Erem Ahmetali, Azra Kocaarslan, Stefan Bräse, Patrick Théato, M. Kasım Şener
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引用次数: 0
Abstract
Nitroxide-mediated polymerization (NMP) and nitroxide exchange reaction (NER) are very efficient methodologies that require only suitable alkoxyamine derivatives and create different polymeric architectures in a controlled manner. Herein, the synthesis of star polymers containing TEMPO-substituted symmetric zinc phthalocyanine (ZnPc) is presented via NMP and NER. Moreover, linear polymer formation is conducted in a single arm on TEMPO-substituted asymmetric ZnPc to elucidate the properties of star polymers. All linear and star polymers are characterized by FT-IR, UV–vis, fluorescence, GPC, NMR, and EPR techniques. The results show that the proposed reactions are capable of forming controlled star-shaped polymers. The increasing arm number (from a single to four arms) results in variable dispersity values (Đ) (1.2–3) due to different arm lengths, especially in NMP. However, this difficulty has been overcome via NER, and star polymers have been successfully synthesized with relatively low molecular weight (30 K > 10 K) and low dispersity (1.2–1.9). The results clearly indicate that while styrene and 4-vinyl benzyl chloride monomers are introduced to the structure equally, star polymers with phthalocyanine can be synthesized in a controlled manner, and their quarternized derivatives have the potential to be effective as photoactive agents in photodynamic therapy.
亚硝基氧化物介导聚合(NMP)和亚硝基氧化物交换反应(NER)是非常有效的方法,只需要合适的烷氧基胺衍生物,就能以可控的方式生成不同的聚合物结构。本文介绍了通过 NMP 和 NER 合成含有 TEMPO 取代的对称酞菁锌(ZnPc)的星形聚合物。此外,还在 TEMPO 取代的不对称 ZnPc 上以单臂方式形成线性聚合物,以阐明星型聚合物的特性。所有线性聚合物和星型聚合物都通过傅立叶变换红外光谱、紫外-可见光谱、荧光、GPC、核磁共振和 EPR 技术进行了表征。结果表明,所提出的反应能够形成可控的星形聚合物。由于臂长不同,臂数的增加(从单臂到四臂)会导致分散度值(Đ)(1.2-3)的变化,尤其是在 NMP 中。不过,这一困难已通过 NER 得到克服,并成功合成了分子量相对较低(30 K > 10 K)、分散度较低(1.2-1.9)的星型聚合物。研究结果清楚地表明,虽然苯乙烯和 4-乙烯基苄基氯单体被平等地引入到结构中,但含有酞菁的星形聚合物可以以可控的方式合成,其四分化衍生物有望成为光动力疗法中有效的光活性剂。
期刊介绍:
Macromolecular Rapid Communications publishes original research in polymer science, ranging from chemistry and physics of polymers to polymers in materials science and life sciences.