Literature DB >> 17814001

Facile catalyst separation without water: fluorous biphase hydroformylation of olefins.

I T Horváth, J Rábai.   

Abstract

A novel concept for performing stoichiometric and catalytic chemical transformations has been developed that is based on the limited miscibility of partially or fully fluorinated compounds with nonfluorinated compounds. A fluorous biphase system (FBS) consists of a fluorous phase containing a dissolved reagent or catalyst and another phase, which could be any common organic or nonorganic solvent with limited or no solubility in the fluorous phase. The fluorous phase is defined as the fluorocarbon (mostly perfluorinated alkanes, ethers, and tertiary amines)-rich phase of a biphase system. An FBS compatible reagent or catalyst contains enough fluorous moieties that it will be soluble only or preferentially in the fluorous phase. The most effective fluorous moieties are linear or branched perfluoroalkyl chains with high carbon number; they may also contain heteroatoms. The chemical transformation may occur either in the fluorous phase or at the interface of the two phases. The application of FBS has been demonstrated for the extraction of rhodium from toluene and for the hydroformylation of olefins. The ability to separate a catalyst or a reagent from the products completely at mild conditions could lead to industrial application of homogeneous catalysts or reagents and to the development of more environmentally benign processes.

Entities:  

Year:  1994        PMID: 17814001     DOI: 10.1126/science.266.5182.72

Source DB:  PubMed          Journal:  Science        ISSN: 0036-8075            Impact factor:   47.728


  47 in total

1.  Potentiometric sensors based on fluorous membranes doped with highly selective ionophores for carbonate.

Authors:  Li D Chen; Debaprasad Mandal; Gianluca Pozzi; John A Gladysz; Philippe Bühlmann
Journal:  J Am Chem Soc       Date:  2011-12-02       Impact factor: 15.419

2.  Preparation of a Highly Fluorophilic Phosphonium Salt and its Use in a Fluorous Anion-Exchanger Membrane with High Selectivity for Perfluorinated Acids.

Authors:  Paul G Boswell; Alyce C Anfang; Philippe Bühlmann
Journal:  J Fluor Chem       Date:  2008-10       Impact factor: 2.050

Review 3.  Fluorous synthesis of heterocyclic systems.

Authors:  Wei Zhang
Journal:  Chem Rev       Date:  2004-05       Impact factor: 60.622

4.  Structural basis for the enhanced stability of highly fluorinated proteins.

Authors:  Benjamin C Buer; Jennifer L Meagher; Jeanne A Stuckey; E Neil G Marsh
Journal:  Proc Natl Acad Sci U S A       Date:  2012-03-12       Impact factor: 11.205

Review 5.  Fluorine: a new element in protein design.

Authors:  Benjamin C Buer; E Neil G Marsh
Journal:  Protein Sci       Date:  2012-02-14       Impact factor: 6.725

6.  De novo design of defined helical bundles in membrane environments.

Authors:  Basar Bilgiçer; Krishna Kumar
Journal:  Proc Natl Acad Sci U S A       Date:  2004-10-14       Impact factor: 11.205

7.  Selective metabolite and peptide capture/mass detection using fluorous affinity tags.

Authors:  Eden P Go; Wilasinee Uritboonthai; Junefredo V Apon; Sunia A Trauger; Anders Nordstrom; Grace O'Maille; Scott M Brittain; Eric C Peters; Gary Siuzdak
Journal:  J Proteome Res       Date:  2007-03-08       Impact factor: 4.466

8.  High lipophilicity of perfluoroalkyl carboxylate and sulfonate: implications for their membrane permeability.

Authors:  Ping Jing; Patrick J Rodgers; Shigeru Amemiya
Journal:  J Am Chem Soc       Date:  2009-02-18       Impact factor: 15.419

9.  A recyclable fluorous organocatalyst for Diels-Alder reactions.

Authors:  Qianli Chu; Wei Zhang; Dennis P Curran
Journal:  Tetrahedron Lett       Date:  2006-12-25       Impact factor: 2.415

10.  A General Approach to Biocompatible Branched Fluorous Tags for Increased Solubility in Perfluorocarbon Solvents.

Authors:  Margeaux A Miller; Ellen M Sletten
Journal:  Org Lett       Date:  2018-10-24       Impact factor: 6.005

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