Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Ievgen Shulov"'
Autor:
Germain A. Brou, Gildas K. Gbassi, Ievgen Shulov, Aidar Seralin, Andrey S. Klymchenko, Thierry F. Vandamme, Nicolas Anton
Publikováno v:
Physical Chemistry Chemical Physics. 25:1177-1186
In this study, we explored how chemical reactions of amphiphile compounds can be characterized and followed-up on model interfaces. A custom-made surfactant containing three alkyne sites was first adsorbed and characterized at a water/oil interface.
Autor:
Damianos Agathangelou, Yves Mély, Andrey S. Klymchenko, Anastasia Ioanna Skilitsi, Stefan Haacke, Jérémie Léonard, Jamie Conyard, Ievgen Shulov
Publikováno v:
Physical Chemistry Chemical Physics
Physical Chemistry Chemical Physics, Royal Society of Chemistry, 2018, 20 (11), pp.7885-7895. ⟨10.1039/C7CP08584B⟩
Physical Chemistry Chemical Physics, 2018, 20 (11), pp.7885-7895. ⟨10.1039/C7CP08584B⟩
Physical Chemistry Chemical Physics, Royal Society of Chemistry, 2018, 20 (11), pp.7885-7895. ⟨10.1039/C7CP08584B⟩
Physical Chemistry Chemical Physics, 2018, 20 (11), pp.7885-7895. ⟨10.1039/C7CP08584B⟩
The excited state intramolecular proton transfer (ESIPT) of 3-hydroxyflavone derivatives results in a fluorescence spectrum composed of two emission bands, the relative intensity of which is strongly influenced by the interaction with the local envir
Autor:
Yves Mély, Emilie Roger, Andrey S. Klymchenko, Thierry F. Vandamme, Nicolas Anton, Halina Anton, Ievgen Shulov, Julien Vermot
Publikováno v:
RSC advances. 2(31)
Dye-loaded lipid nano-droplets present an attractive alternative to inorganic nanoparticles, as they are composed of non-toxic biodegradable materials and easy to prepare. However, to achieve high fluorescence brightness, the nano-droplets have to be
Publikováno v:
Nanoscale. 6:12934-12942
Fluorescent organic nanoparticles (NPs) are attractive alternatives to quantum dots due to their potential biodegradability. However, preparation of fluorescent organic NPs is challenging due to the problem of self-quenching of the encapsulated dyes.
Autor:
Ievgen Shulov, Roman V. Rodik, Youri Arntz, Andreas Reisch, Vitaly I. Kalchenko, Andrey S. Klymchenko
This is the pre-peer reviewed version of the following article: Shulov, I.; Rodik, R. V.; Arntz, Y.; Reisch, A.; Kalchenko, V. I.; Klymchenko, A. S.: Protein-Sized Bright Fluorogenic Nanoparticles Based on Cross-Linked Calixarene Micelles with Cyanin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2659::97e79bcd6aafe07744f1bf9d632f9061
https://zenodo.org/record/579567
https://zenodo.org/record/579567
Autor:
Ievgen Shulov, Andrey S. Klymchenko, Vitaly I. Kalchenko, Roman V. Rodik, Andreas Reisch, Youri Arntz
Publikováno v:
Angewandte Chemie International Edition
The key challenge in the field of fluorescent nanoparticles (NPs) for biological applications is to achieve superior brightness for sizes equivalent to single proteins (3–7 nm). We propose a concept of shell-cross-linked fluorescent micelles, in wh
Publikováno v:
Chemical Communications
Chemical Communications, Royal Society of Chemistry, 2016, 52 (51), pp.7962-7965. ⟨10.1039/c6cc03716j⟩
Chemical Communications, 2016, 52 (51), pp.7962-7965. ⟨10.1039/c6cc03716j⟩
Chem. Commun.
Chemical Communications, Royal Society of Chemistry, 2016, 52 (51), pp.7962-7965. ⟨10.1039/c6cc03716j⟩
Chemical Communications, 2016, 52 (51), pp.7962-7965. ⟨10.1039/c6cc03716j⟩
Chem. Commun.
International audience; A non-coordinating anion, fluorinated tetraphenylborate, assembles specially designed cationic cyanine amphiphiles into 7–8 nm fluorescent nanoparticles that are >40-fold brighter than a single cyanine dye. This kind of anio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c5c76a6cbfaf4093138d46688d346d8a
https://hal.archives-ouvertes.fr/hal-03309601
https://hal.archives-ouvertes.fr/hal-03309601
Autor:
Pascal Villa, Andrey S. Klymchenko, S. Gioria, Dominique Bonnet, Iuliia A. Karpenko, Yves Mély, Ievgen Shulov, Rémy Kreder, Marcel Hibert
Publikováno v:
Chemical communications (Cambridge, England). 51(14)
Herein, we show that a far-red arylidene–squaraine dye is stable against nucleophiles, in contrast to arene–squaraines. Owing to the fluorescence enhancement in apolar media together with high brightness and photostability, this dye was successfu
Autor:
Ievgen Shulov, Andrey S. Klymchenko, Yves Mély, Mayeul Collot, Youri Arntz, Sule Oncul, Andreas Reisch
Publikováno v:
Nanoscale
Nanoscale, Royal Society of Chemistry, 2015, 7, pp.18198-18210
Nanoscale, 2015, 7 (43), pp.18198-18210. ⟨10.1039/c5nr04955e⟩
Nanoscale, Royal Society of Chemistry, 2015, 7 (43), pp.18198-18210. ⟨10.1039/c5nr04955e⟩
Nanoscale, Royal Society of Chemistry, 2015, 7, pp.18198-18210
Nanoscale, 2015, 7 (43), pp.18198-18210. ⟨10.1039/c5nr04955e⟩
Nanoscale, Royal Society of Chemistry, 2015, 7 (43), pp.18198-18210. ⟨10.1039/c5nr04955e⟩
International audience; The key to ultrabright fluorescent nanomaterials is the control of dye emission in the aggregated state. Here, lipophilic rhodamine B derivatives are assembled into nanoparticles (NPs) using tetraphenylborate counterions with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a978b596eec023bb27078d900c95c392
https://hal.archives-ouvertes.fr/hal-01280512
https://hal.archives-ouvertes.fr/hal-01280512