dc.creatorRicci, Claudia Guadalupe
dc.creatorCabrera, Maria Ines
dc.creatorLuna, Julio Alberto
dc.creatorGrau, Ricardo José Antonio
dc.date.accessioned2017-11-21T11:49:06Z
dc.date.accessioned2018-11-06T16:20:19Z
dc.date.available2017-11-21T11:49:06Z
dc.date.available2018-11-06T16:20:19Z
dc.date.created2017-11-21T11:49:06Z
dc.date.issued2002-12
dc.identifierRicci, Claudia Guadalupe; Cabrera, Maria Ines; Luna, Julio Alberto; Grau, Ricardo José Antonio; A Convenient Synthesis of Quaternary Ammonium Gemini Surfactants from Long-chain alkyldimethylamines and Epichlorohydrin; Georg Thieme Verlag Kg; Synlett; 18; 12-2002; 1811-1814
dc.identifier0936-5214
dc.identifierhttp://hdl.handle.net/11336/28564
dc.identifierCONICET Digital
dc.identifierCONICET
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1907179
dc.description.abstractAqueous micellar systems proved to be an excellent reaction medium for the selective synthesis of bis-quaternary ammonium salts 5a-c from epichlorohydrin 2 and long-chain alkyldimethylamines 1a-c, in the presence of the corresponding amine chlorohydrates 3a-c as functional surfactants. Unlike alcohol or alcohol-water mixtures as reaction medium, mono-quaternary ammonium salts 4a-c were formed, if any, in very small amounts under micellar conditions, allowing a more direct and rapid access to these quaternary ammonium gemini surfactants.
dc.languageeng
dc.publisherGeorg Thieme Verlag Kg
dc.relationinfo:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.1055/s-2002-34876
dc.rightshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/
dc.rightsinfo:eu-repo/semantics/restrictedAccess
dc.subjectGemini
dc.subjectSurfactants
dc.subjectQuaternary Ammonium
dc.subjectEpichlorohydrin
dc.titleA Convenient Synthesis of Quaternary Ammonium Gemini Surfactants from Long-chain alkyldimethylamines and Epichlorohydrin
dc.typeArtículos de revistas
dc.typeArtículos de revistas
dc.typeArtículos de revistas


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