Details

Autor(en) / Beteiligte

• Altintas, Ozcan
• Schulze-Suenninghausen, David
• Luy, Burkhard
• Barner-Kowollik, Christopher

Titel

Facile Preparation of Supramolecular H‑Shaped (Ter)polymers via Multiple Hydrogen Bonding

Ist Teil von

• ACS macro letters, 2013-03, Vol.2 (3), p.211-216

Ort / Verlag

United States: American Chemical Society

Erscheinungsjahr

2013

Link zum Volltext

Quelle

Alma/SFX Local Collection

Beschreibungen/Notizen

• A well-defined Hamilton wedge (HW) midchain functionalized block copolymer, i.e., polyethylene glycol-b-polystyrene (PEG-HW-PS, M n,GPC = 5600 Da, PDI = 1.03), was successfully synthesized via a combination of atom transfer radical polymerization (ATRP) and copper-catalyzed azide alkyne cycloaddition (CuAAC). An α,ω-cyanuric acid (CA) difunctional linear homopolymer poly(n-butylacrylate) (CA-PnBA-CA, M n,GPC = 8100 Da, PDI = 1.09) was concomitantly prepared via reversible addition–fragmentation chain transfer (RAFT) polymerization. Supramolecular H-shaped macromolecules werefor the first timeprepared through supramolecular self-assembly between HW and CA recognition motifs to generate (PS-b-PEG)·PnBA·(PS-b-PEG) and (PS-b-PS)·PnBA·(PS-b-PS) in CH2Cl2 or dichloromethane-d 2 at ambient temperature. The self-assembly process (at a total concentration of the two species of close to 4.5 mM) was evidenced by proton nuclear magnetic resonance (1H NMR) spectroscopy, diffusion-ordered NMR spectroscopy (DOSY), and dynamic light scattering (DLS) analyses. The results derived via DOSY NMR experiments and DLS combined with a Job plot analysis and in-depth NMR titration experiments indicate that the formation of supramolecular H-shaped macromolecules in 2:1 stoichiometry is efficiently occurring via the employed complementary recognition motifs with high binding constants (between 1.2 and 1.5 × 105 L mol–1 at ambient temperature).