DOI | Resolve DOI: https://doi.org/10.1021/ol1025958 |
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Author | Search for: Lu, Y.; Search for: Zhou, Y.; Search for: Quan, Y.-W.; Search for: Chen, Q.-M.; Search for: Chen, R.-F.; Search for: Zhang, Z.-Y.; Search for: Fan, Q.-L.; Search for: Huang, W.; Search for: Ding, J.-F.1 |
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Affiliation | - National Research Council of Canada. NRC Institute for Chemical Process and Environmental Technology
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Format | Text, Article |
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Abstract | Monodisperse macrospirocyclic oligomers were prepared using self-condensation of the Friedel-Crafts reaction. Through the C-9s of the central fluorene units of four surrounding oligofluorenes, four carbazole units are connected in a series to form a macrocyclic core. These rodlike oligofluorenes form a rigid three-dimensional structure, affording the resulting macrocyclics a high steric hindrance for close interchain packing. © 2010 American Chemical Society. |
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Publication date | 2011 |
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In | |
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Language | English |
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Peer reviewed | Yes |
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NPARC number | 21271403 |
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Export citation | Export as RIS |
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Report a correction | Report a correction (opens in a new tab) |
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Record identifier | 3a5efdcf-a14c-4623-bb9b-3d39fd2c89bd |
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Record created | 2014-03-24 |
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Record modified | 2020-04-21 |
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