† College of Chemistry, Chemical Engineering and Material Science, Soochow University, Suzhou 215123, P. R. China
‡ College of Chemistry, Xiangtan University, Xiangtan 411105, P. R. China
§ Shanghai Institute of Applied Physics, Chinese Academy of Science, Shanghai 201800, P. R. China
Macromolecules 2014, 47, 3917–3925
We investigate the self-assembly behavior of a series of supramolecular hydrogen bonded polymer complexes P4VP(nCBP)x in which bent-shaped molecules (nCBP, n = 10,12,14) are attached to a poly(4-vinylpridine) (P4VP) backbone via hydrogen bond interaction in both bulk and thin films. The formation of lamellar and hexagonal columnar (ΦH) phases are dependent on the blending ratio of nCBP per vinylpridine unit (x), aliphatic tail length (n), and temperature. When increasing the grafting density x, the phase structure of polymer complexes transform from lamellar to ΦH phase. A nonreversible lamellar to ΦH phase transition appears in the heating process for P4VP(10CBP)x with x ≥ 0.4, P4VP(12CBP)x with x ≥ 0.3, and P4VP(14CBP)x with x ≥ 0.2. The lamellar and ΦH phase are oriented parallel to the substrate in the thin film as verified by both GISAXS and AFM.