Sulfur selenium halides

In spite of the hazardous nature of Sc4N4, this binary selenium nitride has been used for the synthesis of other Se-N compounds, all of which have sulfur analogues (Scheme 5.2). " However, safer alternatives to the use of Sc4N4, e.g., selenium-nitrogen halides and silicon-nitrogen-selenium reagents, are available for the development of Se-N chemistry. ... 

Nitrogen and sodium do not react at any temperature under ordinary circumstances, but are reported to form the nitride or azide under the influence of an electric discharge (14,35). Sodium siHcide, NaSi, has been synthesized from the elements (36,37). When heated together, sodium and phosphoms form sodium phosphide, but in the presence of air with ignition sodium phosphate is formed. Sulfur, selenium, and tellurium form the sulfide, selenide, and teUuride, respectively. In vapor phase, sodium forms haHdes with all halogens (14). At room temperature, chlorine and bromine react rapidly with thin films of sodium (38), whereas fluorine and sodium ignite. Molten sodium ignites in chlorine and bums to sodium chloride (see Sodium COMPOUNDS, SODIUM HALIDES). 

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. 

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