Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Candela Segarra"'
Publikováno v:
ChemistryEurope, Vol 2, Iss 2, Pp n/a-n/a (2024)
Abstract The carbonyl group is arguably the most versatile functional group for synthetic purposes. Here, a series of N,N’‐bis(pyridylideneamide) (bisPYA) complexes of ruthenium(II), [Ru(cym)(bisPYA)Cl]+ (cym=cymene), were synthesized and applied
Externí odkaz:
https://doaj.org/article/a05b9f7ff34640e1ad54eadc77421a5b
Publikováno v:
Angewandte Chemie (International ed. in English). 59(23)
An exceptionally efficient ruthenium-based catalyst for olefin oxidation has been designed by exploiting N,N'-bis(pyridylidene)oxalamide (bisPYA) as a donor-flexible ligand. The dynamic donor ability of the bisPYA ligand, imparted by variable zwitter
Autor:
Urbano Díaz, Geo Paul, Robert Raja, Marta Meazza, Leonardo Marchese, Enrica Gianotti, Fernando Rey, Candela Segarra, Andrea Erigoni, Ivana Miletto, Ramon Rios, Maria Consuelo Hernández-Soto
Publikováno v:
Catalysis Science & Technology
Digital.CSIC. Repositorio Institucional del CSIC
instname
RiuNet. Repositorio Institucional de la Universitat Politécnica de Valéncia
Digital.CSIC. Repositorio Institucional del CSIC
instname
RiuNet. Repositorio Institucional de la Universitat Politécnica de Valéncia
[EN] Two different heterogeneous catalysts carrying aryl-sulfonic moieties, in which the aromatic ring was either fluorinated or not, were successfully synthesized. The multi-step synthetic approaches implemented involved the synthesis of the silyl-d
Publikováno v:
Chemical reviews. 118(19)
Mesoionic carbenes are a subclass of the family of N-heterocyclic carbenes that generally feature less heteroatom stabilization of the carbenic carbon and hence impart specific donor properties and reactivity schemes when coordinated to a transition
Publikováno v:
Catalysis in Chemistry and Biology.
Autor:
Li-Xiong Shao, Rachelle Suen, Helge Müller-Bunz, Kate F. Donnelly, Martin Albrecht, Candela Segarra
Publikováno v:
Organometallics. 34:4076-4084
A ruthenium cymene complex bearing a bidentate ligand composed of the N-mesoionic donor N-[1-methylpyridin-4(1H)-ylidene]amide and the C-mesoionic donor 1,2,3-triazolylidene was prepared. Spectroscopic analyses including UV–vis, electrochemical, an
Autor:
Candela Segarra, Elena Mas-Marzá, Michael K. Whittlesey, John P. Lowe, Rebecca C. Poulten, Mary F. Mahon
Publikováno v:
Organometallics. 31:8584-8590
Thermolysis of Rh(PPh3)4H in the presence of the six-membered N-heterocyclic carbene 1,3-bis(2-propyl)-3,4,5,6-tetrahydropyrimidin-2-ylidine (6-iPr) gave the monocarbene complex Rh(6-iPr)(PPh3)2H as a 1:2 mixture of the cis- and trans-phosphine isome
Publikováno v:
Angewandte Chemie International Edition. 51:10841-10845
Publikováno v:
Advanced Synthesis & Catalysis. 353:2078-2084
The reaction of (pentamethylcyclopentadienyl)iridium dichloride dimer, [IrCp*Cl 2 ] 2 , with bis(2,4,6-trimethylphenyl)formamidine allows the preparation of two new [IrCp*Cl 2 (amidine)] and [IrCp*Cl(amidinate)] complexes, which have been fully chara
Publikováno v:
Organometallics. 30:684-688
Four new Pd(II) complexes containing sulfonate-functionalized N-heterocyclic carbene ligands have been synthesized. All new complexes are palladium bis-NHCs, in which the ligands adopt a monodentate, bis-chelating, and pincer coordination form, so th