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

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• 作者：Ozcan Altintas ; David Schulze-Suenninghausen ; Burkhard Luy ; Christopher Barner-Kowollik
• 刊名：ACS Macro Letters
• 出版年：2013
• 出版时间：March 19, 2013
• 年：2013
• 卷：2
• 期：3
• 页码：211-216
• 全文大小：302K
• 年卷期：v.2,no.3(March 19, 2013)
• ISSN：2161-1653

文摘

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 伪,蠅-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鈥揻ragmentation chain transfer (RAFT) polymerization. Supramolecular H-shaped macromolecules were鈥攆or the first time鈥攑repared through supramolecular self-assembly between HW and CA recognition motifs to generate (PS-b-PEG)路PnBA路(PS-b-PEG) and (PS-b-PS)路PnBA路(PS-b-PS) in CH₂Cl₂ or dichloromethane-d₂ 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 脳 10⁵ L mol^鈥? at ambient temperature).