TY - JOUR
T1 - Self-assembled single-walled carbon nanotube
T2 - Zinc-porphyrin hybrids through ammonium ion-crown ether interaction: Construction and electron transfer
AU - D'Souza, Francis
AU - Chitta, Raghu
AU - Sandanayaka, Atula S.D.
AU - Subbaiyan, Navaneetha K.
AU - D'Souza, Lawrence
AU - Araki, Yasuyuki
AU - Ito, Osamu
PY - 2007/10/24
Y1 - 2007/10/24
N2 - An ammonium ion-crown ether interaction has been successfully used to construct porphyrin-single-walled carbon nanotube (SWNT) donor-acceptor hybrids. The [18]crown-6 to alkyl ammonium ion binding strategy resulted in porphyrin-SWNT nanohybrids that are stable and soluble in DMF. The porphyrin-SWNT hybrids were characterized by spectroscopic, TEM, and electrochemical techniques. Both steady-state and time-resolved emission studies revealed efficient quenching of the singlet excited state of the porphyrins and free-energy calculations suggested that electrontransfer quenching occurred. Nanosecond transient absorption spectral results supported the charge-separation quenching process. Charge-stabilization was also observed for the nanohybrids in which the lifetime of the radical ion pairs was around 100 ns. The present nanohybrids were also used to reduce the hexyl viologen dication (HV 2+) and to oxidize 1-benzyl-1,4-dihydronicotinamide in solution in an electronpooling experiment. Accumulation of the radical cation (HV+) was observed in high yields, which provided additional proof for the occurrence of photoinduced charge separation. The present study demonstrates that a hydrogen-bonding motif is a successful self-assembly method to build SWNTs bearing donor-acceptor nanohybrids, which are useful for light-energy harvesting and photovoltaic applications.
AB - An ammonium ion-crown ether interaction has been successfully used to construct porphyrin-single-walled carbon nanotube (SWNT) donor-acceptor hybrids. The [18]crown-6 to alkyl ammonium ion binding strategy resulted in porphyrin-SWNT nanohybrids that are stable and soluble in DMF. The porphyrin-SWNT hybrids were characterized by spectroscopic, TEM, and electrochemical techniques. Both steady-state and time-resolved emission studies revealed efficient quenching of the singlet excited state of the porphyrins and free-energy calculations suggested that electrontransfer quenching occurred. Nanosecond transient absorption spectral results supported the charge-separation quenching process. Charge-stabilization was also observed for the nanohybrids in which the lifetime of the radical ion pairs was around 100 ns. The present nanohybrids were also used to reduce the hexyl viologen dication (HV 2+) and to oxidize 1-benzyl-1,4-dihydronicotinamide in solution in an electronpooling experiment. Accumulation of the radical cation (HV+) was observed in high yields, which provided additional proof for the occurrence of photoinduced charge separation. The present study demonstrates that a hydrogen-bonding motif is a successful self-assembly method to build SWNTs bearing donor-acceptor nanohybrids, which are useful for light-energy harvesting and photovoltaic applications.
KW - Crown compounds
KW - Donor-acceptor systems
KW - Electron transfer
KW - Nanotubes porphyrinoids
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U2 - 10.1002/chem.200700583
DO - 10.1002/chem.200700583
M3 - Article
C2 - 17625800
AN - SCOPUS:35348944807
SN - 0947-6539
VL - 13
SP - 8277
EP - 8284
JO - Chemistry - A European Journal
JF - Chemistry - A European Journal
IS - 29
ER -