH)] and -[1,2'-(MeS)-3,3'-Co(1,2-CBH)] isomers. The structures of both isomers were studied using DFT quantum chemical calculations. The most preferable geometry of rotamers and the stabilization energy of -methylthio derivatives of cobalt bis(dicarbolide) were calculated.

Stabilization of Pancake Bonding in (TCNQ) Dimers in the Radical-Anionic Salt (N-CH-2-NH-5Cl-Py)(TCNQ)(CHCN) Solvate and Antiferromagnetism Induction.

We report a new antiferromagnetic radical-anion salt (RAS) formed from 7,7,8,8-tetracyanquinonedimethane (TCNQ) anion and 2-amino-5-chloro-pyridine cation with the composition of (N-CH-2-NH-5Cl-Py)(TCNQ)(CHCN). The crystallographic data indicates the formation of (TCNQ) radical-anion π-dimers in the synthesized RAS. Unrestricted density functional theory calculations show that the formed π-dimers characterize with strong π-stacking "pancake" interactions, resulting in high electronic coupling, enabling efficient charge transfer properties, but π-dimers cannot be stable in the isolated conditions as a result of strong Coulomb repulsions.

Crystal structure of bis-(ethyl-enedi-thio)-tetra-thia-fulvalenium μ2-acetato-bis-[tri-bromido-rhenate(III)] 1,1,2-tri-chloro-ethane hemisolvate.

The asymmetric unit of the title salt, (C10H8S8)[Re2Br6(CH3COO)]·0.5C2H3Cl3, contains one bis-(ethyl-enedi-thio)-tetra-thia-fulvalene (ET) radical cation, one μ2-acetato-bis-[tri-bromido-rhenate(III)] anion and a 1,1,2-tri-chloro-ethane mol-ecule with half-occupancy disordered about a twofold rotation axis. The tetra-thia-fulvalene fragment adopts an almost planar configuration typical of the ET radical cation.

Molecular conductors with a 8-hydroxy cobalt bis(dicarbollide) anion.

Molecular conductors based on the 8-hydroxy cobalt bis(dicarbollide) anion, (TMTTF)[8-HO-3,3'-Co(1,2-C2B9H10)(1',2'-C2B9H11)] (1), (BMDT-TTF)[8-HO-3,3'-Co(1,2-C2B9H10) (1',2'-C2B9H11)] (2), and (BEDT-TTF)[8-HO-3,3'-Co(1,2-C2B9H10)(1',2'-C2B9H11)] (3), were synthesized, and their crystal structures and electrical conductivities were determined. Compounds 2 and 3 are isostructural to the corresponding radical-cation salts of the parent cobalt bis(dicarbollide). All of the radical-cation salts prepared were found to be semiconductors.