Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Sergey V. Shevchuk"'
Autor:
Hee Kyung Na, Vincent M. Lynch, Jonathan L. Sessler, Chang-Hee Lee, Dong Hoon Won, Won Seob Cho, Dae Wi Yoon, Sergey V. Shevchuk
Publikováno v:
Journal of the American Chemical Society. 125:7301-7306
Three calix[4]pyrroles bearing m-orcinol-derived diether straps of different lengths on one side of the tetrapyrrolic core have been synthesized and characterized. Structural information for an analogous diester bridged strapped system reported previ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d4fcfb0c49369e16d47b5e41e35653a5
https://doi.org/10.1021/ja029175u
https://doi.org/10.1021/ja029175u
Autor:
Yurii V. Korovin, Andrey I. Gren, Ninel A. Nazarenko, Anna M. Turianskaya, Natalia V. Rusakova, Sergey V. Shevchuk
Publikováno v:
Journal of Fluorescence. 8:225-228
New ytterbium complexes with seven calix[4]resorcinarenes containing methoxycarbonyl, methyldiethylamino groups, and bromine as the substituents in the resorcinol ring and methyl or phenyl substituents in the macro ring were synthesized. The absorpti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ae62ced62932ce64c7d431dde19cdf76
https://doi.org/10.1023/a:1022505716725
https://doi.org/10.1023/a:1022505716725
Autor:
Ninel A. Nazarenko, Anna M. Turianskaya, Yurii V. Korovin, Natalia V. Rusakova, Sergey V. Shevchuk, Yurii E. Shapiro, Andrey I. Gren
Publikováno v:
Analytical Communications. 34:201-204
Calix[4]resorcinarenes, 2,8,14,20-tetramethyl- (L 1 ) and 2,8,14,20-tetraphenyl- (L 2 ) 5,11,17,23-tetradiethylamino- methylpentacyclo[19,3,1,1 3,7 ,1 9,13 ,1 15,19 ]octacosa- 1(25),3,5,7(26)9,11,13(27),15,17,19(28),21,23-dodecan- 4,6,10,12,16,18,22,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a5f3b5c7ce780afa7395e94711ef34d1
https://doi.org/10.1039/a703834h
https://doi.org/10.1039/a703834h
Publikováno v:
Polyhedron. 17:145-147
The protonation of 1,4,7,10-tetraazabicyclododecane (L2), 4,7-dioxa 1,10,13,16-tetraazabicyclo[8.8.2]eicosane (L3) and 1,4,7,10,13,16-hexaazabicyclo[8.8.2]eicosane (L7) was studied by potentiometric methods at 18°C and ionic strength of 0.1 (NaClO4)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6e89ed4893040a1f5be86218f7754de2
https://doi.org/10.1016/s0277-5387(97)00251-9
https://doi.org/10.1016/s0277-5387(97)00251-9