Group 16 elements sulfur compounds

Sulfur [7704-34-9] S, a nonmetallic element, is the second element of Group 16 (VIA) of the Periodic Table, coming below oxygen and above selenium. In massive elemental form, sulfur is often referred to as brimstone. Sulfur is one of the most important taw materials of the chemical industry. It is of prime importance to the fertilizer industry (see Fertilizers) and its consumption is generally regarded as one of the best measures of a nation s industrial development and economic activity (see Sulfur compounds Sulfurremoval and recovery Sulfuric acid and sulfur trioxide). 

Vol 12 PerfluorohaloorganiL Compounds of Main Group Elements Part 2 Compounds of Sulfur (Cuniinuanon) Selenium and Tellurium... 

System No 5 Fluorine Perfluorohaloorganic Compounds of Main Group Elements Supplementary, Vol 1 Compounds with Elements of Mom Groups I to 5 (EKcludtng Nitrogen) and with Sulfur (Partially)... 

The sulfur-rich oxides S 0 and S 02 belong to the group of so-called lower oxides of sulfur named after the low oxidation state of the sulfur atom(s) compared to the best known oxide SO2 in which the sulfur is in the oxidation state +4. Sulfur monoxide SO is also a member of this class but is not subject of this review. The blue-green material of composition S2O3 described in the older literature has long been shown to be a mixture of salts with the cations S4 and Ss and polysulfate anions rather than a sulfur oxide [1,2]. Reliable reviews on the complex chemistry of the lower sulfur oxides have been published before [1, 3-6]. The present review deals with those sulfur oxides which contain at least one sulfur-sulfur bond and not more than two oxygen atoms. These species are important intermediates in a number of redox reactions of elemental sulfur and other sulfur compounds. 

Phenothiazines are well-known as intermediates for pharmaceuticals, and are also active as insecticides and antioxidants. These compounds are usually prepared by the thiation of diphenylamines with elemental sulfur. In this context, the group of Toma has elaborated a synthesis of 3-phthalimidophenothiazine, as shown in Scheme 6.265 [455]. Using a variety of high-boiling solvents under conventional thermal reflux conditions, low isolated yields of the desired product were obtained. The highest conversion and isolated product yield (55%) was achieved by microwave irradiation of a mixture of the starting N-(4-phenylaminophenyl)phthalimide with... 

The oxidative carbonylation of amines to give ureas is at present one of the most attractive ways for synthesizing this very important class of carbonyl compounds via a phosgene-free approach. Ureas find extensive application as agrochemicals, dyes, antioxidants, resin precursors, synthetic intermediates (also for the production of carbamates and isocyanates), and HIV-inhibitors. Many transition metals (incuding Au [244], Co [248,253-255], Cu [242], Mn [249,256-258], Ni [259], Rh [246,247,260-262], Ru [224,260,263] and especially Pd [219,225,226,264-276], and, more recently, W [277-283]) as well as main-group elements (such as sulfur [284-286] and selenium [287— 292]) have been reported to promote the oxidative carbonylation of amines, usually under catalytic conditions. In some cases, carbamates and/or oxamides are formed as byproducts, thus lowering the selectivity of the process. 

Tetracoordinate sulfur compounds containing a lone pair of electrons at sulfur possess a more or less distorted trigonal-bipyramidal structure, in common with the vast majority of other pentacoordinated molecules of the main group elements (189,191,199). A common name, sulfurane, is generally accepted for this type of compound. In principle, sulfuranes are chiral. However, both the number of optically active isomers and their optical stability depend on the nature of substituents bonded to the central sulfur atom, the apicophilicity of the substituents, and the energy required for permutational isomerization processes. In this context it is interesting to note that acyclic sulfuranes with four different ligands should exist in 20 isomeric forms. 

I. Inorganic sulfur compounds containing another (usually more electropositive) element. When the other element is an alkali or alkaline earth, the sulfide is ionic in character. Metal sulfides often have unusual stoichiometries. Examples of sulfides include H2S, Na2S, FeS, and HgS. 2. Organic sulfides are also referred to as thioethers and have the general structure R—S—R. Biochemical examples of sulfides include methionine, cystathionine, and djenkolic acid. If the two R groups are identical, the substance can be referred to as a symmetrical sulfide (biological examples of which are lanthionine and homo-lanthionine). 

The two primary approaches to removal of sulfurous compounds from process gas streams are 1) the direct-oxidation processes and 2) the acid-gas removal systems9,10. in the direct-oxidation processes, hydrogen sulfide is selectively removed from the process gas, and the sulfur is recovered in its elemental form. The acid-gas removal processes, as a group, remove acidic components (H2S, CO2, HCN, etc.) and regenerate these species into a separate side stream. 

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