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  2. Diphenyl sulfide - Wikipedia

    en.wikipedia.org/wiki/Diphenyl_sulfide

    Diphenyl sulfide and its analogues can also be produced by coupling reactions using metal catalysts. [5] It can also be prepared by reduction of diphenyl sulfone. [6] Diphenyl sulfide is a product of the photodegradation of the fungicide edifenphos. [7] Diphenyl sulfide is a precursor to triaryl sulfonium salts, which are used as photoinitiators.

  3. Diphenyl disulfide - Wikipedia

    en.wikipedia.org/wiki/Diphenyl_disulfide

    Hydrogen peroxide can also be used as the oxidant. [2] Ph 2 S 2 is rarely prepared in the laboratory because it is inexpensive, and the precursor has a disagreeable odour. Like most organic disulfides, the C–S–S–C core of Ph 2 S 2 is non-planar with a dihedral angle approaching 85°. [3] Ball-and-stick model of diphenyl disulfide.

  4. Diphenyl sulfone - Wikipedia

    en.wikipedia.org/wiki/Diphenyl_sulfone

    Diphenyl sulfone is an organosulfur compound with the formula (C 6 H 5) 2 SO 2.It is a white solid that is soluble in organic solvents.It is used as a high temperature solvent. Such high temperature solvents are useful for processing highly rigid polymers, e.g., PEEK, which only dissolve in very hot solve

  5. Category:Organosulfur compounds - Wikipedia

    en.wikipedia.org/wiki/Category:Organosulfur...

    Main page; Contents; Current events; Random article; About Wikipedia; Contact us; Pages for logged out editors learn more

  6. 4,6-Dimethyldibenzothiophene - Wikipedia

    en.wikipedia.org/wiki/4,6-Dimethyldibenzothiophene

    4,6-Dimethyldibenzothiophene is an organosulfur compound with the formula (C 6 H 3 CH 3) 2 S.It is one of several dimethyl derivatives of benzothiophene.The compound is of particular interest as an organosulfur contaminant in petroleum that is recalcitrant.

  7. 4,4'-Dichlorodiphenyl sulfone - Wikipedia

    en.wikipedia.org/wiki/4,4'-Dichlorodiphenyl_sulfone

    DCDPS is synthesized via sulfonation of chlorobenzene with sulfuric acid, often in the presence of various additives to optimize the formation of the 4,4′-isomer: . ClC 6 H 5 + SO 3 → (ClC 6 H 4) 2 SO 2 + H 2 O

  8. Dibenzothiophene - Wikipedia

    en.wikipedia.org/wiki/Dibenzothiophene

    Dibenzothiophene (DBT, diphenylene sulfide) is the organosulfur compound consisting of two benzene rings fused to a central thiophene ring. It has the chemical formula C 12 H 8 S. It is a colourless solid that is chemically somewhat similar to anthracene .

  9. Bisphenol - Wikipedia

    en.wikipedia.org/wiki/Bisphenol

    Exceptions include bisphenol S, P, and M. "Bisphenol" is a common name; the letter following denotes the variant, which depends on the additional substituents. Bisphenol A is the most popular representative of the group, with millions of metric tons produced globally in the past decade, often simply called "bisphenol". [3] [4] [5]