Effect of alkyl substitution in 3,3′-Bis(dipyrrin) on chemosensor activity of fluorescent detection of Zn2+ cations
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| 024 | 7 | 0 | |a 10.1134/S107042801508014X |2 doi |
| 035 | |a (NATIONALLICENCE)springer-10.1134/S107042801508014X | ||
| 245 | 0 | 0 | |a Effect of alkyl substitution in 3,3′-Bis(dipyrrin) on chemosensor activity of fluorescent detection of Zn2+ cations |h [Elektronische Daten] |c [N. Dudina, E. Antina, D. Sozonov, A. V'yugin] |
| 520 | 3 | |a New "off-on” Zn2+ fluorescent probes in organic solvents were developed underlain by ligands consisting of deca-, octa-, and tetramethyl-substituted 3,3′-bis(dipyrrins). The coordination of the probes with two Zn2+ ions with the formation of complexes [Zn2L2] is accompanied with a significant (200-550-fold) increase in the fluorescence intensity. The fluorescence response is maximum for the reaction of Zn2+ with tetramethyl-substituted 3,3′-bis(dipyrrin). The presence of cations of Na+, Mg2+, Mn2+, Co2+, Ni2+, Cd2+, Hg2+, and other metals, save Cu2+, does not interfere with the detection of Zn2+ demonstrating the high selectivity of bis(dipyrrin) Zn2+-sensors. | |
| 540 | |a Pleiades Publishing, Ltd., 2015 | ||
| 700 | 1 | |a Dudina |D N. |u Krestov Institute of Solution Chemistry, Russian Academy of Sciences, ul. Akademicheskaya 1, 153045, Ivanovo, Russia |4 aut | |
| 700 | 1 | |a Antina |D E. |u Krestov Institute of Solution Chemistry, Russian Academy of Sciences, ul. Akademicheskaya 1, 153045, Ivanovo, Russia |4 aut | |
| 700 | 1 | |a Sozonov |D D. |u Ivanovo State Chemical Engineering University, Ivanovo, Russia |4 aut | |
| 700 | 1 | |a V'yugin |D A. |u Krestov Institute of Solution Chemistry, Russian Academy of Sciences, ul. Akademicheskaya 1, 153045, Ivanovo, Russia |4 aut | |
| 773 | 0 | |t Russian Journal of Organic Chemistry |d Pleiades Publishing |g 51/8(2015-08-01), 1155-1161 |x 1070-4280 |q 51:8<1155 |1 2015 |2 51 |o 11178 | |
| 856 | 4 | 0 | |u https://doi.org/10.1134/S107042801508014X |q text/html |z Onlinezugriff via DOI |
| 898 | |a BK010053 |b XK010053 |c XK010000 | ||
| 900 | 7 | |a Metadata rights reserved |b Springer special CC-BY-NC licence |2 nationallicence | |
| 908 | |D 1 |a research-article |2 jats | ||
| 949 | |B NATIONALLICENCE |F NATIONALLICENCE |b NL-springer | ||
| 950 | |B NATIONALLICENCE |P 856 |E 40 |u https://doi.org/10.1134/S107042801508014X |q text/html |z Onlinezugriff via DOI | ||
| 950 | |B NATIONALLICENCE |P 700 |E 1- |a Dudina |D N. |u Krestov Institute of Solution Chemistry, Russian Academy of Sciences, ul. Akademicheskaya 1, 153045, Ivanovo, Russia |4 aut | ||
| 950 | |B NATIONALLICENCE |P 700 |E 1- |a Antina |D E. |u Krestov Institute of Solution Chemistry, Russian Academy of Sciences, ul. Akademicheskaya 1, 153045, Ivanovo, Russia |4 aut | ||
| 950 | |B NATIONALLICENCE |P 700 |E 1- |a Sozonov |D D. |u Ivanovo State Chemical Engineering University, Ivanovo, Russia |4 aut | ||
| 950 | |B NATIONALLICENCE |P 700 |E 1- |a V'yugin |D A. |u Krestov Institute of Solution Chemistry, Russian Academy of Sciences, ul. Akademicheskaya 1, 153045, Ivanovo, Russia |4 aut | ||
| 950 | |B NATIONALLICENCE |P 773 |E 0- |t Russian Journal of Organic Chemistry |d Pleiades Publishing |g 51/8(2015-08-01), 1155-1161 |x 1070-4280 |q 51:8<1155 |1 2015 |2 51 |o 11178 | ||