Development of a continuous-flow system for catalysis with palladium(0) particles

Publikation: Beitrag in FachzeitschriftArtikelForschungPeer-Review

Autoren

  • Wladimir Solodenko
  • Hongliang Wen
  • Stefanie Leue
  • Friedrich Stuhlmann
  • Georgia Sourkouni-Argirusi
  • Gerhard Jas
  • Hagen Schönfeld
  • Ulrich Kunz
  • Andreas Kirschning

Organisationseinheiten

Externe Organisationen

  • CHELONA GmbH
  • Technische Universität Clausthal
Forschungs-netzwerk anzeigen

Details

OriginalspracheEnglisch
Seiten (von - bis)3601-3610
Seitenumfang10
FachzeitschriftEuropean Journal of Organic Chemistry
Ausgabenummer17
PublikationsstatusVeröffentlicht - 17 Aug. 2004

Abstract

Heterogeneous catalysis for organic synthesis under continuous-flow conditions becomes possible by a new reactor-based approach. Continuous-flow reactors with a monolithic glass/polymer composite interior are loaded with palladium particles by ion exchange followed by reduction. When incorporated into a continuous-flow setup (PASSflow) this reactor allows the transfer-hydrogenation of alkenes, alkynes, nitro-substituted aromatic compounds and benzyl ethers in the flow-through mode. In addition, the activity of the catalysts is well suited to achieve Suzuki, Sonogashira and Heck cross-coupling reactions in the absence of phosphanes or any other ligands, resulting in a greatly simplified purification. As an extension to this concept a bifunctional support was prepared inside the reactor consisting of Pd particles and an ion-exchange group (hydroxide form). In the Suzuki-Miyaura reaction the reactor serves as a base for immobilisation and activation of the boronic acid as boronate and as a catalyst for promoting the C-C coupling reaction under continuous-flow conditions.

ASJC Scopus Sachgebiete

Zitieren

Development of a continuous-flow system for catalysis with palladium(0) particles. / Solodenko, Wladimir; Wen, Hongliang; Leue, Stefanie et al.
in: European Journal of Organic Chemistry, Nr. 17, 17.08.2004, S. 3601-3610.

Publikation: Beitrag in FachzeitschriftArtikelForschungPeer-Review

Solodenko, W, Wen, H, Leue, S, Stuhlmann, F, Sourkouni-Argirusi, G, Jas, G, Schönfeld, H, Kunz, U & Kirschning, A 2004, 'Development of a continuous-flow system for catalysis with palladium(0) particles', European Journal of Organic Chemistry, Nr. 17, S. 3601-3610. https://doi.org/10.1002/ejoc.200400194
Solodenko, W., Wen, H., Leue, S., Stuhlmann, F., Sourkouni-Argirusi, G., Jas, G., Schönfeld, H., Kunz, U., & Kirschning, A. (2004). Development of a continuous-flow system for catalysis with palladium(0) particles. European Journal of Organic Chemistry, (17), 3601-3610. https://doi.org/10.1002/ejoc.200400194
Solodenko W, Wen H, Leue S, Stuhlmann F, Sourkouni-Argirusi G, Jas G et al. Development of a continuous-flow system for catalysis with palladium(0) particles. European Journal of Organic Chemistry. 2004 Aug 17;(17):3601-3610. doi: 10.1002/ejoc.200400194
Solodenko, Wladimir ; Wen, Hongliang ; Leue, Stefanie et al. / Development of a continuous-flow system for catalysis with palladium(0) particles. in: European Journal of Organic Chemistry. 2004 ; Nr. 17. S. 3601-3610.
Download
@article{1ae94eca02564645ae5e584d2476f7e3,
title = "Development of a continuous-flow system for catalysis with palladium(0) particles",
abstract = "Heterogeneous catalysis for organic synthesis under continuous-flow conditions becomes possible by a new reactor-based approach. Continuous-flow reactors with a monolithic glass/polymer composite interior are loaded with palladium particles by ion exchange followed by reduction. When incorporated into a continuous-flow setup (PASSflow) this reactor allows the transfer-hydrogenation of alkenes, alkynes, nitro-substituted aromatic compounds and benzyl ethers in the flow-through mode. In addition, the activity of the catalysts is well suited to achieve Suzuki, Sonogashira and Heck cross-coupling reactions in the absence of phosphanes or any other ligands, resulting in a greatly simplified purification. As an extension to this concept a bifunctional support was prepared inside the reactor consisting of Pd particles and an ion-exchange group (hydroxide form). In the Suzuki-Miyaura reaction the reactor serves as a base for immobilisation and activation of the boronic acid as boronate and as a catalyst for promoting the C-C coupling reaction under continuous-flow conditions.",
keywords = "Continuous-flow processes, Heterogeneous catalysis, Hydrogenation, Palladium, Supported catalysts",
author = "Wladimir Solodenko and Hongliang Wen and Stefanie Leue and Friedrich Stuhlmann and Georgia Sourkouni-Argirusi and Gerhard Jas and Hagen Sch{\"o}nfeld and Ulrich Kunz and Andreas Kirschning",
year = "2004",
month = aug,
day = "17",
doi = "10.1002/ejoc.200400194",
language = "English",
pages = "3601--3610",
journal = "European Journal of Organic Chemistry",
issn = "1434-193X",
publisher = "Wiley-VCH Verlag",
number = "17",

}

Download

TY - JOUR

T1 - Development of a continuous-flow system for catalysis with palladium(0) particles

AU - Solodenko, Wladimir

AU - Wen, Hongliang

AU - Leue, Stefanie

AU - Stuhlmann, Friedrich

AU - Sourkouni-Argirusi, Georgia

AU - Jas, Gerhard

AU - Schönfeld, Hagen

AU - Kunz, Ulrich

AU - Kirschning, Andreas

PY - 2004/8/17

Y1 - 2004/8/17

N2 - Heterogeneous catalysis for organic synthesis under continuous-flow conditions becomes possible by a new reactor-based approach. Continuous-flow reactors with a monolithic glass/polymer composite interior are loaded with palladium particles by ion exchange followed by reduction. When incorporated into a continuous-flow setup (PASSflow) this reactor allows the transfer-hydrogenation of alkenes, alkynes, nitro-substituted aromatic compounds and benzyl ethers in the flow-through mode. In addition, the activity of the catalysts is well suited to achieve Suzuki, Sonogashira and Heck cross-coupling reactions in the absence of phosphanes or any other ligands, resulting in a greatly simplified purification. As an extension to this concept a bifunctional support was prepared inside the reactor consisting of Pd particles and an ion-exchange group (hydroxide form). In the Suzuki-Miyaura reaction the reactor serves as a base for immobilisation and activation of the boronic acid as boronate and as a catalyst for promoting the C-C coupling reaction under continuous-flow conditions.

AB - Heterogeneous catalysis for organic synthesis under continuous-flow conditions becomes possible by a new reactor-based approach. Continuous-flow reactors with a monolithic glass/polymer composite interior are loaded with palladium particles by ion exchange followed by reduction. When incorporated into a continuous-flow setup (PASSflow) this reactor allows the transfer-hydrogenation of alkenes, alkynes, nitro-substituted aromatic compounds and benzyl ethers in the flow-through mode. In addition, the activity of the catalysts is well suited to achieve Suzuki, Sonogashira and Heck cross-coupling reactions in the absence of phosphanes or any other ligands, resulting in a greatly simplified purification. As an extension to this concept a bifunctional support was prepared inside the reactor consisting of Pd particles and an ion-exchange group (hydroxide form). In the Suzuki-Miyaura reaction the reactor serves as a base for immobilisation and activation of the boronic acid as boronate and as a catalyst for promoting the C-C coupling reaction under continuous-flow conditions.

KW - Continuous-flow processes

KW - Heterogeneous catalysis

KW - Hydrogenation

KW - Palladium

KW - Supported catalysts

UR - http://www.scopus.com/inward/record.url?scp=4544298371&partnerID=8YFLogxK

U2 - 10.1002/ejoc.200400194

DO - 10.1002/ejoc.200400194

M3 - Article

AN - SCOPUS:4544298371

SP - 3601

EP - 3610

JO - European Journal of Organic Chemistry

JF - European Journal of Organic Chemistry

SN - 1434-193X

IS - 17

ER -

Von denselben Autoren