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恶唑并二氢卟吩21. 合成β-四苯基和β-四(五氟苯基)卟吩内酯及其锌(II)和铂(II)配合物的最有效方法。

Oxazolochlorins 21. Most Efficient Access to -Tetraphenyl- and -Tetrakis(pentafluorophenyl)porpholactones, and Their Zinc(II) and Platinum(II) Complexes.

作者信息

Thuita Damaris, Damunupola Dinusha, Brückner Christian

机构信息

Department of Chemistry, University of Connecticut, Unit 3060, Storrs, CT 06269-3060, USA.

出版信息

Molecules. 2020 Sep 22;25(18):4351. doi: 10.3390/molecules25184351.

Abstract

-Phenyl- and -pentafluorophenyl-porpholactones, their metal complexes, as well as porphyrinoids directly derived from them are useful in a number of technical and biomedical applications, and more uses are expected to be discovered. About a dozen competing and complementary pathways toward their synthesis were reported. The suitability of the methods changes with the -aryl group and whether the free base or metal derivatives are sought. These circumstances make it hard for anyone outside of the field of synthetic porphyrin chemistry to ascertain which pathway is the best to produce which specific derivative. We report here on what we experimentally evaluated to be the most efficient pathways to generate the six key compounds from the commercially available porphyrins, -tetraphenylporphyrin (TPP) and -tetrakis(pentafluorophenyl)porphyrin (TPP): free base -tetraphenylporpholactone (TPL) and -tetrakis(pentafluorophenyl)porpholactone (TPL), and their platinum(II) and zinc(II) complexes TPLPt, TPLPt, TPLZn, and TPLZn, respectively. Detailed procedures are provided to make these intriguing molecules more readily available for their further study.

摘要

苯基和五氟苯基卟吩内酯、它们的金属配合物以及直接由它们衍生而来的类卟啉在许多技术和生物医学应用中都很有用,并且预计会发现更多用途。据报道,有大约十二条相互竞争和互补的合成途径。这些方法的适用性会随着芳基以及所需的是游离碱还是金属衍生物而变化。这些情况使得合成卟啉化学领域之外的任何人都难以确定哪种途径最适合生产哪种特定衍生物。我们在此报告我们通过实验评估得出的从市售卟啉——四苯基卟啉(TPP)和四(五氟苯基)卟啉(TPP)生成六种关键化合物的最有效途径:游离碱四苯基卟吩内酯(TPL)和四(五氟苯基)卟吩内酯(TPL),以及它们的铂(II)和锌(II)配合物TPLPt、TPLPt、TPLZn和TPLZn。提供了详细的步骤,以便更方便地获得这些有趣的分子用于进一步研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ffc0/7570530/e5fbed92603c/molecules-25-04351-sch001.jpg

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