ELECTROCHEMICAL PROPERTIES OF TETRAETHYNYLETHENES, FULLY CROSS-CONJUGATED PI-CHROMOPHORES, AND TETRAETHYNYLETHENE-BASED CARBON-RICH MOLECULAR RODS AND DEHYDROANNULENES
C. Boudon et al., ELECTROCHEMICAL PROPERTIES OF TETRAETHYNYLETHENES, FULLY CROSS-CONJUGATED PI-CHROMOPHORES, AND TETRAETHYNYLETHENE-BASED CARBON-RICH MOLECULAR RODS AND DEHYDROANNULENES, Journal of electroanalytical chemistry [1992], 394(1-2), 1995, pp. 187-197
The redox properties of tetraethynylethenes and carbon-rich molecular
rods and dehydroannulenes built from these fully cross-conjugated mole
cular construction units are reported here for the first time. All mon
omeric and oligomeric cyclic and acyclic tetraethynylethenes are diffi
cult to oxidize but undergo stepwise reductions, with the number of di
stinct steps increasing with the length of the linearly conjugated all
-carbon backbone and the size of the a system. The reductions are also
facilitated when the length of the carbon backbone and the number of
a electrons in the molecules increase.