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
.jpg)
- Institución
- Consejo Nacional de Investigaciones Científicas y Técnicas
- OAI Identificador
- oai:ri.conicet.gov.ar:11336/279816
Ver los metadatos del registro completo
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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 |
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2025-02 |
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info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion http://purl.org/coar/resource_type/c_6501 info:ar-repo/semantics/articulo |
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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 |
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http://hdl.handle.net/11336/279816 |
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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 |
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eng |
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eng |
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application/pdf application/pdf |
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Wiley VCH Verlag |
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Wiley VCH Verlag |
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