New dimeric surfactants from alkyl glucosides

Carbohydrate containing dimeric (or gemini) surfactants were synthesized starting from D-glucose. Three different spacers (glutaryl, succinyl and terephthaloyl) were used to link the sugar moieties through O-2 or O-6. The critical micellar concentration (CMC) for these new compounds was ten-fold sma...

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Publicado: 1999
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Acceso en línea:https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_00404020_v55_n44_p12711_Castro
http://hdl.handle.net/20.500.12110/paper_00404020_v55_n44_p12711_Castro
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id paper:paper_00404020_v55_n44_p12711_Castro
record_format dspace
spelling paper:paper_00404020_v55_n44_p12711_Castro2023-06-08T15:04:13Z New dimeric surfactants from alkyl glucosides Dimers Esters Glycosides Surfactants alkyl aryl ether glucose glucoside surfactant article concentration (parameters) dimerization esterification hydrogenation micelle nuclear magnetic resonance spectroscopy priority journal reaction analysis structure analysis surface tension synthesis Carbohydrate containing dimeric (or gemini) surfactants were synthesized starting from D-glucose. Three different spacers (glutaryl, succinyl and terephthaloyl) were used to link the sugar moieties through O-2 or O-6. The critical micellar concentration (CMC) for these new compounds was ten-fold smaller than that of their monomeric counterpart. 1999 https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_00404020_v55_n44_p12711_Castro http://hdl.handle.net/20.500.12110/paper_00404020_v55_n44_p12711_Castro
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
topic Dimers
Esters
Glycosides
Surfactants
alkyl aryl ether
glucose
glucoside
surfactant
article
concentration (parameters)
dimerization
esterification
hydrogenation
micelle
nuclear magnetic resonance spectroscopy
priority journal
reaction analysis
structure analysis
surface tension
synthesis
spellingShingle Dimers
Esters
Glycosides
Surfactants
alkyl aryl ether
glucose
glucoside
surfactant
article
concentration (parameters)
dimerization
esterification
hydrogenation
micelle
nuclear magnetic resonance spectroscopy
priority journal
reaction analysis
structure analysis
surface tension
synthesis
New dimeric surfactants from alkyl glucosides
topic_facet Dimers
Esters
Glycosides
Surfactants
alkyl aryl ether
glucose
glucoside
surfactant
article
concentration (parameters)
dimerization
esterification
hydrogenation
micelle
nuclear magnetic resonance spectroscopy
priority journal
reaction analysis
structure analysis
surface tension
synthesis
description Carbohydrate containing dimeric (or gemini) surfactants were synthesized starting from D-glucose. Three different spacers (glutaryl, succinyl and terephthaloyl) were used to link the sugar moieties through O-2 or O-6. The critical micellar concentration (CMC) for these new compounds was ten-fold smaller than that of their monomeric counterpart.
title New dimeric surfactants from alkyl glucosides
title_short New dimeric surfactants from alkyl glucosides
title_full New dimeric surfactants from alkyl glucosides
title_fullStr New dimeric surfactants from alkyl glucosides
title_full_unstemmed New dimeric surfactants from alkyl glucosides
title_sort new dimeric surfactants from alkyl glucosides
publishDate 1999
url https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_00404020_v55_n44_p12711_Castro
http://hdl.handle.net/20.500.12110/paper_00404020_v55_n44_p12711_Castro
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