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Tetrasulphur tetranitride

Reaction of tetrasulphur tetranitride antimony pentachloride complex (S4N4.SbCl5) with a series of primary (3-enaminones and P-enamino esters 79 in toluene at 100 °C gave reasonable yields of 3,4-disubstituted 1,2,5-thiadiazoles 80. The formation of 80 was explained by the same mechanism as that proposed for the formation of 1,2,5-thiadiazoles from 3,5-disubstituted isoxazoles with S4N4.SbCl5 complex <00H159>. [Pg.200]

Tetrasulphur tetranitride, N4S4, is produced when dry NHg is passed into a solution of SgClg in dry ether, separating as orange crystals, m.p. 178°. [Pg.338]

When tetrasulphur tetranitride (p. 338) at low pressure is heated to 300 the ring is broken and a polymer, (SN) , is produced as fibrous crystals with a metallic lustre. The material, which is a semi-conductor, probably has the structure ... [Pg.564]

Since decomposition of tetrasulphur tetranitride with alkali gives ammonia, and reduction with stannous chloride followed by decomposition with alkali also gives ammonia, there canbe no NN links in molecule. [Pg.149]

When a 2-halophenoI is heated with (the explosive) tetrasulphur tetranitride, both substituents are usually displaced and a thiadiazole ring is formed, but exceptions to this rule are observed, for example, 4-t-butyl-2-chlorophenol gives 6 t-butyl-4-chloro-2,I,3-benzothiadiazole as the major product (56% yield) and... [Pg.570]

Phenols which are unsubstituted at C-2 and/or C-6 are cyclized by heating with the explosive tetrasulphur tetranitride. 2-Naphthol also gives a high yield of the... [Pg.637]

Nitroxides, Hydroxylamines, and Nitroso- and Nitro-compounds. The chemistry of the magic radical , bistrifluoromethyl nitroxide, and related compounds particularly (CF3)jN OH and [(CFj),N O],Hg has been dealt with at some length in the review literature full details of the work on reactions between (i) the nitroxide and tetrasulphur tetranitride -> N4S4[O N(CF8)2]4, also obtainable from (CFj),N-0- + N4S4H4 or N3S3CI3 and [(CF3)jN-0]jHg + N3S3CI3, (ii) the mercurial [(CF3)3N-0]3Hg and thiazyl fluoride - ... [Pg.223]

Decahydroazecines (454) and (455) are described, and the reaction of tetrasulphur tetranitride with norbomene has been shown to yield the exo-cis structure (456), elucidated by i.r., n.m.r., and u.v. studies. Compounds (457) and (458) are other ten-membered ring heterocyclic structures described this year. ... [Pg.342]

Studies which have involved Lewis acid-base adducts of organoboranes include the following the adducts of phenyl boron dichloride with tetrasulphur tetranitride, dibromomethylborane and bromodimethylborane with pyridine, 4-methylpyridine, trimethylamine and trimethylphosphine, monoalkylboranes with A AWW -tetramethylethylenediamine, diethylboron esters of alkane-nitronic acids with pyridine, and triarylboranes with guanidine,urea, methylurea, and thiourea. ... [Pg.40]

Further additions to norbornenes are extensively reported. Tetrasulphur tetranitride adds to norbornene and to norbornadiene and structure (116) is proposed for the adduct of norbornene. However, structure (117) or even... [Pg.340]

Liquid ammonia solutions. Sulphur and tetrasulphur tetranitride (S4N4) 245... [Pg.763]

Ditosylsulphurdi-imine acts as an oxidizing agent, converting hydro-quinone into quinone, thiophenol into diphenyl disulphide, hydrazobenzene into azobenzene, and 1,4-dihydronaphthalene into naphthaiene." The same di-imine reacted with dimethylaminotrimethylstannane such that the latter reagent added separately across each S=N bond. The same reagent reacted with tetrasulphur tetranitride to form the di-imine (131), which reacted with... [Pg.371]


See other pages where Tetrasulphur tetranitride is mentioned: [Pg.445]    [Pg.90]    [Pg.14]    [Pg.425]    [Pg.148]    [Pg.156]    [Pg.752]    [Pg.131]    [Pg.445]    [Pg.90]    [Pg.14]    [Pg.425]    [Pg.148]    [Pg.156]    [Pg.752]    [Pg.131]   


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