Kirk-Othmer Encyclopedia of Chemical Technology 2005
DOI: 10.1002/0471238961.sulfkult.a01
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Sulfur‐Containing Polymers

Abstract: This review describes methods of synthesis and some more interesting properties of the various new sulfur‐containing polymers, with particular regard for their potential application possibilities. Also, some new or improved methods of synthesizing already known polymers are discussed. Polysulfides, including poly(monosulfide)s and poly(disulfide)s are the subject of many detailed studies. In the last decade, extensive efforts have been devoted to the synthesis of cyclic oligomers (macrocyclic aromati… Show more

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Cited by 5 publications
(4 citation statements)
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“…The viscous oil was mixed with a small amount of diethylether and purified by flash chromatography onto silica (eluent: diethylether). BPA2 was collected as a yellow viscous oil after evaporation of the solvent (48.2 g, isolated yield 95 %); 1 ) was added to trap residual copper and the mixture was stirred at rt for 4 h. The resin was filtered and stored to be recycled. The solvent was removed under vacuum to yield a yellowish oil M2 (59.6 g, isolated yield 93 %); 1 H NMR (400 MHz, DMSO-d 6 ) δ 4.87 (d, J = 4 Hz, 2H), 4.69 (d, J = 4 Hz, 2H), 3.56 (t, J = 6.6 Hz, 4H), 3.51 (s, 4H), 2.68 (t, J = 6.6 Hz, 4H), 2.54 (m, 4H), 2.14 (m, 4H), 1.60 (s, 6H); 13…”
Section: Chemsuschemmentioning
confidence: 99%
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“…The viscous oil was mixed with a small amount of diethylether and purified by flash chromatography onto silica (eluent: diethylether). BPA2 was collected as a yellow viscous oil after evaporation of the solvent (48.2 g, isolated yield 95 %); 1 ) was added to trap residual copper and the mixture was stirred at rt for 4 h. The resin was filtered and stored to be recycled. The solvent was removed under vacuum to yield a yellowish oil M2 (59.6 g, isolated yield 93 %); 1 H NMR (400 MHz, DMSO-d 6 ) δ 4.87 (d, J = 4 Hz, 2H), 4.69 (d, J = 4 Hz, 2H), 3.56 (t, J = 6.6 Hz, 4H), 3.51 (s, 4H), 2.68 (t, J = 6.6 Hz, 4H), 2.54 (m, 4H), 2.14 (m, 4H), 1.60 (s, 6H); 13…”
Section: Chemsuschemmentioning
confidence: 99%
“…Sulfur-containing polymers have caught interest of researchers and material manufacturers by virtue of their attractive properties, rendering them particularly suitable for a high diversity of applications such as engineering plastics, optics and optoelectronics, adhesives, or electrolytes. [1] Intensive research in this field is evidenced by the large panel of recently developed polymer scaffolds embedding sulfur atoms in their backbone. [2] Poly(monothiocarbonate)s (PMTCs) is an appealing class of these polymers as the sulfur atom integrated in the carbonate unit thoroughly modifies their chemical and physical properties [3,4] compared to their polycarbonate analogues.…”
Section: Introductionmentioning
confidence: 99%
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“…The addition reaction is an elegant, atom-efficient way of producing a variety of sulfides, which are in great demand in material, polymer, and chemical science [ 4 , 5 , 6 , 7 , 8 , 9 ]. Investigation of the procedure for the direct involvement of the components of crude oil in chemical syntheses requires an efficient methodology of component assignment.…”
Section: Introductionmentioning
confidence: 99%