Literature DB >> 16217817

Supramolecular approaches to generate libraries of chelating bidentate ligands for homogeneous catalysis.

Bernhard Breit1.   

Abstract

The process of catalyst discovery and development relying on combinatorial methods has suffered so far from the difficult access to structurally diverse and large libraries of ligands, in particular the structurally more complex class of bidentate ligands. A completely new approach to streamline the difficult ligand synthesis process is to use structurally less complex monodentate ligands that self-assemble in the coordination sphere of a metal center through noncovalent attractive ligand-ligand interactions to generate bidentate, chelating ligands. When complementary attractive ligand-ligand interactions are employed, it is even possible to generate libraries of defined chelate-ligand catalysts by simply mixing two different monomeric ligands. This Minireview summarizes the first approaches and results in this new field of combinatorial homogeneous catalysis.

Entities:  

Mesh:

Substances:

Year:  2005        PMID: 16217817     DOI: 10.1002/anie.200501798

Source DB:  PubMed          Journal:  Angew Chem Int Ed Engl        ISSN: 1433-7851            Impact factor:   15.336


  13 in total

1.  Self-assembled nanospheres with multiple endohedral binding sites pre-organize catalysts and substrates for highly efficient reactions.

Authors:  Qi-Qiang Wang; Sergio Gonell; Stefan H A M Leenders; Maximilian Dürr; Ivana Ivanović-Burmazović; Joost N H Reek
Journal:  Nat Chem       Date:  2016-01-11       Impact factor: 24.427

2.  Ligand scaffold optimization of a supramolecular hydrogenation catalyst: Analyzing the influence of key structural subunits on reactivity and selectivity.

Authors:  Nathan C Thacker; Shin A Moteki; James M Takacs
Journal:  ACS Catal       Date:  2012-11-05       Impact factor: 13.084

3.  Excess substrate is a spectator ligand in a rhodium-catalyzed asymmetric [2 + 2 + 2] cycloaddition of alkenyl isocyanates with tolanes.

Authors:  Mark Emil Oinen; Robert T Yu; Tomislav Rovis
Journal:  Org Lett       Date:  2009-11-05       Impact factor: 6.005

Review 4.  Supramolecular Approaches To Control Activity and Selectivity in Hydroformylation Catalysis.

Authors:  Sandra S Nurttila; Pim R Linnebank; Tetiana Krachko; Joost N H Reek
Journal:  ACS Catal       Date:  2018-03-09       Impact factor: 13.084

5.  XBphos-Rh: a halogen-bond assembled supramolecular catalyst.

Authors:  Lucas Carreras; Marta Serrano-Torné; Piet W N M van Leeuwen; Anton Vidal-Ferran
Journal:  Chem Sci       Date:  2018-02-19       Impact factor: 9.825

6.  Rational Optimization of Supramolecular Catalysts for the Rhodium-Catalyzed Asymmetric Hydrogenation Reaction.

Authors:  Julien Daubignard; Remko J Detz; Anne C H Jans; Bas de Bruin; Joost N H Reek
Journal:  Angew Chem Int Ed Engl       Date:  2017-09-12       Impact factor: 15.336

7.  Novel Chiral Bis-Phosphoramides as Organocatalysts for Tetrachlorosilane-Mediated Reactions.

Authors:  Sergio Rossi; Marco Ziliani; Rita Annunziata; Maurizio Benaglia
Journal:  Molecules       Date:  2017-12-08       Impact factor: 4.411

8.  A supramolecularly tunable chiral diphosphine ligand: application to Rh and Ir-catalyzed enantioselective hydrogenation.

Authors:  Xi-Chang Zhang; Yi-Hu Hu; Chuan-Fu Chen; Qiang Fang; Li-Yao Yang; Ying-Bo Lu; Lin-Jie Xie; Jing Wu; Shijun Li; Wenjun Fang
Journal:  Chem Sci       Date:  2016-03-31       Impact factor: 9.825

9.  Cofactor Controlled Encapsulation of a Rhodium Hydroformylation Catalyst.

Authors:  Lukas J Jongkind; Johannes A A W Elemans; Joost N H Reek
Journal:  Angew Chem Int Ed Engl       Date:  2019-01-29       Impact factor: 15.336

10.  Catalysis of transesterification reactions by a self-assembled nanosystem.

Authors:  Davide Zaramella; Paolo Scrimin; Leonard J Prins
Journal:  Int J Mol Sci       Date:  2013-01-21       Impact factor: 5.923

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.