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Thermal Fusion Reactions of meso-(3-Thienyl) Groups in [26]Hexaphyrins to Produce Möbius Aromatic Molecules
Fuse to twist: Simple thermal reactions of meso‐(3‐thienyl) groups in Hückel‐aromatic [26]hexaphyrins (see picture, left; N blue, S yellow, F green) provide 3‐thienyl‐fused [28]hexaphyrins (right) that have Möbius aromatic character, as indicated by a number of spectroscopic methods....
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Published in: | Angewandte Chemie (International ed.) 2009-01, Vol.48 (36), p.6687-6690 |
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Main Authors: | , , , , , , |
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cited_by | cdi_FETCH-LOGICAL-c4337-2024184819ee86f0ad51e10909a6f7d90e75cf98649d50c27a3ac8c04963926c3 |
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container_end_page | 6690 |
container_issue | 36 |
container_start_page | 6687 |
container_title | Angewandte Chemie (International ed.) |
container_volume | 48 |
creator | Inoue, Mitsunori Kim, Kil Suk Suzuki, Masaaki Lim, Jong Min Shin, Jae-Yoon Kim, Dongho Osuka, Atsuhiro |
description | Fuse to twist: Simple thermal reactions of meso‐(3‐thienyl) groups in Hückel‐aromatic [26]hexaphyrins (see picture, left; N blue, S yellow, F green) provide 3‐thienyl‐fused [28]hexaphyrins (right) that have Möbius aromatic character, as indicated by a number of spectroscopic methods. |
doi_str_mv | 10.1002/anie.200902677 |
format | article |
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subjects | aromaticity electronic structure hexaphyrins Möbius aromaticity porphyrinoids |
title | Thermal Fusion Reactions of meso-(3-Thienyl) Groups in [26]Hexaphyrins to Produce Möbius Aromatic Molecules |
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