首页> 外文期刊>Journal of Porphyrins and Phthalocyanines >Realizing metalloporphyrin functionalization of 4-vinylpyridine copolymer via axial coordination reaction
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Realizing metalloporphyrin functionalization of 4-vinylpyridine copolymer via axial coordination reaction

机译:通过轴向配位反应实现4-乙烯基吡啶共聚物的金属卟啉官能化

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摘要

Cobalt tetra(para-chlorophenyl)porphyrin (CoTCPP) and zinc tetraphenyl porphyrin (ZnTPP) were linked on the side chains of the copolymer of 4-vinylpyridine (4VP) and styrene (St), P(4VP-co-St), via axial coordination reactions, respectively, and the metalloporphyrin-functionalized macromolecules, CoTCPP-P(4VP-co-St) and ZnTPP-P(4VP-co-St), were prepared. Their chemical structures were characterized by FTIR and 1H NMR. The spectral properties of the two macromolecular axial coordination complexes were mainly studied, and their photophysical behavior were discussed in depth. The experimental results show that the metalloporphyrin-functionalized macromolecules, CoTCPP-P(4VP-co-St) and ZnTPP-P(4VP-co-St), can be prepared favorably through axial coordination reaction with the side pyridine groups of the copolymer P(4VP-co-St) as ligands. The two complexes have characteristic spectra similar to that of the small molecular metalloporphyrins, CoTCPP and ZnTPP, respectively. At the same time, they also display the characteristic spectroscopic property of axial coordination complexes: the electronic adsorption spectra of CoTCPP-P(4VP-co-St) and ZnTPP-P(4VP-co-St) red-shifted obviously as compared to that of CoTCPP and ZnTPP, and the fluorescence emission of ZnTPP-P(4VP-co-St) blue-shifted apparently with respect to that of ZnTPP. For CoTCPP-P(4VP-co-St) and ZnTPP-P(4VP-co-St), some polymer effects were found: (1) the bonding degree of the small molecular metalloporphyrin, CoTCPP or ZnTPP, on the side chains of the copolymer P(4VP-co-St) has a limit value because of the steric hindrance and there is a bonding degree difference between the actual value and the theoretical value; (2) for ZnTPP-P(4VP-co-St), slight energy transfer between adjacent ZnTPP units on an identical macromolecule occurs, leading to slight static quench of the fluorescence emission as the bonding density of ZnTPP units on theside chains of the copolymer P(4VP-co-St) reaches a certain value.
机译:四(对氯苯基)卟啉钴(CoTCPP)和四苯基卟啉锌(ZnTPP)在4-乙烯基吡啶(4VP)和苯乙烯(St)P(4VP-co-St)共聚物的侧链上通过分别制备了轴向配位反应和金属卟啉官能化的大分子CoTCPP-P(4VP-co-St)和ZnTPP-P(4VP-co-St)。它们的化学结构通过FTIR和1H NMR表征。主要研究了两种大分子轴向配位配合物的光谱性质,并对它们的光物理行为进行了深入讨论。实验结果表明,通过与共聚物P的侧吡啶基团进行轴向配位反应,可以很好地制备金属卟啉官能化的大分子CoTCPP-P(4VP-co-St)和ZnTPP-P(4VP-co-St)。 (4VP-co-St)作为配体。两种配合物的特征光谱分别类似于小分子金属卟啉CoTCPP和ZnTPP。同时,它们还显示了轴向配位配合物的特征光谱性质:与之相比,CoTCPP-P(4VP-co-St)和ZnTPP-P(4VP-co-St)的电子吸附光谱明显偏红。 CoTCPP和ZnTPP的荧光发射,并且ZnTPP-P(4VP-co-St)的荧光发射相对于ZnTPP明显蓝移。对于CoTCPP-P(4VP-co-St)和ZnTPP-P(4VP-co-St),发现了一些聚合物效应:(1)小分子金属卟啉,CoTCPP或ZnTPP在侧链上的键合度共聚物P(4VP-co-St)由于位阻而具有极限值,在实际值与理论值之间存在键合度差。 (2)对于ZnTPP-P(4VP-co-St),在相同大分子上相邻ZnTPP单元之间会发生轻微的能量转移,随着ZnTPP单元在共聚物侧链上的键合密度的增加,导致荧光发射的轻微静态猝灭P(4VP-co-St)达到一定值。

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