z-logo
Premium
Catalytically Active Palladium Nanoparticle‐Cored Ferrocenyl‐Terminated Dendrimers
Author(s) -
Lu Feng,
Didier Astruc
Publication year - 2015
Publication title -
european journal of inorganic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.667
H-Index - 136
eISSN - 1099-0682
pISSN - 1434-1948
DOI - 10.1002/ejic.201501103
Subject(s) - dendrimer , chemistry , catalysis , palladium , styrene , nanomaterials , nanoparticle , branching (polymer chemistry) , fourier transform infrared spectroscopy , supramolecular chemistry , combinatorial chemistry , polymer chemistry , organic chemistry , nanotechnology , chemical engineering , molecule , copolymer , polymer , materials science , engineering
Nanoparticle‐cored (NP‐cored) ferrocenyl dendrimers are precise multifunctional supramolecular nanomaterials owing to their active central and terminal groups and high (1→3) branching connectivity. For instance, catalysis in the interior of the metallodendrimer remains intriguing, especially because sulfur ligands have the reputation to inhibit catalytic reactions on surfaces. A nonaferrocenyl thiol dendron, 1 , was utilized to prepare PdNP‐cored metallodendrimers (FcD‐PdNPs) 2 , which were characterized by 1 H, 13 C NMR and FTIR spectroscopy, elemental analysis, and TEM. The ratio of precursor complex [PdCl 2 (MeCN) 2 ] to dendron 1 was demonstrated to play a key role in the effectiveness of 2 as catalyst in Suzuki–Miyaura and styrene hydrogenation reactions, and a ratio of 5:1 optimized intradendritic catalytic activity for styrene hydrogenation at room temp. and 1 atm H 2 .

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom