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Light-controlled switching of the spin state of iron(III)

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dc.contributor.author Sreejith, S
dc.contributor.author Peters, M
dc.contributor.author Steinborn, K
dc.contributor.author Krahwinkel, B
dc.contributor.author Sonnichsen, F D
dc.contributor.author Grote, D
dc.contributor.author Sander, W
dc.contributor.author Lohmiller, T
dc.contributor.author Rudiger, O
dc.contributor.author Herges, R
dc.date.accessioned 2019-07-08T13:56:12Z
dc.date.available 2019-07-08T13:56:12Z
dc.date.issued 2018-11-12
dc.identifier.citation Nature Communications; 9(1):4750 en_US
dc.identifier.uri https://www.nature.com/articles/s41467-018-07023-1
dc.identifier.uri http://10.10.100.66:8080/xmlui/handle/123456789/3389
dc.description.abstract Controlled switching of the spin state of transition metal ions, particularly of FeII and FeIII, is a prerequisite to achieve selectivity, efficiency, and catalysis in a number of metalloenzymes. Here we report on an iron(III) porphyrin with a photochromic axial ligand which, upon irradiation with two different wavelengths reversibly switches its spin state between low-spin (S = 1/2) and high-spin (S = 5/2) in solution (DMSO-acetone, 2:598). The switching efficiency is 76% at room temperature. The system is neither oxygen nor water sensitive, and no fatigue was observed after more than 1000 switching cycles. Concomitant with the spin-flip is a change in redox potential by ~60 mV. Besides serving as a simple model for the first step of the cytochrome P450 catalytic cycle, the spin switch can be used to switch the spin-lattice relaxation time T1 of the water protons by a factor of 15. en_US
dc.language.iso en en_US
dc.publisher Nature en_US
dc.title Light-controlled switching of the spin state of iron(III) en_US
dc.type Article en_US


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  • 2018
    Journal Articles authored by NIIST researchers published in 2018

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