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scopus(12)
2,2,3,3′-Tetraphenyl-7,7′-biquinoxaline
ArticleAbstract: In the crystal structure of the title compound, C40H26N4, mol-ecules reside on crystallographic centPalabras claves:Autores:César H. Zambrano, Dueno E.E., Gibson R.J.P., Pike R., Salvatore R.N.Fuentes:scopus2,2′,3,3′-Tetramethyl-6,6′-biquinoxaline
ArticleAbstract: The molecule of the title compound, C 20H 18N 4, has twofold rotational symmetry. Each aromatic ringPalabras claves:Autores:César H. Zambrano, Dueno E.E., Gibson R.J.P., Kass J.P., Pike R., Salvatore R.N.Fuentes:scopus2,8,14,20-Tetra-kis(4-hydroxy-phen-yl)-pyrogallol[4]arene dimethyl-formamide hexa-solvate
ArticleAbstract: The title compound, C52H40O16·6C3H7NO, is shown to adopt a macrocyclic chair conformation. The asymmPalabras claves:Autores:César H. Zambrano, Dueno E.E., Hunter A.D., Ray T.A., Salvatore R.N., Zeller M.Fuentes:scopus2,8,14,20-Tetraphenylpyrogallol[4]arene dimethylformamide octasolvate
ArticleAbstract: The title compound, C52H40O12· 8C3H7NO, contains substituted pyrogallolarene molecules accompanied bPalabras claves:Autores:César H. Zambrano, Dueno E.E., Hunter A.D., Kass J.P., Zeller M.Fuentes:scopus2,8,14,20-para-Methoxy-tetra-phenyl-pyrogallol[4]arene dimethyl-formamide hexa-solvate
ArticleAbstract: The title compound, C56H48O16·6C3H7NO, adopts a macrocyclic chair conformation in the solid state. TPalabras claves:Autores:César H. Zambrano, Dueno E.E., Salvatore R.N., Thomas R., Zeller M.Fuentes:scopus7,8-Dichloro-1,2,3,4-tetra-hydro-phenazine
ArticleAbstract: In the structure of the title compound, C12H10Cl2N2, the cyclo-hexene ring adopts a half-chair confoPalabras claves:Autores:Barger B., César H. Zambrano, Dueno E.E., Gibson R.J.P., Pike R.Fuentes:scopus7,8-Dichloro-2,3-diphenylquinoxaline
ArticleAbstract: The title compound, C20H12Cl2N 2, was synthesized from the reaction of equimolar amounts of 4,5-dichPalabras claves:Autores:César H. Zambrano, Dueno E.E., Fronczek F.R., Gibson R.J.P., Kass J.P.Fuentes:scopusA theoretical study of the conformational preference of alkyl-and aryl-substituted pyrogallol[4]arenes and evidence of the accumulation of negative electrostatic potential within the cavity of their rccc conformers
ArticleAbstract: We report a theoretical study of the structural and electronic properties of the rccc and rctt confoPalabras claves:conformational preference, DFT, Electrostatic potential, Macromolecules, PyrogallolAutores:César H. Zambrano, Dueno E.E., Fernando Javier Torres, Miguel Angel Méndez, Robert A. Cazar, Sebastián ManzanoFuentes:scopusCrystal structure of 2, 8, 14, 20-tert-butylpyrogallol[4]arene
ArticleAbstract: The aromatic derivative 2, 8, 14, 20-tert-butylpyrogallol[4]arene was synthesized by the acid catalyPalabras claves:Crown conformation, Crystal structure, tert-butyl, Pyrogallol[4]areneAutores:César H. Zambrano, Dueno E.E., Hunter A.D., Ray T.A., Salvatore R.N., Zeller M.Fuentes:scopusCrystal structure of 2,8,14,20-tetranaphthylpyrogallol[4]arene
ArticleAbstract: The aromatic derivative 2,8,14,20-tetranaphthylpyrogallol[4]arene was synthesized by the acid catalyPalabras claves:Chair conformation, Crystal structure, Naphthyl, Pyrogallol[4]areneAutores:César H. Zambrano, Dueno E.E., Kass J.P., Ke Y., Zhou H.C.Fuentes:scopus