A new bimetallic platform comprising a six-coordinate Fe(ONO) unit bound to an (ONO)M (M = Fe, Zn) has been discovered ((ONO)H = bis(3,5-di--butyl-2-phenol)amine). Reaction of Fe(ONO) with either (ONO)Fe(py) or with (ONO)FeCl under reducing conditions led to the formation of the bimetallic complex Fe(ONO), which includes unique five- and six-coordinate iron centers. Similarly, the reaction of Fe(ONO) with the new synthon (ONO˙)Zn(py) led to the formation of the heterobimetallic complex FeZn(ONO), with a six-coordinate iron center and a five-coordinate zinc center. Both bimetallic complexes were characterized by single-crystal X-ray diffraction studies, solid-state magnetic measurements, and multiple spectroscopic techniques. The magnetic data for FeZn(ONO) are consistent with a ground state = 3/2 spin system, generated from a high-spin iron(ii) center that is antiferromagnetically coupled to a single (ONO˙) radical ligand. In the case of Fe(ONO), the magnetic data revealed a ground state = 7/2 spin system arising from the interactions of one high-spin iron(ii) center, one high-spin iron(iii) center, and two (ONO˙) radical ligands.
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http://dx.doi.org/10.1039/c5sc03006d | DOI Listing |
J Inorg Biochem
January 2025
IRCCS Fondazione Bietti, Roma, Italy. Electronic address:
Nitrite (NO) interacts with myoglobin (Mb) and hemoglobin (Hb) behaving as a ligand of both the ferrous (i.e., Mb(II) and Hb(II)) and ferric (i.
View Article and Find Full Text PDFPhys Chem Chem Phys
March 2019
State Key Laboratory of Structural Chemistry, Fujian Institute of Research on the Structure of Matter, Chinese Academy of Sciences, Fuzhou 350002, People's Republic of China. and Center for Advanced Marine Materials and Smart Sensors, Minjiang University, Fuzhou 350116, China.
A direct NO-releasing reaction of nitrite catalyzed by [N(afa)Fe(OTf)] (afa (azafulvene-amine); OTf (trifluoromethanesulfonate); Cy (cyclohexyl)) was investigated using density functional theory (DFT) with D3 dispersion correction. The complex featured a secondary coordination sphere that facilitated the formation of the iron-oxo product [N(afa)FeO] with three (Fe)OH-N hydrogen bonds. As a high-spin iron(ii), the O-binding initial intermediate Fe(O)-nitrito was thermodynamically favorable in the S = 2 state.
View Article and Find Full Text PDFJ Inorg Biochem
January 2017
Department of Chemistry, University of Cyprus, P.O. Box 20537, 1678 Nicosia, Cyprus. Electronic address:
The coordination of nitrite in myoglobin (Mb) has been characterized by resonance Raman spectroscopy and the frequencies of the nitrite bound to the heme Fe as well to the 2-vinyl have been computed by density functional theory (DFT) calculations. The DFT Natural Bond Orbital (NBO) analysis and the extensive isotope-labeling in the resonance Raman experiments indicate that NO (O1NO2) is bound to the heme Fe via O1. Based on the vibrational characterization of the reversible transition between low and high spin FeONO/2-nitrovinyl species, we suggest that the key step that triggers the spin-change is the increase of the proximal FeN bond length.
View Article and Find Full Text PDFJ Am Chem Soc
December 2009
Department of Chemistry and Biochemistry, University of Oklahoma, 620 Parrington Oval, Norman, Oklahoma 73019, USA.
It is now well-established that mammalian heme proteins are reactive with various nitrogen oxide species and that these reactions may play significant roles in mammalian physiology. For example, the ferrous heme protein myoglobin (Mb) has been shown to reduce nitrite (NO(2)(-)) to nitric oxide (NO) under hypoxic conditions. We demonstrate here that the distal pocket histidine residue (His64) of horse heart metMb(III) (i.
View Article and Find Full Text PDFJ Inorg Biochem
August 2006
Department of Chemistry and Biochemistry, University of Oklahoma, 620 Parrington Oval, Norman, OK 73019, USA.
Nitrite is an important species in the global nitrogen cycle, and the nitrite reductase enzymes convert nitrite to nitric oxide (NO). Recently, it has been shown that hemoglobin and myoglobin catalyze the reduction of nitrite to NO under hypoxic conditions. We have determined the 1.
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