Zobrazeno 1 - 10
of 58
pro vyhledávání: '"Tatiana Woller"'
Publikováno v:
Frontiers in Chemistry, Vol 9 (2021)
In the search for new nonlinear optical (NLO) switching devices, expanded porphyrins have emerged as ideal candidates thanks to their tunable chemical and photophysical properties. Introducing meso-substituents to these macrocycles is a successful st
Externí odkaz:
https://doaj.org/article/e3a4deec6ef948e08b3c97e6103e5f9b
Autor:
Xavier Deraet, Tatiana Woller, Ruben Van Lommel, Prof. Frank De Proft, Prof. Guido Verniest, Prof. Mercedes Alonso
Publikováno v:
ChemistryOpen, Vol 8, Iss 6, Pp 788-806 (2019)
Abstract The performance of density functionals and wavefunction methods for describing the thermodynamics and kinetics of hydride reductions of 2‐substituted cyclohexanones has been evaluated for the first time. A variety of exchange correlation f
Externí odkaz:
https://doaj.org/article/daab18043050465b9d999f373b1c5d60
Autor:
Munck, Sebastian, Christopher Cawthorne, Tatiana Woller, Benjamin Pavie, Alexander Botzki, Frank Vernaillen, Raf De Coster, Paul Borgermans, Ingrid Barcena Roig, Mariana Montes
To make modern data management and analysis that is committed to FAIR principles and improved reproducibility a reality, Flanders BioImaging in a team effort with the Flemish supercomputing center (Vlaams Supercomputer Centrum, VSC) and KU Leuven’s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0263866ee0711bf3cf5f6bbb732fad60
Autor:
Irene Casademont‐Reig, Tatiana Woller, Victor García, Julia Contreras‐García, William Tiznado, Miquel Torrent‐Sucarrat, Eduard Matito, Mercedes Alonso
Publikováno v:
Chemistry – A European Journal. 29
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::331d6587f5d77891e06a91d78202be47
https://doi.org/10.1002/chem.202300066
https://doi.org/10.1002/chem.202300066
Publikováno v:
Physical Chemistry Chemical Physics.
Combining meso-substitutions and core-modifications in the 28R → 30R hexaphyrin-based switch can synergistically improve the contrast between the nonlinear optical responses of the ON and OFF states by 10-fold compared to the unsubstituted switch.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0e9e25dbf109468bef0f6d600cd6eb44
https://doi.org/10.1039/d3cp01240a
https://doi.org/10.1039/d3cp01240a
Autor:
Irene Casademont‐Reig, Tatiana Woller, Victor García, Julia Contreras‐García, William Tiznado, Miquel Torrent‐Sucarrat, Eduard Matito, Mercedes Alonso
Publikováno v:
Chemistry – A European Journal. 29
Despite the central role of aromaticity in the chemistry of expanded porphyrins, the evaluation of aromaticity remains difficult for these extended macrocycles. The presence of multiple conjugation pathways and different planar and nonplanar π-conju
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fb4f39d0e82101618d8c822025a537f3
https://doi.org/10.1002/chem.202202264
https://doi.org/10.1002/chem.202202264
Summary report about a workshop on research data management and data deposition for biological images. This workshop took place on 23/06/2022 and was organized by VIB and Flanders Bioimaging consortium in collaboration with Elixir Belgium and Flemish
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9151a5d4af139933c6dffb320ed2c67f
Publikováno v:
Molecules, Vol 23, Iss 6, p 1333 (2018)
With their versatile molecular topology and aromaticity, porphyrinoid systems combine remarkable chemistry with interesting photophysical properties and nonlinear optical properties. Hence, the field of application of porphyrinoids is very broad rang
Externí odkaz:
https://doaj.org/article/52c50c23217047af99b99c6b3c128c49
Publikováno v:
The Journal of Physical Chemistry C. 123:7318-7335
Expanded porphyrins are currently recognized as the ideal test bed to explore the correlation between molecular properties and (anti)aromaticity since they can adopt different π-conjugation topologies and change easily the number of π-electrons alo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eeec59c066c66df67cdce9eb9c10338a
https://doi.org/10.1021/acs.jpcc.8b10908
https://doi.org/10.1021/acs.jpcc.8b10908
Autor:
Jolien Bertouille, Ruben Van Lommel, Niko Van den Brande, Thomas M. A. Barlow, Tatiana Woller, Steven Ballet, Tess De Maeseneer, Joost Brancart, Richard Hoogenboom, Valentin Lacanau, Annemieke Madder, Mercedes Alonso, Wouter Vandeplassche, Paula Moldenaers, Frank De Proft, Charlotte Martin, Tom Bettens
Publikováno v:
MATERIALS ADVANCES
Non-covalent interactions involving aromatic rings play a central role in many areas of modern chemistry. In medicinal and bioorganic chemistry, the intermolecular interactions between the aromatic side chains of amino acids, such as phenylalanine an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1d01db94ac78b2982fab7dd99b7495be
https://biblio.ugent.be/publication/8724360
https://biblio.ugent.be/publication/8724360