Reference Type | Journal (article/letter/editorial) |
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Title | Synthesis of Rigid Stepladder Polymers via Scandium-Catalyzed Polyspiroannulation of Quinoline with Alkyne |
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Journal | Journal of the American Chemical Society |
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Authors | Shao, Jingjing | Author |
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Huang, Lin | Author |
Lou, Shao-Jie | Author |
Ohno, Aya | Author |
Yamada, Yoichi M. A. | Author |
Nishiura, Masayoshi | Author |
Murahashi, Tetsuro | Author |
Hou, Zhaomin | Author |
Year | 2025 (January 15) | Volume | 147 |
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Issue | 2 |
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Publisher | American Chemical Society (ACS) |
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DOI | doi:10.1021/jacs.4c15046Search in ResearchGate |
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| Generate Citation Formats |
Mindat Ref. ID | 18051738 | Long-form Identifier | mindat:1:5:18051738:5 |
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GUID | 0 |
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Full Reference | Shao, Jingjing, Huang, Lin, Lou, Shao-Jie, Ohno, Aya, Yamada, Yoichi M. A., Nishiura, Masayoshi, Murahashi, Tetsuro, Hou, Zhaomin (2025) Synthesis of Rigid Stepladder Polymers via Scandium-Catalyzed Polyspiroannulation of Quinoline with Alkyne. Journal of the American Chemical Society, 147 (2). doi:10.1021/jacs.4c15046 |
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Plain Text | Shao, Jingjing, Huang, Lin, Lou, Shao-Jie, Ohno, Aya, Yamada, Yoichi M. A., Nishiura, Masayoshi, Murahashi, Tetsuro, Hou, Zhaomin (2025) Synthesis of Rigid Stepladder Polymers via Scandium-Catalyzed Polyspiroannulation of Quinoline with Alkyne. Journal of the American Chemical Society, 147 (2). doi:10.1021/jacs.4c15046 |
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In | (2025, January) Journal Of The American Chemical Society Vol. 147 (2). American Chemical Society (ACS) |
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These are the references the publisher has listed as being connected to the article. Please check the article itself for the full list of references which may differ. Not all references are currently linkable within the Digital Library.
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 | Lou, Shao-Jie, Zhang, Liang, Luo, Yong, Nishiura, Masayoshi, Luo, Gen, Luo, Yi, Hou, Zhaomin (2020) Regiodivergent CâH Alkylation of Quinolines with Alkenes by Half-Sandwich Rare-Earth Catalysts. Journal of the American Chemical Society, 142 (42) 18128-18137 doi:10.1021/jacs.0c08362 |
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| The 6-(trimethylsilylethynyl)-substituted
quinoline was chosen due to its easier availability compared to other
regioisomers. |
| Not Yet Imported: - journal-article : 10.1039/b708534f
If you would like this item imported into the Digital Library, please contact us quoting Journal ID |
| This might be due to
the larger steric bulk of the methyl group, which could induce more
frustrated chain packing, thereby enhancing the surface area. For
a previous example of the influence of methyl substituents on the
BET surface area, see ref (3e). |
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