Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Magdalena Olesińska"'
Autor:
Magdalena Olesińska-Mönch, Claire Deo
Publikováno v:
Chemical Communications. 59:660-669
Fluorescence microscopy has revolutionised our understanding of biological systems, enabling the visualisation of biomolecular structures and dynamics in complex systems. The possibility to reversibly control the optical or biochemical properties of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e81a0460427bcadf85b22aa858b19342
https://doi.org/10.1039/d2cc05870g
https://doi.org/10.1039/d2cc05870g
Autor:
Magdalena Olesińska, Cinzia Pezzella, Patrick Shahgaldian, Philippe F.-X. Corvini, Seyed Amirabbas Nazemi, Chia-Wei Lin, Simona Varriale
Publikováno v:
Chemical Communications. 57:11960-11963
We report a method of glycosylated enzymes' surface immobilisation and stabilisation. The enzyme is immobilised at the surface of silica nanoparticles through the reversible covalent binding of vicinal diols of the enzyme glycans with a surface-attac
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::30de5278ea99949bead2c1ecf2400953
https://doi.org/10.1039/d1cc04916j
https://doi.org/10.1039/d1cc04916j
Publikováno v:
Chemical science. 13(30)
Extended polymeric structures based on redox-active species are of great interest in emerging technologies related to energy conversion and storage. However, redox-active monomers tend to inhibit radical polymerisation processes and hence, increase p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3f7df105dee56d1b029884947e206f0a
https://pubmed.ncbi.nlm.nih.gov/35975157
https://pubmed.ncbi.nlm.nih.gov/35975157
Autor:
Daniel Antón-García, Oren A. Scherman, István Szabó, Magdalena Olesińska, Michael R. Wasielewski, Youn Jue Bae, Guanglu Wu, Edina Rosta
Publikováno v:
Chemical Science
A modular strategy has been employed to develop a new class of fluorescent molecules, which generates discrete, dimeric stacked fluorophores upon complexation with multiple cucurbit[8]uril macrocycles. The multiple constraints result in a “static
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dd740b651348ccd4b3d34c6427c60ed2
https://www.repository.cam.ac.uk/handle/1810/325657
https://www.repository.cam.ac.uk/handle/1810/325657
Autor:
Daniel Antón-García, Guanglu Wu, Magdalena Olesińska, Oren A. Scherman, Edina Rosta, Silvia Gómez-Coca, István Szabó
Publikováno v:
Olesińska, M, Wu, G, Gómez-Coca, S, Antón-García, D, Szabó, I, Rosta, E & Scherman, O A 2019, ' Modular supramolecular dimerization of optically tunable extended aryl viologens ', Chemical Science, vol. 10, no. 38, pp. 8806-8811 . https://doi.org/10.1039/c9sc03057c
Chemical Science
Chemical Science
Cucurbit[8]uril (CB[8]) mediated assembly of extended aryl viologens (EVs) into optically tunable dimers is reported for the first time. We show that the modular design and synthesis of a new class of π-conjugated viologen derivatives with rigid aro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e7fd0e491b3d74276581430fba865e0a
Autor:
Ben Schoenaers, Magdalena Olesińska, David E. Clarke, Tobias Mönch, Andre Stesmans, Oren A. Scherman
A pentapeptide sequence was functionalized with an asymmetric arylated methyl-viologen (AVI3D2) and through controllable β-sheet self-assembly, conductive nanofibers were formed. Using a combination of spectroscopic techniques and conductive atomic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::32eef66a6ea3d5c739e882cf4344b716
Supramolecular chemistry utilizing the macrocyclic hosts cyclodextrins (CDs) and cucurbit[n]urils (CB[n]s) is traditionally performed in aqueous media; however, their solubility is typically poor, especially for the family of CB[n]s. Through derivati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ad0962bbd0651310543e7f47ce6f1cdf
Publikováno v:
Journal of the American Chemical Society. 139(8)
A 1:1 binding stoichiometry of a host-guest complex need not consist of a single host and guest. Diarylviologens containing electron-donating substituents complexed with cucurbit[8]uril (CB[8]) in a 1:1 stoichiometry exhibit abnormally large binding
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::a05221831dc1bd9882e65e1d0f5e780c
https://pubmed.ncbi.nlm.nih.gov/28198190
https://pubmed.ncbi.nlm.nih.gov/28198190
Publikováno v:
Chemistry (Weinheim an der Bergstrasse, Germany). 21(28)
Understanding how the spatial ordering of liquid crystalline nanoparticles can be controlled by different factors is of great importance in the further development of their photonic applications. In this paper, we report a new key parameter to contro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7113742bbd1b050db9aee627feb43c69
https://pubmed.ncbi.nlm.nih.gov/26037593
https://pubmed.ncbi.nlm.nih.gov/26037593
Publikováno v:
Nanoscale Advances. 5(1):81-87
Gold nanoparticles (AuNPs), owing to their intrinsic plasmonic properties, are widely used in applications ranging from nanotechnology and nanomedicine to catalysis and bioimaging. Capitalising on the ability of AuNPs to generate nanoscale heat upon
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::65981be7dd88d8093f26f3c635607467