Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Marius Lupu"'
Autor:
Reijo Sillanpää, Mikko M. Hänninen, Ariadna Pepiol, Zsolt Kelemen, Francesc Teixidor, Clara Viñas, Marius Lupu
Publikováno v:
Chemical Communications
Digital.CSIC. Repositorio Institucional del CSIC
instname
Digital.CSIC. Repositorio Institucional del CSIC
instname
Four-fold aryl substituted o-carborane derivatives with defined patterns of substitution at the antipodal region of the cluster carbon atoms have been achieved. It is proven that this region is congested but lacks steric hindrance. Also, the two anti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f81f7f7e756d551bf035f0c94da885a8
https://doi.org/10.1039/c9cc04526k
https://doi.org/10.1039/c9cc04526k
Publikováno v:
Journal of Organometallic Chemistry. 798:171-181
The preparation of Cc-monosubstituted closo and nido carborane derivatives, mono-, di and tetraiodinated is reported. Some of these mono-to poly-iodinated nido carboranes are studied in terms of the acidity of the open face bridging proton, their che
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::50091fb075a5aef4366d45165a6a2797
https://doi.org/10.1016/j.jorganchem.2015.05.053
https://doi.org/10.1016/j.jorganchem.2015.05.053
Autor:
Marcin Chmielewski, Marius Lupu, Slawomir Janczak, Sandra Bałabańska, Zbigniew J. Lesnikowski, Agnieszka B. Olejniczak, Clara Viñas
Publikováno v:
Chemistry – A European Journal. 21:15118-15122
A synthetic strategy for functionalization of the three vertices of o-carborane and the attachment of the obtained triped to the solid support was developed. Further functionalization of the triped with short DNA sequences by automated DNA synthesis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5fef77f182d9eec43f44010f527c925c
https://doi.org/10.1002/chem.201502822
https://doi.org/10.1002/chem.201502822
Autor:
Slawomir, Janczak, Agnieszka, Olejniczak, Sandra, Balabańska, Marcin K, Chmielewski, Marius, Lupu, Clara, Viñas, Zbigniew J, Lesnikowski
Publikováno v:
Chemistry (Weinheim an der Bergstrasse, Germany). 21(43)
A synthetic strategy for functionalization of the three vertices of o-carborane and the attachment of the obtained triped to the solid support was developed. Further functionalization of the triped with short DNA sequences by automated DNA synthesis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::1524f11162ba6d09c4247682898bbe64
https://pubmed.ncbi.nlm.nih.gov/26346614
https://pubmed.ncbi.nlm.nih.gov/26346614
Publikováno v:
Dipòsit Digital de la UB
Universidad de Barcelona
Universidad de Barcelona
The metallacarborane [3,3'-Co(1,2-closo-C2B9H11)2](-) has been synthesized. This species allows the formation of redox couples in which both partners are negatively charged. The E1/2 potential can be tuned by adjusting the nature and number of substi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ee14e80f04cd845f2b5e2ede77bbe8c4
http://hdl.handle.net/2445/159723
http://hdl.handle.net/2445/159723
Publikováno v:
Angewandte Chemie (International ed. in English). 50(52)
Step by step: The cluster [3,3'-Co(1,2-C(2)B(9)H(11))(2)](-) is an excellent platform for making a stepwise tunable redox potential system by dehydroiodination. With the addition of up to eight iodine substituents (purple; see picture), there is a fa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::563ec57fd379861377dd2904bd08949d
https://pubmed.ncbi.nlm.nih.gov/22052578
https://pubmed.ncbi.nlm.nih.gov/22052578
Publikováno v:
Chemistry: A European Journal. 21(36):12778
o-Carborane (C2 B10 H12 ) was adapted to perform as the core of globular macromolecules, dendrons or dendrimers. To meet this objective, precisely defined substitution patterns of terminal olefin groups on the carborane framework were subjected to He
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f603f48a4e60e0eb893bf385fcc2ad04
http://juuli.fi/Record/0009321515
http://juuli.fi/Record/0009321515