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New supramolecular transition metal catalysts
Author(s) -
Reetz Manfred T.
Publication year - 1998
Publication title -
journal of heterocyclic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.321
H-Index - 59
eISSN - 1943-5193
pISSN - 0022-152X
DOI - 10.1002/jhet.5570350506
Subject(s) - chemistry , transition metal , catalysis , supramolecular chemistry , combinatorial chemistry , supramolecular catalysis , nanotechnology , organic chemistry , molecule , materials science
The covalent connection of a catalytically active transition metal center with a water‐soluble receptor (host molecule) generates a new type of supramolecular catalyst in which the features of molecular recognition, phase transfer catalysis and transition metal catalysis are combined in a single system. The first examples of this principle make use of commercially available β‐cyclodextrin (β‐CD) as the receptor and rhodium complexes of diphosphanes as the catalytically active center, these being covalently connected to one another via a spacer. In competitive hydrogenation of certain olefins, unusual degrees of substrate selectivity based on molecular recognition are observed, not possible by conventional transition metal catalysts. The two‐phase (water/organic) hydrogenation of nitro‐aromatics also is a smooth process catalyzed by these supramolecular complexes. They also constitute an unusually active catalyst system for the selective hydroformylation of higher olefins such as 1‐octene in a two‐phase system. Dendrimers having diphosphane moieties on the surface provide ligands for transition metals, the corresponding metal complexes ( e.g. , Pd) functioning as efficient catalysts which can be recycled due to their nanoscopic properties.