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Zn-polyphenol chelation: Complexes with quercetin, (+)-catechin, and derivatives: II Electrochemical and EPR studies

In this work, we have studied the formation of complexes between flavonols, (quercetin, rutin, quercitrin, kaempferol, luteolin, tamarixetin) and flavanols ((+)-catechin, (-)-epicatechin), flavanonol, (+)-taxifolin, and Zn acetate in two hydro-organic media at neutral pH in the absence of oxygen. The complexation was first studied by cyclic voltammetry. Then preparative electrolysis have been attempted followed by coulometry, UV-Vis optical absorption and circular dicroism spectroscopies for characterizing the oxidized compounds. Spectroelectrochemistries monitored either in the UV-Vis or in the EPR spectrometers at room temperature have been also used and we have identified o-semi-quinone intermediates in some cases. Different behaviour vis-a-vis the complexation by Zn2+ according to the molecular structures of these different families of polyphenols have been found. Some of them are more easily oxidizible.

Zn-polyphenol chelation: Complexes with quercetin, (+)-catechin, and derivatives: II Electrochemical and EPR studies

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Reference£º
Iron Catalysis in Organic Synthesis | Chemical Reviews,
Iron Catalysis in Organic Synthesis: A Critical Assessment of What It Takes To Make This Base Metal a Multitasking Champion

 

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The study of regioselectivity of ferrocenylalkylation of N, S-heterocycles in aqueous-organic media

Regioselectivity of ferrocenylalkylation reaction of mercaptoheterocycles with ferrocenylcarbinoles in biphasic aqueous-organic media was studied. The structures of compounds were assigned on the basis of NMR spectra and 1H/13C heteronuclear correlations. X-ray determination of molecular structures of 1-(ferrocenyl(phenyl)methyl)pyrrolidine-2-thione 5f, 4, 5-dihydro-1-(1-ferrocenylmethyl)-1H-imidazole-2-thiol 7a and 4, 5-dihydro-1-(1-ferrocenyl-2methylpropyl)-1H-imidazole-2-thiol 7e were carried out.

The study of regioselectivity of ferrocenylalkylation of N, S-heterocycles in aqueous-organic media

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Reference£º
Iron Catalysis in Organic Synthesis | Chemical Reviews,
Iron Catalysis in Organic Synthesis: A Critical Assessment of What It Takes To Make This Base Metal a Multitasking Champion

 

The Absolute Best Science Experiment for Vinylferrocene

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Antimicrobial activity of organometallic isonicotinyl and pyrazinyl ferrocenyl-derived complexes

Isonicotinyl and pyrazinyl ferrocenyl-derived complexes were prepared using various hydrazides and ferrocenyl aldehydes. Three heterobimetallic complexes were also synthesized from the Schiff base-derived isonicotinyl ferrocene complex using various platinum group metal dimers based on ruthenium, rhodium and iridium. All complexes were evaluated in vitro for antimycobacterial and antiparasitic activity. Against Mycobacterium tuberculosis H37Rv, the platinum group metal complexes showed glycerol-dependent antimycobacterial activity. The antiplasmodial activities against the NF54 chloroquine-sensitive strain of Plasmodium falciparum of some compounds were moderate, while some complexes also showed promising activity against Trichomonas vaginalis. Incorporation of the ferrocenyl-salicylaldimine moiety resulted in enhanced antimicrobial activity compared to the non-ferrocenyl compound in some cases. The bimetallic iridium-ferrocene isonicotinyl complex exhibited superior antitrichomonal activity relative to its organic counterpart, isoniazid. Furthermore, all these compounds, when screened on several normal flora bacteria of humans, showed no effect on the microbiome, emphasizing the selection of these compounds for these pathogens. The promising antimicrobial activities of the complexes thus supports incorporation of ferrocene as part of existing antimicrobial therapies in order to alter their biological activities favorably.

Antimicrobial activity of organometallic isonicotinyl and pyrazinyl ferrocenyl-derived complexes

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Reference£º
Iron Catalysis in Organic Synthesis | Chemical Reviews,
Iron Catalysis in Organic Synthesis: A Critical Assessment of What It Takes To Make This Base Metal a Multitasking Champion

 

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A has cytotoxicity to tumor targeting effects of ferrocene base Uygur formic acid/paclitaxel nano particle and its application (by machine translation)

A has cytotoxicity to tumor targeting effects of ferrocene base Uygur formic acid/paclitaxel nano particle and its in the preparation of medicament for treating tumor application, belongs to the technical field of medicament. The invention preparation of nano particle retains the tretinoin inhibiting tumor stem cell proliferation, inducing activity, taxol can be carried at the same time the role of anti-personnel tumor stem cell outside of the common tumor cells; and the nano-particles to a tumor cell in a high concentration of reduced glutathione sensitive, into tumor cells can be rapidly cleavage after the release of the paclitaxel, exposed tretinoin functional group, their role; in the normal cell because less reductive glutathione content, will not be released or very few release, to reduce the toxic effect of the normal cells. At the same time, the nano-particle portable and transfer Micro – RNA into a cell to play a relevant role in, thus can be used for preparing medicaments for treating tumors. (by machine translation)

A has cytotoxicity to tumor targeting effects of ferrocene base Uygur formic acid/paclitaxel nano particle and its application (by machine translation)

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Reference£º
Iron Catalysis in Organic Synthesis | Chemical Reviews,
Iron Catalysis in Organic Synthesis: A Critical Assessment of What It Takes To Make This Base Metal a Multitasking Champion

 

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Metallocenes meet porphyrinoids: Consequences of a “fusion”

Historic as well as new developments in chemistry of metallocenyl-containing porphyrins, phthalocyanines, naphthalocyanines, tetraazaporphyrins, subphthalocyanines, subporphyrins, BODIPYs, azaBODIPYs, and related systems were overviewed. Synthetic pathways for preparation as well as the redox and photophysical properties of metallocenyl-type compounds in which organometallic substituents connected to the respective core pi-system via (i) equatorial covalent bond; (ii) axial covalent or coordination bond; (iii) beta,beta’-fusion into the aromatic system; and (iv) eta5- or eta6-bonds to the central metal ion are discussed.

Metallocenes meet porphyrinoids: Consequences of a “fusion”

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Reference£º
Iron Catalysis in Organic Synthesis | Chemical Reviews,
Iron Catalysis in Organic Synthesis: A Critical Assessment of What It Takes To Make This Base Metal a Multitasking Champion

 

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Application of 1271-48-3, The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.1271-48-3, Name is 1,1′-Ferrocenedicarboxaldehyde, molecular formula is C12H10FeO2. In a Article£¬once mentioned of 1271-48-3

Synthesis of ferrocene tethered open and macrocyclic bis-beta-lactams and bis-beta-amino acid derivatives

New bioorganometallic ferrocene derivatives are synthesized through a Diversity Oriented Synthesis strategy. Easily available ferrocene bisimines have been transformed into open ferrocenyl bis-beta-lactams. These compounds have demonstrated to be versatile synthons used in further transformations into new ferrocene bis-beta-amino acids. Carefully selected substituents submitted to ring closing metathesis (RCM) and Cu-catalyzed oxidative alkyne coupling conditions have also allowed the conversion of open substrates into ferrocenic macrocyclic bis-beta-lactams. The Royal Society of Chemistry 2009.

Synthesis of ferrocene tethered open and macrocyclic bis-beta-lactams and bis-beta-amino acid derivatives

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Reference£º
Iron Catalysis in Organic Synthesis | Chemical Reviews,
Iron Catalysis in Organic Synthesis: A Critical Assessment of What It Takes To Make This Base Metal a Multitasking Champion

 

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TRIHYDRIDOSILYL-TERMINATED POLYSILANES AND METHODS OF PREPARATION

Novel trihydridosilyl-terminated polysilanes and methods for their synthesis, which are applicable to other polysilanes, are provided. The synthetic methods provide for facile preparation of products with minimal handling of pyrophoric intermediates and byproducts. The novel compounds contain at least three silicon-silicon bonds and at least one terminal silicon atom having three hydrogen substituents.

TRIHYDRIDOSILYL-TERMINATED POLYSILANES AND METHODS OF PREPARATION

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Reference£º
Iron Catalysis in Organic Synthesis | Chemical Reviews,
Iron Catalysis in Organic Synthesis: A Critical Assessment of What It Takes To Make This Base Metal a Multitasking Champion

 

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In heterogeneous catalysis, the catalyst is in a different phase from the reactants. Application In Synthesis of 1,1′-Ferrocenedicarboxaldehyde, At least one of the reactants interacts with the solid surface in a physical process called adsorption in such a way. 1271-48-3, name is 1,1′-Ferrocenedicarboxaldehyde. In an article£¬Which mentioned a new discovery about 1271-48-3

A simple method for desymmetrizing 1,1?-ferrocenedicarboxaldehyde

A simple chromatography-free method for desymmetrizing ferrocene is described starting from the readily available dialdehyde. Oxidation of 1,1?-ferrocenedicarboxaldehyde in a water/acetonitrile mixture with KMnO4 produced 1?-formyl-ferrocenecarboxylic acid. The same reaction carried out in a water/acetone mixture produced 1?-[(E)-3-oxo- but-1-enyl]-ferrocenecarboxylic acid.

A simple method for desymmetrizing 1,1?-ferrocenedicarboxaldehyde

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Reference£º
Iron Catalysis in Organic Synthesis | Chemical Reviews,
Iron Catalysis in Organic Synthesis: A Critical Assessment of What It Takes To Make This Base Metal a Multitasking Champion

 

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The stability of nonporous and macroporous titania thin films in aqueous electrolyte solutions

A simple electrochemical approach was used to evaluate the stability and porosity of titania and silica thin films spin coated on electrode surfaces. This approach involved monitoring the magnitude of the Faradaic current of diffusing redox probes at the modified electrode surfaces over the course of a week to 4.5 months. Relatively nonporous films were examined as well as films templated with polystyrene latex spheres. The results show that templated titania films were significantly more porous compared to non-templated films. After the defect sites in the templated films were blocked, their long-term stability in aqueous electrolyte was evaluated. For titania, blocking was done by spin coating a dilute titania sol on the top of the film whereas for silica, the film was soaked in octyltrimethoxysilane. Both types of titania films (templated and non-templated) were found to be significantly more stable than the corresponding silica films, showing no signs of deterioration in simple electrolyte solutions during the entire evaluation period. In contrast, silica films showed significant deterioration in as little as 3 days. The enhanced stability of the titania films relative to silica films in near neutral electrolyte solutions was attributed to the differences in the point of zero charge of the oxide films.

The stability of nonporous and macroporous titania thin films in aqueous electrolyte solutions

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Reference£º
Iron Catalysis in Organic Synthesis | Chemical Reviews,
Iron Catalysis in Organic Synthesis: A Critical Assessment of What It Takes To Make This Base Metal a Multitasking Champion

 

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Synthesis of mono and doubly alkynyl substituted ferrocene and its crystal engineering using -C-H¡¤¡¤¡¤O supramolecular synthon

Mono and doubly alkynyl substituted ferrocene complexes, [Fc(CH2OCH2C{triple bond, long}CH)n], 2-3 (2: n = 1; 3: n = 2; Fc = ferrocene) have been synthesized from the room temperature reaction of mono and 1,1?-dihydroxymethyl ferrocene, Fc(CH2OH)n, 1a-b (1a: n = 1; 1b: n = 2) and propargyl bromide, in modest to good yields. These new ferrocene derivatives have been characterized by mass, IR, 1H, 13C NMR spectroscopy, and molecular structures of compound 2 and 3 were unequivocally established by single crystal X-ray diffraction study. The crystal structure analysis revealed that 2 and 3 consist of infinite 1D zig-zag hydrogen bonded chains and 2D microporous hydrogen bonded network of molecules, linked by intermolecular C-H¡¤¡¤¡¤O hydrogen bonding. The molecular structures of both 2 and 3 are further stabilized by C-H¡¤¡¤¡¤pi interactions.

Synthesis of mono and doubly alkynyl substituted ferrocene and its crystal engineering using -C-H¡¤¡¤¡¤O supramolecular synthon

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Reference£º
Iron Catalysis in Organic Synthesis | Chemical Reviews,
Iron Catalysis in Organic Synthesis: A Critical Assessment of What It Takes To Make This Base Metal a Multitasking Champion