1966
DOI: 10.1002/macp.1966.020910109
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Reaktionsfähige hochpolymere auf polystyrolbasis als träger von proteinen und enzymen

Abstract: ZUSAMMENFASSUNG:Durch SUMMARY:Reactive, hydrophilic, insoluble polymers which contain nitrofluorobenzenesulfofonyl groups were prepared by FRIEDEL-CRAFTS reaction of 4-fluorobenzenesulfonyl chloride with polystyrene and subsequent sulfonation and nitration.Reactive, hydrophilic, insoluble polymers containing dinitrofluorophenyl groups were prepared by nitration of copolymers obtained from 4-or 3-fluorostyrene, methacrylic acid, and divinylbenzene.The chemical reactivity of these polymers especially their abil… Show more

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Cited by 33 publications
(11 citation statements)
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“…The use of synthetic polymeric carriers bearing halogen atoms can be dated back to the beginning of the 1960s [266,267]. These synthetic polymeric carriers bearing halogen atoms were synthesized from monomers bearing fluoro groups, for example I, II, III, and IV in Scheme 3.58, with co-monomers such as acrylic acid or divinylbenzene.…”
Section: Polymers Bearing Halogen Atomsmentioning
confidence: 99%
See 1 more Smart Citation
“…The use of synthetic polymeric carriers bearing halogen atoms can be dated back to the beginning of the 1960s [266,267]. These synthetic polymeric carriers bearing halogen atoms were synthesized from monomers bearing fluoro groups, for example I, II, III, and IV in Scheme 3.58, with co-monomers such as acrylic acid or divinylbenzene.…”
Section: Polymers Bearing Halogen Atomsmentioning
confidence: 99%
“…Following this work, other synthetic polymers, for example a copolymer of methacrylic acid m-fluoroanilide with methacrylic acid, divinylbenzene or fluorostyrene, have been synthesized since the 1960s [266][267][268][269]. In general, there has been almost no further interest in this type of polymer since the 1970s.…”
Section: Polymers Bearing Halogen Atomsmentioning
confidence: 99%
“…De nombreuses enzymes ont 6th fixees sur divers supports insolubles [l] : polym&res d'acides amin& 123, polymeres synthetiques [3,4] , membranes au collodion [5], derives de la cellulose [6-81, Stphadex [9], verre poreux [lo, 111. L'invertase a deja Btb insolubilisee par fucation sur copolymere nitrl d'acide metacrylique et de m-fluoroanilide d'acide metacrylique [4] ainsi que sur DEAE-cellulose [8] .…”
Section: Introductionunclassified
“…L'invertase a deja Btb insolubilisee par fucation sur copolymere nitrl d'acide metacrylique et de m-fluoroanilide d'acide metacrylique [4] ainsi que sur DEAE-cellulose [8] .…”
Section: Introductionunclassified
“…The following derivatives of synthetic polymers were reacted with proteins: polymeric carboxylic or sulphonic acid chlorides of ion exchange resins, diazotized poly-aminostyrene, poly-isocyanatostyrene, poly-isothiocyanatostyrene (Manecke & Gunzel, 1967), copolymers of N-carboxylic acid anhydrides of L-leucine and p-amino-DL-phenylalanine as diazonium salt (Cebra, Givol, Silman & Katchalski, 1961), diazotized polymers to react copolymers of N-carboxytyrosine anhydride with trypsin , nitrated copolymers of methacrylic acid, methacryl-3fluoroanilide and divinylbenzene, nitrated copolymers of methacrylic acid, 2-, 3-or 4-fluorostyrene and divinylbenzene (Manecke & Forster, 1966), reaction products of polystyrene with 4-fluorobenzenesulphonyl chloride, subsequently sulphonated and nitrated (Manecke & Forster, 1966). Starting from reactive monomers of m-isothiocyanatostyrene (Manecke & Gunzel, 1967) and vinylisothiocyanate (Manecke & Giinzel, unpublished work) are the only examples which were polymerized to yield polymers reactive with proteins (for other references see Manecke, 1962).…”
mentioning
confidence: 99%