有机化学 ›› 2019, Vol. 39 ›› Issue (10): 2973-2979.DOI: 10.6023/cjoc201904038 上一篇    下一篇

所属专题: 有机超分子化学合辑

研究简报

两亲聚肽/螺烯的电荷复合自组装行为研究

王婧琳a, 沈程硕b, 唐颂超a*(), 姚远a*()   

  1. a 华东理工大学材料科学与工程学院 高分子材料与工程教研室 上海 200237
    b 上海交通大学化学化工学院 上海 200240
  • 收稿日期:2019-04-15 修回日期:2019-05-07 发布日期:2019-05-21
  • 通讯作者: 唐颂超,姚远 E-mail:schtang@ecust.edu.cn;yaoyuan@ecust.edu.cn
  • 基金资助:
    国家自然科学基金(No. 51573088)

Study of Charge-Conjugated Self-Assembly Behavior of Amphiphilic Block Copolypeptides/Helicene

Wang, Jinglina, Shen, Chengshuob, Tang, Songchaoa*(), Yao, Yuana*()   

  1. a Teaching and Research Department of Polymer Materials and Engineering, School of Materials Science and Engineering, East China University of Science and Technology, Shanghai 200237
    b School of Chemistry and Chemical Engineering, Shanghai Jiao Tong University, Shanghai 200240
  • Received:2019-04-15 Revised:2019-05-07 Published:2019-05-21
  • Contact: Tang, Songchao,Yao, Yuan E-mail:schtang@ecust.edu.cn;yaoyuan@ecust.edu.cn
  • Supported by:
    Project supported by the National Natural Science Foundation of China(No. 51573088)

研究了包含聚肽嵌段的两亲共聚物聚乙二醇-b-聚(L-谷氨酸)(PEG-b-PGlu)与4-甲基-4-氮杂[4]螺烯鎓离子(Me[4]H)的电荷复合自组装行为, 讨论了聚肽链段长度、谷氨酸单元与螺烯物质的量比、pH值等因素对组装体形貌的影响. 研究发现, 当刚-柔型嵌段聚合物与刚性、大尺寸并具有诱导作用的小分子共同组装时, 遵循与柔性大分子电荷复合组装完全不同的规律. PEG-b-PGlu/Me[4]H的电荷复合组装体形貌由π-π堆叠作用、两亲嵌段聚肽的亲疏水比、PGlu链段的刚硬程度共同决定, 这些作用在组装过程中相互制约, 当π-π堆叠作用占主导地位时, 得到以指针状和条带状等平面结构为主的组装形貌.

关键词: 电荷复合自组装, 两亲嵌段共聚物, 螺烯

Amphiphilic block copolypeptides of polyethylene glycol-b-poly(L-glutamic acid) (PEG-b-PGlu) were synthesized to self-assemble with 4-methyl-4-aza[4]helicene onium ion (Me[4]H) in water through charge-conjugation. The morphology of the assemblies was studied by varying PGlu block length, the molar ratio of Glu unit/Me[4]H and pH value. It was found that when rigid-flexible block copolymers were assembled together with small molecules which had rigid, large size and inductive effect, they would follow a completely different law from the charge-conjugated assembly of flexible macromolecules. The self-assemblies were controlled by the π-π stacking of helicene, together with the volume fraction of the hydrophobic parts and the rigidity of PGlu segments. These effects restricted each other in the assembly process. When π-π stacking was dominant, assembly morphologies with pointer-like and strip-like planar structures were obtained.

Key words: charge-conjugated self-assembly, amphiphilic block copolymer, helicene