Department of Chemistry and Molecular Design Institute, New York University, New York, NY, 10003, USA.
Macromol Rapid Commun. 2013 Oct;34(19):1518-23. doi: 10.1002/marc.201300501. Epub 2013 Aug 19.
A triblock copolymer containing the complementary hydrogen bonding recognition pair ureidoguanosine-diaminonaphthyridine (UG-DAN) as pendant functional groups is synthesized using ring-opening metathesis polymerization (ROMP). The norbornene-based DAN monomer is shown to allow for a controlled polymerization when polymerized in the presence of a modified-UG molecule that serves as a protecting group, subsequently allowing for the fabrication of functionalized triblock copolymers. The self-assembly of the copolymers was characterized using dynamic light scattering and (1) H NMR spectroscopy. It is demonstrated that the polymers self-assemble via complementary hydrogen bonding motifs even at low dilutions, indicating intramolecular interactions.
一种三嵌段共聚物,含有互补氢键识别对尿嘧啶脱氧核苷-二氨基萘啶(UG-DAN)作为侧基官能团,是使用开环复分解聚合(ROMP)合成的。当使用作为保护基团的改性 UG 分子存在时,基于降冰片烯的 DAN 单体显示出可控制的聚合,随后允许制备官能化的三嵌段共聚物。使用动态光散射和(1)H NMR 光谱对共聚物的自组装进行了表征。结果表明,即使在低稀释度下,聚合物也通过互补氢键模体自组装,表明存在分子内相互作用。