Tunable Supramolecular Hexagonal Columnar Structures of Hydrogen-Bonded Copolymers Containing Two Different Sized Dendritic Side Chains.
Yongchen CaiMeiqing ZhengYalan ZhuXiao-Fang ChenChristopher Y LiPublished in: ACS macro letters (2017)
Polymer structures with tunable symmetry and sizes are desired for applications such as lithography, filtration membranes, and separation. Here we report the self-assembled supramolecular hexagonal columnar (Φ H ) structures with tunable lattice size varying from 5 to 7 nm by constructing hydrogen-bonded copolymers bearing poly(4-vinylpyridine) (P4VP) and two dendritic molecular additives, 1-[4'-(3″,4″,5″-tridecyloxybenzoyloxy)phenyleneoxycarbonyl]-3-[(4″-hydroxyphenyl)oxycarbonyl]benzene (12CBP) and 4-hydroxyphenyl (3,4,5-tridecyloxy)benzoate (12CTB). Despite the distinct molecular size difference between 12CBP and 12CTB, the resulting ternary supramolecular copolymers, P4VP(12CBP) x (12CTB) y , possess a homogeneous Φ H phase at x ≥ 0.1 and y ≥ 0.2. Each column is constructed with P4VP as the backbone tethered with mixed side chains. The column diameter is between the size of the corresponding P4VP(12CBP) x + y and P4VP(12CTB) x + y and could be easily tuned by varying x and y . The enhancement of Φ H in supramolecular copolymers is attributed to the entropy effect of the mixed side chain and enthalpy effect from hydrogen bonding interaction of the P4VP backbone and two molecules (12CBP and 12CTB).