Zobrazeno 1 - 10
of 702
pro vyhledávání: '"L. Bossi"'
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 15, Iss 1, Pp 2344-2354 (2019)
We present a new series of photochromic 1,2-bis(2-ethylbenzo[b]thiophen-3-yl)perfluorocyclopentenes with an oxidized benzothiophene core (O) or a nonoxidized one, decorated with mono- (Th1) and bithiophene (Th2) units attached to positions 6 and 6′
Externí odkaz:
https://doaj.org/article/74feb1bda7cf465e95ff9d0e68cfe7be
Autor:
Richard Lincoln, Mariano L. Bossi, Michael Remmel, Elisa D’Este, Alexey N. Butkevich, Stefan W. Hell
Publikováno v:
Nature Chemistry
The controlled switching of fluorophores between non-fluorescent and fluorescent states is central to every superresolution fluorescence microscopy (nanoscopy) technique, and the exploration of radically new switching mechanisms remains critical to b
Publikováno v:
Molecular Photoswitches. :605-626
Publikováno v:
Small
The introduction of MINFLUX nanoscopy allows single molecules to be localized with one nanometer precision in as little as one millisecond. However, current applications have so far focused on increasing this precision by optimizing photon collection
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2bce257426d794ac4055ca47dc91fe06
https://hdl.handle.net/21.11116/0000-000C-860E-E21.11116/0000-000D-04C7-E
https://hdl.handle.net/21.11116/0000-000C-860E-E21.11116/0000-000D-04C7-E
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
N-Cyanorhodamines: cell-permeant, photostable and bathochromically shifted analogues of fluoresceins
Publikováno v:
Chemical Science
Fluorescein and its analogues have found only limited use in biological imaging because of the poor photostability and cell membrane impermeability of their O-unprotected forms. Herein, we report rationally designed N-cyanorhodamines as orange- to re
Autor:
Kakishi Uno, Dojin Kim, Jonas Bucevicius, Mariano L. Bossi, Vladimir N. Belov, Stefan W. Hell
Publikováno v:
Organic Chemistry Frontiers
Asymmetric diarylethenes with benzo[b]thiophen-3-yl and 2-thienyl residues having variable oxidation degrees (S and/or SO2) remained unexplored. These photochromes provide reversibly photoswitchable absorbance and multicolor emission modulation. Here
Publikováno v:
Journal of the American Chemical Society
We designed caging-group-free photoactivatable live-cell permeant dyes with red fluorescence emission and ∼100 nm Stokes shifts based on a 1-vinyl-10-silaxanthone imine core structure. The proposed fluorophores undergo byproduct-free one- and two-p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3462aac118d9c63984d7937b6be1b006
https://hdl.handle.net/21.11116/0000-000C-AB01-221.11116/0000-000C-AB03-0
https://hdl.handle.net/21.11116/0000-000C-AB01-221.11116/0000-000C-AB03-0
Publikováno v:
ChemPhotoChem
Searching for photoconvertible or photoactivatable dyes, we considered trimethine (Cy3) and pentamethine (Cy5) fluorophores with a 4-amino-1-diazo-2-butanone fragment (H2N(CH2)2COCH=N2) attached to the meso (γ) position of the polymethine chain via
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a2028d0375d64d8637b01405b46a934f
https://hdl.handle.net/21.11116/0000-000B-7615-921.11116/0000-000B-7617-7
https://hdl.handle.net/21.11116/0000-000B-7615-921.11116/0000-000B-7617-7