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| Novel expanded porphyrinoids with multiple-inner-ring-fusion and/or tunable aromaticity |
| Wei Miao, Zhaoyang Zhu, Zhongxin Li, Erhong Hao, Lijuan Jiao |
| Laboratory of Functional Molecular Solids, Ministry of Education, School of Chemistry and Materials Science, Anhui Normal University, Wuhu 241002, China |
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| Guide Novel expanded porphyrinoids with advanced structure features have a wide range of benefits (such as multi-metal coordination and facile tunable aromaticity) not offered by their normal porphyrin analogues. Considering research efforts have been devoted to address their limited synthetic accessibility issue. This review highlights some of these recent synthetic progresses towards these novel expanded porphyrinoids. |
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Abstract Novel expanded porphyrinoids with advanced structure features (such as multiple-inner-ring-fusion) have a wide range of benefits (such as multi-metal coordination and facile tunable aromaticity) not offered by their normal porphyrin analogues, and have found wide applications as sensors, fluorescent probes, novel ligands and functionalized NIR organic dyes in various research fields. However, the structures of these expanded porphyrinoids are scarce due to their limited synthetic accessibility. Herein, we summarized the lately reported efficient synthesis of novel expanded porphyrinoids with multipleinner-ring-fusion (up to six-inner-ring-fusion) and smaragdyrins with tunable aromaticity. Their synthesis is either based on an oxidative ring cyclization on linear/macrocyclic oligopyrroles containing N-confused pyrrole unit(s) or a straightforward double SNAr reaction on readily available 3,5-dibromoBODIPY, respectively.
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Received: 03 July 2019
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| Fund: We thank the National Nature Science Foundation of China (Nos. 21672006, 21672007 and 21871006) for supporting this work. |
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Corresponding Authors:
Lijuan Jiao
E-mail: jiao421@ahnu.edu.cn
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