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Heterogenization of a Cobalt Porphyrin Catalyst Investigated by Scanning Probe Microscopy and X-Ray Photoelectron Spectroscopy: The Effect on Catalysis of Oxidation Reactions
Mälardalens högskola, Akademin för hållbar samhälls- och teknikutveckling.
2008 (engelsk)Doktoravhandling, med artikler (Annet vitenskapelig)
Abstract [en]

Construction of advanced materials through self-assembly on the molecular level is an important route to achieve novel functionality. Self-assembly of thiols onto gold has during the last decades shown greate promise in the creation of functional nanomaterials, such as sensors or catalysts, but for many applications silicon should be a better substrate since it offers semiconducting properties and better processing abilities in addition to being cheaper. This work describes an efficient novel method to incorporate reactive disulfide bonds onto a silica surface under mild reaction conditions. The reactive thiol groups introduced onto the silica surface will be oxidized but is then converted into highly reactive thiopyridyl groups, which can easily be utilized for further organic synthesis involving thiol-containing molecules.

Cobalt tetraarylporphyrins with thioacetate-functionalized carbon chains on the aryl groups were synthesized (CoTPP-L) and were used as a model system for investigating catalytic activity in homogeneous and heterogeneous oxidation catalysis. For heterogeneous catalysis CoTPP-L was immobilized onto gold surfaces through thiol-gold self-assembly, and onto silica surfaces by the above mentioned disulfide exchange method.

The properties of the molecular layers were characterized on the molecular level by means of X-ray photoelectron spectroscopy (XPS) and scanning probe microscopy (SPM). The immobilization on gold surfaces took place through the formation of multiple thiolate bonds and it could be controlled by varying the preparation scheme. More thiolate bonds form if the thioacetyl protective groups of the thiol linkers are cleaved off prior to immobilization. The CoTPP-L molecules were in all cases found to form stable disordered monolayers on gold surfaces. On silica surfaces the CoTPP-L forms patchwise multilayers.

The catalytic performance of the heterogenized systems (CoTPP-L immobilized onto gold or silicon wafers) was evaluated and it was found that the strong inactivation observed for their homogeneous congener was avoided. As a result, the turnover number per molecule in heterogeneous catalysis was at least 100 times higher than that of the corresponding homogeneous catalyst. It is thus demonstrated that the performance of these catalysts can be dramatically improved if the catalyst arrangement can be controlled on the molecular level. Work is ongoing to extend the system to high surface area materials.

sted, utgiver, år, opplag, sider
Akademin för hållbar samhälls- och teknikutveckling , 2008.
Serie
Mälardalen University Press Dissertations, ISSN 1651-4238 ; 57
HSV kategori
Forskningsprogram
Bioteknik/kemiteknik
Identifikatorer
URN: urn:nbn:se:mdh:diva-492ISBN: 978-91-85485-71-0 (tryckt)OAI: oai:DiVA.org:mdh-492DiVA, id: diva2:121040
Disputas
2008-03-07, Filen, Verktyget, Smedjegatan 37, Eskilstuna, 10:00
Opponent
Veileder
Tilgjengelig fra: 2008-02-06 Laget: 2008-02-06
Delarbeid
1. Novel method for preparation of disulfides on silicon
Åpne denne publikasjonen i ny fane eller vindu >>Novel method for preparation of disulfides on silicon
Vise andre…
2001 (engelsk)Inngår i: Langmuir, ISSN 0743-7463, Vol. 17, nr 2, s. 6056-6058Artikkel i tidsskrift (Fagfellevurdert) Published
Abstract [en]

This work describes an efficient novel method to incorporate reactive disulfide bonds onto a silica surface under mild reaction conditions. The reactive thiol groups introduced onto the silicon surface in the first reaction step will be oxidized but easily converted into highly reactive thiopyridyl groups, which can therefore easily be utilized for further organic synthesis involving thiol-containing molecules. This is done in a way that yields approximately a monolayer of reactant on the surface, thereby not adding to the roughness of the surface, of special importance, for instance, for single molecule interaction studies.

HSV kategori
Identifikatorer
urn:nbn:se:mdh:diva-4161 (URN)10.1021/la0155092 (DOI)000171305700008 ()2-s2.0-0035797975 (Scopus ID)
Tilgjengelig fra: 2008-02-06 Laget: 2008-02-06 Sist oppdatert: 2015-07-08bibliografisk kontrollert
2. Synthesis of thioacetate-functionalized cobalt(II) porphyrins and their immobilization on gold surface - Characterization by X-ray photoelectron spectroscopy
Åpne denne publikasjonen i ny fane eller vindu >>Synthesis of thioacetate-functionalized cobalt(II) porphyrins and their immobilization on gold surface - Characterization by X-ray photoelectron spectroscopy
Vise andre…
2006 (engelsk)Inngår i: European Journal of Organic Chemistry, ISSN 1434-193X, nr 5, s. 1193-1199Artikkel i tidsskrift (Fagfellevurdert) Published
Abstract [en]

Cobalt tetraarylporphyrins 1-Co and 2-Co with thioacetate-functionalized carbon chains on the aryl groups were synthesized. The cobalt porphyrin 2-Co was immobilized on a gold surface after deprotection of the S-acetyl group. The immobilized porphyrin was studied by X-ray Photoelectron Spectroscopy (XPS) and the results suggest that a complete monolayer of porphyrins is formed.

HSV kategori
Identifikatorer
urn:nbn:se:mdh:diva-4162 (URN)10.1002/ejoc.200500656 (DOI)000235821600014 ()2-s2.0-33644761874 (Scopus ID)
Tilgjengelig fra: 2008-02-06 Laget: 2008-02-06 Sist oppdatert: 2015-07-08bibliografisk kontrollert
3. Activity boost of a biomimetic oxidation catalyst by immobilization onto a gold surface
Åpne denne publikasjonen i ny fane eller vindu >>Activity boost of a biomimetic oxidation catalyst by immobilization onto a gold surface
Vise andre…
2006 (engelsk)Inngår i: Journal of Catalysis, ISSN 0021-9517, Vol. 244, nr 1, s. 86-91Artikkel i tidsskrift (Fagfellevurdert) Published
Abstract [en]

Thiol-functionalized cobalt porphyrins were used as a model system for investigating catalytic activity in homogeneous and heterogeneous oxidation catalysis. Self-assembled monolayers of thiol-functionallized cobalt porphyrins were prepared on a gold surface and served as heterogeneous catalysts. These immobilized molecules prevented the strong inactivation observed for their homogeneous congener. As a result, the turnover number per molecule in heterogeneous catalysis was at least 100 times higher than that of the corresponding homogeneous catalyst. It is atypical for a heterogenized catalyst to outperform its homogeneous congener. The properties of the molecular layers were characterized on the molecular level by means of X-ray photoelectron spectroscopy (XPS) and scanning tunneling microscopy (STM). The results demonstrate that the performance of these biomimetic catalysts can be dramatically improved if the catalyst arrangement can be controlled on the molecular level.

HSV kategori
Identifikatorer
urn:nbn:se:mdh:diva-4163 (URN)10.1016/j.jcat.2006.08.017 (DOI)000242130100010 ()2-s2.0-33749622371 (Scopus ID)
Tilgjengelig fra: 2008-02-06 Laget: 2008-02-06 Sist oppdatert: 2015-07-08bibliografisk kontrollert
4. Electronic and structural studies of immobilized thiol-derivatized cobalt porphyrins on gold surfaces
Åpne denne publikasjonen i ny fane eller vindu >>Electronic and structural studies of immobilized thiol-derivatized cobalt porphyrins on gold surfaces
Vise andre…
2007 (engelsk)Inngår i: Applied Surface Science, ISSN 0169-4332, Vol. 253, nr 18, s. 7540-7548Artikkel i tidsskrift (Fagfellevurdert) Published
Abstract [en]

The immobilisation of thiol-derivatized cobalt porphyrins on gold surfaces has been studied in detail by means of combined scanning tunnelling microscopy (STM) and X-ray photoelectron spectroscopy (XPS). S-thioacetyl has been used as a protective group for the thiol. Different routes for deprotection of the acetyl groups were performed in acidic and in basic conditions. The results show the formation of monolayer films for the different preparation schemes. The immobilisation of the molecules on the gold surface takes place through the thiol-linkers by the formation of multiple thiolate bonds. In the case of layers formed with protected porphyrins approximately 60% of the linkers are bonded to the gold surface whereas for deprotected layers the amount of bonded linkers is increased up to about 80%. STM measurements revealed that the molecules arrange in a disordered overlayer and do not exhibit mobility on the gold surface. Annealing experiments have been performed in order to test the stability of the porphyrin layers. Disordered patterns have been observed in the STM images after annealing at T= 400 degrees C. XPS revealed that the sulphur content disappeared completely after annealing at T= 180 degrees C and that the molecules did undergo significant modifications.

HSV kategori
Identifikatorer
urn:nbn:se:mdh:diva-4164 (URN)10.1016/j.apsusc.2007.03.066 (DOI)000247863800034 ()2-s2.0-34249905896 (Scopus ID)
Tilgjengelig fra: 2008-02-06 Laget: 2008-02-06 Sist oppdatert: 2015-07-02bibliografisk kontrollert
5. The performance of a biomimetic oxidation catalyst immobilized on silicon wafers: A comparison with the catalyst in solution and immobilized on gold
Åpne denne publikasjonen i ny fane eller vindu >>The performance of a biomimetic oxidation catalyst immobilized on silicon wafers: A comparison with the catalyst in solution and immobilized on gold
Vise andre…
(engelsk)Manuskript (Annet vitenskapelig)
HSV kategori
Identifikatorer
urn:nbn:se:mdh:diva-4165 (URN)
Tilgjengelig fra: 2008-02-06 Laget: 2008-02-06 Sist oppdatert: 2017-02-22bibliografisk kontrollert

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