Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Sylwia Kostera"'
Publikováno v:
ACS Catalysis. 13:5236-5244
Autor:
Stefan Weber, Maurizio Peruzzini, Luca Gonsalvi, Sylwia Kostera, Luis F. Veiros, Karl Kirchner
Publikováno v:
Organometallics
Organometallics (Online) 40 (2021): 1213–1220. doi:10.1021/acs.organomet.0c00710
info:cnr-pdr/source/autori:Sylwia Kostera, Stefan Weber, Maurizio Peruzzini, Luis F. Veiros, Karl Kirchner, and Luca Gonsalvi/titolo:Carbon Dioxide Hydrogenation to Formate Catalyzed by a Bench-Stable, Non-Pincer-Type Mn(I) Alkylcarbonyl Complex/doi:10.1021%2Facs.organomet.0c00710/rivista:Organometallics (Online)/anno:2021/pagina_da:1213/pagina_a:1220/intervallo_pagine:1213–1220/volume:40
Organometallics (Online) 40 (2021): 1213–1220. doi:10.1021/acs.organomet.0c00710
info:cnr-pdr/source/autori:Sylwia Kostera, Stefan Weber, Maurizio Peruzzini, Luis F. Veiros, Karl Kirchner, and Luca Gonsalvi/titolo:Carbon Dioxide Hydrogenation to Formate Catalyzed by a Bench-Stable, Non-Pincer-Type Mn(I) Alkylcarbonyl Complex/doi:10.1021%2Facs.organomet.0c00710/rivista:Organometallics (Online)/anno:2021/pagina_da:1213/pagina_a:1220/intervallo_pagine:1213–1220/volume:40
The catalytic reduction of carbon dioxide is a process of growing interest for the use of this simple and abundant molecule as a renewable building block in C1-chemical synthesis and for hydrogen storage. The well-defined, bench-stable alkylcarbonyl
Publikováno v:
ChemCatChem (Internet) 12 (2020): 4625–4631. doi:10.1002/cctc.202000469
info:cnr-pdr/source/autori:Kostera, Sylwia; Peruzzini, Maurizio; Kirchner, Karl; Gonsalvi, Luca/titolo:Mild and Selective Carbon Dioxide Hydroboration to Methoxyboranes Catalyzed by Mn(I) PNP Pincer Complexes/doi:10.1002%2Fcctc.202000469/rivista:ChemCatChem (Internet)/anno:2020/pagina_da:4625/pagina_a:4631/intervallo_pagine:4625–4631/volume:12
info:cnr-pdr/source/autori:Kostera, Sylwia; Peruzzini, Maurizio; Kirchner, Karl; Gonsalvi, Luca/titolo:Mild and Selective Carbon Dioxide Hydroboration to Methoxyboranes Catalyzed by Mn(I) PNP Pincer Complexes/doi:10.1002%2Fcctc.202000469/rivista:ChemCatChem (Internet)/anno:2020/pagina_da:4625/pagina_a:4631/intervallo_pagine:4625–4631/volume:12
Well-defined Mn(I)-PNP pincer-type complexes were tested as non-precious transition metal catalysts for the selective reduction of CO2 to boryl-protected MeOH in the presence of hydroboranes (HBpin, 9-BBN) and borates as Lewis acids (LA) additives. T
Publikováno v:
New Journal of Chemistry. 44:10786-10795
Among the broad palette of POSS hybrids, the mono-functionalized ones can be considered as attractive starting blocks for further structural expansion. In this paper, we report on the poorly known group represented by N-containing derivatives which h
Publikováno v:
CO2 Hydrogenation Catalysis, edited by Yuichiro Himeda, pp. 53–88. Wheinheim: Wiley-VCH-Weinheim, 2021
info:cnr-pdr/source/autori:Luca Gonsalvi, Antonella Guerriero, Sylwia Kostera/titolo:Homogeneously Catalyzed CO2 Hydrogenation to Formic Acid%2FFormate with Non-precious Metal Catalysts/titolo_volume:CO2 Hydrogenation Catalysis/curatori_volume:Yuichiro Himeda/editore: /anno:2021
CO2 Hydrogenation Catalysis
info:cnr-pdr/source/autori:Luca Gonsalvi, Antonella Guerriero, Sylwia Kostera/titolo:Homogeneously Catalyzed CO2 Hydrogenation to Formic Acid%2FFormate with Non-precious Metal Catalysts/titolo_volume:CO2 Hydrogenation Catalysis/curatori_volume:Yuichiro Himeda/editore: /anno:2021
CO2 Hydrogenation Catalysis
In this chapter, the main results described in the literature for CO2 hydrogenation to formic acid and formates, using non-precious (mainly first-row) transition metals, are summarized. Particular attention is given to illustrate the different classe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::37f6fee957c5cf7331d95bbbfb6d1312
Publikováno v:
Dalton Transactions. 46:11552-11555
A ruthenium-hydride complex, [Ru(H)(Cl)(CO)(PCy3)2], was found to be active in the highly selective redistribution of primary and secondary amines bearing an α-hydrogen atom. This new deaminative coupling of amines enables the highly selective synth
Publikováno v:
RSC Advances. 6:39947-39954
A selective and efficient catalytic method was developed for the synthesis of new styryl-conjugated silyl-ferrocene materials. The use of an effective palladium catalytic system [Pd(η2-dba)(P(o-tolyl)3)2] (3) with a K3PO4 base solution allowed us to
Publikováno v:
Tetrahedron Letters. 55:3055-3058
This work describes very precise and controlled catalytic transformations as useful tools for the synthesis of new trans-π-conjugated molecular and macromolecular organosilicon compounds. Several distyryl-arenes were obtained efficiently via silylat
Publikováno v:
Dalton transactions (Cambridge, England : 2003). 44(2)
The ruthenium hydride complex-catalyzed N-silylation of primary and secondary amines with substituted vinylsilanes, with the general formula R(1)CH=CHSiR (where R(1) = H, Ph, n-Bu, Si(OEt)3), leading to the formation of a Si-N bond with the evolution
Publikováno v:
ChemInform. 45
Silylative coupling of distyrylarenes with vinyltrimethylsilane provides new E,E-bis(silyl)arenes with excellent selectivity.