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  • 1
    Electronic Resource
    Electronic Resource
    Silicon-modified carbohydrate surfactants VI: Synthesis of carbosilane, silane, polysilane and non-permethylated siloxane derivatives; the wetting behaviour of epoxy-modified precursor liquids on non-polar surfacesIn remembrance of Professor Dr Edwin Hengge (1998)
    New York, NY [u.a.] : Wiley-Blackwell
    Applied Organometallic Chemistry 12 (1998), S. 47-58 
    Details
    ISSN: 0268-2605
    Keywords: surfactants ; carbohydrate ; carbosilane ; silane ; wetting ; surface tension ; Chemistry ; Industrial Chemistry and Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The synthesis of carbohydrate surfactants bearing carbosilane, silane, polysilane and non-permethylated siloxane moieties is described. These surfactants consist of three structural elements: (1) a silicon-containing moiety, (2) a spacer and (3) a carbohydrate unit. Additionally two different types of mixed structures have been synthesized: (a) single-chained carbosilane-siloxane surfactants and (b) double-chained combinations of carbo- silanes, silanes and siloxanes. The wetting behaviour of the key intermediates, the allyl glycidyl derivatives, has been investigated by static surface tension (γlv, σ) and wetting tension (γsv-γsl, α) measurements on a non-polar perfluorinated surface (FEP® plate). The contact angles obtained for these pure liquids are not a linear function of the surface tension but depend on the polarity of the substructures. © 1998 John Wiley & Sons, Ltd.
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
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    Paper (German National Licenses)
  • 2
    Electronic Resource
    Electronic Resource
    Silicon-Modified Carbohydrate Surfactants II: Siloxanyl Moieties Containing Branched Structures (1996)
    New York, NY [u.a.] : Wiley-Blackwell
    Applied Organometallic Chemistry 10 (1996), S. 437-450 
    Details
    ISSN: 0268-2605
    Keywords: siloxanes ; surfactant ; carbohydrate ; amino ; regioselective ; Chemistry ; Industrial Chemistry and Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Branched siloxanyl-modified carbohydrate surfactants have been synthesized by coupling mono-, di- and poly-functional siloxanes to carbohydrate units either via a branched spacer or by attaching a separate modifying element to a straight-chained structure. Hydrophilic as well as extremely hydrophobic elements have been incorporated successfully. Siloxanyl-modified carbohydrates bearing a secondary amino function were alkylated in regioselective reactions by different epoxides ranging from glycidol- to siloxanyl-modified allyl glycidyl ether derivatives. Alternatively, carbohydrate-modified piperazinyl structures yielded cyclic subunits after alkylation. Structures bearing two identical hydrophilic groups are accessible by alkylation of carbohydrate-modified bisamides. The derivatives synthesized were characterized by means of GC, NMR and elemental analysis.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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    Paper (German National Licenses)
  • 3
    Electronic Resource
    Electronic Resource
    Silicon-Modified Carbohydrate Surfactants III: Cationic and Anionic Compounds (1997)
    New York, NY [u.a.] : Wiley-Blackwell
    Applied Organometallic Chemistry 11 (1997), S. 523-538 
    Details
    ISSN: 0268-2605
    Keywords: silicon-modified ; carbohydrate ; surfactant ; Chemistry ; Industrial Chemistry and Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Ionic siloxanyl-modified carbohydrate surfactants have been synthesized by alkylation/esterification of precursors containing tertiary amino functions. Depending on the reaction strategy, the siloxanyl moiety is part of the alkylating agent or the substrate. Polyhydroxylated tertiary amines can be quaternized by siloxanyl-modified chloroacetic acid esters or epoxysiloxanes in the presence of glacial acetic acid. The esterification of tertiary amines bearing carbohydrate and siloxanyl subunits by cyclic acid anhydrides yields, after neutralization, carboxylate salts. The reaction of hydroxyl groups and sulfamic acid leads to sulfates. The new substances were characterized by means of 13C NMR spectroscopy, gas chromatography, elemental analysis and their solubility profile. © 1997 John Wiley & Sons, Ltd.
    Additional Material: 16 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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    Paper (German National Licenses)
  • 4
    Electronic Resource
    Electronic Resource
    Silicon-modified carbohydrate surfactants. IV. The impact of substructures on the wetting behaviour of siloxanyl-modified carbohydrate surfactants on low-energy surfaces (1997)
    New York, NY [u.a.] : Wiley-Blackwell
    Applied Organometallic Chemistry 11 (1997), S. 617-632 
    Details
    ISSN: 0268-2605
    Keywords: siloxanyl-modified ; carbohydrate ; surfactant ; wetting behaviour ; Chemistry ; Industrial Chemistry and Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The siloxanyl-modified carbohydrate surfactants investigated consist of the four structural elements: (1) siloxanyl moiety; (2) spacer; (3) carbohydrate unit; and (4) modifying element. By static surface tension (γsν  -  γsβ α) measurements the contact angles of the aqueous surfactant solutions above the critical micelle formation concentration (cmc) on nonpolar perfluorinated surfaces (FEP® plate) were determined. Although the siloxanyl units were found to have a high capacity to level out the interfacial properties, both surface tension and wetting tension react independently to defined changes in the chemical structure of the surfactant molecules. The results of spreading experiments on polyproylene show good correlation with the dependences found by wetting meaurements. © 1997 John Wiley & Sons, Ltd.
    Additional Material: 17 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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    Paper (German National Licenses)
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