Sulfur organosulfur

Sulfur Organosulfur compounds present in the sample react with Raney nickel to produce nickel sulfides. Nickel sulfides... 

Stability Proceed as directed under Stability, Appendix VII. Sulfur Organosulfur compounds present in the sample react with Raney nickel to produce nickel sulfides. Nickel sulfides are treated with a strong acid to produce hydrogen sulfide, which is trapped and titrated with mercuric acetate using a dithizone indicator. 

Organosulfur Halides. When sulfur is directly linked only to an organic radical and to a halogen atom, the radical name is attached to the word sulfur and the name(s) and number of the halide(s) are stated as a separate word. Alternatively, the name can be formed from R—SOH, a sulfenic acid whose radical prefix is sulfenyl-. For example, CH3CH2—S — Br would be named either ethylsulfur monobromide or ethanesulfenyl bromide. When another principal group is present, a composite prefix is formed from the number and substitutive name(s) of the halogen atoms in front of the syllable thio. For example, BrS—COOH is (bromothio)formic acid. 

Organosulfur Adsorbates on Metal and Semiconductor Surfaces. Sulfur compounds (qv) and selenium compounds (qv) have a strong affinity for transition metal surfaces (206—211). The number of reported surface-active organosulfur compounds that form monolayers on gold includes di- -alkyl sulfide (212,213), di- -alkyl disulfides (108), thiophenols (214,215), mercaptopyridines (216), mercaptoanilines (217), thiophenes (217), cysteines (218,219), xanthates (220), thiocarbaminates (220), thiocarbamates (221), thioureas (222), mercaptoimidazoles (223—225), and alkaneselenoles (226) (Fig. 11). However, the most studied, and probably most understood, SAM is that of alkanethiolates on Au(lll) surfaces. 

The chemistry of organic sulfur compounds is very rich and organosulfur compounds are incorporated into many molecules. Thiols, or mercaptans as they were originally called, are essential as feedstocks in the manufacture of many types of mbber (qv) and plastics (qv). They are utilized as intermediates in agricultural chemicals, pharmaceuticals (qv), ia flavors and fragrances, and as animal feed supplements. Many reviews have been undertaken on the chemistry of the thiols, regarding both their preparation and their reactions (1 7). 

J. W. Eitzgerald, "Naturally Occurring Organosulfur Compounds in Soil," inJ. O. Ntiagu, ed.. Sulfur in the Environment, Part II Ecological Impacts, Wiley-lnterscience, New York, 1978, pp. 391—443. 

Multiple reactors achieve 95-96% conversion and recovery, and stringent air pollution legislation has now pushed this to 99%. A similar sequence of reactions is used for sulfur production from crude oil except that the organosulfur compounds must first be removed from the refinery feed and converted to H2S by a hydrogenation process before the sulfur can be recovered. 

Although desulfurization is a process, which has been in use in the oil industry for many years, renewed research has recently been started, aimed at improving the efficiency of the process. Envii onmental pressure and legislation to further reduce Sulfur levels in the various fuels has forced process development to place an increased emphasis on hydrodesulfurization (HDS). For a clear comprehension of the process kinetics involved in HDS, a detailed analyses of all the organosulfur compounds clarifying the desulfurization chemistry is a prerequisite. The reactivities of the Sulfur-containing structures present in middle distillates decrease sharply in the sequence thiols sulfides thiophenes benzothiophenes dibenzothio-phenes (32). However, in addition, within the various families the reactivities of the Substituted species are different. 

Sulfur in crude oils is mainly present in the form of organosulfur compounds. Hydrogen sulfide is the only important inorganic sulfur compound found in crude oil. Its presence, however, is harmful because of its corrosive nature. Organosulfur compounds may generally be classified as acidic and non-acidic. Acidic sulfur compounds are the thiols (mercap-tans). Thiophene, sulfides, and disulfides are examples of non-acidic sulfur compounds found in crude fractions. Extensive research has been carried out to identify some sulfur compounds in a narrow light petroleum fraction.Examples of some sulfur compounds from the two types are ... 

Unexpectedly, neither direct complexation nor the deoxygenated complexes 95 or 96136,137 were observed in the reaction of diphenylthiirene oxide (18a) with iron nonacarbonyl. Instead, the red organosulfur-iron complex 97138 was isolated12, which required the cleavage of three carbon-sulfur bonds in the thiirene oxide system (see equation 33). The mechanism of the formation of 97 from 18a is as yet a matter of speculation. 

For a review of sulfur-Containing neighboring groups, see Block, E. Reactions of Organosulfur Compounds, Academic Press NY, 1978, p. 141. 

The demand for environment-friendly fuels requires the removal of organosulfur compounds present in crade-oil fractions. SO2 or SO3 contribute to the formation of acid rain and have an effect on pollution control devices [9]. Very stringent environmental regulations will limit the sulfur levels in diesel fuels in EU to less than 10 ppm by the end of 2010 [10]. The conventional sulfur-compound... 

FIGURE 2.4 Organosulfur compounds used as sources of sulfur by algae. 

B. M. Trost and L. S. Melvin, Jr., Sulfur Ylides, Academic Press, New York, 1975 E. Block, Reactions of Organosulfur Compounds, Academic Press, New York, 1978. 

Scarso A, Rebek Jr J (2006) Chiral Spaces in Supramolecular Assemblies. 265 1-46 Schaumann E (2007) Sulfur is More Than the Fat Brother of Oxygen. An Overview of Organosulfur Chemistry. 274 1-34... 

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