Journalartikel
Autorenliste: Tran-Van, AF; Huxol, E; Basler, JM; Neuburger, M; Adjizian, JJ; Ewels, CP; Wegner, HA
Jahr der Veröffentlichung: 2014
Seiten: 1594-1597
Zeitschrift: Organic Letters
Bandnummer: 16
Heftnummer: 6
ISSN: 1523-7060
DOI Link: https://doi.org/10.1021/ol500194s
Verlag: 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.
Zitierstile
Harvard-Zitierstil: 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-Zitierstil: 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