Related Experiment Video
Updated: Aug 17, 2026

Catalytic Reactions at Amine-Stabilized and Ligand-Free Platinum Nanoparticles Supported on Titania During Hydrogenation of Alkenes and Aldehydes
Published on: June 24, 2022
New directions in supramolecular transition metal catalysis
Matthew J Wilkinson1, Piet W N M van Leeuwen, Joost N H Reek
1van't Hoff Institute for Molecular Sciences, University of Amsterdam, Nieuwe Achtergracht 166, 1018 WV Amsterdam, The Netherlands.
Abstract:
Supramolecular chemistry has grown into a major scientific field over the last thirty years and has fueled numerous developments at the interfaces with biology and physics, clearly demonstrating its potential at a multidisciplinary level. Simultaneously, organometallic chemistry and transition metal catalysis have matured in an incredible manner, broadening the pallet of tools available for chemical conversions. The interface between supramolecular chemistry and transition metal catalysis has received surprisingly little attention. It provides, however, novel and elegant strategies that could lead to new tools in the search for effective catalysts, as well as the possibility of novel conversions induced by metal centres that are in unusual environments. This perspective describes new approaches to transition metal catalyst development that evolve from a combination of supramolecular strategies and rational ligand design, which may offer transition metal catalysts for future applications.
Related Concept Videos
Reduction of Alkenes: Asymmetric Catalytic Hydrogenation
The metal catalyst used can be either heterogeneous or homogeneous. When hydrogenation of an alkene generates a chiral center, a pair of enantiomeric products is expected to form. However, an enantiomeric excess of one of the products can be facilitated using an enantioselective reaction or an...
Heterogeneous Catalysis
Introduction to Mechanisms of Enzyme Catalysis
Introduction to Mechanisms of Enzyme Catalysis
Metal-Ligand Bonds
In these complexes, transition metals form coordinate covalent bonds, a kind of Lewis acid-base interaction in which both of the electrons in the bond are contributed by a donor (Lewis base) to an electron acceptor (Lewis acid). The Lewis acid in...
Properties of Organometallic Compounds

