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Эта публикация цитируется в 4 научных статьях (всего в 4 статьях)
The reactivity of calyx[4]resorcinolarene anions towards p-nitrophenyl esters of tetracoordinated phosphorus acids
I. S. Ryzhkinaa, L. A. Kudryavtsevaa, E. Kh. Kazakovaa, A. R. Burilova, A. I. Konovalovb a A.E. Arbuzov Institute of Organic and Physical Chemistry, FRC Kazan Scientific Center of the Russian Academy of Sciences, Kazan, Russian Federation
b Alexander Butlerov Institute of Chemistry, Kazan Federal University, Kazan, Russian Federation
Аннотация:
The results of a kinetic study have shown that the reactivity of monomeric forms of amphiphilic tetra- ([H4L]4–) and octa- ([L]8–) anions of calyx[4]resorcinolarenes (H8L) towards p-nitrophenyl esters of tetracoordinated phosphorus acids in aqueous dimethylformamide (50 vol.% of DMF) is determined by the nucleophilic centres of the anions, whereas an increase in the concentration of H8L inhibits the process, which is due to the formation of aggregates.
Образец цитирования:
I. S. Ryzhkina, L. A. Kudryavtseva, E. Kh. Kazakova, A. R. Burilov, A. I. Konovalov, “The reactivity of calyx[4]resorcinolarene anions towards p-nitrophenyl esters of tetracoordinated phosphorus acids”, Mendeleev Commun., 7:3 (1997), 88–90
Образцы ссылок на эту страницу:
https://www.mathnet.ru/rus/mendc4797 https://www.mathnet.ru/rus/mendc/v7/i3/p88
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