Journal article
Authors list: Tran-Van, AF; Huxol, E; Basler, JM; Neuburger, M; Adjizian, JJ; Ewels, CP; Wegner, HA
Publication year: 2014
Pages: 1594-1597
Journal: Organic Letters
Volume number: 16
Issue number: 6
ISSN: 1523-7060
DOI Link: https://doi.org/10.1021/ol500194s
Publisher: American Chemical Society
Abstract:
A new modular approach to the smallest substituted cycloparaphenylenes (CPPs) is presented. This versatile method permits access to substituted CPPs, choosing the substituent at a late stage of the synthesis. Variously substituted [8]CPPs have been synthesized, and their properties analyzed. The structural characteristics of substituted CPPs are close to those of unsubstituted CPPs. However, their optoelectronic behavior differs remarkably due to the larger torsion angle between the phenyl units.
Citation Styles
Harvard Citation style: Tran-Van, A., Huxol, E., Basler, J., Neuburger, M., Adjizian, J., Ewels, C., et al. (2014) Synthesis of Substituted [8]Cycloparaphenylenes by [2+2+2] Cycloaddition, Organic Letters, 16(6), pp. 1594-1597. https://doi.org/10.1021/ol500194s
APA Citation style: Tran-Van, A., Huxol, E., Basler, J., Neuburger, M., Adjizian, J., Ewels, C., & Wegner, H. (2014). Synthesis of Substituted [8]Cycloparaphenylenes by [2+2+2] Cycloaddition. Organic Letters. 16(6), 1594-1597. https://doi.org/10.1021/ol500194s
