Tag: M.W:200-300

Related Products of 14098-44-3, An article , which mentions 14098-44-3, molecular formula is C14H20O5. The compound – Benzo-15-crown-5 played an important role in people’s production and life.

Two ditopic uranyl salophen receptors with benzo-15-crown-5 and benzo-18-crown-6 units (R1 and R2, respectively) have been synthesized from commercially available starting materials. Comprehensive studies on the solid-state ion pair complexation with various alkali and ammonium halides have been conducted. From the 19 obtained solid-state structures (6 structures with R1, 13 structures with R2), three general interaction motifs I-III have been observed. Interaction motif I has a separated ion pair with the cation coordinated to the crown ether unit, and the anion or oxygen containing solvent molecule coordinated to the uranyl center. The interaction motif II manifests a polymeric structure with a contact ion pair between the uranyl-coordinated anion and cation coordinated in the crown ether in the adjacent receptor. Interaction motif III consists of a more general stacked packing structure of the receptors with or without ion pairs. From the obtained solid-state structures, the complex R2·NaI shows an interesting formation of infinite coordination polymeric structure where the crown ether complexed sodium cations and the O=U=O units of the adjacent receptors form a nearly linear 1-D chains. In the course of this work also the first solid-state structure of uranyl salophen acetate complex was obtained (R2·KAcO).

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Chiral Catalysts,
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14098-44-3, Name is Benzo-15-crown-5, molecular formula is C14H20O5, belongs to chiral-catalyst compound, is a common compound. In a patnet, once mentioned the new application about 14098-44-3, Recommanded Product: Benzo-15-crown-5

Nanocomposites of benzo 15-crown-5 ether substituted oligo phenylene vinylene (CE-OPV) were prepared by solution intercalation into a surface treated bentone clay, B34, in both the presence and absence of Eu3+ ions, and were characterized using X-ray diffraction (XRD) and fluorescence techniques. The intercalation of B34 by CE-OPV increases the d-spacing (gallery height) of B34, the increase being more in the presence of metal ion than in its absence. The increase in d-spacing of a related material, poly[1,4,-(2,5-bis (tetra ethylene oxide substituted)) phenylene vinylene (EO-PPV)] due to intercalation into clay is greater than that by CE-OPV. Results on intercalation of small benzo-crown ether molecules themselves into B34 in the presence and absence of Eu3+, are also presented to help elucidate the process. The fluorescence emission maxima of the nanocomposites of CE-OPV, CE-OPV-Eu 3+ and EO-PPV showed a steady blue shift as a function of B34 composition and the results are explained in terms of partial intercalation of the fluorophores into the clay.

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Chiral Catalysts,
Chiral catalysts – SlideShare

In an article, published in an article, once mentioned the application of 14098-44-3, Name is Benzo-15-crown-5,molecular formula is C14H20O5, is a conventional compound. this article was the specific content is as follows.SDS of cas: 14098-44-3

The present paper reports the crystal structure and luminescent properties of bis(benzo-15-crown-5)europium(II) diperchlorate. The structure is composed of complex bis(benzo-15-crown-5)europium(II) cations and perchlorate anions. The complex cation is centrosymmetric, and the metal ion is surrounded by 10 oxygen atoms of two ligand molecules. The compound shows very bright luminescence at 23450 cm-1. The emission parameters (wavelength and the average lifetime of the excited state) are compared to those previously reported for the analogous complex in methanol solutions. Wiley-VCH Verlag GmbH, 69451 Weinheim, Germany, 2002.

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Reference：
Chiral Catalysts,
Chiral catalysts – SlideShare

The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.94-91-7, Name is N,N’-Bis(salicylidene)-1,2-propanediamine, molecular formula is C17H18N2O2. In a Article，once mentioned of 94-91-7, Application In Synthesis of N,N’-Bis(salicylidene)-1,2-propanediamine

The composition and structure of the mononuclear Pt(II) complexes with N,N?-bis(salicylidene)-ethylenediamine (salen) and polymers on its basis were studied by X-ray photoelectron spectroscopy. The Pt(salen) polymer contains platinum in two oxidation states Pt(II) and Pt(IV), and the atomic Pt(II)/Pt(IV) ratio depends on the conditions of the electrochemical synthesis. The presence of platinum in different oxidation states previews the exchange character of the bonds between metal centers and the reversibility of the reaction 2Pt(III) ? Pt(II) + Pt(IV). The supporting electrolyte – tetrabuthylammonium perchlorate (Bu4NClO4) – stabilizes the electrically excited complex [Pt(III)(salen)]-. This complex, formed as a result of electron transfer from Pt(II) onto the ligand, is the central component of the processes taking place upon the synthesis of Pt(salen) polymers and determines their unique photochemical properties. A redox reaction mechanism in the electrode-polymer-electrolytic medium system with the initial mononuclear complex is suggested.

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Reference：
Chiral Catalysts,
Chiral catalysts – SlideShare

33100-27-5, Name is 1,4,7,10,13-Pentaoxacyclopentadecane, molecular formula is C10H20O5, belongs to chiral-catalyst compound, is a common compound. In a patnet, once mentioned the new application about 33100-27-5, Computed Properties of C10H20O5

Addition of 15-crown-5 to [GdF(AsF6)2], both dissolved in liquid SO2, and crystallisation at -30C has led to the isolation of the tetranuclear ionic complex [Gd4F7(15-crown-5) 4][AsF6]5·6SO2 which is stable up to -10C where SO2 loss leads to loss of crystallinity. The Royal Society of Chemistry 2005.

Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law.Computed Properties of C10H20O5. In my other articles, you can also check out more blogs about 33100-27-5

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Chiral Catalysts,
Chiral catalysts – SlideShare

The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.94-91-7, Name is N,N’-Bis(salicylidene)-1,2-propanediamine, molecular formula is C17H18N2O2. In a Article，once mentioned of 94-91-7, category: chiral-catalyst

Six boron compounds have been synthesized through the combination of phenylboronic acid and various Salen (N,N?-ethylenebis(2-hydroxy)benzylidenimine) ligands. They contain seven- and eight-membered heterocycles with a bridging oxygen and have the formula: L[(PhB)2(mu-O)] (L= Acmen (1), Salen(tBu) (2), Sal(2-OH)pen (3), Salpen(tBu) (4), Acpen (5) and L[B2(mu-O)(O2BPh)] (L = Acen (6), Salmen (7)). Compounds 6 and 7 are interesting trinuclear boron derivatives with two four-coordinate and one three-coordinate boron atoms. The compounds have been characterized by MP, MS, IR, EA and 1H- and 11B-NMR, by 11B-MAS for 6 and 7 and by X-ray crystallography for 2, 4-7.

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Chiral Catalysts,
Chiral catalysts – SlideShare

A catalyst don’t appear in the overall stoichiometry of the reaction it catalyzes, but it must appear in at least one of the elementary reactions in the mechanism for the catalyzed reaction. 4488-22-6, Name is [1,1′-Binaphthalene]-2,2′-diamine, molecular formula is C20H16N2. In a Patent，once mentioned of 4488-22-6, Application In Synthesis of [1,1′-Binaphthalene]-2,2′-diamine

In one aspect, the present disclosure provides diaryl compounds of the formula presented herein. The application also provides compositions and methods of treatment thereof. In some embodiments, these compounds are used in the treatment of bacterial infections or in the treatment of cancer.

Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law.Application In Synthesis of [1,1′-Binaphthalene]-2,2′-diamine. In my other articles, you can also check out more blogs about 4488-22-6

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Chiral Catalysts,
Chiral catalysts – SlideShare

Related Products of 23190-16-1. Let’s face it, organic chemistry can seem difficult to learn. Especially from a beginner’s point of view. Like 23190-16-1, Name is (1R,2S)-(−)-2-Amino-1,2-diphenylethanol. In a document type is Article, introducing its new discovery.

A series of chiral sulfamide-amine alcohols (SAA) (1-6) has been easily synthesized from commercially available chiral amino alcohols. In the absence of Ti(OiPr)4, ligand 4 catalyzed the asymmetric addition of diethylzinc to aromatic aldehydes with moderate to good yields and enantioselectivities.

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Reference：
Chiral Catalysts,
Chiral catalysts – SlideShare

Application of 33100-27-5, An article , which mentions 33100-27-5, molecular formula is C10H20O5. The compound – 1,4,7,10,13-Pentaoxacyclopentadecane played an important role in people’s production and life.

The reaction between 1-phenyl-tetrazole-5-thione (1) and the metal hydroxides MOH (M = Li, Na, K, Rb, Cs) in the presence of crown ethers led to the alkali metal complexes, [Li(15-crown-5)(SCN4Ph)] (2), [Na(15-crown-5)(SCN4Ph)] (5), [K(18-crown-6)(SCN4Ph)] (4), [Rb(18-crown-6)(SCN4Ph)] (5), [Cs(15-crown-5)2][SCN4Ph] (6), [{Cs(15-crown-5)(SCN4Ph)}] (6a), [Cs(18-crown-6)(SCN4Ph)] (7), [Cs(dibenzo-24-crown-8)(SCN4Ph)] (8) and [Cs2(dibenzo-24-crown-8)3(SCN4Ph)2] (8a). Compounds 2?8 were characterized by physical and analytical methods. X-ray diffraction studies performed on these compounds reveal that crown ether moiety precludes the ionic lattice formation. The tetrazole anion coordinates to the metal cation in a bidentate N,S fashion in 3?5 with the formation of a four-membered MSCN ring, whereas in 2, monodentate coordination through a N atom is observed. In contrast, cesium complexes 6, 6a, 7, 8 and 8a show a variety of structural arrangements including monomeric, dimeric and polymeric species, depending on the size of crown ether employed.

I hope this article can help some friends in scientific research. I am very proud of our efforts over the past few months and hope to 33100-27-5, help many people in the next few years., Application of 33100-27-5

Reference：
Chiral Catalysts,
Chiral catalysts – SlideShare

The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.33100-27-5, Name is 1,4,7,10,13-Pentaoxacyclopentadecane, molecular formula is C10H20O5. In a Article，once mentioned of 33100-27-5, COA of Formula: C10H20O5

The complexes between lysine-containing peptides (M) and crown ethers (CEs, 18C6, 15C5, 12C4) have been studied by the electrospray ionization (ESI) mass spectrometry. The maximum number of CEs attached has been found to be the same as that of the alkyl-amino side chains of lysine and as that of the protons attached. Examination of the breakdown plots of the abundances of the ions observed against the cone voltage (CV) has shown that mass spectrometric fragmentation pathways of [M + nH + (CE)n]+n may involve a loss of a neutral CE molecule as well as protonated one. The decrease in the CE cavity (the use of 12C4 or 15C5 instead of 18C6) leads to a dramatic lowering in the stability of the complexes in the gas phase but not in solution. Attachment of a CE to peptides increases their hydrophobicity, and therefore proceeds with lower efficiency in water than in methanol. Copyright

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Reference：
Chiral Catalysts,
Chiral catalysts – SlideShare