250687-30-0Relevant articles and documents
Advances in the synthesis of functionalised pyrrolotetrathiafulvalenes
O'Driscoll, Luke J.,Andersen, Sissel S.,Solano, Marta V.,Bendixen, Dan,Jensen, Morten,Duedal, Troels,Lycoops, Jess,Van Der Pol, Cornelia,Sorensen, Rebecca E.,Larsen, Karina R.,Myntman, Kenneth,Henriksen, Christian,Hansen, Stinne W.,Jeppesen, Jan O.
supporting information, p. 1112 - 1122 (2015/08/18)
The electron-donor and unique redox properties of the tetrathiafulvalene (TTF, 1) moiety have led to diverse applications in many areas of chemistry. Monopyrrolotetrathiafulvalenes (MPTTFs, 4) and bispyrrolotetrathiafulvalenes (BPTTFs, 5) are useful struc
Binding studies between triethylene glycol-substituted monopyrrolotetrathiafulvalene derivatives and cyclobis(paraquat-p-phenylene)
Nygaard, Sune,Hansen, Camilla N.,Jeppesen, Jan O.
, p. 1617 - 1626 (2007/10/03)
The synthesis of several π-electron-donating monopyrrolotetrathiafulvalene (MPTTF) derivatives, which conceptually can be divided into three classes containing none, one, or two triethylene glycol (TEG) substituents, is described. In all cases, the comple
Pyrrolo annelated tetrathiafulvalenes: The parent systems
Jeppesen, Jan Oskar,Takimiya, Kazuo,Jensen, Frank,Becher, Jan
, p. 1291 - 1294 (2008/02/09)
The synthesis of the parent bis(pyrrolo[3,4-d])tetrathiafulvalene via a nonclassical and simple pyrrole synthesis is reported, together with a detailed study of the fundamental redox behavior of some of this class of heterocycles.
