Zobrazeno 1 - 10
of 169
pro vyhledávání: '"Maria Carmela Iapalucci"'
Autor:
Guido Bussoli, Cristiana Cesari, Cristina Femoni, Maria Carmela Iapalucci, Silvia Ruggieri, Cristina Tiozzo, Stefano Zacchini
Publikováno v:
Results in Chemistry, Vol 4, Iss , Pp 100435- (2022)
This paper presents a deepening on the investigation of the Rh-Sn system of heterometallic carbonyl clusters. More specifically, we herein report the synthesis and isolation of the new [Rh7Sn4Cl10(CO)14]5− (1) compound and the atomically precise [R
Externí odkaz:
https://doaj.org/article/36be2d4ac7224c5c96a82f88343e5322
Publikováno v:
ACS Omega, Vol 3, Iss 10, Pp 13239-13250 (2018)
Externí odkaz:
https://doaj.org/article/0c0053262a3842628230d67f7f5a3f23
Autor:
Cristiana Cesari, Beatrice Berti, Francesco Calcagno, Cristina Femoni, Marco Garavelli, Maria Carmela Iapalucci, Ivan Rivalta, Stefano Zacchini
Publikováno v:
Molecules, Vol 26, Iss 6, p 1529 (2021)
The reaction of [Co(CO)4]− (1) with M(I) compounds (M = Cu, Ag, Au) was reinvestigated unraveling an unprecedented case of polymerization isomerism. Thus, as previously reported, the trinuclear clusters [M{Co(CO)4}2]− (M = Cu, 2; Ag, 3; Au, 4) we
Externí odkaz:
https://doaj.org/article/7ba8399171764d249818680b49515e9d
Autor:
Cristiana Cesari, Beatrice Berti, Tiziana Funaioli, Cristina Femoni, Maria Carmela Iapalucci, Daniele Pontiroli, Giacomo Magnani, Mauro Riccò, Marco Bortoluzzi, Federico Maria Vivaldi, Stefano Zacchini
Publikováno v:
Inorganic Chemistry. 61:12534-12544
The molecular Pt nanocluster [Pt27(CO)31]4- (14-) was obtained by thermal decomposition of [Pt15(CO)30]2- in tetrahydrofuran under a H2 atmosphere. The reaction of 14- with increasing amounts of HBF4·Et2O afforded the previously reported [Pt26(CO)32
Autor:
Cristiana Cesari, Beatrice Berti, Marco Bortoluzzi, Cristina Femoni, Tiziana Funaioli, Federico Maria Vivaldi, Maria Carmela Iapalucci, Stefano Zacchini
Molecular alloy Pt–Ni nanoclusters of increasing sizes were synthesized, their structures determined by X-ray crystallography, Pt–Ni distribution computationally investigated, and the effect of Pt–Ni replacement electrochemically studied.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0bbd015f35966298ca3ce16e671b7535
https://hdl.handle.net/10278/5017185
https://hdl.handle.net/10278/5017185
Autor:
Maria Carmela Iapalucci, Beatrice Berti, Cristiana Cesari, Cristina Femoni, Marco Bortoluzzi, Federico Vacca, Rita Mazzoni, Stefano Zacchini
Publikováno v:
Inorganic Chemistry
The thermal reactions of [NEt4][Fe(CO)4(AuNHC)] [NHC = IMes ([NEt4][1]) or IPr ([NEt4][2]); IMes = C3N2H2(C6H2Me3)2; IPr = C3N2H2(C6H3iPr2)2], Fe(CO)4(AuNHC)2 [NHC = IMes (3) or IPr (4)], Fe(CO)4(AuIMes)(AuIPr) (5), and Fe(CO)4(AuNHC)(AuPPh3) [NHC =
Autor:
Cristiana, Cesari, Marco, Bortoluzzi, Cristina, Femoni, Maria, Carmela Iapalucci, Stefano, Zacchini
Publikováno v:
Dalton transactions (Cambridge, England : 2003). 51(6)
The elusive mono-hydride tri-anion [HRu
Autor:
Cristiana Cesari, Marco Bortoluzzi, Francesca Forti, Lisa Gubbels, Cristina Femoni, Maria Carmela Iapalucci, Stefano Zacchini
The reactions of [HRu3(CO)11]- (1) with M(I) (M = Cu, Ag, and Au) compounds such as [Cu(CH3CN)4][BF4], AgNO3, and Au(Et2S)Cl afford the 2-D molecular alloy clusters [CuRu6(CO)22]- (2), [AgRu6(CO)22]- (3), and [AuRu5(CO)19]- (4), respectively. The rea
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3f4cef2cf3c18129c03d5b654ad7342d
https://hdl.handle.net/10278/5007600
https://hdl.handle.net/10278/5007600
Autor:
Cristiana Cesari, Marco Bortoluzzi, Cristina Femoni, Maria Carmela Iapalucci, Stefano Zacchini
The elusive mono-hydride tri-anion [HRu4(CO)12]3- (4) has been isolated and fully characterized for the first time. Cluster 4 can be obtained by the deprotonation of [H3Ru4(CO)12]- (2) with NaOH in DMSO. A more convenient synthesis is represented by
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::268e99e2de16e605223a2e24c7018900
http://hdl.handle.net/10278/3751508
http://hdl.handle.net/10278/3751508
Autor:
Gabriele Manca, Fabrizia Fabrizi de Biani, Maddalena Corsini, Cristiana Cesari, Cristina Femoni, Maria Carmela Iapalucci, Stefano Zacchini, Andrea Ienco
Publikováno v:
Inorganic chemistry (Online) 61 (2022): 3484–3492. doi:10.1021/acs.inorgchem.1c03386
info:cnr-pdr/source/autori:Gabriele Manca, Fabrizia Fabrizi de Biani, Maddalena Corsini, Cristiana Cesari, Cristina Femoni, Maria Carmela Iapalucci, Stefano Zacchini, Andrea Ienco/titolo:Inverted Ligand Field in a Pentanuclear Bow Tie Au%2FFe Carbonyl Cluster/doi:10.1021%2Facs.inorgchem.1c03386/rivista:Inorganic chemistry (Online)/anno:2022/pagina_da:3484/pagina_a:3492/intervallo_pagine:3484–3492/volume:61
info:cnr-pdr/source/autori:Gabriele Manca, Fabrizia Fabrizi de Biani, Maddalena Corsini, Cristiana Cesari, Cristina Femoni, Maria Carmela Iapalucci, Stefano Zacchini, Andrea Ienco/titolo:Inverted Ligand Field in a Pentanuclear Bow Tie Au%2FFe Carbonyl Cluster/doi:10.1021%2Facs.inorgchem.1c03386/rivista:Inorganic chemistry (Online)/anno:2022/pagina_da:3484/pagina_a:3492/intervallo_pagine:3484–3492/volume:61
Gold chemistry has experienced in the last decades exponential attention for a wide spectrum of chemical applications, but the +3 oxidation state, traditionally assigned to gold, remains somewhat questionable. Herein, we present a detailed analysis o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f79c55c4b1c343e7617a18549dda0c9c