1,4-BIS(1,2,6-TRIPHENYL-4-PYRIDYL)BENZENE AS A NOVEL HYDROPHOBIC ELECTRON RELAY FOR DIHYDROGEN EVOLUTION IN PHOTOCATALYTIC SYSTEMS BASED ONLIPID VESICLES
Ev. Efimova et al., 1,4-BIS(1,2,6-TRIPHENYL-4-PYRIDYL)BENZENE AS A NOVEL HYDROPHOBIC ELECTRON RELAY FOR DIHYDROGEN EVOLUTION IN PHOTOCATALYTIC SYSTEMS BASED ONLIPID VESICLES, Journal of photochemistry and photobiology. A, Chemistry, 83(2), 1994, pp. 153-159
1,4-Bis(1,2,6-triphenyl-4-pyridyl)benzene (''benzoviologen'') is an ef
ficient lipophilic reversible electron relay, which can be used to bui
ld structurally organized molecular systems based on lipid vesicles fo
r photocatalytic water cleavage. Benzoviologen has an advantage over t
he widely used conventional lipophilic viologens, since its reduced fo
rms possess more negative reduction potentials. This promotes photosti
mulated transmembrane electron transfer and catalytic water reduction
at neutral or even slightly basic pH. The kinetic properties of benzov
iologen and its capacity to produce one- and two-electron-reduced form
s were studied. The ability to couple vectorial transmembrane electron
phototransfer with dihydrogen evolution from water over a dispersed P
d catalyst was proven experimentally.