2009
DOI: 10.1016/j.jcis.2008.12.007
|View full text |Cite
|
Sign up to set email alerts
|

Contribution of 1H NMR to the investigation of the adsorption of cationic Gemini surfactants with oligooxyethylene spacer group onto silica

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
3
1
1

Citation Types

0
5
0

Year Published

2010
2010
2017
2017

Publication Types

Select...
9

Relationship

0
9

Authors

Journals

citations
Cited by 29 publications
(5 citation statements)
references
References 39 publications
0
5
0
Order By: Relevance
“…43 An alternative approach, often providing reliable results, consists of monitoring the variation of the chemical shift of both the surfactant and analyte for solution of increasing relative concentration. [44][45][46][47][48] To make sure that the peak shift is caused by close contact between the solute and the surfactant, the determination of the peak separation between methylene units belonging to the apolar portion of the surfactant is followed. This separation changes with the amount of the solute, clearly excluding other solvation effects and confirming the close contact between the most sensitive methylene unit and the solute.…”
Section: Instrumental Investigations On Micellar Systemsmentioning
confidence: 99%
“…43 An alternative approach, often providing reliable results, consists of monitoring the variation of the chemical shift of both the surfactant and analyte for solution of increasing relative concentration. [44][45][46][47][48] To make sure that the peak shift is caused by close contact between the solute and the surfactant, the determination of the peak separation between methylene units belonging to the apolar portion of the surfactant is followed. This separation changes with the amount of the solute, clearly excluding other solvation effects and confirming the close contact between the most sensitive methylene unit and the solute.…”
Section: Instrumental Investigations On Micellar Systemsmentioning
confidence: 99%
“…[21][22][23][24] The aggregation properties of gemini lipids strongly depend on the nature and length of the spacer between the two head groups. [25][26][27][28][29] The introduction of oxygen into the spacer can affect the orientation in a different fashion; thus, the spacer chain containing oxyethylene functionalities folds in association with water molecules of the interfacial region, this additional hydration reduces the coulumbic repulsions between two cationic heads 30 and might improve the interaction between the GCLs and DNA. Such interfacial polarity has been found to inuence the membrane properties of lipid aggregates as well as many crucial biological events.…”
Section: Introductionmentioning
confidence: 99%
“…Notably, these γ CAC values were significantly lower than those of hydrocarbon-based surfactants (30-40 mN/m) [31] and were similar to those reported for other trisiloxane surfactants (20-25 mN/m) [7,8] and fluorosurfactants (18-28 mN/m) [9], which might be attributed to the two hydrophobic trisiloxane groups of the gemini surfactant molecules better facilitating the self assembly into aggregates and more efficiently decreasing the surface tension than the corresponding monomeric surfactants. Moreover, other physicochemical parameters (Γ CAC , A CAC , △G θ mic , and △G θ ads ) related to surface activity were calculated according to previous studies [32][33][34][35]. The variables Г max and A CAC are also related to m and n, and an increase in the spacer group (CH 2 ) resulted in a slight decrease in Г max and an increase in A CAC .…”
Section: Surface Activities and Aggregation Properties Of Surfactantsmentioning
confidence: 99%