2012
DOI: 10.1021/ol300555a
|View full text |Cite
|
Sign up to set email alerts
|

Amphiphiles Based on d-Glucose: Efficient Low Molecular Weight Gelators

Abstract: A series of novel amphiphiles were synthesized based entirely on renewable resources. Besides their efficacy as supramolecular gelators in a wide variety of organic solvents and also water, their surface properties as surfactants and emulsifiers have been determined. A methodical study revealed that the length of the hydrocarbon chains has a dramatic and decisive influence on the thermal stabilities of the obtained hydrogels.

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
3
1
1

Citation Types

0
39
0

Year Published

2014
2014
2019
2019

Publication Types

Select...
7
2

Relationship

2
7

Authors

Journals

citations
Cited by 32 publications
(39 citation statements)
references
References 60 publications
0
39
0
Order By: Relevance
“…Multiple, directional hydroxyl groups in the sugar part make it easier for sugar surfactants to form hydrogen‐bonding networks . The advantage of hydrogen‐bond formation is that sugar surfactants can form gels in various solvents, including water, organic solvents, and RTILs …”
Section: Introductionmentioning
confidence: 99%
“…Multiple, directional hydroxyl groups in the sugar part make it easier for sugar surfactants to form hydrogen‐bonding networks . The advantage of hydrogen‐bond formation is that sugar surfactants can form gels in various solvents, including water, organic solvents, and RTILs …”
Section: Introductionmentioning
confidence: 99%
“…At present, carbohydrate-based supramolecular hydrogels have begun to emerge as valuable scaffolds for multivalent carbohydrate recognition, [73][74][75] showing tight and specific binding to host cells. As one of the most important functional biomolecules, carbohydrates often play an extremely important role in a wide range of basic biological phenomena through carbohydrate-mediated multivalent interactions.…”
Section: Bioactive Propertiesmentioning
confidence: 99%
“…1A) according to a published procedure. 36,37 Briey, we prepared 6-O-acylated fatty acid ester of D-glucose by reacting it with O-O 0 -dilauroyltartaric acid anhydride. In a Teon lm tightened, septum-capped test tube 100 mg of 1 and 330 mL DI water were placed and then heated in an oven to 125 C for 2.5 h. Upon completion of the carbonization, the reaction mixture was cooled to room temperature yielding a brown precipitate indicating the formation of carbon dots and puried for further work.…”
Section: C-dot-hydrogel Synthesismentioning
confidence: 99%