Аннотация:
The meso-acrylic 1,3,5,7-tetramethyl-BODIPY derivative was obtained from 2,4-dimethylpyrrole and ethyl 4-chloro-4-oxobutanoate and its crystal structure was characterized by X-ray diffraction. This 8-alkenyl-BODIPY dye is originally nonfluorescent, but turns-on fluorescence upon the double bond reduction.
Тип публикации:
Статья
Язык публикации: английский
Образец цитирования:
A. A. Pakhomov, Yu. N. Kononevich, A. A. Korlyukov, V. I. Martynov, A. M. Muzafarov, “Synthesis, crystal structure and optical properties of a new meso-acrylate BODIPY dye”, Mendeleev Commun., 26:3 (2016), 196–198
Образцы ссылок на эту страницу:
https://www.mathnet.ru/rus/mendc2156
https://www.mathnet.ru/rus/mendc/v26/i3/p196
Эта публикация цитируется в следующих 13 статьяx:
A. Yu. Frolova, S. V. Kutyakov, V. I. Martynov, S. M. Deyev, A. A. Pakhomov, “BODIPY Dye Derivative for Irreversible Fluorescent Labeling of Eukaryotic Cells and Their Simultaneous Cytometric Analysis”, Acta Naturae, 15:4 (2024), 92
José G. Becerra-González, Eduardo Peña-Cabrera, José L. Belmonte-Vázquez, “From blue to red. Reaching the full visible spectrum with a single fluorophore: BODIPY”, Tetrahedron, 168 (2024), 134334
Alexey A. Pakhomov, Anna V. Efremova, Yuriy N. Kononevich, Dmitriy S. Ionov, Margarita A. Maksimova, Alexander D. Volodin, Alexander A. Korlyukov, Nikita O. Dubinets, Vladimir I. Martynov, Anatoly A. Ivanov, Aziz M. Muzafarov, “NIR‐I Fluorescent Probes Based on Distyryl‐BODIPYs with Two‐Photon Excitation in NIR‐II Window**”, ChemPhotoChem, 7:5 (2023)
Oksana Desiatkina, Ghalia Boubaker, Nicoleta Anghel, Yosra Amdouni, Andrew Hemphill, Julien Furrer, Emilia Păunescu, “Synthesis, Photophysical Properties and Biological Evaluation of New Conjugates BODIPY: Dinuclear Trithiolato‐Bridged Ruthenium(II)‐Arene Complexes”, ChemBioChem, 23:23 (2022)
В. И. Мартынов, А. А. Пахомов, “Флуоресцентные производные BODIPY как репортеры молекулярных процессов в живой клетке”, Усп. хим., 90:10 (2021), 1213–1262; V. I. Martynov, A. A. Pakhomov, “BODIPY derivatives as fluorescent reporters of molecular activities in living cells”, Russian Chem. Reviews, 90:10 (2021), 1213–1262
Hasrat Ali, Brigitte Guérin, Johan E. van Lier, “gem-Dibromovinyl boron dipyrrins: synthesis, spectral properties and crystal structures”, Dalton Trans., 48:30 (2019), 11492
E. V. Rumyantsev, Y. S. Marfin, “Boron Dipirrins: Mechanism of Formation, Spectral and Photophysical Properties, and Directions of Functionalization”, Russ J Gen Chem, 89:12 (2019), 2682
S. A. Gorbatov, M. A. Kozlov, I. E. Zlobin, A. V. Kartashov, I. V. Zavarzin, Yu. A. Volkova, “Highly selective BODIPY-based fluorescent probe for Zn2+ imaging in plant roots”, Mendeleev Commun., 28:6 (2018), 615–617
Alexey A. Pakhomov, Igor E. Deyev, Natalia M. Ratnikova, Stepan P. Chumakov, Veronika B. Mironiuk, Yuriy N. Kononevich, Aziz M. Muzafarov, Vladimir I. Martynov, “BODIPY-Based Dye for No-Wash Live-Cell Staining and Imaging”, BioTechniques, 63:2 (2017), 77
A. A. Pakhomov, V. B. Mironiuk, Yu. N. Kononevich, A. A. Korlyukov, A. D. Volodin, T. A. Priakhina, V. I. Martynov, A. M. Muzafarov, “Synthesis and crystal structure of a meso-decene-BODIPY dye as a functional bright fluorophore for silicone matrices”, Mendeleev Commun., 27:4 (2017), 363–365
V. E. Shershov, V. E. Kuznetsova, S. A. lapa, M. A. Spitsyn, T. O. Guseinov, Ya. V. Tkachev, A. S. Zasedatelev, A. V. Chudinov, “Synthesis and characterization of novel zwitterionic heptamethine indocyanine fluorophores”, Mendeleev Commun., 27:4 (2017), 360–362
Antonio Prlj, Alberto Fabrizio, Clemence Corminboeuf, “Rationalizing fluorescence quenching in meso-BODIPY dyes”, Phys. Chem. Chem. Phys., 18:48 (2016), 32668
Обратная связь: