Self-assembled single-walled carbon nanotube:zinc-porphyrin hybrids through ammonium ion-crown ether interaction:: Construction and electron transfer

被引:59
作者
D'Souza, Francis
Chitta, Raghu
Sandanayaka, Atula S. D.
Subbaiyan, Navaneetha K.
D'Souza, Lawrence
Araki, Yasuyuki
Ito, Osamu
机构
[1] Wichita State Univ, Dept Chem, Wichita, KS 67260 USA
[2] Tohoku Univ, Inst Multidisciplinary Res Adv Mat, Aoba Ku, Sendai, Miyagi 9808577, Japan
[3] Univ Illinois, Dept Chem Engn, Chicago, IL 60607 USA
关键词
crown compounds; donor-acceptor systems; electron transfer; nanotubes; porphyrinoids;
D O I
10.1002/chem.200700583
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
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 electron-transfer 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 us. The present nanohybrids were also used to reduce the hexyl viologen dication (HV2+) and to oxidize 1-benzyl-1,4-dihydronicotinamide in solution in an electron-pooling experiment. Accumulation of the radical cation (HV center dot+) 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.
引用
收藏
页码:8277 / 8284
页数:8
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