| Reference Type | Journal (article/letter/editorial) |
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| Title | 3-Fluoro-2,4,5-triphenylfuran |
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| Journal | Acta Crystallographica Section E Structure Reports Online |
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| Authors | Jacobsen, Jesse M. | Author |
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| Arimitsu, Satoru | Author |
| Hammond, Gerald B. | Author |
| Mashuta, Mark S. | Author |
| Year | 2007 (November 1) | Volume | 63 |
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| Issue | 11 |
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| Publisher | International Union of Crystallography (IUCr) |
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| DOI | doi:10.1107/s1600536807049902Search in ResearchGate |
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| Generate Citation Formats |
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| Mindat Ref. ID | 467220 | Long-form Identifier | mindat:1:5:467220:7 |
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| GUID | 0 |
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| Full Reference | Jacobsen, Jesse M., Arimitsu, Satoru, Hammond, Gerald B., Mashuta, Mark S. (2007) 3-Fluoro-2,4,5-triphenylfuran. Acta Crystallographica Section E Structure Reports Online, 63 (11) doi:10.1107/s1600536807049902 |
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| Plain Text | Jacobsen, Jesse M., Arimitsu, Satoru, Hammond, Gerald B., Mashuta, Mark S. (2007) 3-Fluoro-2,4,5-triphenylfuran. Acta Crystallographica Section E Structure Reports Online, 63 (11) doi:10.1107/s1600536807049902 |
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| In | (2007, November) Acta Crystallographica Section E Structure Reports Online Vol. 63 (11) International Union of Crystallography (IUCr) |
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| Abstract/Notes | The title compound, C22H15FO, is the first example of a crystallographically characterized fully substituted fluorofuran. Although the F atom does not appear to participate in aryl–π attractions or classical hydrogen bonding, the title compound does contain four unique intermolecular π–π stacking interactions that have an atom-to-centroid range of 3.53 (4)–3.64 (4) Å. The phenyl ring located between the F and O atoms is only 9.55 (7)° from being coplanar with the furan ring, whereas the other aromatic planes form angles of 41.71 (1) and 20.45 (1)° with the ring. |
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