Purpurinimide-fullerene dyads: introduction of fullerene moiety at various peripheral positions of the purpurinimide system

Organic Letters
Guolin LiRavindra K Pandey

Abstract

[reaction: see text] Fullerene was regioselectively introduced at various peripheral positions of N-hexyl-purpurinimide for photoinduced electron transfer studies. Remarkably different effects of the position of the fullerene moiety in the formation of atropisomers were observed.

References

Jul 1, 1990·Journal of Medicinal Chemistry·R K PandeyT J Dougherty
Feb 12, 2000·Angewandte Chemie·F P Montforts, O Kutzki
Feb 15, 2001·Accounts of Chemical Research·D GustA L Moore
Mar 10, 2001·Journal of Photochemistry and Photobiology. B, Biology·D GustA L Moore
Feb 19, 2002·Chemical Reviews·Nazario MartínIgnacio Pérez
Apr 19, 2002·Journal of the American Chemical Society·Sergei SmirnovFranz-Peter Montforts
Oct 18, 2003·Chemphyschem : a European Journal of Chemical Physics and Physical Chemistry·Jeong-Hyon HaYoung Key Shim

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Citations

Jun 26, 2007·The Journal of Organic Chemistry·Chinnasamy MuthiahJonathan S Lindsey
Jun 22, 2006·Lasers in Surgery and Medicine·Ravindra K PandeyThomas J Dougherty
Feb 4, 2010·The Journal of Organic Chemistry·Marcin PtaszekJonathan S Lindsey

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