期刊
CHEMISTRY-A EUROPEAN JOURNAL
卷 27, 期 12, 页码 4053-4063出版社
WILEY-V C H VERLAG GMBH
DOI: 10.1002/chem.202003327
关键词
energy transfer; porphyrinoids; self-assembly; structure elucidation; zinc
资金
- Kakenhi, MEXT, Japan [18K05156]
- National Research Foundation of Korea (NRF) - Korea government (MSIT) [2020R1A5A1019141]
- Grants-in-Aid for Scientific Research [18K05156] Funding Source: KAKEN
This study focused on the self-assembly of zinc porphyrin derivatives with meta-pyridyl groups in chloroform, revealing a unique trimer structure with a triangular cone shape. Incorporation of a porphyrin-ferrocene dyad into the assemblies led to a rare light-harvesting/charge-separation system with energy gradient and reductive quenching.
Self-assembly of porphyrins is a fascinating topic, not only for mimicking chlorophyll assemblies in photosynthetic organisms, but also for the potential of creating molecular-level devices. Herein, zinc porphyrin derivatives bearing a meta-pyridyl group at the meso position were prepared and their assemblies studied in chloroform. Among the porphyrins studied, one with a carbamoylpyridyl moiety gave a distinct H-1 NMR spectrum in CDCl3, which allowed the supramolecular structure in solution to be probed in detail. Ring-current-induced chemical-shift changes in the H-1 NMR spectrum, together with vapor-pressure osmometry and diffusion-ordered NMR spectroscopy, among other evidence, suggested that the porphyrin molecules form a trimer with a triangular cone structure. Incorporation of a directly linked porphyrin-ferrocene dyad with the same assembling properties in the assemblies led to a rare example of a light-harvesting/charge-separation system in which an energy gradient is incorporated and reductive quenching occurs.
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