Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Marina Juribašić Kulcsar"'
Autor:
Marina Juribašić Kulcsar, Marko Robić, Alen Bjelopetrović, Darko Babić, Manda Ćurić, Ivan Halasz
Publikováno v:
Organometallics. 38:4479-4484
The solvent-free ball-milling method for substitution of anionic ligands in organopalladium compounds was developed. Reactions of acetate, acetylacetonate, chloride, or tetrafluoroborate of mono- or dicyclopalladated azobenzenes with alkali salts of
Autor:
Zrinka Duvnjak, Marina Juribašić Kulcsar, Manda Ćurić, Alen Bjelopetrović, Darko Babić, Ivan Džajić, Ivan Halasz, Ana Budimir, Dajana Barišić, Manuel Martínez
Publikováno v:
Inorganic Chemistry
Dipòsit Digital de la UB
Universidad de Barcelona
Dipòsit Digital de la UB
Universidad de Barcelona
Palladium C–H bond activation in azobenzenes with R1 and R2 at para-positions of the phenyl rings (R1=N(Me)2, R2=H (L1); R1=N(Me)2, R2=Cl (L2); R1=N(Me)2, R2=I (L3); R1=–N(Me)2, R2=NO2 (L4); R1=H, R2=H (L5)) and their already monopalladated deriv
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2f0d78676acbf8bf78ad1622b820e14a
https://doi.org/10.1021/acs.inorgchem.0c02418
https://doi.org/10.1021/acs.inorgchem.0c02418
Autor:
Mario Cetina, Krunoslav Užarević, Martina Tireli, Stipe Lukin, Marina Juribašić Kulcsar, Ivan Halasz, Dijana Žilić, Silvana Raić-Malić, Silvija Maračić
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 13, Iss 1, Pp 2352-2363 (2017)
Beilstein Journal of Organic Chemistry
Beilstein Journal of Organic Chemistry
Copper-catalyzed mechanochemical click reactions using Cu(II), Cu(I) and Cu(0) catalysts have been successfully implemented to provide novel 6-phenyl-2-(trifluoromethyl)quinolines with a phenyl-1,2,3-triazole moiety at O-4 of the quinoline core. Mill
Autor:
Marina Juribašić Kulcsar, Krunoslav Užarević, Ana Budimir, Andrea Monas, Stipe Lukin, Manda Ćurić, Janez Plavec, Ivan Halasz, Franziska Emmerling
Publikováno v:
Inorganic Chemistry. 56:5342-5351
N−H bond activation of gaseous ammonia is achieved at room temperature in a reversible solvent-free reaction using a solid dicyclopalladated azobenzene complex. Monitoring of the gas−solid reaction in real-time by in situ solid-state Raman spectr
Autor:
Stipe Lukin, Ivan Halasz, Ana Budimir, Krunoslav Užarević, Alen Bjelopetrović, Manda Ćurić, Marina Juribašić Kulcsar, Dajana Barišić, Ivica Đilović
Publikováno v:
Chemistry-A European Journal
Mechanism of solid-state C–H bond activation by various Pd(II) catalysts under milling conditions has been studied by in situ Raman spectroscopy. Common Pd(II) precursors, i.e. PdCl2, [Pd(OAc)2]3, PdCl2(MeCN)2 and [Pd(MeCN)4][BF4]2, have been emplo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f9a0532e7f98ef48b45c5c0840f17b8a
https://www.bib.irb.hr/943515
https://www.bib.irb.hr/943515
Autor:
Krunoslav Užarević, Martina Tireli, Nikola Bregović, Marina Juribašić Kulcsar, Dajana Barišić, Nikola Cindro, Vladislav Tomišić
Publikováno v:
Chemistry – A European Journal. 25:4533-4533
A series of aromatic bis-urea derivatives was prepared and their proton dissociation, as well as anion binding properties in DMSO were investigated. To this end, UV/Vis and 1 H NMR spectroscopies and computational methods were employed. The synthesiz
Autor:
Dajana Barišić, Vladislav Tomišić, Marina Juribašić Kulcsar, Nikola Cindro, Martina Tireli, Krunoslav Užarević, Nikola Bregović
Publikováno v:
Chemistry – A European Journal. 25:4530-4530
Publikováno v:
Chemical Communications
Room-temperature accelerated aging in the solid state has been applied for atom- and energy-efficient activation of either one or two C–H bonds of azobenzene and methyl orange by palladium(II) acetate. Organopalladium complexes are prepared in quan
Autor:
Martina Tireli, Nikola Biliškov, Nikola Cindro, Marina Juribašić Kulcsar, Manda Ćurić, Mladen Borovina, Davor Gracin, Ivan Halasz, Krunoslav Užarević
Publikováno v:
Chemical Communications
In situ Raman spectroscopy was employed to study the course of a mechanochemical nucleophilic substitution on a carbonyl group. We describe evidence of base catalysis, akin to catalysis in solution, achieved by liquid-assisted grinding.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f77554cd6d60cc8e6b0ed48c83a0254c
http://fulir.irb.hr/2574/
http://fulir.irb.hr/2574/
Autor:
Martina Tireli, Silvija Maračić, Stipe Lukin, Marina Juribašić Kulcsár, Dijana Žilić, Mario Cetina, Ivan Halasz, Silvana Raić-Malić, Krunoslav Užarević
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 13, Iss 1, Pp 2352-2363 (2017)
Copper-catalyzed mechanochemical click reactions using Cu(II), Cu(I) and Cu(0) catalysts have been successfully implemented to provide novel 6-phenyl-2-(trifluoromethyl)quinolines with a phenyl-1,2,3-triazole moiety at O-4 of the quinoline core. Mill
Externí odkaz:
https://doaj.org/article/532d798ec62246a6bbb4e792cccb7ac8