Some scientific research about Dibenzo-18-crown-6

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14187-32-7, Name is Dibenzo-18-crown-6, molecular formula is C20H24O6, belongs to chiral-catalyst compound, is a common compound. In a patnet, once mentioned the new application about 14187-32-7, Application In Synthesis of Dibenzo-18-crown-6

A new method is developed for the sulfonation of benzocrown ethers with potassium sulfate in polyphosphoric acid. The reaction takes place spontaneously and gives high yields of the sulfonic acids.

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Reference:
Chiral Catalysts,
Chiral catalysts – SlideShare

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A new chemosensor, 2,3,15,16-tetrakis(pyridin-2-yl)-7,8,10,11,20,21,23,24- octahydro[1,4,7,10,13,16]hexaoxacyclooctadecino[2,3-g:11,12-g?] diquinoxaline (1), containing 2,3-bis(pyridin-2-yl)quinoxaline and crown ether moieties, has been designed and found to be a ratiometric and selective fluorescent detector of Zn2+ over a wide range of tested metal ions. The addition of Zn2+ to the solution of 1 in acetonitrile induced the formation of a 1:2 ligand-metal complex, 1-Zn2+, which exhibits a remarkable enhanced fluorescent emission centered at 460 nm, with the disappearance of the fluorescent emission of 1 centered at 396 nm due to the mechanism of internal charge transfer. In contrast, the presence of K + results in the fluorescence quenching of 1 and 1-Zn2+ through the photoinduced electron-transfer mechanism. These results demonstrate that 1 can perform as not only an INHIBIT logic gate but also an “off-on-off” molecular switch triggered by Zn2+ and K +. The structure of complex 1-Zn2+ has been characterized by single-crystal X-ray crystallography, mass spectrometry, and 1H NMR titration experiments. Density functional theory calculation results on 1 and the 1-Zn2+ complex are well consistent with the experimental results.

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Reference:
Chiral Catalysts,
Chiral catalysts – SlideShare

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In 1967 Pedersen described dibenzo-18-crown-6 (1).We report the preparation of its isomeric dihydroxy derivatives 2c and 3c.Nitration of 1 in acetic acid and chloroform yields the dinitro compounds 2a and 3a. 2a and 3a have different solubility in ethylene glycol monomethyl ether and can be separated.Catalytic reduction of the dinitro derivatives with hydrazine and Raney nickel leads to the diamines 2b and 3b.The diazonium salts of 2b and 3b are heated in dilute sulfuric acid and yield the phenols 2c and 3c. – Key words: Dibenzo-18-crown-6, Isomeric Dihydroxy Derivatives

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Reference:
Chiral Catalysts,
Chiral catalysts – SlideShare

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Several new K and Hg(II) complexes derived from crown ethers (DC18C6, DB18C6) have been prepared by tribochemistry reactions. The isolated solid complexes have been characterized by I.R. spectral measurements. The isolated solid complexes are compared with the corresponding metal complexes prepared in solution. Also, the IR and NMR spectra of the solid complexes have been used to determine the strength of bond between Hg(II) ion and the crown ether.

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Reference:
Chiral Catalysts,
Chiral catalysts – SlideShare

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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. 14187-32-7, Name is Dibenzo-18-crown-6, molecular formula is C20H24O6. In a Article,once mentioned of 14187-32-7, SDS of cas: 14187-32-7

Abstrac: A new complex [K(Db18C6)(THF)] 3 + [Fe(NCS)6]3- ? 0.31 H2O (I) was prepared and studied by X-ray diffraction (space group C2/c, a = 21.954, b = 26.496, c = 15.902 A, beta = 102.24, Z = 4; direct method, leastsquares refinement in the anisotropic approximation to R = 0.098 for 5944 independent reflections; CAD4 automated diffractometer, lambdaMoK alpha). The [Fe(NCS)6]3- anion (on twofold axis) having a slightly distorted octahedral structure is connected by two K-S bonds with two complex cations connected by a twofold axis. Two independent complex cations [K(Db18C6)(THF)]+ are of the host-guest type, one being statistically disordered with respect to the twofold axis with site populations of 0.5. The coordination polyhedra of K+ are a distorted hexagonal bipyramid and pyramid.

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Reference:
Chiral Catalysts,
Chiral catalysts – SlideShare

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The standard enthalpies of combustion of three crown-ethers were determined calorimetrically and their standard enthalpies of formation were calculated.The energy contributions to the standard enthalpies of formation of individual fragments of the crown-ethers were calculated by the method of group contributions.The ring strain energies were evaluated.

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Reference:
Chiral Catalysts,
Chiral catalysts – SlideShare

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A practical, two-step synthesis of crown ether functionalized pyrimidines has been developed. The reaction conditions have been optimized, and the protocol is generalized for series of substrates. These newly synthesized compounds exhibited antimicrobial activity against bacterial strains Staphylcoccus aureus (Gram-positive) and Escherichia coli (Gram-negative). These compounds were also found to be potent antifungal agents Aspergillus niger and Candida albicans strains, respectively.

Sometimes chemists are able to propose two or more mechanisms that are consistent with the available data.Safety of Dibenzo-18-crown-6, If a proposed mechanism predicts the wrong experimental rate law, however, the mechanism must be incorrect.Welcome to check out more blogs about 14187-32-7, in my other articles.

Reference:
Chiral Catalysts,
Chiral catalysts – SlideShare

A new application about Dibenzo-18-crown-6

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The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.14187-32-7, Name is Dibenzo-18-crown-6, molecular formula is C20H24O6. In a Article,once mentioned of 14187-32-7, Application In Synthesis of Dibenzo-18-crown-6

[K(dibenzo-18-crown-6)]+ (KC) cations are used for cocrystallization with manganese halides, producing isostructural single crystals of organic-inorganic hybrid complexes, [K(dibenzo-18-crown-6)]2MnX4 (abbreviated (KC)2MnX4) (X=Cl, Br), which feature one-dimensional (1D) morphology and green phosphorescence with considerable photoluminescence quantum yields (PLQYs) accompanied by excellent optical waveguide behavior with a low loss coefficient. More interestingly, (KC)2MnX4 crystallizes in the monoclinic space group Cc belonging to the achiral point group m (Cs), where the noncentrosymmetric arrangement of racemic units, with right- and left-handed rotating optical axes, endows these achiral single crystals with circularly polarized luminescence (CPL), observed for the first time.

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Reference:
Chiral Catalysts,
Chiral catalysts – SlideShare

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A new synthetic route to the molecular clip with diphenylglycoluril and dibenzo-18-crown-6 using protection-deprotection protocol is proposed. Yield of desired compound has increased from 10-15% to 41%. Starting from 4,5-dibromobenzene-1,2-diol 4,5-dibromodibenzo-18-crown-6 and then tetrabromo-substituted molecular clip were obtained. The target molecular clip was obtained by bromine cleavage by hydrogenolysis. Stability constants were determined by spectrophotometric titration with alkali metal cations and paraquat. Quantum-chemical calculations confirm the assumption of additional stabilization of complex with K+ by pi?pi stacking between the terminal aromatic fragments with formation of a ?pseudocryptand? type structure. The structures of complexes of the molecular clips with paraquat were determined by X-ray crystallography.

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Reference:
Chiral Catalysts,
Chiral catalysts – SlideShare

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Abstract: A new nano-size crown ether-based ionic liquid on the basis of dibenzo-18-crown-6 ([DB-18-C-6K+][OH?] nIL) has been synthesized via a simple procedure and characterized through fourier transform infrared spectroscopy, nuclear magnetic resonance spectroscopy, high-resolution scanning electron microscopy, energy-dispersive X-ray spectroscopy, thermogravimetric/differential thermal analysis, and UV?Vis spectroscopy techniques The obtained catalyst has been utilized for the one-pot, four-component synthesis of spiro[indoline-3,2?-quinoline] derivatives from the combination of isatins, amines, dimedone, and dialkylacetylenedicarboxylates. The advantages of this protocol included the use of common and easily-available starting materials, utilizing ambient temperature, non-toxic and inexpensive reagent usage, high yields of products, and operationally simple procedure.

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Reference:
Chiral Catalysts,
Chiral catalysts – SlideShare