Interplay of electrostatic and hydrophobic effects with binding of cationic gemini surfactants and a conjugated polyanion: Experimental and molecular modeling studies

• Type: Article in International Scientific Journal
• Date: 2007

Authors

Hugh D Burrows (Author) Other; Maria J Tapia (Author) Other; Claudia L Silva (Author) Other; Alberto A C C Pais (Author) Other; Sofia M Fonseca (Author) Other; Joao Pina (Author) Other; Seixas S de Melo (Author) Other; Yujie J Wang (Author) FCUP; Eduardo F Marques (Author) FCUP; Matti Knaapila (Author) Other; Andrew P Monkman (Author) Other; Vasil M Garamus (Author) Other; Swapna Pradhan (Author) Other; Ullrich Scherf (Author) Other

Journal

Title: Journal of Physical Chemistry B

Vol. 111

Pages: 4401-4410

ISSN: 1520-6106

Publisher: American Chemical Society

Indexing

ISI Web of Knowledge - 64 Citations

Scopus - 69 Citations

Scientific classification

FOS: Natural sciences > Chemical sciences

Other information

Authenticus ID: P-004-A53

DOI: 10.1021/jp070100s

Abstract (EN): Understanding factors responsible for the fluorescence behavior of conjugated polyelectrolytes and modulation of their behavior are important for their application as functional materials. The interaction between the anionic poly{1,4-phenylene-[9,9-bis(4-phenoxy-butylsulfonate)]fluorene-2,7-diyl}copolymer (PBS-PFP) and cationic gemini surfactants alpha,omega-(CmH2m+1N+(CH3)(2))(2)(CH2)(s)(Br-)(2) (m-s-m; m = 12, s = 2, 3, 5, 6, 10, and 12) has been studied experimentally in aqueous solution. These surfactants are chosen to see whether molecular recognition and self-assembly occurs between the oppositely charged conjugated polyelectrolyte and gemini surfactant when the spacer length on the surfactant is similar to the intercharge separation on the polymer. Without surfactants, PBS-PFP exists as aggregates. These are broken up upon addition of gemini surfactants. However, as anticipated, the behavior strongly depends upon spacer length (s). Fluorescence measurements show three surfactant concentration regimes: At low concentrations (< 2 x 10(-6) M) quenching occurs and is most marked with the small spacer 12-2-12; at intermediate concentrations (similar to 2 x 10(-6)-10(-3) M), fluorescence intensity is constant, with a 12-carbon spacer 12-12-12 showing the strongest fluorescence; above the critical micelle concentration (CMC; similar to 10(-3) M) increases in emission intensity are seen in all cases and are largest with the intermediate spacers 12-5-12 and 12-6-12, where the spacer length most closely matches the distance between monomer units on the polymer. With longer spacer length surfactants, surface tension measurements for concentrations below the CMC reveal the presence of polymer-surfactant aggregates at the air-water interface, possibly reflecting increased hydrophobicity. Above the CMC, small-angle neutron scattering experiments for the 12-6-12 system show the presence of spherical aggregates, both for the pure surfactant and for polyelectrolyte/gemini mixtures. Molecular dynamics simulations help rationalize these observations and show that there is a very fine balance between electrostatic and hydrophobic interactions. With the shortest spacer 12-2-12, Coulombic interactions are dominant, while for the longest spacer 12-12-12 the driving force involves hydrophobic interactions. Qualitatively, with the intermediate 12-5-12 and 12-6-12 systems, the optimum balance is observed between Coulombic and hydrophobic interactions, explaining their strong fluorescence enhancement.

Language: English

Type (Professor's evaluation): Scientific