Stable Antiaromatic [24]Hexaphyrin(1.1.0.0.1.0) and Its Metal Complexes
- Authors
- Liu, Yang; Xu, Ling; Rao, Yutao; Kim, Jinseok; Yin, Bangshao; Zhou, Mingbo; Oh, Juwon; Kim, Dongho; Song, Jianxin; Osuka, Atsuhiro
- Issue Date
- Nov-2023
- Publisher
- AMER CHEMICAL SOC
- Citation
- ORGANIC LETTERS, v.25, no.45, pp 8121 - 8126
- Pages
- 6
- Journal Title
- ORGANIC LETTERS
- Volume
- 25
- Number
- 45
- Start Page
- 8121
- End Page
- 8126
- URI
- https://scholarworks.bwise.kr/sch/handle/2021.sw.sch/25638
- DOI
- 10.1021/acs.orglett.3c03231
- ISSN
- 1523-7060
1523-7052
- Abstract
- 5,10,23-Trimesityl-substituted [24]hexaphyrin(1.1.0.0.1.0) was synthesized as a stable antiaromatic molecule by base-catalyzed twofold SNAr reaction and was reduced to the corresponding [26]hexaphyrin, which was an unstable aromatic molecule because it easily oxidized to the [24]hexaphyrin. The [24]hexaphyrin served as a ligand to give the bis-Pd-II complex and tris-Rh-I complex with unique structures. The former complex has two square-planar-coordinated Pd-II ions bridged by an acetate anion and shows a strong paratropic ring current, while the latter complex has three Rh-I ions coordinated with two pyrrolic nitrogen atoms and two carbonyl groups, but one carbonyl group is shared with two Rh-I ions in a unique manner.
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Collections - College of Natural Sciences > Department of Chemistry > 1. Journal Articles
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