Category: 63295-48-7

Sabenya, Gerard; Lazaro, Laura; Gamba, Ilaria; Martin-Diaconescu, Vlad; Andris, Erik; Weyhermuller, Thomas; Neese, Frank; Roithova, Jana; Bill, Eckhard; Lloret-Fillol, Julio; Costas, Miquel published an article about the compound: Iron(III) trifluoromethanesulfonate( cas:63295-48-7,SMILESS:O=S(C(F)(F)F)([O-])=O.O=S(C(F)(F)F)([O-])=O.O=S(C(F)(F)F)([O-])=O.[Fe+3] ).HPLC of Formula: 63295-48-7. Aromatic heterocyclic compounds can be classified according to the number of heteroatoms or the size of the ring. The authors also want to convey more information about this compound (cas:63295-48-7) through the article.

Iron complex [FeIII(N3)(MePy2tacn)](PF6)2 (1), containing a neutral triazacyclononane-based pentadentate ligand, and a terminally bound azide ligand has been prepared and spectroscopically and structurally characterized. Structural details, magnetic susceptibility data, and Mossbauer spectra demonstrate that 1 has a low-spin (S = 1/2) ferric center. X-ray diffraction anal. of 1 reveals remarkably short Fe-N (1.859 Å) and long FeN-N2 (1.246 Å) distances, while the FT-IR spectra show an unusually low N-N stretching frequency (2019 cm-1), suggesting that the FeN-N2 bond is particularly weak. Photolysis of 1 at 470 or 530 nm caused N2 elimination and generation of a nitrido species that on the basis of Mossbauer, magnetic susceptibility, EPR, and X-ray absorption in conjunction with d. functional theory computational analyses is formulated as [FeV(N)(MePy2tacn)]2+ (2). Results indicate that 2 is a low-spin (S = 1/2) iron(V) species, which exhibits a short Fe-N distance (1.64 Å), as deduced from extended X-ray absorption fine structure anal. Compound 2 is only stable at cryogenic (liquid N2) temperatures, and frozen solutions as well as solid samples decompose rapidly upon warming, producing N2. However, the high-valent compound could be generated in the gas phase, and its reactivity against olefins, sulfides, and substrates with weak C-H bonds studied. Compound 2 proved to be a powerful two-electron oxidant that can add the nitrido ligand to olefin and sulfide sites as well as oxidize cyclohexadiene substrates to benzene in a formal H2-transfer process. In summary, compound 2 constitutes the first case of an octahedral FeV(N) species prepared within a neutral ligand framework and adds to the few examples of FeV species that could be spectroscopically and chem. characterized.

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The three-dimensional configuration of the ester heterocycle is basically the same as that of the carbocycle. Compound: Iron(III) trifluoromethanesulfonate(SMILESS: O=S(C(F)(F)F)([O-])=O.O=S(C(F)(F)F)([O-])=O.O=S(C(F)(F)F)([O-])=O.[Fe+3],cas:63295-48-7) is researched.Related Products of 600-05-5. The article 《Synthesis, characterization, and crystal structures of 2-[(3-chloropyridin-2-yl)hydrazonemethyl]-6-ethoxyphenol and its iron(III) complex》 in relation to this compound, is published in Inorganic and Nano-Metal Chemistry. Let’s take a look at the latest research on this compound (cas:63295-48-7).

A new Schiff base 2-[(3-chloropyridin-2-yl)hydrazonemethyl]-6-ethoxyphenol (HL) and its new iron(III) complex were synthesized and characterized by elemental anal., IR spectra, and single-crystal x-ray determination The Schiff base was crystallized in the triclinic space group P1_, and the complex was crystallized in the monoclinic space group Cc. The particular interest is to study the coordination behavior of the Schiff base with iron. Single-crystal X-ray diffraction indicated that the Schiff base ligand coordinates to the Fe atom through the phenolate O, imine N, and pyridine N atoms. The asym. unit of the Schiff base contains two Schiff base mols. and one methanol mol. The asym. unit of the complex contains two mononuclear iron(III) complex cations and two trifluoromethylsulfate anions. The Fe atom is six-coordinated in an octahedral geometry. The coordination of the Schiff base to the Fe atom is also reflected in the IR spectra. Crystal structures of the compounds are stabilized by hydrogen bonds.

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The chemical properties of alicyclic heterocycles are similar to those of the corresponding chain compounds. Compound: Iron(III) trifluoromethanesulfonate, is researched, Molecular C3F9FeO9S3, CAS is 63295-48-7, about A bioinspired iron catalyst for nitrate and perchlorate reduction, the main research direction is bioinspired iron catalyst nitrate perchlorate reduction water wastewater.Synthetic Route of C3F9FeO9S3.

Nitrate and perchlorate have considerable use in technol., synthetic materials, and agriculture; as a result, they have become pervasive water pollutants. Industrial strategies to chem. reduce these oxyanions often require the use of harsh conditions, but microorganisms can efficiently reduce them enzymically. We developed an Fe catalyst inspired by the active sites of nitrate reductase and (per)chlorate reductase enzymes. The catalyst features a secondary coordination sphere that aids in oxyanion deoxygenation. Upon reduction of the oxyanions, an Fe(III)-oxo is formed, which in the presence of protons and electrons regenerates the catalyst and releases water.

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SDS of cas: 63295-48-7. The fused heterocycle is formed by combining a benzene ring with a single heterocycle, or two or more single heterocycles. Compound: Iron(III) trifluoromethanesulfonate, is researched, Molecular C3F9FeO9S3, CAS is 63295-48-7, about Fe(OTf)3 versus Bi(OTf)3 as Mild Catalysts in Epoxide Oxidative Ring-Opening, Urea α-Diketone Condensation, and Glycoluril Diether Synthesis. Author is Mandadapu, Vijaybabu; Wu, Feng; Day, Anthony I..

The salt Fe(OTf)3 has been shown to function as an effective catalyst in three different reactions, epoxide oxidative ring-opening to an α-hydroxy ketone, urea α-diketone condensation to form glycolurils, and glycoluril diether synthesis by formaldehyde condensation. In each of these reactions, Fe(OTf)3 was compared to Bi(OTf)3, a viable alternative catalyst with few or no prior examples of this type. Differences and advantages are highlighted but in most cases yields were generally high, and both catalysts outperformed conventional acid catalyzed methods.

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Related Products of 63295-48-7. Aromatic compounds can be divided into two categories: single heterocycles and fused heterocycles. Compound: Iron(III) trifluoromethanesulfonate, is researched, Molecular C3F9FeO9S3, CAS is 63295-48-7, about Solution processed intrinsically conductive polymer films with high thermoelectric properties and good air stability. Author is Yao, Hongyan; Fan, Zeng; Li, Pengcheng; Li, Bichen; Guan, Xin; Du, Donghe; Ouyang, Jianyong.

It is important to study thermoelec. (TE) materials because they can directly convert heat into electricity. Although intrinsically conducting polymers have the advantages of nontoxicity, low cost, high mech. flexibility and low thermal conductivity, their thermoelec. properties must be significantly improved for practical application. Here, we report a solution-processed conducting polymer, poly(3,4-ethylenedioxythiophene):trifluoromethanesulfonate (PEDOT:OTf), with very high TE properties. As-prepared PEDOT:OTf films from their precursor solution can exhibit a power factor of 346 ± 39 μW m-1 K-2. The power factor can be further enhanced by a post treatment with NaOH or a reducing agent like glucose or ascorbic acid. The NaOH treatment can give rise to a power factor of 568 ± 64 μW m-1 K-2 with a Seebeck coefficient of 49.2 ± 1.4 μV K-1 and an elec. conductivity of 2342 ± 98 S cm-1. This power factor is higher than those obtained by treatment with the reducing agents. The different power factors by NaOH and reducing agent treatments are attributed to their different effects on the doping. The NaOH treatment can remove the protonic doping while the reducing agents can lower the normal oxidation level of PEDOT. The charge carriers due to protonic acid doping have lower energy, and thus the removal of protonic acid doping can significantly enhance the Seebeck coefficient while not lowering the elec. conductivity too much.

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Name: Iron(III) trifluoromethanesulfonate. The fused heterocycle is formed by combining a benzene ring with a single heterocycle, or two or more single heterocycles. Compound: Iron(III) trifluoromethanesulfonate, is researched, Molecular C3F9FeO9S3, CAS is 63295-48-7, about Synthesis of Trifluoromethyl- and Ester Group-Substituted α-Carbolines via Iron-Catalyzed Tandem Cyclization Reaction. Author is Xu, Yumin; Chen, Xiaoqian; Gao, Yiqin; Yan, Zicong; Wan, Changfeng; Liu, Jin-Biao; Wang, Zhiyong.

An efficient approach to prepare trifluoromethyl-α-carbolines and ester group-substituted α-carbolines via the tandem cyclization reaction of 2-(2-aminophenyl)acetonitriles and trifluoromethyl 1,3-diones or β,γ-unsaturated α-ketoesters is reported. The transformation proceeded smoothly in the presence of catalytic environmental-benign iron salts, which were used to prepare the desired products in moderate to good yields.

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The chemical properties of alicyclic heterocycles are similar to those of the corresponding chain compounds. Compound: Iron(III) trifluoromethanesulfonate, is researched, Molecular C3F9FeO9S3, CAS is 63295-48-7, about S to O and O to S linkage isomerization in sulfoxide complexes of pentaammineruthenium, the main research direction is linkage isomerization kinetics ruthenium sulfoxide; ammine ruthenium DMSO linkage isomerism; aquation isomerization kinetics ruthenium DMSO; reduction potential ruthenium linkage isomer.Synthetic Route of C3F9FeO9S3.

When Ru(NH3)5(Me2SO)2+ is oxidized to the 3+ state, S → O isomerization takes place at a specific rate of (7.0 ± 0.5) × 10-2 s-1 (24 × 10-2 s-1 for the methioninesulfonate complex). Aquation is quite slow, kaq being 7.7 × 10-5 s-1 (6.2 × 10-5 s-1). On reduction to the 2+ state, O → S isomerization takes place, the values of kism being 30 ± 7 s-1 (99 ± 7 s-1). Aquation accompanies isomerization in the 2+ species and kaq ≈ 10 s-1 (30 s-1). The shift from the S- to the O-bound form changes the 3+/2+ reduction potential from 1.0 to 0.01 V.

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Synthetic Route of C3F9FeO9S3. So far, in addition to halogen atoms, other non-metallic atoms can become part of the aromatic heterocycle, and the target ring system is still aromatic. Compound: Iron(III) trifluoromethanesulfonate, is researched, Molecular C3F9FeO9S3, CAS is 63295-48-7, about One-pot solvent-free synthesis of quinolines by C-H activation/C-C Bond formation catalyzed by recyclable iron(III) triflate.

A novel application of highly stable Fe(OTf)3 as an efficient catalyst for a carbon-carbon bond formation by the activation of a terminal alkyne carbon-hydrogen (C-H) bond under solvent-free reaction conditions is described. Notably, this protocol of green synthesis (green chem.), which produced quinolines by a reaction of amines, aldehydes and terminal aryl alkynes, shows attractive characteristics including concise one-pot reaction conditions, high atom economy, very limited energy consumption and the sequential catalytic process requires only a catalytic (5 mol%) amount of Fe(OTf)3 and short reaction time. Meanwhile, the catalyst was easily recovered from the reaction system and reused smoothly with only a little loss of activity. The synthesis of the target compounds was achieved using (aryl)alkynes, aryl aldehydes and aryl amines as starting materials. The title compounds thus formed included 2,4-diphenylquinoline, 2-(2,4-dichlorophenyl)-6-methyl-4-phenylquinoline (I), the crystal structure of which was determined, and 6-methyl-4-phenyl-2-(2-thienyl)quinoline, etc.

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Application In Synthesis of Iron(III) trifluoromethanesulfonate. The mechanism of aromatic electrophilic substitution of aromatic heterocycles is consistent with that of benzene. Compound: Iron(III) trifluoromethanesulfonate, is researched, Molecular C3F9FeO9S3, CAS is 63295-48-7, about Vapor phase synthesized poly(3,4-ethylenedioxythiophene)-trifluoromethanesulfonate as a transparent conductor material. Author is Brooke, Robert; Franco-Gonzalez, Juan Felipe; Wijeratne, Kosala; Pavlopoulou, Eleni; Galliani, Daniela; Liu, Xianjie; Valiollahi, Roudabeh; Zozoulenko, Igor V.; Crispin, Xavier.

Inorganic transparent conductive oxides have dominated the market as transparent electrodes due to their high conductivity and transparency. Here, we report the fabrication and optimization of the synthesis of poly(3,4-ethylenedioxythiophene) trifluoromethanesulfonate via vapor phase polymerization for the potential replacement of such inorganic materials. The parameters and conditions of the polymerization were investigated and an elec. conductivity of 3800 S cm-1 and 4500 S cm-1 after acid treatment were obtained while maintaining an absorbance similar to that of com. indium tin oxide. This increase in elec. conductivity was rationalized exptl. and theor. to an increase in the oxidation level and a higher order of crystallinity which does not disrupt the π-π stacking of PEDOT chains.

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Most of the compounds have physiologically active properties, and their biological properties are often attributed to the heteroatoms contained in their molecules, and most of these heteroatoms also appear in cyclic structures. A Journal, European Journal of Organic Chemistry called Highly Selective Formation of β-Glycosides of N-Acetylglucosamine Using Catalytic Iron(III) Triflate, Author is Stevenin, Arnaud; Boyer, Francois-Didier; Beau, Jean-Marie, which mentions a compound: 63295-48-7, SMILESS is O=S(C(F)(F)F)([O-])=O.O=S(C(F)(F)F)([O-])=O.O=S(C(F)(F)F)([O-])=O.[Fe+3], Molecular C3F9FeO9S3, Product Details of 63295-48-7.

Efficient and highly selective glycosylation reactions of peracetylated β-D-N-acetylglucosamine are described using catalytic iron(III) triflate and 2,4,6-tri-tert-butylpyrimidine (TTBP) under microwave conditions. We have demonstrated that the formation of β-(1→6) and β-(1→3) linked disaccharides are obtained in high yields in the presence of various protecting groups.

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Piperidine – Wikipedia,
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