Issue 7, 2002

Abstract

Fullerene–porphyrin conjugates coordinated with Fe and Zn ions (1·Fe and 1·Zn) were designed and synthesized. Compounds 1·Fe and 1·Zn were reconstituted into apomyoglobin successfully to produce C60-modified myoglobins, 1·Fe-Mb and 1·Zn-Mb, respectively. The axial-ligand exchange reaction revealed that 1·Fe-Mb maintains the intrinsic properties of native Mb, except for the autooxidation rate constant, suggesting similar microenvironment of the porphyrin moieties in the proteins. Cyclic voltammogram (CV) of a graphite electrode modified with a film of 1·Fe-Mb–didodecyldimethylammonium bromide (DDAB) showed two reversible redox couples with E0′ = −206 and −1048 mV which are attributable to Fe2+/3+ and the reduction of the porphyrin ring, respectively. Differential pulse voltammogram of an electrode modified with a 1·Fe-Mb–tridodecylmethylammonium bromide (TDAB) film in water containing 0.5 M tetraethylammonium chloride and 10 mM 2,2′,2″-nitrilotriethanol showed three cathodic peaks at E½,1 = −372, E½,2 = −555, and E½,3 = −1028 mV which are attributable to Fe2+/3+, C600/1−, and the reduction of the porphyrin ring, respectively. The electrodes modified with 1·Fe-Mb and 1·Zn-Mb gave anodic photocurrent coupled with on–off light irradiation. The action spectrum of photocurrent for a 1·Zn-Mb–DDAB film was in accord with the UV–vis absorption spectrum of 1·Zn-Mb. Transient absorption spectra of 1·Zn in benzonitrile and 1·Zn-Mb in a 50 mM phosphate buffer at 100 ns after the ns-laser light pulse irradiation at 532 nm showed three absorption maxima at 700, 830, and 1000 nm which are assignable to the triplet excited state of C60 (3C60*), the triplet excited state of the zinc porphyrin (3ZnP*), and C60 radical anion (C60˙), respectively. Existence of the apparent C60˙ indicates the generation of charge-separation state, ZnP˙+–C60˙. The rate constants for the generation of the charge separation states in 1·Zn and 1·Zn-Mb calculated from the fluorescence data were 8.2 × 108 s−1 and 6.4 × 108 s−1, respectively, and the corresponding quantum yields were 0.62 and 0.59.

Graphical abstract: Design, synthesis and photophysical properties of C60-modified proteins

Article information

Article type
Paper
Submitted
31 Jan 2002
Accepted
22 Feb 2002
First published
28 Mar 2002

J. Mater. Chem., 2002,12, 2026-2033

Design, synthesis and photophysical properties of C60-modified proteins

H. Murakami, R. Matsumoto, Y. Okusa, T. Sagara, M. Fujitsuka, O. Ito and N. Nakashima, J. Mater. Chem., 2002, 12, 2026 DOI: 10.1039/B201145J

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