Some mixed-valence Fe(II) Fe(III) complexes of thiocarboxylic acids and straight chain fatty acids with general formula [Fe(II)Fe(III)(2)O(SOCR)(6)(H(2)O)(3)] and [Fe(II)Fe(III)(2)O(SOCR)(3)(OOCR')(3)(CH(3)OH)(3)] (where, R=CH(3) or C(6)H(5) and R'=C(13)H(27), C(15)H(31) or C(17)H(35)) were synthesized and characterized by elemental analyses, spectral (infrared, electronic and Mössbauer) studies, molar conductance and magnetic susceptibility measurements. The infrared spectra suggested bridging nature of carboxylate and thiocarboxylate anions along with upsilon(asym)(Fe(3)O) vibrations in the complexes. Mössbauer studies revealed two resolved quadrupole doublets at 120-315 K confirming the presence of Fe(II) and Fe(III) moieties in the complexes. This was supported by the observed electronic spectral bands in the complexes at room temperature. The spectrum showed a band at around 13,800 cm(-1) which indicated an intervalence-transfer. Magnetic susceptibility measurements showed weak antiferromagnetic coupling related to mixed-valence pairs with S(2)=2, em leader S(1)=S(3)=5/2 spin exchange model. Conductance data indicated, the complexes were non-electrolytes in nitrobenzene. A structure has been established on the basis of these studies.
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http://dx.doi.org/10.1016/s1386-1425(02)00232-9 | DOI Listing |
Environ Res
January 2025
Ministry of Ecology and Environment South China Institute of Environmental Sciences, Guangzhou 510655, China; Key Laboratory of Water Environmental Simulation and Pollution Control, Ministry of Ecology and Environment, Guangzhou 510655, China. Electronic address:
Iron-activated peroxyacetic acid (PAA) represents an innovative advanced oxidation process (AOP). However, the efficiency of PAA activation by Fe(III) is often underestimated due to the widespread assumption that Fe(III) exhibits much lower ability than Fe(II) to activate PAA. Herein, the oxidative degradation of Rhodamine B (RhB) by Fe(III)-activated PAA process was investigated, and some new insights into the performance and mechanism of the Fe(III)/PAA system were presented.
View Article and Find Full Text PDFFront Microbiol
January 2025
College of Grassland Science, Xinjiang Agricultural University, Urumqi, China.
Iron (Fe) minerals possess a huge specific surface area and high adsorption affinity, usually considered as "rust tanks" of organic carbon (OC), playing an important role in global carbon storage. Microorganisms can change the chemical form of Fe by producing Fe-chelating agents such as side chains and form a stable complex with Fe(III), which makes it easier for microorganisms to use. However, in seasonal frozen soil thawing, the succession of soil Fe-cycling microbial communities and their coupling relationship with Fe oxides and Fe-bound organic carbon (Fe-OC) remains unclear.
View Article and Find Full Text PDFJ Pharm Sci
January 2025
Department of Pharmaceutical Chemistry, University of Kansas, 2093 Constant Avenue, Lawrence, KS 66047, USA. Electronic address:
Iron-catalyzed oxidation reactions are common degradation pathways in pharmaceutical formulations. Buffers can influence oxidation reactions promoted by iron (Fe) and hydrogen peroxide (H₂O₂). However, mechanistically, the specific role of buffers in such reactions is not well understood.
View Article and Find Full Text PDFInorg Chem
January 2025
State Key Laboratory of Clean and Efficient Coal Utilization, Taiyuan University of Technology, Taiyuan 030024, China.
The low sulfur selectivity of Fe-based HS-selective catalytic oxidation catalysts is still a problem, especially at a high O content. This is alleviated here through anchoring FeO nanoclusters on UiO-66 via the formation of Fe-O-Zr bonds. The introduced FeO species exist in the form of Fe and Fe.
View Article and Find Full Text PDFJ Inorg Biochem
March 2025
Centro de Química Estrutural, Institute of Molecular Sciences, Departamento de Química e Bioquímica, Faculdade de Ciências, Universidade de Lisboa, Campo Grande, 1749-016 Lisboa, Portugal.
Due to their diverse chemical properties and high ability to interact with biological molecules and cellular processes, transition metal-based compounds have emerged as promising candidates for cancer therapy. Iron complexes are among them, however, there is a gap in the comprehensive analysis of heterometallic iron complexes in the anticancer field. This review aims to fill this gap by summarizing recent progress in the study of Fe(II) and Fe(III) heterobimetallic complexes for anticancer applications and to gather important insights and future perspectives, with special emphasis on their theranostic capabilities.
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