Publications by authors named "Lakhemici Kaboub"

In the title compound, CHN ·2Cl·2HO, the two pyridine side arms are not coplanar, with the terminal pyridine rings subtending a dihedral angle of 26.45 (6)°. In the crystal, hydrogen bonds, inter-molecular C-H⋯Cl contacts and a weak C-H⋯O inter-action connect the mol-ecule with neighbouring chloride counter-anions and lattice water mol-ecules.

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A new bis-TTF donor (TTF is tetrathiafulvalene) containing a pyridine diester spacer, namely bis{2-[(6,7-tetramethylene-3-methylsulfanyltetrathiafulvalen-2-yl)sulfanyl]ethyl} pyridine-2,6-dicarboxylate-tetracyanoquinodimethane-dichloromethane (2/1/2), 2C(33)H(33)NO(4)S(12) x C(12)H(4)N(4) x 2 CH(2)Cl(2), has been synthesized and its electron-donating ability determined by cyclic voltammetry. The electrical conductivity and crystal structure of this donor-acceptor (DA) complex with TCNQ (tetracyanoquinodimethane) as the acceptor are presented. The TCNQ moiety lies across a crystallographic inversion centre.

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The title compound, C(30)H(28)N(2)S(16), is a precursor to hybrid magnetic materials. The complete molecule is generated by a crystallographic inversion centre. In the crystal structure, the TTF core is not planar and adopts a chair conformation; the two C(3)S(2) rings are folded around the S⋯S hinges, the dihedral angles being 17.

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We report the synthesis and properties of eight new tetrathiafulvalene (TTF) derivatives containing two different functionalities, prepared with the aim of obtaining stable organic materials. The four acetoxyphenyl- and four hydroxyphenyl TTFs were synthesized via Wittig-type condensations. The electrochemical properties of these redox-active molecules were studied by cyclic voltammetry.

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Metallic thin films of the single-component, neutral, molecular solid Ni(tmdt)2 have been prepared by electrocrystallization on passivated silicon substrates. Metallicity is achieved down to 6 K despite the polycrystalline morphology.

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