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dc.contributor.authorSreejith, S-
dc.contributor.authorPeters, M-
dc.contributor.authorSteinborn, K-
dc.contributor.authorKrahwinkel, B-
dc.contributor.authorSonnichsen, F D-
dc.contributor.authorGrote, D-
dc.contributor.authorSander, W-
dc.contributor.authorLohmiller, T-
dc.contributor.authorRudiger, O-
dc.contributor.authorHerges, R-
dc.date.accessioned2019-07-08T13:56:12Z-
dc.date.available2019-07-08T13:56:12Z-
dc.date.issued2018-11-12-
dc.identifier.citationNature Communications; 9(1):4750en_US
dc.identifier.urihttps://www.nature.com/articles/s41467-018-07023-1-
dc.identifier.urihttp://10.10.100.66:8080/xmlui/handle/123456789/3389-
dc.description.abstractControlled 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.isoenen_US
dc.publisherNatureen_US
dc.titleLight-controlled switching of the spin state of iron(III)en_US
dc.typeArticleen_US
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