The DOI matches its Crossref record; 26 of the 26 references it cites were found in a registry or an index.
α-Oligofurans
Abstract
A new type of organic electronic material, consisting of long alpha-oligofurans containing up to nine rings, was synthesized and characterized. alpha-Oligofurans are highly fluorescent, with a quantum yield in the range 58-74%. They are more rigid than the corresponding oligothiophenes, with tighter herringbone packing. The calculated twisting energy of oligofurans is significantly higher than that of other conjugated heterocycles. Despite their greater rigidity, oligofurans are more soluble than oligothiophenes. The introduced long oligofurans fulfill the most important requirements for a wide range of applications as organic electronic materials.
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Cites
Handbook of conducting polymers
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The Larger Acenes: Versatile Organic Semiconductors
Anthony, J. E. (2008) · Angewandte Chemie International Edition · doi:10.1002/anie.200604045 · Cited by 2,100
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(2008) · Elsevier eBooks · doi:10.1016/b978-0-08-045316-3.x0001-4 · Cited by 1,496
Simple Chemical Transformation of Lignocellulosic Biomass into Furans for Fuels and Chemicals
Binder, J. B., & Raines, R. T. (2009) · Journal of the American Chemical Society · doi:10.1021/ja808537j · Cited by 1,490
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Cited by
Yiu, A. T., Beaujuge, P. M., Lee, O. P., Woo, C. H., Toney, M. F., & Fréchet, J. M. J. (2012) · Journal of the American Chemical Society · doi:10.1021/ja2089662 · Cited by 491
Xiong, Y., Tao, J., Wang, R., Qiao, X., Yang, X., Wang, D., Wu, H., & Li, H. (2016) · Advanced Materials · doi:10.1002/adma.201600120 · Cited by 123
Metadata
- Authors
- Gidron, O., Diskin-Posner, Y., & Bendikov, M.
- Venue
- Journal of the American Chemical Society
- Publisher
- American Chemical Society (ACS)
- Published
- 2010-01-29
- Volume
- 132
- Issue
- 7
- Pages
- 2148-2150
- ISSN
- 0002-7863 (ISSN-L)
- 1520-5126
- OpenAlex
- W4250615106
- Cited by
- 269
- References
- 26
- FWCI
- 16.70
- Type
- journal article
- Language
- en
- Open access
- closed
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