Academic Journal

An N-heterocyclic carbene ligand promotes highly selective alkyne semihydrogenation with copper nanoparticles supported on passivated silica

التفاصيل البيبلوغرافية
العنوان: An N-heterocyclic carbene ligand promotes highly selective alkyne semihydrogenation with copper nanoparticles supported on passivated silica
المؤلفون: Kaeffer, Nicolas, id_orcid:0 000-0002-3166-8551, Liu, Hsueh-Ju, Lo, Hung-Kun, Fedorov, Alexey, id_orcid:0 000-0001-9814-6726, Copéret, Christophe, id_orcid:0 000-0001-9660-3890
المصدر: Chemical Science, 9 (24)
بيانات النشر: Royal Society of Chemistry
سنة النشر: 2018
المجموعة: ETH Zürich Research Collection
الوصف: We report a surface organometallic route that generates copper nanoparticles (NPs) on a silica support while simultaneously passivating the silica surface with trimethylsiloxy groups. The material is active for the catalytic semihydrogenation of phenylalkyl-, dialkyl- and diaryl-alkynes and displays high chemo- and stereoselectivity at full alkyne conversion to corresponding (Z)-olefins in the presence of an N-heterocyclic carbene (NHC) ligand. Solid-state NMR spectroscopy using the NHC ligand 13C-labeled at the carbenic carbon reveals a genuine coordination of the carbene to Cu NPs. The presence of distinct Cu surface environments and the coordination of the NHC to specific Cu sites likely account for the increased selectivity. ; ISSN:2041-6520 ; ISSN:2041-6539
نوع الوثيقة: article in journal/newspaper
وصف الملف: application/application/pdf
اللغة: English
Relation: info:eu-repo/semantics/altIdentifier/wos/000436027800008; http://hdl.handle.net/20.500.11850/274422
DOI: 10.3929/ethz-b-000274422
الاتاحة: https://hdl.handle.net/20.500.11850/274422
https://doi.org/10.3929/ethz-b-000274422
Rights: info:eu-repo/semantics/openAccess ; http://creativecommons.org/licenses/by-nc/3.0/ ; Creative Commons Attribution-NonCommercial 3.0 Unported
رقم الانضمام: edsbas.3090964E
قاعدة البيانات: BASE
الوصف
DOI:10.3929/ethz-b-000274422