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.