Literature DB >> 16276555

Reactions in micellar systems.

Torsten Dwars1, Eckhard Paetzold, Günther Oehme.   

Abstract

The notion of "green chemistry" has encouraged even synthetic organic chemists to include water as a solvent. Incredible selectivities and activities can be achieved through the addition of amphiphiles with a defined structure. The morphology of supramolecular assemblies or associates formed by surfactants vary according to the temperature and concentration. As a rule, reactions are typically conducted using simple spherical aggregates, that is, micelles in the nanometer range. The strong polarity gradient present between the hydrophilic surface and the hydrophobic core of the micelle means that both nonpolar and polar reagents can be solubilized. This solubilization results in reactants becoming more concentrated within the micelle than in the surrounding water phase and leads to an acceleration of the reaction and causes selective effects. The kinetic treatment of reactions in micellar systems can be accomplished by considering them as microheterogeneous two-phase systems.

Entities:  

Year:  2005        PMID: 16276555     DOI: 10.1002/anie.200501365

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


  45 in total

Review 1.  High-definition self-assemblies driven by the hydrophobic effect: synthesis and properties of a supramolecular nanocapsule.

Authors:  Simin Liu; Bruce C Gibb
Journal:  Chem Commun (Camb)       Date:  2008-06-06       Impact factor: 6.222

2.  Entropic factors provide unusual reactivity and selectivity in epoxide-opening reactions promoted by water.

Authors:  Jeffery A Byers; Timothy F Jamison
Journal:  Proc Natl Acad Sci U S A       Date:  2013-09-17       Impact factor: 11.205

3.  Miyaura Borylations of Aryl Bromides in Water at Room Temperature.

Authors:  Bruce H Lipshutz; Ralph Moser; Karl R Voigtritter
Journal:  Isr J Chem       Date:  2010-12-01       Impact factor: 3.333

4.  Materials chemistry: catalytic accordions.

Authors:  Nicolas Giuseppone; Jean-François Lutz
Journal:  Nature       Date:  2011-05-05       Impact factor: 49.962

5.  Catalytic Y-tailed amphiphilic homopolymers - aqueous nanoreactors for high activity, low loading SCS pincer catalysts.

Authors:  Joseph P Patterson; Pepa Cotanda; Elizabeth G Kelley; Adam O Moughton; Annhelen Lu; Thomas H Epps; Rachel K O'Reilly
Journal:  Polym Chem       Date:  2013-01-28       Impact factor: 5.582

6.  HandaPhos: A General Ligand Enabling Sustainable ppm Levels of Palladium-Catalyzed Cross-Couplings in Water at Room Temperature.

Authors:  Sachin Handa; Martin P Andersson; Fabrice Gallou; John Reilly; Bruce H Lipshutz
Journal:  Angew Chem Int Ed Engl       Date:  2016-02-29       Impact factor: 15.336

7.  "Nok": a phytosterol-based amphiphile enabling transition-metal-catalyzed couplings in water at room temperature.

Authors:  Piyatida Klumphu; Bruce H Lipshutz
Journal:  J Org Chem       Date:  2014-01-21       Impact factor: 4.354

8.  "Click" and Olefin Metathesis Chemistry in Water at Room Temperature Enabled by Biodegradable Micelles.

Authors:  Bruce H Lipshutz; Zarko Bošković; Christopher S Crowe; Victoria K Davis; Hannah C Whittemore; David A Vosburg; Anna G Wenzel
Journal:  J Chem Educ       Date:  2013-11-12       Impact factor: 2.979

9.  Pd-catalyzed synthesis of allylic silanes from allylic ethers.

Authors:  Ralph Moser; Takashi Nishikata; Bruce H Lipshutz
Journal:  Org Lett       Date:  2010-01-01       Impact factor: 6.005

10.  On the synergism between H2O and a tetrahydropyran template in the regioselective cyclization of an epoxy alcohol.

Authors:  Jeffery A Byers; Timothy F Jamison
Journal:  J Am Chem Soc       Date:  2009-05-13       Impact factor: 15.419

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