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Influence of the structure of nonionic surfactants and the length of alkyl substituents of calix[4]resorcinarenes on their solubility, acid-base, and complexation propertiesRegularities of solubilization of calix[4]resorcinarenes (H8L) with the variable length

Influence of the structure of nonionic surfactants and the length of alkyl substituents of calix[4]resorcinarenes on their solubility, acid-base, and complexation propertiesRegularities of solubilization of calix[4]resorcinarenes (H8L) with the variable length

Atmospheric and high pressure ene reaction of norbornene with 4-phenyl-3H-1,2,4-triazole-3,5(4H)-dione of norbornene with 4-phenyl-3H-1,2,4-triazole-3,5(4H)-dione in toluene, which is accompanied by Wagner

Ene reaction of 4-phenyl-3H-1,2,4-triazole-3,5(4H)-dione with dicyclopentadiene-phenyl-3H-1,2,4-triazole-3,5(4H)-dione in benzene, toluene, acetonitrile, 1,2-dichloroetane

pH-driven variation of the outer-sphere binding mode of cis-[Co(Ad)(en)2Cl]Cl (en-ethylendiamine, ad-adeninate) with p-sulfonatothiacalix[4]arene-sulfonatothiacalix[4]arene (STCA) to study the inclusion complex formation at wide range of pH 2-10. It was shown by 1H

Ene Reaction of β-Pinene with 4-Phenyl-3H-1,2,4-triazole-3,5(4H)-dione: Effects of Temperature, High Pressure, and Solvent Nature pressure on the rate of the ene reaction of 4-phenyl-3H-1,2,4-triazole-3,5(4H)-dione with β-pinene have

Atmospheric and high pressure ene reaction of norbornene with 4-phenyl-3H-1,2,4-triazole-3,5(4H)-dione of norbornene with 4-phenyl-3H-1,2,4-triazole-3,5(4H)-dione in toluene, which is accompanied by Wagner

Ene reaction of 4-phenyl-3H-1,2,4-triazole-3,5(4H)-dione with dicyclopentadiene-phenyl-3H-1,2,4-triazole-3,5(4H)-dione in benzene, toluene, acetonitrile, 1,2-dichloroetane

[2π + 2π]-Cycloaddition of biadamantylidene to 4-phenyl-3H-1,2,4-triazole-3,5(4H)-dione. Effects of temperature, high pressure, and solvent pressure on the rate of the reaction of biadamantylidene with 4-phenyl-3H-1,2,4-triazole-3,5(4H)-dione have

Aggregation and counter ion binding ability of sulfonatomethylcalix[4] resorcinarenes in aqueous solutions1H NMR spectroscopy, 1H NMR spin-lattice relaxation, conductivity and pH-metric titration data have

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