Chemistry:4,4'-Dichlorodiphenyl sulfone
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| Names | |
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| Preferred IUPAC name
1,1′-Sulfonylbis(4-chlorobenzene) | |
Other names
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3D model (JSmol)
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| Properties | |
| C12H8Cl2O2S | |
| Molar mass | 287.15 g·mol−1 |
| Appearance | White solid |
| Melting point | 148 °C (298 °F; 421 K) |
| Boiling point | 397 °C (747 °F; 670 K) |
| Insoluble | |
| Hazards | |
| Safety data sheet | External MSDS |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
 verify (what is   ?)
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4,4′-Dichlorodiphenyl sulfone (DCDPS) is an organic compound with the formula (ClC6H4)2SO2. Classified as a sulfone,[1] this white solid is most commonly used as a precursor to polymers that are rigid and temperature-resistant such as PES or Udel.[2]
Synthesis and reactions
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:
- ClC6H5 + SO3 → (ClC6H4)2SO2 + H2O
It can also be produced by chlorination of diphenylsulfone.[3]
With chloride substituents activated toward substitution, DCDPS is useful in the production of polysulfones:
- n (ClC6H4)2SO2 + n NaO−X−ONa → [(O−X−OC6H4)2SO2]n + 2n NaCl
Further reading
- Graybill, Bruce M. (1967). "Synthesis of aryl sulfones". The Journal of Organic Chemistry 32 (9): 2931–2933. doi:10.1021/jo01284a075.
- Udel Polysulfone Design Guide (Report). Alpharetta, GA: Solvay Advanced Polymers. pp. 7–10.
- Radel PPSU, Veradel PESU and Acudel modified PPSU Design Guide by Solvay
References
- ↑ Sime, J. G; Abrahams, S. C. (1960). "The crystal and molecular structure of 4,4′-dichlorodiphenyl sulphone". Acta Crystallographica 13 (1): 1–9. doi:10.1107/S0365110X60000017. http://journals.iucr.org/q/issues/1960/01/00/a02720/a02720.pdf.
- ↑ Parker, David; Bussink, Jan; Grampel, Hendrik T.; Wheatley, Gary W.; Dorf, Ernst‐Ulrich; Ostlinning, Edgar; Reinking, Klaus; Schubert, Frank et al.. "Ullmann's Encyclopedia of Industrial Chemistry". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a21_449.pub3.
- ↑ Kovacic, Peter; Brace, Neal O. (1954). "Chlorination of Aromatic Compounds with Metal Chlorides". Journal of the American Chemical Society 76 (21): 5491–5494. doi:10.1021/ja01650a069.
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