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Synthesis, characterization, and photoinduced electron transfer in functionalized single wall carbon nanohorns.

Authors :
Cioffi C
Campidelli S
Sooambar C
Marcaccio M
Marcolongo G
Meneghetti M
Paolucci D
Paolucci F
Ehli C
Rahman GM
Sgobba V
Guldi DM
Prato M
Source :
Journal of the American Chemical Society [J Am Chem Soc] 2007 Apr 04; Vol. 129 (13), pp. 3938-45. Date of Electronic Publication: 2007 Mar 08.
Publication Year :
2007

Abstract

Single-wall carbon nanohorns (SWNHs) are a new class of material that is closely related to single-wall carbon nanotubes. Here, we describe the synthesis and characterization of a series of SWNHs functionalized with ethylene glycol chains and porphyrins. Functionalization of carbon nanohorns has been achieved using two different synthetic protocols: (1) direct attack of a free amino group on the nanohorn sidewalls (nucleophilic addition) and (2) amidation reaction of the carboxylic functions in oxidized nanohorns. The nanohorn derivatives have been characterized by a combination of several techniques, and the electronic properties of the porphyrin/nanohorn assemblies (SWNH/H2P) have been investigated by electrochemistry, spectroelectrochemistry, and a series of steady-state and time-resolved spectroscopy. The cyclic voltammetry curve of nanohorn/porphyrin conjugate 6 showed a continuum of faradic and pseudocapacitive behavior, which is associated with multiple-electron transfers to and from the SWNHs. Superimposed on such a pseudocapacitive current, the curve also displays three discrete reduction peaks at -2.26, -2.57, and -2.84 V and an oxidation peak at 1.12 V (all attributed to the porphyrin moiety). Steady-state and time-resolved fluorescence demonstrated a quenching of the fluorescence of the porphyrin in SWNH/H2P conjugates 5 and 6 compared to the reference free base porphyrin. Transient absorption spectra permitted the electron-transfer process between the porphyrins and the carbon nanostructures to be highlighted.

Details

Language :
English
ISSN :
0002-7863
Volume :
129
Issue :
13
Database :
MEDLINE
Journal :
Journal of the American Chemical Society
Publication Type :
Academic Journal
Accession number :
17343379
Full Text :
https://doi.org/10.1021/ja068007p