Functionalization and metathesis polymerization induced self-assembly of an alternating copolymer into giant vesicles.
Functionalization and metathesis polymerization induced self-assembly of an alternating copolymer into giant vesicles.
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官能化和复分解聚合诱导交替共聚物自组装成巨型囊泡
DOI:
10.1039/d1ra00835h
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发表时间:
2021-04-21
期刊:
影响因子:
3.9
通讯作者:
Li X
中科院分区:
文献类型:
--
作者:
Song W;Shen J;Li X
A facile fabrication of spherical vesicles and micelles by acyclic diene metathesis (ADMET) polymerization and alternative metathesis polymerization (ALTMET) was investigated. We utilize fluorine (FL) and perylene diimide-based (PDI) α,ω-dienes and α,ω-diacrylates to provide a series of homopolymers and alternating copolymers. When using α,ω-dienes as model monomers, TEM measurement indicates that the aromatic FL and PDI building block induced polymers to generate medium-sized (30–50 nm and 90–120 nm, respectively) micelles and vesicles. It was amazing that alternating copolymers derived from PDI α,ω-dienes and FL α,ω-diacrylates spontaneously form giant vesicles with sizes in the range of 0.7 μm to 2.5 μm. The controlled self-assembly of the organic polymer mediated by ADMET and ALTMET techniques avoided extremely annoying post treatment. Therefore, this work establishes a new, versatile synthetic strategy to create nanoparticles having tunable morphologies with potential application as molecular payload delivery vehicles. Fluorine (FL) and perylene diimide-based (PDI) α,ω-dienes and α,ω-diacrylates were used to synthesise a series of homopolymers and alternating copolymers and provide spherical vesicles and micelles by metathesis polymerization.
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