Issue 39, 2010

Electron transfer reaction of light harvestingzinc naphthalocyanine–subphthalocyanine self-assembled dyad: spectroscopic, electrochemical, computational, and photochemical studies

Abstract

Electron transfer reaction of a self-assembled donor–acceptor dyad formed by axial coordination of zinc naphthalocyanine, ZnNc, and subphthalocyanine appended with pyridine coordinating ligand, SubPc(py), was investigated in the present study. The SubPc(Py) : ZnNc self-assembled dyad absorbs the light in a wide section of the UV/Vis/NIR spectra. The formation constant of SubPc(py) : ZnNc in o-dichlorobenzene was found to be 1.2 × 105 M−1 from the steady-state absorption and emission measurements, suggesting stable complex formation. The geometric and electronic calculations by using ab initio B3LYP/6-311G methods showed the majority of the highest occupied frontier molecular orbital (HOMO) on the zinc naphthalocyanine entity, while the lowest unoccupied molecular orbital (LUMO) was on the subphthalocyanine entity, suggesting that the charge-separated state of the supramolecular complex is (SubPc(py))˙ : ZnNc˙+. The electrochemical results suggest the exothermic charge-separation process via the singlet states of both SubPc(py) and ZnNc entities. Upon coordination the pyridine appended subphthalocyanine to ZnNc; the main quenching pathway involved charge separation via the singlet excited states of ZnNc and SubPc(py). A clear evidence of the intramolecular electron transfer from the singlet state of ZnNc to SubPc(py) was monitored by femtosecond laser photolysis in o-dichlorobenzene by observing the characteristic absorption band of the ZnNc radical cation in the NIR region at 960 nm. The rate of charge-separation process was found to be 1.3 × 1010 s−1, indicating fast and efficient charge separation. The rate of charge recombination and the lifetime of the charge-separated state were found to be 1.0 × 109 s−1 and 1 ns, respectively. The absorption in a wide section of the solar spectrum and high charge-separation/charge-recombination ratio suggests the usefulness of self-assembled SubPc(Py) : ZnNc for being a photosynthetic model.

Graphical abstract: Electron transfer reaction of light harvesting zinc naphthalocyanine–subphthalocyanine self-assembled dyad: spectroscopic, electrochemical, computational, and photochemical studies

Supplementary files

Article information

Article type
Paper
Submitted
19 May 2010
Accepted
08 Jul 2010
First published
27 Aug 2010

Phys. Chem. Chem. Phys., 2010,12, 12746-12752

Electron transfer reaction of light harvesting zinc naphthalocyaninesubphthalocyanine self-assembled dyad: spectroscopic, electrochemical, computational, and photochemical studies

M. E. El-Khouly, Phys. Chem. Chem. Phys., 2010, 12, 12746 DOI: 10.1039/C0CP00612B

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements