pH‐Modulated 1D Hierarchical Self‐Assembly of a Brush‐Like Poly‐Para‐Phenylene Homopolymer

Author:

Zhang Xiaomin1,Liu Bohao2,Xu Fugui3,Ning Lijian1,Zhou Qian1,Zhang Qichun4,Mai Yiyong3,Gong Qiuyu2,Huang Yinjuan1ORCID

Affiliation:

1. State Key Laboratory for Mechanical Behavior of Materials Shaanxi International Research Center for Soft Matter School of Materials Science and Engineering Xi'an Jiaotong University Xi'an 710049 P. R. China

2. Department of Thoracic Surgery The First Affiliated Hospital of Xi'an Jiaotong University Xi'an 710061 P. R. China

3. School of Chemistry and Chemical Engineering Shanghai Key Laboratory of Electrical Insulation and Thermal Ageing Shanghai Jiao Tong University 800 Dongchuan Road Shanghai 200240 P. R. China

4. Department Materials Science and Engineering Department of Chemistry & Center of Super‐Diamond and Advanced Films (COSDAF) City University of Hong Kong Kowloon, Hong Kong SAR 999077 P. R. China

Abstract

AbstractThe controllable self‐assembly of conjugated homopolymers, especially homopolymers without other segments (a prerequisite for phase separation), which can afford chances to achieve tunable optical/electronic properties, remains a great challenge due to their poor solubility and has remained rarely documented. Herein, a conjugated homopolymer (DPPP‐COOH) is synthesized, which has a unique brush‐like structure with a conjugated dendritic poly‐para‐phenylene (DPPP) backbone and alkyl‐carboxyl side chains at both edges of the backbone. The introduction of carboxyl makes the brush‐like homopolymer exhibit pH‐modulated 1D hierarchical self‐assembly behavior in dilute solution, and allows for flexible morphological regulation of the assemblies, forming some uncommon superstructures including ultralong nanowires (at pH 7), superhelices (at pH 10) and “single‐wall” nanotubes (at pH 13), respectively. Furthermore, the good aqueous dispersibility and 1D feature endow the superstructures formed in a high‐concentration neutral solution with high broad‐spectrum antibacterial performance superior to that of many conventional 1D materials.

Funder

National Natural Science Foundation of China

Publisher

Wiley

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