2002
DOI: 10.1016/s0020-1693(01)00761-7
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Synthesis, molecular structure and magnetic properties of [Fe6(μ3-O)2(OPri)2(μ-OPri)6(O2CPh)2(μ-O2CPh)4]

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Cited by 16 publications
(9 citation statements)
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“…This is a reflection of the diverse areas to which such chemistry is relevant, from magnetic materials to mineralogy and biology. Molecular oxide-bridged iron(III) clusters with structural or other relevance to minerals such as hematite or ferrihydrite, the iron-oxo-hydroxo core of the iron storage protein ferritin, and biomineralization in general are some of the areas of interest in high-nuclearity Fe chemistry. Smaller nuclearity molecules are also of biological interest, such as those containing the [Fe 2 (μ-O)(O 2 CR) 2 ] 2+ core of the oxygen carrier protein hemerythrin and the related cores in other dinuclear Fe proteins such as ribonucleotide reductases, purple acid phosphatases, and methane monooxygenases …”
Section: Introductionmentioning
confidence: 99%
“…This is a reflection of the diverse areas to which such chemistry is relevant, from magnetic materials to mineralogy and biology. Molecular oxide-bridged iron(III) clusters with structural or other relevance to minerals such as hematite or ferrihydrite, the iron-oxo-hydroxo core of the iron storage protein ferritin, and biomineralization in general are some of the areas of interest in high-nuclearity Fe chemistry. Smaller nuclearity molecules are also of biological interest, such as those containing the [Fe 2 (μ-O)(O 2 CR) 2 ] 2+ core of the oxygen carrier protein hemerythrin and the related cores in other dinuclear Fe proteins such as ribonucleotide reductases, purple acid phosphatases, and methane monooxygenases …”
Section: Introductionmentioning
confidence: 99%
“…Iron plays an important role in diverse areas of nature, from mineralogy to biology. Its most common oxidation state is 3+, which is found in oxide-based minerals such as hematite or ferrihydrite, 11 as well as in a number of biological systems. Of particular interest is the biomineralization of the element and its deposition into iron storage proteins.…”
Section: Introductionmentioning
confidence: 99%
“…In this way, [Fe 4 O 2 (O 2 CPh) 8 -(py) 2 ] was converted with Al(OR) 3 (R ) Pr i , Bu) to the hexanuclear product [Fe 6 O 2 (OR) 8 (O 2 CPh) 6 ]. 11 A related method uses the relative acidity of alcohols to transform iron(III) salts or (more rarely) preformed Fe x clusters into alkoxide-containing complexes in the absence of more aggressive alkoxide sources. These controlled alcoholysis reactions take place under milder conditions than the aforementioned metathesis reactions.…”
Section: Introductionmentioning
confidence: 99%
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“…Very recently, a similar reaction was reported that employed aluminum alkoxides in a reaction with a preformed cluster rather than a simple iron salt. In this way, [Fe 4 O 2 (O 2 CPh) 8 (py) 2 ] was converted with Al (OR) 3 (R = Pr i , Bu) to the hexanuclear product [Fe 6 O 2 (OR) 8 (O 2 CPh) 6 ] [26].…”
Section: Metathesis Reactionmentioning
confidence: 99%