Pyrene dimerization into 1, 1′-dipyrenyl
VA Nefedov
Index: Nefedov Russian Journal of Organic Chemistry, 2007 , vol. 43, # 8 p. 1163 - 1166
Full Text: HTML
Citation Number: 5
Abstract
Abstract Treatment of pyrene and some its derivatives with Cu (II) tetrafluoroborate or perchlorate in CH 3 CN cleanly led to the formation of 1, 1′-dipyrenyls. The other polycyclic hydrocarbons (anthracene, perylene) under the same conditions provide cation-radicals. 1, 1′-Dipyrenyl strongly differs from pyrene in the chemical behavior: it does not undergo either formylation by Vilsmeier reaction, neither acylation (AcCl, ZnCl 2) or nitration (by ...
Related Articles:
[Buchanan, A. C.; Dworkin, A. S.; Smith, G. P. Journal of the American Chemical Society, 1980 , vol. 102, # 16 p. 5262 - 5265]
[Guenther, Howard; Kovacic, Peter Synthetic Communications, 1984 , vol. 14, # 5 p. 413 - 428]
[Wahl, Peter; Krieger, Claus; Schweitzer, Dieter; Staab, H. A. Chemische Berichte, 1984 , vol. 117, # 1 p. 260 - 276]