6 research outputs found
Crystal structure of 25,27-dipropoxy-26,28-dihydroxycalix[4]arene, C\u3csub\u3e34\u3c/sub\u3eH\u3csub\u3e36\u3c/sub\u3eO\u3csub\u3e4\u3c/sub\u3e
New calix[4]arene-based amides - Their synthesis, conformation, complexation
New chiral calix[4]arene-based diol-diamides 1a, 1b, tetraamides 2a, 2b and 7 as well as achiral diamide 3 and tetraamides 4-6 were prepared. The conformation of 1 has been studied in solution by NMR and in solid state by X-ray crystallography. The pinched-cone conformation of the calix[4]arene skeleton in 1 was found to be stabilized by a circular array of hydrogen bonds formed by two phenolic O-H and two amidic N-H bonds at lower rim. Whereas no significant complexation of Na+ was observed in solution for diamides 1 and 3, tetraamides 2, 4, 5, and 6 give strong complexes with Na+ as confirmed by NMR titrations of 2 and 4. The influence of anions and the solvents used on complexation ability of 2 towards Na+ is negligible
New calix[4]arene-based amides - Their synthesis, conformation, complexation
New chiral calix[4]arene-based diol-diamides 1a, 1b, tetraamides 2a, 2b and 7 as well as achiral diamide 3 and tetraamides 4-6 were prepared. The conformation of 1 has been studied in solution by NMR and in solid state by X-ray crystallography. The pinched-cone conformation of the calix[4]arene skeleton in 1 was found to be stabilized by a circular array of hydrogen bonds formed by two phenolic O-H and two amidic N-H bonds at lower rim. Whereas no significant complexation of Na+ was observed in solution for diamides 1 and 3, tetraamides 2, 4, 5, and 6 give strong complexes with Na+ as confirmed by NMR titrations of 2 and 4. The influence of anions and the solvents used on complexation ability of 2 towards Na+ is negligible
New calix[4]arene-based amides - Their synthesis, conformation, complexation
New chiral calix[4]arene-based diol-diamides 1a, 1b, tetraamides 2a, 2b and 7 as well as achiral diamide 3 and tetraamides 4-6 were prepared. The conformation of 1 has been studied in solution by NMR and in solid state by X-ray crystallography. The pinched-cone conformation of the calix[4]arene skeleton in 1 was found to be stabilized by a circular array of hydrogen bonds formed by two phenolic O-H and two amidic N-H bonds at lower rim. Whereas no significant complexation of Na+ was observed in solution for diamides 1 and 3, tetraamides 2, 4, 5, and 6 give strong complexes with Na+ as confirmed by NMR titrations of 2 and 4. The influence of anions and the solvents used on complexation ability of 2 towards Na+ is negligible
New calix[4]arene-based amides - Their synthesis, conformation, complexation
New chiral calix[4]arene-based diol-diamides 1a, 1b, tetraamides 2a, 2b and 7 as well as achiral diamide 3 and tetraamides 4-6 were prepared. The conformation of 1 has been studied in solution by NMR and in solid state by X-ray crystallography. The pinched-cone conformation of the calix[4]arene skeleton in 1 was found to be stabilized by a circular array of hydrogen bonds formed by two phenolic O-H and two amidic N-H bonds at lower rim. Whereas no significant complexation of Na+ was observed in solution for diamides 1 and 3, tetraamides 2, 4, 5, and 6 give strong complexes with Na+ as confirmed by NMR titrations of 2 and 4. The influence of anions and the solvents used on complexation ability of 2 towards Na+ is negligible