Tuning the morphology of triblock terpoly(2-oxazoline)s containing a 2-phenyl-2-oxazoline block with varying fluorine contentElectronic supplementary information (ESI) available: SEC traces of the terpolymers and corresponding 1H NMR spectra. See DOI: 10.1039/c3sm50159k
The formation of nanostructures in triblock terpolymers consisting of poly[2-ethyl-2-oxazoline- block -2-(1-ethylpentyl)-2-oxazoline- block -2-(Xfluorophenyl)-2-oxazoline] (X = di, tri, tetra and penta) was investigated in water. For this purpose a gradually increasing degree of fluorination was int...
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Main Authors | , , , , , |
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Format | Journal Article |
Language | English |
Published |
05.06.2013
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Online Access | Get full text |
ISSN | 1744-683X 1744-6848 |
DOI | 10.1039/c3sm50159k |
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Summary: | The formation of nanostructures in triblock terpolymers consisting of poly[2-ethyl-2-oxazoline-
block
-2-(1-ethylpentyl)-2-oxazoline-
block
-2-(Xfluorophenyl)-2-oxazoline] (X = di, tri, tetra and penta) was investigated in water. For this purpose a gradually increasing degree of fluorination was introduced in the molecular structures and its influence on the self-assembly was studied. It can be demonstrated that the basic form of aggregation of these systems resembles rod-like micelles, which tend, upon introduction of fluorinated blocks, to aggregate first into 2-dimensional and later into 3-dimensional super-aggregates. In the case of di- and pentafluorinated terpolymers well-defined structures were observed, which represent likely intermediate, stable transient structures formed during an assumed rod-to-vesicle transition. DLS and cryo-TEM were utilized to analyze the structural features of these nanostructures and a model for their further assembly into super-structures was developed.
The assembly of triblock terpolymers consisting of poly[2-ethyl-2-oxazoline-
b
-2-(1-ethylpentyl)-2-oxazoline-
b
-2-(2,6-Xfluorophenyl)-2-oxazoline] (X = di, tri, tetra and penta) was investigated in water. |
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Bibliography: | 1 Electronic supplementary information (ESI) available: SEC traces of the terpolymers and corresponding H NMR spectra. See DOI 10.1039/c3sm50159k |
ISSN: | 1744-683X 1744-6848 |
DOI: | 10.1039/c3sm50159k |