Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Nathalie Mehanna"'
Autor:
Martina Austeri, Renaud Bach, Nathalie Mehanna, Ankit Sharma, Franck Torricelli, Walid Zeghida, Jérôme Lacour
Publikováno v:
CHIMIA, Vol 62, Iss 11 (2008)
Externí odkaz:
https://doaj.org/article/532cd6f140834003bbc1f68d2f960bbb
Autor:
Martini Austeri, Renaud Bach, Nathalie Mehanna, Roman Novikov, Ankit Sharma, Franck Torricelli, Jérôme Lacour
Publikováno v:
CHIMIA, Vol 62, Iss 1-2 (2008)
Externí odkaz:
https://doaj.org/article/176439d5577f42e9827e8c5b5ef3fbc2
Autor:
Martini Austeri, Renaud Bach, Nathalie Mehanna, Roman Novikov, Ankit Sharma, Franck Torricelli, Jérôme Lacour
Publikováno v:
CHIMIA, Vol 61, Iss 12 (2007)
Externí odkaz:
https://doaj.org/article/989924e70cd94bbbafbc950c598535a5
Autor:
Martina Austeri, David Linder, Nathalie Mehanna, Roman Novikov, Franck Torricelli, Jérôme Lacour
Publikováno v:
CHIMIA, Vol 61, Iss 10 (2007)
Externí odkaz:
https://doaj.org/article/5ea83d19ad954926b063b373be99ae49
Autor:
Jérôme Lacour, Martin Hammarson, Benoît Laleu, Alexandre Fürstenberg, Nathalie Mehanna, Oksana Kel, Bo Albinsson, Eric Vauthey, Cyril Nicolas
Publikováno v:
Chemistry-a European Journal
Chem. Eur. J.
Chemistry-A European Journal, Vol. 19, No 22 (2013) pp. 7173-7180
Chem. Eur. J.
Chemistry-A European Journal, Vol. 19, No 22 (2013) pp. 7173-7180
The interaction of a series of chiral cationic [4]helicene derivatives, which differ by their substituents, with double-stranded DNA has been investigated by using a combination of spectroscopic techniques, including time-resolved fluorescence, fluor
Publikováno v:
Chirality. 24:928-935
1,13-Dimethoxyquinacridinium ions of type 3 are highly configurationally stable [4]helicenes that can be synthesized in racemic form in a single step from tris(2,6-dimethoxyphenyl)methylium ion. Previously, it had been shown that the single enantiome
Publikováno v:
Journal of Organic Chemistry
Journal of Organic Chemistry, Vol. 76, No 8 (2011) pp. 2716-2722
Journal of Organic Chemistry, Vol. 76, No 8 (2011) pp. 2716-2722
Using a two-step reduction/metalation procedure, highly stable chiral carbenium ions are transformed into reactive carbanion intermediates. Interesting polar ketone and thioamide products are the results of this umpolung that occurs with complete ret
Publikováno v:
Photochemical and Photobiological Sciences, Vol. 11, No 4 (2012) pp. 623-631
Photochem. Photobiol. Sci.
Photochem. Photobiol. Sci.
The photophysical properties of a series of helicene cations in various solvents have been investigated using stationary and time-resolved spectroscopy. These compounds fluoresce in the near infrared region with a quantum yield ranging between 2 and
Publikováno v:
Chirality, Vol. 24, No 11 (2012) pp. 928-935
Chirality
Chirality
1,13-Dimethoxyquinacridinium ions of type 3 are highly configurationally stable [4]helicenes that can be synthesized in racemic form in a single step from tris(2,6-dimethoxyphenyl)methylium ion. Previously, it had been shown that the single enantiome
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::1997c91f4fa822e8a2b8595caf540bb6
https://archive-ouverte.unige.ch/unige:23577
https://archive-ouverte.unige.ch/unige:23577
Publikováno v:
Dalton Transactions, Vol. 41, No 22 (2012) pp. 6777-6782
A new tripodal ligand has been designed by coupling pyridyldicarbonyl binding strands with a triazatriangulenium platform (TATA). The complexation reaction with europium provides a C(3)-symmetrical mononuclear compound that is characterized with NMR,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::45587d7aa2267a04172f3ceed6f24a6f
https://archive-ouverte.unige.ch/unige:20423
https://archive-ouverte.unige.ch/unige:20423