Towards Surface‐Enhanced Homogeneous Catalysis: Tailoring the Enrichment of Metal Complexes at Ionic Liquid Surfaces

Autores
Hemmeter, Daniel; Haumann, Marco; Williams, Federico José; Koller, Thomas M.; Wasserscheid, Peter; Meyer, Karsten; Maier, Florian; Steinruck, Hans Peter
Año de publicación
2025
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
When talking about homogeneous catalyst systems, it has long been assumed that the system at hand consists of a transition metal complex in solution with the liquid interface representing the composition of the bulk solution. Now, in light of considerable developments in the study of metal complexes dissolved in ionic liquids with their negligible vapor pressures, more detailed studies of the composition at the liquid/gas interface became possible. These investigations revealed pronounced surface enrichment and segregation effects of high relevance for practical applications. This article reviews recent advancements in tailoring the interfacial composition of ionic liquid-based catalytic systems. A particular focus is dedicated to surface enrichment phenomena, and a variety of parameters are presented for deliberate control of the local concentration of the complexes at the surface, that is, the nature of the ligands, the bulk concentration, the temperature, and the nature of the IL solvent. As experimental methods, angle-resolved X-ray photoelectron spectroscopy (ARXPS) and vacuum-based pendant-drop surface tension measurements were applied. The reviewed results are intended to provide the basis for the advancement of catalytic systems with high surface areas, such as in supported ionic liquid phase (SILP) catalysis, where the interface design is directly interconnected with catalytic performance.
Fil: Hemmeter, Daniel. Universitat Erlangen-Nuremberg; Alemania
Fil: Haumann, Marco. Universitat Erlangen-Nuremberg; Alemania
Fil: Williams, Federico José. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Ciudad Universitaria. Instituto de Química, Física de los Materiales, Medioambiente y Energía. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales. Instituto de Química, Física de los Materiales, Medioambiente y Energía; Argentina
Fil: Koller, Thomas M.. Universitat Erlangen-Nuremberg; Alemania
Fil: Wasserscheid, Peter. Universitat Erlangen-Nuremberg; Alemania
Fil: Meyer, Karsten. Universitat Erlangen-Nuremberg; Alemania
Fil: Maier, Florian. Universitat Erlangen-Nuremberg; Alemania
Fil: Steinruck, Hans Peter. Universitat Erlangen-Nuremberg; Alemania
Materia
ionic liquids
XPS
complex
catalysis
Nivel de accesibilidad
acceso abierto
Condiciones de uso
https://creativecommons.org/licenses/by/2.5/ar/
Repositorio
CONICET Digital (CONICET)
Institución
Consejo Nacional de Investigaciones Científicas y Técnicas
OAI Identificador
oai:ri.conicet.gov.ar:11336/279816

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spelling Towards Surface‐Enhanced Homogeneous Catalysis: Tailoring the Enrichment of Metal Complexes at Ionic Liquid SurfacesHemmeter, DanielHaumann, MarcoWilliams, Federico JoséKoller, Thomas M.Wasserscheid, PeterMeyer, KarstenMaier, FlorianSteinruck, Hans Peterionic liquidsXPScomplexcatalysishttps://purl.org/becyt/ford/1.4https://purl.org/becyt/ford/1When talking about homogeneous catalyst systems, it has long been assumed that the system at hand consists of a transition metal complex in solution with the liquid interface representing the composition of the bulk solution. Now, in light of considerable developments in the study of metal complexes dissolved in ionic liquids with their negligible vapor pressures, more detailed studies of the composition at the liquid/gas interface became possible. These investigations revealed pronounced surface enrichment and segregation effects of high relevance for practical applications. This article reviews recent advancements in tailoring the interfacial composition of ionic liquid-based catalytic systems. A particular focus is dedicated to surface enrichment phenomena, and a variety of parameters are presented for deliberate control of the local concentration of the complexes at the surface, that is, the nature of the ligands, the bulk concentration, the temperature, and the nature of the IL solvent. As experimental methods, angle-resolved X-ray photoelectron spectroscopy (ARXPS) and vacuum-based pendant-drop surface tension measurements were applied. The reviewed results are intended to provide the basis for the advancement of catalytic systems with high surface areas, such as in supported ionic liquid phase (SILP) catalysis, where the interface design is directly interconnected with catalytic performance.Fil: Hemmeter, Daniel. Universitat Erlangen-Nuremberg; AlemaniaFil: Haumann, Marco. Universitat Erlangen-Nuremberg; AlemaniaFil: Williams, Federico José. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Ciudad Universitaria. Instituto de Química, Física de los Materiales, Medioambiente y Energía. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales. Instituto de Química, Física de los Materiales, Medioambiente y Energía; ArgentinaFil: Koller, Thomas M.. Universitat Erlangen-Nuremberg; AlemaniaFil: Wasserscheid, Peter. Universitat Erlangen-Nuremberg; AlemaniaFil: Meyer, Karsten. Universitat Erlangen-Nuremberg; AlemaniaFil: Maier, Florian. Universitat Erlangen-Nuremberg; AlemaniaFil: Steinruck, Hans Peter. Universitat Erlangen-Nuremberg; AlemaniaWiley VCH Verlag2025-02info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/279816Hemmeter, Daniel; Haumann, Marco; Williams, Federico José; Koller, Thomas M.; Wasserscheid, Peter; et al.; Towards Surface‐Enhanced Homogeneous Catalysis: Tailoring the Enrichment of Metal Complexes at Ionic Liquid Surfaces; Wiley VCH Verlag; Angewandte Chemie; 64; 14; 2-2025; 1-261433-7851CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/url/https://onlinelibrary.wiley.com/doi/10.1002/anie.202422693info:eu-repo/semantics/altIdentifier/doi/10.1002/anie.202422693info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2026-02-06T13:13:14Zoai:ri.conicet.gov.ar:11336/279816instacron:CONICETInstitucionalhttp://ri.conicet.gov.ar/Organismo científico-tecnológicoNo correspondehttp://ri.conicet.gov.ar/oai/requestdasensio@conicet.gov.ar; lcarlino@conicet.gov.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:34982026-02-06 13:13:15.07CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse
dc.title.none.fl_str_mv Towards Surface‐Enhanced Homogeneous Catalysis: Tailoring the Enrichment of Metal Complexes at Ionic Liquid Surfaces
title Towards Surface‐Enhanced Homogeneous Catalysis: Tailoring the Enrichment of Metal Complexes at Ionic Liquid Surfaces
spellingShingle Towards Surface‐Enhanced Homogeneous Catalysis: Tailoring the Enrichment of Metal Complexes at Ionic Liquid Surfaces
Hemmeter, Daniel
ionic liquids
XPS
complex
catalysis
title_short Towards Surface‐Enhanced Homogeneous Catalysis: Tailoring the Enrichment of Metal Complexes at Ionic Liquid Surfaces
title_full Towards Surface‐Enhanced Homogeneous Catalysis: Tailoring the Enrichment of Metal Complexes at Ionic Liquid Surfaces
title_fullStr Towards Surface‐Enhanced Homogeneous Catalysis: Tailoring the Enrichment of Metal Complexes at Ionic Liquid Surfaces
title_full_unstemmed Towards Surface‐Enhanced Homogeneous Catalysis: Tailoring the Enrichment of Metal Complexes at Ionic Liquid Surfaces
title_sort Towards Surface‐Enhanced Homogeneous Catalysis: Tailoring the Enrichment of Metal Complexes at Ionic Liquid Surfaces
dc.creator.none.fl_str_mv Hemmeter, Daniel
Haumann, Marco
Williams, Federico José
Koller, Thomas M.
Wasserscheid, Peter
Meyer, Karsten
Maier, Florian
Steinruck, Hans Peter
author Hemmeter, Daniel
author_facet Hemmeter, Daniel
Haumann, Marco
Williams, Federico José
Koller, Thomas M.
Wasserscheid, Peter
Meyer, Karsten
Maier, Florian
Steinruck, Hans Peter
author_role author
author2 Haumann, Marco
Williams, Federico José
Koller, Thomas M.
Wasserscheid, Peter
Meyer, Karsten
Maier, Florian
Steinruck, Hans Peter
author2_role author
author
author
author
author
author
author
dc.subject.none.fl_str_mv ionic liquids
XPS
complex
catalysis
topic ionic liquids
XPS
complex
catalysis
purl_subject.fl_str_mv https://purl.org/becyt/ford/1.4
https://purl.org/becyt/ford/1
dc.description.none.fl_txt_mv When talking about homogeneous catalyst systems, it has long been assumed that the system at hand consists of a transition metal complex in solution with the liquid interface representing the composition of the bulk solution. Now, in light of considerable developments in the study of metal complexes dissolved in ionic liquids with their negligible vapor pressures, more detailed studies of the composition at the liquid/gas interface became possible. These investigations revealed pronounced surface enrichment and segregation effects of high relevance for practical applications. This article reviews recent advancements in tailoring the interfacial composition of ionic liquid-based catalytic systems. A particular focus is dedicated to surface enrichment phenomena, and a variety of parameters are presented for deliberate control of the local concentration of the complexes at the surface, that is, the nature of the ligands, the bulk concentration, the temperature, and the nature of the IL solvent. As experimental methods, angle-resolved X-ray photoelectron spectroscopy (ARXPS) and vacuum-based pendant-drop surface tension measurements were applied. The reviewed results are intended to provide the basis for the advancement of catalytic systems with high surface areas, such as in supported ionic liquid phase (SILP) catalysis, where the interface design is directly interconnected with catalytic performance.
Fil: Hemmeter, Daniel. Universitat Erlangen-Nuremberg; Alemania
Fil: Haumann, Marco. Universitat Erlangen-Nuremberg; Alemania
Fil: Williams, Federico José. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Ciudad Universitaria. Instituto de Química, Física de los Materiales, Medioambiente y Energía. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales. Instituto de Química, Física de los Materiales, Medioambiente y Energía; Argentina
Fil: Koller, Thomas M.. Universitat Erlangen-Nuremberg; Alemania
Fil: Wasserscheid, Peter. Universitat Erlangen-Nuremberg; Alemania
Fil: Meyer, Karsten. Universitat Erlangen-Nuremberg; Alemania
Fil: Maier, Florian. Universitat Erlangen-Nuremberg; Alemania
Fil: Steinruck, Hans Peter. Universitat Erlangen-Nuremberg; Alemania
description When talking about homogeneous catalyst systems, it has long been assumed that the system at hand consists of a transition metal complex in solution with the liquid interface representing the composition of the bulk solution. Now, in light of considerable developments in the study of metal complexes dissolved in ionic liquids with their negligible vapor pressures, more detailed studies of the composition at the liquid/gas interface became possible. These investigations revealed pronounced surface enrichment and segregation effects of high relevance for practical applications. This article reviews recent advancements in tailoring the interfacial composition of ionic liquid-based catalytic systems. A particular focus is dedicated to surface enrichment phenomena, and a variety of parameters are presented for deliberate control of the local concentration of the complexes at the surface, that is, the nature of the ligands, the bulk concentration, the temperature, and the nature of the IL solvent. As experimental methods, angle-resolved X-ray photoelectron spectroscopy (ARXPS) and vacuum-based pendant-drop surface tension measurements were applied. The reviewed results are intended to provide the basis for the advancement of catalytic systems with high surface areas, such as in supported ionic liquid phase (SILP) catalysis, where the interface design is directly interconnected with catalytic performance.
publishDate 2025
dc.date.none.fl_str_mv 2025-02
dc.type.none.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
http://purl.org/coar/resource_type/c_6501
info:ar-repo/semantics/articulo
format article
status_str publishedVersion
dc.identifier.none.fl_str_mv http://hdl.handle.net/11336/279816
Hemmeter, Daniel; Haumann, Marco; Williams, Federico José; Koller, Thomas M.; Wasserscheid, Peter; et al.; Towards Surface‐Enhanced Homogeneous Catalysis: Tailoring the Enrichment of Metal Complexes at Ionic Liquid Surfaces; Wiley VCH Verlag; Angewandte Chemie; 64; 14; 2-2025; 1-26
1433-7851
CONICET Digital
CONICET
url http://hdl.handle.net/11336/279816
identifier_str_mv Hemmeter, Daniel; Haumann, Marco; Williams, Federico José; Koller, Thomas M.; Wasserscheid, Peter; et al.; Towards Surface‐Enhanced Homogeneous Catalysis: Tailoring the Enrichment of Metal Complexes at Ionic Liquid Surfaces; Wiley VCH Verlag; Angewandte Chemie; 64; 14; 2-2025; 1-26
1433-7851
CONICET Digital
CONICET
dc.language.none.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv info:eu-repo/semantics/altIdentifier/url/https://onlinelibrary.wiley.com/doi/10.1002/anie.202422693
info:eu-repo/semantics/altIdentifier/doi/10.1002/anie.202422693
dc.rights.none.fl_str_mv info:eu-repo/semantics/openAccess
https://creativecommons.org/licenses/by/2.5/ar/
eu_rights_str_mv openAccess
rights_invalid_str_mv https://creativecommons.org/licenses/by/2.5/ar/
dc.format.none.fl_str_mv application/pdf
application/pdf
dc.publisher.none.fl_str_mv Wiley VCH Verlag
publisher.none.fl_str_mv Wiley VCH Verlag
dc.source.none.fl_str_mv reponame:CONICET Digital (CONICET)
instname:Consejo Nacional de Investigaciones Científicas y Técnicas
reponame_str CONICET Digital (CONICET)
collection CONICET Digital (CONICET)
instname_str Consejo Nacional de Investigaciones Científicas y Técnicas
repository.name.fl_str_mv CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicas
repository.mail.fl_str_mv dasensio@conicet.gov.ar; lcarlino@conicet.gov.ar
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