A mono-TTF-annulated porphyrin as a fluorescence switch.
Annulation of one TTF unit directly to the porphyrin chromophore produces an almost nonfluorescent species which can be transformed into a fluorescent species by oxidation of the TTF unit.
Biomedical subjects
Publications and source records attributed to Jan O Jeppesen.
Annulation of one TTF unit directly to the porphyrin chromophore produces an almost nonfluorescent species which can be transformed into a fluorescent species by oxidation of the TTF unit.
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[reaction: see text] A novel type of tetrathiafulvalene-cage 4 containing three monopyrrolo-tetrathiafulvalene units has been prepared employing a general and efficient synthetic approach. X-ray crystal structure analysis revealed that the cage is able to accommodate solvent molecules within a cavity in the solid state.
Addressing an array of bistable [2]rotaxanes through a two-dimensional crossbar arrangement provides the device element of a current-driven molecular electronic circuit. The development of the [2]rotaxane switches through an iterative, evolutionary process is described. The arrangement reported here allows both memory and logic functions to use the same elements.
A general and efficient four-step synthesis of a tetrathiafulvalene-belt 6, starting from the monopyrrolo-tetrathiafulvalene building block 1, is described, together with its 7,7,8,8-tetracyano-p-quinodimethane charge transfer complex. The complexation of the electron acceptor 7,7,8,8-tetracyano-p-quinodimethane by the tetrathiafulvalene-belt 6 was investigated both in solution and in the solid state. [reaction: see text]