Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Orsino, Alessio F."'
Autor:
Verhoeven, Dide G. A., Orsino, Alessio F., Bienenmann, Roel L. M., Lutz, Martin, Moret, Marc-etienne, Sub Organic Chemistry and Catalysis, Sub Crystal and Structural Chemistry, Organic Chemistry and Catalysis, Crystal and Structural Chemistry
Publikováno v:
Organometallics, 39(4), 623. American Chemical Society
Activation of a Si–H bond is commonly a critical step in catalytic hydrosilylation reactions. Herein, we investigate the cooperative reactivity of Ni(0) centers bearing a side-bound imine ligand toward silanes. Such complexes activate a Si–H bond
Autor:
Orsino, Alessio F., Gutiérrez Del Campo, Manuel, Lutz, Martin, Moret, Marc-etienne, Sub Organic Chemistry and Catalysis, Sub Crystal and Structural Chemistry, Organic Chemistry and Catalysis, Crystal and Structural Chemistry
Publikováno v:
ACS Catalysis, 9, 2458. American Chemical Society
ACS Catalysis
ACS Catalysis
Adaptive ligands, which can adapt their coordination mode to the electronic structure of various catalytic intermediates, offer the potential to develop improved homogeneous catalysts in terms of activity and selectivity. 2,2′-Diphosphinobenzopheno
Autor:
Orsino, Alessio F., Moret, Marc Etienne, Sub Organic Chemistry and Catalysis, Organic Chemistry and Catalysis
Publikováno v:
Organometallics, 39(10), 1998. American Chemical Society
π-coordinating units incorporated in the supporting ligand of an organometallic complex may open up specific reactive pathways. The diphosphine ketone supported nickel complex [(p-tolL1)Ni(BPI)] (p-tol1; p-tolL1 = 2,2′-bis(di-p-tolylphosphino)benz
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::23062cc2318fb65a1b44abb93d71f67d
https://dspace.library.uu.nl/handle/1874/411228
https://dspace.library.uu.nl/handle/1874/411228
Autor:
Verhoeven, Dide G. A., Negenman, Hidde A., Orsino, Alessio F., Lutz, Martin, Moret, Marc-etienne, Organic Chemistry and Catalysis, Crystal and Structural Chemistry, Sub Organic Chemistry and Catalysis, Sub Crystal and Structural Chemistry
Publikováno v:
Inorganic Chemistry, 57(17). American Chemical Society
Ligands that can adapt their coordination mode to the electronic properties of a metal center are of interest to support catalysis or small molecule activation processes. In this context, the ability of imine moieties to bind in either an η1(N)-fash
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cc91d0c1c32d2123dddf9a7c89d92ab5
https://dspace.library.uu.nl/handle/1874/369295
https://dspace.library.uu.nl/handle/1874/369295
Versatile Coordination and C-C Coupling of Diphosphine-Tethered Imine Ligands with Ni(II) and Ni(0).
Autor:
Verhoeven DGA; Organic Chemistry and Catalysis, Debye Institute for Nanomaterials Science, Faculty of Science , Utrecht University , Universiteitsweg 99 , 3584 CG , Utrecht , The Netherlands., Negenman HA; Organic Chemistry and Catalysis, Debye Institute for Nanomaterials Science, Faculty of Science , Utrecht University , Universiteitsweg 99 , 3584 CG , Utrecht , The Netherlands., Orsino AF; Organic Chemistry and Catalysis, Debye Institute for Nanomaterials Science, Faculty of Science , Utrecht University , Universiteitsweg 99 , 3584 CG , Utrecht , The Netherlands., Lutz M; Crystal and Structural Chemistry, Bijvoet Center for Biomolecular Research, Faculty of Science , Utrecht University , Padualaan 8 , 3584 CH , Utrecht , The Netherlands., Moret ME; Organic Chemistry and Catalysis, Debye Institute for Nanomaterials Science, Faculty of Science , Utrecht University , Universiteitsweg 99 , 3584 CG , Utrecht , The Netherlands.
Publikováno v:
Inorganic chemistry [Inorg Chem] 2018 Sep 04; Vol. 57 (17), pp. 10846-10856. Date of Electronic Publication: 2018 Aug 16.