TY - JOUR
T1 - Construction of oriented π-electron arrays based on two-dimensional supramolecular organizates
AU - Shimomura, Masatsugu
AU - Karthaus, Olaf
AU - Ijiro, Kuniharu
PY - 1996/1/1
Y1 - 1996/1/1
N2 - Two-dimensional supramolecular organizates are shown to be powerful tools for constructing oriented π-electron arrays, which are applicable to molecular photonics devices and artificial photosynthesis. Complementary hydrogen bonding at the interface of an amphiphilic nucleobase monolayer can form two-dimensional stacking of base-pairs, which is expected to be an electron medium for photoinduced electron transfer as well as double-strand DNAs. DNAs are also immobilized as a monomolecular film of the polyion-complex with an amphiphilic cationic intercalator. A new type of monolayer-forming stilbene amphiphile having a trinitrofluorenylidene group is prepared for designing spatially separated electron donor and acceptor layers.
AB - Two-dimensional supramolecular organizates are shown to be powerful tools for constructing oriented π-electron arrays, which are applicable to molecular photonics devices and artificial photosynthesis. Complementary hydrogen bonding at the interface of an amphiphilic nucleobase monolayer can form two-dimensional stacking of base-pairs, which is expected to be an electron medium for photoinduced electron transfer as well as double-strand DNAs. DNAs are also immobilized as a monomolecular film of the polyion-complex with an amphiphilic cationic intercalator. A new type of monolayer-forming stilbene amphiphile having a trinitrofluorenylidene group is prepared for designing spatially separated electron donor and acceptor layers.
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U2 - 10.1016/0968-5677(96)00032-6
DO - 10.1016/0968-5677(96)00032-6
M3 - Article
AN - SCOPUS:0030106285
SN - 0968-5677
VL - 3
SP - 61
EP - 65
JO - Supramolecular Science
JF - Supramolecular Science
IS - 1-3
ER -