Zobrazeno 1 - 10
of 33
pro vyhledávání: '"Matti Virkki"'
Autor:
Sami Vesamäki, Henning Meteling, Roshan Nasare, Antti Siiskonen, Jani Patrakka, Nelmary Roas-Escalona, Markus Linder, Matti Virkki, Arri Priimagi
Publikováno v:
Communications Materials, Vol 5, Iss 1, Pp 1-11 (2024)
Abstract Azobenzenes are versatile photoswitches that garner interest in applications ranging from photobiology to energy storage. Despite their great potential, transforming azobenzene-based discoveries and proof-of-concept demonstrations from the l
Externí odkaz:
https://doaj.org/article/d7badcfad9d348c49f6f2b1848622403
Autor:
Jelle E. Stumpel, Marco Saccone, Valentina Dichiarante, Ossi Lehtonen, Matti Virkki, Pierangelo Metrangolo, Arri Priimagi
Publikováno v:
Molecules, Vol 22, Iss 11, p 1844 (2017)
In recent years, supramolecular complexes comprising a poly(4-vinylpyridine) backbone and azobenzene-based halogen bond donors have emerged as a promising class of materials for the inscription of light-induced surface-relief gratings (SRGs). The stu
Externí odkaz:
https://doaj.org/article/dd170d4194ef490d95d7313d69f3f7eb
Publikováno v:
Photochemical & Photobiological Sciences. 21:1719-1734
Azobenzenes have many faces. They are well-known as dyes, but most of all, azobenzenes are versatile photoswitchable molecules with powerful photochemical properties. Azobenzene photochemistry has been extensively studied for decades, but only relati
Autor:
Kim Kuntze, Jani Viljakka, Matti Virkki, Chung-Yang (Dennis) Huang, Stefan Hecht, Arri Priimagi
Through simple synthetic derivatisation, the parent indigo dye becomes a red-light E-Z photoswitch exhibiting negative photochromism and tuneable thermal isomerisation kinetics. These attributes make indigo derivatives extremely attractive for applic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d82cf43841aab8fcf09fc8a9f6b17334
https://trepo.tuni.fi/handle/10024/146794
https://trepo.tuni.fi/handle/10024/146794
Autor:
Jussi, Isokuortti, Kim, Kuntze, Matti, Virkki, Zafar, Ahmed, Elina, Vuorimaa-Laukkanen, Mikhail A, Filatov, Andrey, Turshatov, Timo, Laaksonen, Arri, Priimagi, Nikita A, Durandin
Publikováno v:
Chemical Science
Developing azobenzene photoswitches capable of selective and efficient photoisomerization by long-wavelength excitation is an enduring challenge. Herein, rapid isomerization from the Z- to E-state of two ortho-functionalized bistable azobenzenes with
Autor:
Mikhail A. Filatov, Nikita A. Durandin, Jussi Isokuortti, Elina Vuorimaa-Laukkanen, Zafar Ahmed, Andrey Turshatov, Timo Laaksonen, Arri Priimagi, Kim Kuntze, Matti Virkki
Designing azobenzene photoswitches capable of selective and efficient photoisomerization by long wavelength excitation is a long-standing challenge. Indirect excitation can expand the properties of the photoswitching system beyond the intrinsic limit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4b3ba2459052ff7ef1543dbeae538f14
https://doi.org/10.26434/chemrxiv.14134595
https://doi.org/10.26434/chemrxiv.14134595
Publikováno v:
Scientific Reports
Autor:
Matthias Spengler, Matti Virkki, Marco Saccone, Kim Kuntze, Christoph Wölper, Pierangelo Metrangolo, Robert Gehrke, Michael Pfletscher, Georg Jansen, Michael Giese, Arri Priimagi
Publikováno v:
Chemistry of Materials
A new strategy for controlling the liquid crystalline and photophysical properties of supramolecular mesogens assembled via halogen bonding is reported. Changing the degree of fluorination at the halogen-bond donor of the supramolecular liquid crysta
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7b52f50b4306bb65e90513e12a748edc
http://hdl.handle.net/10447/398742
http://hdl.handle.net/10447/398742
Autor:
Pierangelo Metrangolo, Pierre-François Brevet, Matti Virkki, Maurizio Sironi, Valentina Dichiarante, Martti Kauranen, Arri Priimagi, Alessandra Forni, Anthony Maurice
Publikováno v:
Physical Chemistry Chemical Physics
Physical Chemistry Chemical Physics, Royal Society of Chemistry, 2018, 20 (45), pp.28810-28817. ⟨10.1039/c8cp05392h⟩
PCCP. Physical chemistry chemical physics
20 (2018): 28810–28817. doi:10.1039/c8cp05392h
info:cnr-pdr/source/autori:Virkki, Matti; Maurice, Anthony; Forni, Alessandra; Sironi, Maurizio; Dichiarante, Valentina; Brevet, Pierre-Francois; Metrangolo, Pierangelo; Kauranen, Martti; Priimagi, Arri/titolo:On the molecular optical nonlinearity of halogen-bond-forming azobenzenes/doi:10.1039%2Fc8cp05392h/rivista:PCCP. Physical chemistry chemical physics (Print)/anno:2018/pagina_da:28810/pagina_a:28817/intervallo_pagine:28810–28817/volume:20
Physical Chemistry Chemical Physics, Royal Society of Chemistry, 2018, 20 (45), pp.28810-28817. ⟨10.1039/c8cp05392h⟩
PCCP. Physical chemistry chemical physics
20 (2018): 28810–28817. doi:10.1039/c8cp05392h
info:cnr-pdr/source/autori:Virkki, Matti; Maurice, Anthony; Forni, Alessandra; Sironi, Maurizio; Dichiarante, Valentina; Brevet, Pierre-Francois; Metrangolo, Pierangelo; Kauranen, Martti; Priimagi, Arri/titolo:On the molecular optical nonlinearity of halogen-bond-forming azobenzenes/doi:10.1039%2Fc8cp05392h/rivista:PCCP. Physical chemistry chemical physics (Print)/anno:2018/pagina_da:28810/pagina_a:28817/intervallo_pagine:28810–28817/volume:20
We study hyper-Rayleigh scattering and computed molecular hyperpolarizability in a series of azobenzene chromophores in chloroform and dimethylformamide as solvents. The chromophores form halogen or hydrogen bonds of varying strength with dimethylfor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fc4a6b12c1aed7660827f75cf6ce971f
https://hal-univ-lyon1.archives-ouvertes.fr/hal-02289845
https://hal-univ-lyon1.archives-ouvertes.fr/hal-02289845
Autor:
Saccone, Marco, FERNÁNDEZ PALACIO, FRANCISCO ADALBERTO, Cavallo, Gabriella, Dichiarante, Valentina, Matti, Virkki, Terraneo, Giancarlo, Priimagi, Arri, Pierangelo, Metrangolo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3731::b839b30dbd80d1cea525d2784227dbc2
http://hdl.handle.net/11311/1045520
http://hdl.handle.net/11311/1045520