ArticleAngewandte Chemie (International ed. in English)2016
Synthesis of Five-Porphyrin Nanorings by Using Ferrocene and Corannulene Templates.
Article in Angewandte Chemie (International ed. in English), 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.
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Who cites it
9 citing papers in PubMed, 62 citations in OpenAlex.
- Template-directed self-assembly of porphyrin nanorings through an imine condensation reaction.Chemical science · 2025Article
- Magnetically Induced Current Densities in Zinc Porphyrin Nanoshells.The journal of physical chemistry. A · 2022Article
- Straightforward and Controlled Synthesis of Porphyrin-Phthalocyanine-Porphyrin Heteroleptic Triple-Decker Assemblies.Chemistry (Weinheim an der Bergstrasse, Germany) · 2020Article
- A Convenient Synthesis of Pentaporphyrins and Supramolecular Complexes with a Fulleropyrrolidine.Molecules (Basel, Switzerland) · 2019Article
- Molecular Engineering of Free-Base Porphyrins as Ligands-The N-H⋅⋅⋅X Binding Motif in Tetrapyrroles.Angewandte Chemie (International ed. in English) · 2019Review
- Single-Acetylene Linked Porphyrin Nanorings.Journal of the American Chemical Society · 2017Article
- Hierarchical Corannulene-Based Materials: Energy Transfer and Solid-State Photophysics.Angewandte Chemie (International ed. in English) · 2017Article
- Article
- Synthesis of Five-Porphyrin Nanorings by Using Ferrocene and Corannulene Templates.Angewandte Chemie (International ed. in English) · 2016Article
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Authors and funding
7 authors at 1 institution in 1 country.
Funding
Abstract
The smallest and most strained member of a family of π-conjugated cyclic porphyrin oligomers was synthesized by using pentapyridyl templates based on ferrocene and corannulene. Both templates are effective for directing the synthesis of the butadiyne-linked cyclic pentamer, despite the fact that the radii of their N5 donor sets are too small by 0.5 Å and 0.9 Å, respectively (from DFT calculations). The five-porphyrin nanoring exhibits a structured absorption spectrum and its fluorescence extends to 1200 nm, reflecting strong π conjugation and Herzberg-Teller vibronic coupling.
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