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Chalcogenide halide compounds synthesis

Chemical shifts, in NMR, 4 234-245 Chemical transport reactions, and synthesis of chalcogenide halide compounds, 23 330-332. 364, 368-369... [Pg.45]

Very little is known about chalcogenide halides of Group IVB elements. Although the existence of sulfide chlorides (45, 274, 329, 365) and of a selenide chloride (329) of titanium was claimed in early publications, their true composition, and even their existence, remains doubtful. They have usually been obtained by the reaction of titanium chlorides with sulfur and selenium, respectively, or with hydrogen sulfide. The synthesis of a pure compound, TiSClj, was published in 1959 (113). It is an intermediate of the reaction of TiCU with HjS. [Pg.364]

Thus far, only metal-oxide nanotubes have been synthesized by this process. Whereas crystalline nanotubes were obtained from 2D (layered) oxides, various 3D oxide compounds resulted in semicrystalline or amorphous nanotubes, only. In principle, this kind of process could be extended to the synthesis of nanotubes from chalcogenide and halide compounds in the future. [Pg.285]

X-ray crystallography, 40 20-21 synthetic models, 40 23-48 xanthane oxidase, 40 21-23 chalcogenide halides, 23 370-377, 413 Chevrel phases, 23 376-377 metal-metal bonding, 23 330, 373 structural data, 23 373-376 as superconductors, 23 376 synthesis, 23 371-372 chloride, 46 4-24, 35-44 heterocations of, 9 290, 291 cluster compounds, 44 45-46 octahedral, 44 47-49, 53-63 electronic structure, 44 55-63 molecular structure, 44 53-54 synthesis, 44 47-49 rhomboidal, 44 75-82 solid-state clusters and, 44 66-72, 74-75, 80-82, 85-87 tetrahedral, 44 72-75 triangular, 44 82-87 cofactor, 40 2, 4-12 anaerobic isolation, 40 5 molybdopterin and, 40 4-8 reduced form, 40 12 synthesis, 40 8-12 xanthine oxidase, 45 60-63 complexes... [Pg.188]

Low-temperature solvents are not readily available for many refractory compounds and semiconductors of interest. Molten salt electrolysis is utilized in many instances, as for the synthesis and deposition of elemental materials such as Al, Si, and also a wide variety of binary and ternary compounds such as borides, carbides, silicides, phosphides, arsenides, and sulfides, and the semiconductors SiC, GaAs, and GaP and InP [16], A few available reports regarding the metal chalcogenides examined in this chapter will be addressed in the respective sections. Let us note here that halide fluxes provide a good reaction medium for the crystal growth of refractory compounds. A wide spectrum of alkali and alkaline earth halides provides... [Pg.83]

Substitution reactions involving silylated chalcogen reagents represent a powerful approach in metal-group-XVI cluster synthesis.Compounds such as E(TMS)2 and RE-TMS react readily with metal salts to form metal chalcogenide or chalcogenolate bonds (Equations (13)-(15)). The driving force for the reaction is the thermodynamically favorable formation of an X—Si bond and elimination of X-TMS (where X = halide, OAc, etc.). [Pg.61]


See other pages where Chalcogenide halide compounds synthesis is mentioned: [Pg.332]    [Pg.350]    [Pg.401]    [Pg.12]    [Pg.48]    [Pg.61]    [Pg.332]    [Pg.350]    [Pg.401]    [Pg.50]    [Pg.94]    [Pg.239]    [Pg.435]    [Pg.531]    [Pg.219]    [Pg.51]    [Pg.24]    [Pg.178]    [Pg.235]    [Pg.17]    [Pg.133]    [Pg.118]    [Pg.264]    [Pg.19]   


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Chalcogenide

Chalcogenide halide compounds

Chalcogenide halides

Chalcogenide halides synthesis

Chalcogenides

Chalcogenides synthesis

Compounds chalcogenides

Halides compounds

Halides synthesis

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