Supramolecular approaches in transition‐metal catalysis, including catalyst encapsulation, have attracted considerable attention. Compared to enzymes, supramolecular catalysts in general are less complex. Enzyme activity is often controlled by the use of smaller cofactor molecules, which is important in order to control reactivity in complex mixtures of molecules. Interested in increasing complexity and allowing control over supramolecular catalyst formation in response to external stimuli, we designed a catalytic system that only forms an efficient supramolecular complex when a small cofactor molecule is added to the solution. This in turn affects both the activity and selectivity when applied in a hydroformylation reaction. This contribut...
Herein, we report a supramolecular rhodium complex that can form dimeric or monomeric Rh-species cat...
The coordination mode of a monodentate phosphoroamidite ligand in a rhodium complex can be switched ...
International audienceRegio-and enantioselective hydroformylation of styrenes is attained upon embed...
Contains fulltext : 201676.pdf (publisher's version ) (Open Access
Traditional homogeneous catalysis applies catalysts based on organometallic complexes which are tune...
The development of catalysts has enabled highly specialized processes that are of great value to man...
The hydroformylation reaction is one of the most intensively explored reactions in the field of homo...
Size‐selective hydroformylation of terminal alkenes was attained upon embedding a rhodium bisphosphi...
In this thesis supramolecular strategies were investigated to obtain control over the regioselectivi...
De werking van metaalcomplexen als katalysator in industriële processen is anders dan de manier waar...
his study reveals that, in contrast to expectations, supramolecular encapsulated rhodium catalysts c...
Chemical processes proceed much faster and more selectively in the presence of appropriate catalysts...
Chemical processes proceed much faster and more selectively in the presence of appropriate catalysts...
Chemical processes proceed much faster and more selectively in the presence of appropriate catalysts...
Herein, we report a supramolecular rhodium complex that can form dimeric or monomeric Rh-species cat...
Herein, we report a supramolecular rhodium complex that can form dimeric or monomeric Rh-species cat...
The coordination mode of a monodentate phosphoroamidite ligand in a rhodium complex can be switched ...
International audienceRegio-and enantioselective hydroformylation of styrenes is attained upon embed...
Contains fulltext : 201676.pdf (publisher's version ) (Open Access
Traditional homogeneous catalysis applies catalysts based on organometallic complexes which are tune...
The development of catalysts has enabled highly specialized processes that are of great value to man...
The hydroformylation reaction is one of the most intensively explored reactions in the field of homo...
Size‐selective hydroformylation of terminal alkenes was attained upon embedding a rhodium bisphosphi...
In this thesis supramolecular strategies were investigated to obtain control over the regioselectivi...
De werking van metaalcomplexen als katalysator in industriële processen is anders dan de manier waar...
his study reveals that, in contrast to expectations, supramolecular encapsulated rhodium catalysts c...
Chemical processes proceed much faster and more selectively in the presence of appropriate catalysts...
Chemical processes proceed much faster and more selectively in the presence of appropriate catalysts...
Chemical processes proceed much faster and more selectively in the presence of appropriate catalysts...
Herein, we report a supramolecular rhodium complex that can form dimeric or monomeric Rh-species cat...
Herein, we report a supramolecular rhodium complex that can form dimeric or monomeric Rh-species cat...
The coordination mode of a monodentate phosphoroamidite ligand in a rhodium complex can be switched ...
International audienceRegio-and enantioselective hydroformylation of styrenes is attained upon embed...