A series of fluorinated gemini pyridinium amphiphiles have been prepared, purified and fully characterized. The synthesis was performed using alkyl trifluoromethanesulfonates as the quaternizing agents, provided very good yields and overcame problems arising with other less powerful alkylating agents. The use of different characterization techniques, such as conductivity and surface tension measurements, shed light on the aggregation process. The title products showed interesting, unusual properties, which could be interpreted in view of a peculiar aggregating behaviour. This family of compounds is very interesting for their possible transfection activity and application in gene therapy.

Synthesis and Characterization of Highly Fluorinated Gemini Pyridinium Surfactants

QUAGLIOTTO, Pierluigi;BAROLO, CLAUDIA;BARBERO, Nadia;BARNI, Ermanno;VISCARDI, Guido
2009-01-01

Abstract

A series of fluorinated gemini pyridinium amphiphiles have been prepared, purified and fully characterized. The synthesis was performed using alkyl trifluoromethanesulfonates as the quaternizing agents, provided very good yields and overcame problems arising with other less powerful alkylating agents. The use of different characterization techniques, such as conductivity and surface tension measurements, shed light on the aggregation process. The title products showed interesting, unusual properties, which could be interpreted in view of a peculiar aggregating behaviour. This family of compounds is very interesting for their possible transfection activity and application in gene therapy.
2009
-
3167
3177
http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1099-0690
Surfactants; Cationic Surfactants; Fluorinated Surfactants; Amphiphiles; Gemini Pyridinium Amphiphiles; Structure-Activity Relationships; Aqueous Micellar-Solutions; Partial Molar Enthalpies; Alkanediyl-Alpha; Omega-Bis(Dimethylalkylammonium Bromide) Surfactants; Air-Water-Interface; Thermodynamic Properties; Aggregation Properties; Gene Delivery; In-Vivo; Biocompatibility Evaluation
Quagliotto P; Barolo C; Barbero N; Barni E ; Compari C; Fisicaro E; Viscardi G
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2318/73689
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