Ultrafast photodriven intramolecular electron transfer from a zinc porphyrin to a readily reduced diiron hydrogenase model complex

Amanda P S Samuel, Dick T Co, Charlotte L. Stern, Michael R Wasielewski

Research output: Contribution to journalArticle

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Abstract

Diiron complexes modeled on the active site of the [FeFe] hydrogenases having the general formula [Fe2(μ-R)(CO)6-n(L) n], where commonly R = alkyl or aryl dithiolate and L = CO, CN -, or PR3, are a promising class of catalysts for use in photodriven H2 production. However, many of these catalysts are difficult to photoreduce using chromophores that absorb visible light. Here we report the synthesis and spectroscopic characterization of a naphthalene-4,5-dicarboximide-1,8-dithiolate diiron complex [NMI-Fe 2S2(CO)6, 1] and a covalently linked, fixed-distance zinc 5,10,15-tri-n-pentyl-20-phenylporphyrin-NMI-Fe 2S2(CO)6 donor-acceptor dyad (2). The electron-withdrawing nature of the NMI group makes the diiron complex among the most easily reduced hydrogenase mimics reported to date (-0.74 V vs SCE). In the presence of triflic acid, the cyclic voltammogram of 1 showed an increase in current at the first reduction wave at -0.78 V and a new reduction wave at -1.4 V. As the acid concentration was increased, the current at -0.78 V remained constant while the current at -1.4 V increased significantly, which is consistent with a catalytic proton reduction process. Selective photoexcitation of the Zn porphyrin in 2 with 553 nm, 110 fs laser pulses in both toluene and CH2Cl2 yielded transient absorption spectra showing a distinct peak at 616 nm, which has been assigned to [NMI-Fe2S 2(CO)6] on the basis of spectroelectrochemical measurements on 1. The 616 nm peak was used to monitor the charge separation (CS) and charge recombination (CR) dynamics of 2, which yielded τCS = 12 ± 1 ps and τCR = 3.0 ± 0.2 ns in toluene and τCS = 24 ± 1 ps and τCR = 57 ± 1 ps in CH2Cl2. Photoexcitation of the disulfide precursor to 2 in both toluene and CH 2Cl2 produced only the singlet and triplet excited states of the Zn porphyrin, showing that electron transfer is favorable only when the diiron complex is present. Photoexcitation of 2 in the presence of trifluoroacetic acid was shown to generate H2.

Original languageEnglish
Pages (from-to)8813-8815
Number of pages3
JournalJournal of the American Chemical Society
Volume132
Issue number26
DOIs
Publication statusPublished - Jul 7 2010

Fingerprint

Hydrogenase
Photoexcitation
Porphyrins
Carbon Monoxide
Toluene
Zinc
Electrons
Genetic Recombination
Trifluoroacetic acid
Catalysts
Acids
Naphthalene
Chromophores
Excited states
Absorption spectra
Laser pulses
Protons
Trifluoroacetic Acid
Disulfides
Catalytic Domain

ASJC Scopus subject areas

  • Chemistry(all)
  • Catalysis
  • Biochemistry
  • Colloid and Surface Chemistry
  • Medicine(all)

Cite this

Ultrafast photodriven intramolecular electron transfer from a zinc porphyrin to a readily reduced diiron hydrogenase model complex. / Samuel, Amanda P S; Co, Dick T; Stern, Charlotte L.; Wasielewski, Michael R.

In: Journal of the American Chemical Society, Vol. 132, No. 26, 07.07.2010, p. 8813-8815.

Research output: Contribution to journalArticle

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