Zobrazeno 1 - 10
of 21
pro vyhledávání: '"Marconi N. Peñas-Defrutos"'
Autor:
Sara Fernández-Moyano, Guillermo Marcos-Ayuso, Marconi N. Peñas-Defrutos, Camino Bartolomé, Pablo Espinet
Publikováno v:
Chemical Communications. 59:1975-1978
Producción Científica
19F NMR monitoring shows that heating trans-[AuIIIRf2I2]− solutions (Rf = C6F3Cl2-3,5) leads to formation of cis-[AuRf2I2]−, [AuRf3I]− and [AuRfI3]−via kinetic competition between isomerization and Rf/I scrambling
19F NMR monitoring shows that heating trans-[AuIIIRf2I2]− solutions (Rf = C6F3Cl2-3,5) leads to formation of cis-[AuRf2I2]−, [AuRf3I]− and [AuRfI3]−via kinetic competition between isomerization and Rf/I scrambling
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::63e515375bb901548cd3ca5ed27f2f1e
https://doi.org/10.1039/d2cc06415d
https://doi.org/10.1039/d2cc06415d
Publikováno v:
Dalton Transactions. 52:3265-3269
Producción Científica
Complexes trans-[PdX2L2] (X = Cl and Br), where L is 1-(PR2),2-(CH[double bond, length as m-dash]CH–C(O)Ph)-C6F4 (R = Ph, Cy, and iPr), display phosphorescent emission in the solid state, whereas due to their substantia
Complexes trans-[PdX2L2] (X = Cl and Br), where L is 1-(PR2),2-(CH[double bond, length as m-dash]CH–C(O)Ph)-C6F4 (R = Ph, Cy, and iPr), display phosphorescent emission in the solid state, whereas due to their substantia
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c010b67f367ba09522aa899bde568366
https://doi.org/10.1039/d3dt00408b
https://doi.org/10.1039/d3dt00408b
Autor:
Guillermo Marcos-Ayuso, Marconi N. Peñas-Defrutos, Ana M. Gallego, Max García-Melchor, Jesús M. Martínez-Ilarduya, Pablo Espinet
Publikováno v:
Journal of the American Chemical Society. 145:527-536
Producción Científica
The synthesis of aryl–alkynyl compounds is usually achieved via Sonogashira catalysis, but this is inefficient for fluorinated aryls. An alternative method reported by Shirakawa and Hiyama, using alkynylstannanes and he
The synthesis of aryl–alkynyl compounds is usually achieved via Sonogashira catalysis, but this is inefficient for fluorinated aryls. An alternative method reported by Shirakawa and Hiyama, using alkynylstannanes and he
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f76668a750195a9f0143b23d7b458b28
https://doi.org/10.1021/jacs.2c10842
https://doi.org/10.1021/jacs.2c10842
Autor:
Yun Ji Park, Marconi N. Peñas-Defrutos, Michael J. Drummond, Zachary Gordon, Oscar R. Kelly, Ian J. Garvey, Kelly L. Gullett, Max García-Melchor, Alison R. Fout
Publikováno v:
Inorganic Chemistry. 61:8182-8192
The reduction of nitrite (NO
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::edcdd67a0b9713d26c72eb0e614ded1f
https://doi.org/10.1021/acs.inorgchem.2c00462
https://doi.org/10.1021/acs.inorgchem.2c00462
Autor:
Andreu Tortajada, Leonie J. Bole, Manting Mu, Martin Stanford, Marconi N. Peñas-Defrutos, Max García-Melchor, Eva Hevia
Producción Científica
The deprotonative metalation of organic molecules has become a convenient route to prepare functionalised aromatic substrates. Amongst the different metallating reagents available, sodium bases have recently emerged as a
The deprotonative metalation of organic molecules has become a convenient route to prepare functionalised aromatic substrates. Amongst the different metallating reagents available, sodium bases have recently emerged as a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3386ba4c5dbef0c2535648666af1d151
https://doi.org/10.1039/d3sc01705b
https://doi.org/10.1039/d3sc01705b
Autor:
Guillermo, Marcos-Ayuso, Marconi N, Peñas-Defrutos, Ana M, Gallego, Max, García-Melchor, Jesús M, Martínez-Ilarduya, Pablo, Espinet
Publikováno v:
Journal of the American Chemical Society.
The synthesis of aryl-alkynyl compounds is usually achieved via Sonogashira catalysis, but this is inefficient for fluorinated aryls. An alternative method reported by Shirakawa and Hiyama, using alkynylstannanes and hemilabile PN ligands, works appa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::9d1333a5135f118342f23162cb462cd8
https://pubmed.ncbi.nlm.nih.gov/36542758
https://pubmed.ncbi.nlm.nih.gov/36542758
Publikováno v:
Chemical communications (Cambridge, England). 58(69)
Agostic interactions were observed in the bound mesityl group in a series of iron compounds bearing a bis(NHC) pincer CCC ligand. The L-type ligand on [(CCC)Fe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::18cd54b46ac93844dc57dc800f839c35
https://pubmed.ncbi.nlm.nih.gov/35959650
https://pubmed.ncbi.nlm.nih.gov/35959650
Publikováno v:
UVaDOC. Repositorio Documental de la Universidad de Valladolid
instname
instname
Producción Científica
The E phosphine ligands (R = Ph, o-Tol, Cy), abbreviated as RPEWO-F4, are stable in solution, but they develop a rich reactivity on coordination to PdCl2. The chelate P-olefin coordination to PdCl2 leads eventually to a Z
The E phosphine ligands (R = Ph, o-Tol, Cy), abbreviated as RPEWO-F4, are stable in solution, but they develop a rich reactivity on coordination to PdCl2. The chelate P-olefin coordination to PdCl2 leads eventually to a Z
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e604cd38c351864fc60da6c558fbe958
https://doi.org/10.1021/acs.organomet.0c00019
https://doi.org/10.1021/acs.organomet.0c00019
Producción Científica
Agostic interactions were observed in the bound mesityl group in a series of iron compounds bearing a bis(NHC) pincer CCC ligand. The L-type ligand on [(CCC)FeIIMes(L)] complexes influences the strength of the agostic int
Agostic interactions were observed in the bound mesityl group in a series of iron compounds bearing a bis(NHC) pincer CCC ligand. The L-type ligand on [(CCC)FeIIMes(L)] complexes influences the strength of the agostic int
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cbf3a798d3a430ee87e821a769c67dc3
https://doi.org/10.1039/d2cc03260k
https://doi.org/10.1039/d2cc03260k
Publikováno v:
Inorganic chemistry. 60(18)
Analysis of the bonding contributions in molecules [M
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::69aa22d62d0643da28835bccd1bec0de
https://pubmed.ncbi.nlm.nih.gov/34498456
https://pubmed.ncbi.nlm.nih.gov/34498456