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Updated: Sep 22, 2025

Anionic Polymerization of an Amphiphilic Copolymer for Preparation of Block Copolymer Micelles Stabilized by π-π Stacking Interactions
Published on: October 10, 2016
Structural Study of Four-Armed Amphiphilic Star-Block Copolymers: Pristine and End-Linked Tetronic T1307
Kell Mortensen1, Masahiko Annaka2
1Niels Bohr Institute, University of Copenhagen, Copenhagen, Denmark.
Abstract:
We present a comparative structural study of 30 wt % aqueous suspensions of two related systems based on 4-arm PEO-PPO type of macromolecules (Tetronic T1307, BASF) with the PPO block near the star center. One system concerns the pristine 4-arm PEO-PPO star block copolymer T1307. The second system is a 1:1 blend consisting of, respectively, tetra-amine (TAT) and tetra-N-hydroxysuccinimide (TNT) terminated T1307. The two systems show common characteristics which are also known from linear PEO-PPO type of copolymers (Pluronic, BASF): at low temperatures the measured structure is dominated by the characteristics of individual molecules, while at higher temperatures hydrophobic effects of the PPO domains cause self-assembly into spherical or rodlike micelles. These micelles form in both systems ordered mesophases. The pristine T1307 copolymer suspension behaves generally very similarly to linear PEO-PPO type of di- and triblock copolymers: unimers at low temperatures associating into micelles at higher temperatures, forming subsequently cubic and hexagonal phases upon further increase in temperatures. The cubic phase of the 30 wt % Tetronic T1307 has FCC symmetry. The structure of the cross-linked 30 wt % 1:1 TAT-TNT system is basically organized into two-dimensional network sheets. At low temperatures the system is rather disordered but still with a sharp correlation peak which is associated with the distance between neighboring network sheets. Upon raising temperatures, PPO self-assembly causes organization across neighboring sheets, resulting in cylinder-like assemblies perpendicular to the sheets. These cylinders form hexagonal structure.
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