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Iron biomimetic

Key Words Nonheme, Iron, Biomimetic, Bio-inspired, Cytochrome P450, Rieske dioxygenases. Hydrogen peroxide. Peroxide activation. Homogeneous catalysis, c/s-Dihydroxylation, Mechanism, Catalytic additives. Asymmetric... [Pg.451]

Scheme 14 Biomimetic ligands used in iron-catalyzed alkane oxidation... Scheme 14 Biomimetic ligands used in iron-catalyzed alkane oxidation...
In recent years, several model complexes have been synthesized and studied to understand the properties of these complexes, for example, the influence of S- or N-ligands or NO-releasing abilities [119]. It is not always easy to determine the electronic character of the NO-ligands in nitrosyliron complexes thus, forms of NO [120], neutral NO, or NO [121] have been postulated depending on each complex. Similarly, it is difficult to determine the oxidation state of Fe therefore, these complexes are categorized in the Enemark-Feltham notation [122], where the number of rf-electrons of Fe is indicated. In studies on the nitrosylation pathway of thiolate complexes, Liaw et al. could show that the nitrosylation of complexes [Fe(SR)4] (R = Ph, Et) led to the formation of air- and light-sensitive mono-nitrosyl complexes [Fe(NO)(SR)3] in which tetrathiolate iron(+3) complexes were reduced to Fe(+2) under formation of (SR)2. Further nitrosylation by NO yields the dinitrosyl complexes [(SR)2Fe(NO)2], while nitrosylation by NO forms the neutral complex [Fe(NO)2(SR)2] and subsequently Roussin s red ester [Fe2(p-SR)2(NO)4] under reductive elimination forming (SR)2. Thus, nitrosylation of biomimetic oxidized- and reduced-form rubredoxin was mimicked [121]. Lip-pard et al. showed that dinuclear Fe-clusters are susceptible to disassembly in the presence of NO [123]. [Pg.209]

One-step hydroxylation of aromatic nucleus with nitrous oxide (N2O) is among recently discovered organic reactions. A high eflSciency of FeZSM-5 zeolites in this reaction relates to a pronounced biomimetic-type activity of iron complexes stabilized in ZSM-5 matrix. N2O decomposition on these complexes produces particular atomic oj gen form (a-oxygen), whose chemistry is similar to that performed by the active oxygen of enzyme monooxygenases. Room temperature oxidation reactions of a-oxygen as well as the data on the kinetic isotope effect and Moessbauer spectroscopy show FeZSM-5 zeolite to be a successfiil biomimetic model. [Pg.493]

Results discussed above show in several lines a distinct biomimetic-type activity of iron complexes stabilized in the ZSM-S matrix. The most important feature is their unique ability to coordinate a very reactive a-oxygen form which is similar to the active oxygen species of MMO. At room temperature a-oxygen provides various oxidation reactions including selective hydroxylation of methane to methanol. Like in biological oxidation, the rate determining step of this reaction involves the cleavage of C-H bond. [Pg.501]

Bakke et al. (1982) have shown how montmorillonite catalyses chlorination and nitration of toluene nitration leads to 56 % para and 41 % ortho derivative compared to approximately 40 % para and 60 % ortho derivatives in the absence of the catalyst. Montmorillonite clays have an acidity comparable to nitric acid / sulphuric acid mixtures and the use of iron-exchanged material (Clayfen) gives a remarkable improvement in the para, ortho ratio in the nitration of phenols. The nitration of estrones, which is relevant in making various estrogenic drugs, can be improved in a remarkable way by using molecular engineered layer structures (MELS), while a reduction in the cost by a factor of six has been indicated. With a Clayfen type catalyst, it seems possible to manipulate the para, ortho ratio drastically for a variety of substrates and this should be useful in the manufacture of fine chemicals. In principle, such catalysts may approach biomimetic chemistry our ability to predict selectivity is very limited. [Pg.154]

Shiryaeva IM, Collman JP, Boulatov R, Sunderland CJ. 2003. Nonideal electrochemical behavior of biomimetic iron porphyrins Interfacial potential distribution across multilayer films. Anal Chem 79 494. [Pg.692]

Conventional MS in the energy domain has contributed a lot to the understanding of the electronic ground state of iron centers in proteins and biomimetic models ([55], and references therein). However, the vibrational properties of these centers, which are thought to be related to their biological function, are much less studied. This is partly due to the fact that the vibrational states of the iron centers are masked by the vibrational states of the protein backbone and thus techniques such as Resonance Raman- or IR-spectroscopy do not provide a clear picture of the vibrational properties of these centers. A special feature of NIS is that it directly reveals the fraction of kinetic energy due to the Fe motion in a particular vibrational mode. [Pg.528]

P. Calvert and A. Broad, Biomimetic routes to magnetic iron oxide-polymer composites. In K.L. Mittal (Ed.), Polymers in Information Storage Technology, Plenum Press, New York, 1991, p. 257. [Pg.382]

Selective Conversion of Hydrocarbons with H202 Using Biomimetic Non-heme Iron and Manganese Oxidation Catalysts... [Pg.654]

A mild aerobic palladium-catalyzed 1,4-diacetoxylation of conjugated dienes has been developed and is based on a multistep electron transfer46. The hydroquinone produced in each cycle of the palladium-catalyzed oxidation is reoxidized by air or molecular oxygen. The latter reoxidation requires a metal macrocycle as catalyst. In the aerobic process there are no side products formed except water, and the stoichiometry of the reaction is given in equation 19. Thus 1,3-cyclohexadiene is oxidized by molecular oxygen to diacetate 39 with the aid of the triple catalytic system Pd(II)—BQ—MLm where MLm is a metal macrocyclic complex such as cobalt tetraphenylporphyrin (Co(TPP)), cobalt salophen (Co(Salophen) or iron phthalocyanine (Fe(Pc)). The principle of this biomimetic aerobic oxidation is outlined in Scheme 8. [Pg.667]

Griinsteudel H (1998) Nuclear Resonant Scattering of Synchrotron Radiation on Iron Containing Biomimetic Compounds. PhD Thesis, Shaker, Liibeck... [Pg.180]

Biomimetic iron(III) tris-hydroxamates (diferric helices) have been reviewed briefly. [Pg.511]

The intermolecular coupling of phenols is used extensively in what are believed to be biomimetic alkaloid syntheses. Aqueous solutions of iron(lll) salts are most frequently used as the oxidising agent and the dimerization process must involve phenoxy radicals. Examples are the dimerization of orcinol 21 [114] and the formation of bis-benzyltetrahydroisoquinolines 22 [115],... [Pg.209]

The physical and coordination chemistry of hydroxamate-based iron chelators, their thermodynamic, kinetic, structural, spectroscopic and surface properties, have been extensively reviewed Therefore, only selective aspects that are relevant for the design of biomimetic siderophore analogs will be discussed. [Pg.753]

Biomimetic analogs with conformational restrained iron(III) complexes represent the... [Pg.765]


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See also in sourсe #XX -- [ Pg.102 ]




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