(Perylene)Co(mnt)2(CH2Cl2)0.5: a mixed perylenecobalt complex as molecular and polymeric conductor
Autor: | S Vansmaalen, Manuel Almeida, R.T. Henriques, [No Value] Gama, Gregoire Bonfait, Jl Deboer, Auke Meetsma |
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Přispěvatelé: | Molecular Inorganic Chemistry |
Jazyk: | angličtina |
Rok vydání: | 1992 |
Předmět: |
Phase transition
Stereochemistry (PERYLENE)2 PT(MNT)2 Crystal structure Biochemistry Catalysis Metal chemistry.chemical_compound Colloid and Surface Chemistry Electrical resistivity and conductivity MAGNETIC-PROPERTIES Seebeck coefficient SCATTERING business.industry General Chemistry Magnetic susceptibility FAMILY Crystallography Semiconductor chemistry visual_art visual_art.visual_art_medium COMPLEXES business Perylene ORGANIC CONDUCTORS |
Zdroj: | Journal of the American Chemical Society, 114(6), 1986-1989. AMER CHEMICAL SOC |
ISSN: | 0002-7863 |
DOI: | 10.1021/ja00032a008 |
Popis: | Single crystals of the quasi-one-dimensional conductor (perylene)Co-bis(maleonitriledithiolate)(CH2Cl2)0.5 were prepared by electrocrystallization. The structure at room temperature is incommensurate with modulation wave vector (0.22a*, -0.13b*, -0.36c*). At T = 295 K it crystallizes in space group P1BAR with Z = 2 and lattice parameters a = 6.551 (2) angstrom, b = 11.732 (2) angstrom, c = 16.481 (2) angstrom, alpha = 92.08 (1)-degrees, beta = 95.30 (1)-degrees, gamma = 94.62 (1)-degrees, and V = 1251.1 (5) angstrom 3. The structure consists of almost regular perylene stacks and polymeric chains of dimerized Co-bis(dithiolate) units along the a axis, with the solvent molecules disordered in the free spaces. At room temperature, electrical conductivity (sigma(RT) congruent-to 60 OMEGA-1 cm-1) and absolute thermoelectric power (S(RT) = -8-mu-V K-1) approach metallic behavior at high temperatures. These transport properties and magnetic susceptibility measurements show a metal to insulator transition at 272-277 K and a second semiconductor to semiconductor phase transition at ca. 170-190 K, both with a remarkable hysteresis. |
Databáze: | OpenAIRE |
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