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CO2-Reactive Ionic Liquid Surfactants for the Control of Colloidal Morphology
Author(s) -
Paul Brown,
Vishnu Sresht,
Hüseyin Burak Eral,
Andrew M. Fiore,
César de la FuenteNúñez,
Marcus O’Mahony,
Gabriel Mendes,
William T. Heller,
Patrick S. Doyle,
Daniel Blankschtein,
T. Alan Hatton
Publication year - 2017
Publication title -
langmuir
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.042
H-Index - 333
eISSN - 1520-5827
pISSN - 0743-7463
DOI - 10.1021/acs.langmuir.7b00679
Subject(s) - counterion , pulmonary surfactant , bromide , chemistry , micelle , chemical engineering , small angle neutron scattering , microemulsion , neutron scattering , chemical physics , colloid , dynamic light scattering , organic chemistry , nanoparticle , scattering , ion , aqueous solution , optics , engineering , biochemistry , physics
This article reports on a new class of stimuli-responsive surfactant generated from commercially available amphiphiles such as dodecyltrimethylammmonium bromide (DTAB) by substitution of the halide counterion with counterions such as 2-cyanopyrrolide, 1,2,3-triazolide, and L-proline that complex reversibly with CO 2 . Through a combination of small-angle neutron scattering (SANS), electrical conductivity measurements, thermal gravimetric analysis, and molecular dynamics simulations, we show how small changes in charge reorganization and counterion shape and size induced by complexation with CO 2 allow for fine-tunability of surfactant properties. We then use these findings to demonstrate a range of potential practical uses, from manipulating microemulsion droplet morphology to controlling micellar and vesicular aggregation. In particular, we focus on the binding of these surfactants to DNA and the reversible compaction of surfactant-DNA complexes upon alternate bubbling of the solution with CO 2 and N 2 .

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