1228675-10-2Relevant articles and documents
Design, synthesis and redox properties of a fluorene platform linking two different Bodipy dyes
Bura, Thomas,Ziessel, Raymond
, p. 2875 - 2879 (2010)
Several new fluorophores have been prepared by grafting boradiazaindacene (red absorbing) and/or styrylboradiazaindacene (blue absorbing) units as terminal energy acceptors onto a fluorene-derived platform. In one case, an amino-bis(bipyridine) pocket has been attached to enable strong binding of transition metal ions. The stepwise syntheses were largely based on Pd-catalysed cross-coupling reactions. The electrochemistry of the dyes has been analysed by reference to the properties of the various synthetic intermediates, protonation of the tertiary amine site present in the bis(bipyridine) species enabling processes involving this centre to be distinguished from those associated with the boradiazaindacene (Bodipy) unit.
Molecular logics: A mixed bodipy-bipyridine dye behaving as a concealable molecular switch
Puntoriero, Fausto,Nastasi, Francesco,Bura, Thomas,Ziessel, Raymond,Campagna, Sebastiano,Giannetto, Antonino
, p. 948 - 952 (2011/06/22)
A species based on a bodipy chromophore and containing bipyridine chelating sites behaves as a concealable molecular switch, featuring part of the properties of D-latch circuits by integrating two logic gates, a NOR and an INHIBIT gate, with both gates sh
