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Supramolecular Porphyrin Nanostructures Based on Coordination-Driven Self-Assembly and Their Visible Light Catalytic Degradation of Methylene Blue Dye

机译:基于协调驱动的自组装的超分子卟啉纳米结构及其亚甲基蓝染料的可见光催化降解

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摘要

A series of porphyrin triads (1–4), in which each triad is composed of a Sn(IV) porphyrin and two free-base (or Zn(II)) porphyrins, was synthesized and their self-assembled nanostructures were studied. Depending on the substituent on porphyrin moieties, each triad was self-assembled into a different nanostructure. In particular, the cooperative coordination of 3-pyridyl groups in the Sn(IV) porphyrin with the axial Zn(II) porphyrins in triad 4 leads to forming uniform nanofibers with an average width of 10–22 nm. Other triads without the coordinating interaction between the central Sn(IV) porphyrin and the axial porphyrins formed irregularly shaped aggregates in contrast. The morphologies of nanofiber changed drastically upon the addition of pyrrolidine, in which pyrrolidine molecules break down the self-assembly process by coordinating with the axial Zn(II) porphyrins. All porphyrin aggregates exhibited efficient photocatalytic performances on the degradation of methylene blue dye under visible light irradiation. The degradation efficiencies after 2 h were observed to be between 70% and 95% for the aggregates derived from the four triads.
机译:一系列卟啉三元(1-4),其中每个三合会由Sn(IV)卟啉和两个自由碱(或Zn(或Zn(II))卟啉合成,并研究了它们的自组装纳米结构。取决于卟啉部分的取代基,每个三合会都被自组装成不同的纳米结构。特别地,在三合会4中具有轴向Zn(II)卟啉的Sn(IV)卟啉中的3-吡啶基的协同配位导致形成均匀的纳米纤维,平均宽度为10-22nm。其他三合会而没有中央Sn(IV)卟啉和轴向卟啉之间的坐标相互作用形成不规则形状的聚集体。在加入吡咯烷后,纳米纤维的形态变化,其中吡咯烷分子通过与轴向Zn(II)卟啉配位来分解自组装过程。所有卟啉聚集体在可见光照射下表现出高效的光催化性能对亚甲基蓝染料的降解。衍生自四种三合会的聚集体,观察到2小时后的降解效率为70%至95%。

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