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  • 1.
    Abrahamsson, Maria
    et al.
    Uppsala University, Disciplinary Domain of Science and Technology, För teknisk-naturvetenskapliga fakulteten gemensamma enheter, Accelerator mass spectrometry group. Uppsala University, Disciplinary Domain of Science and Technology, Chemistry, Department of Physical Chemistry.
    Wolpher, Henriette
    Johansson, Olof
    Larsson, Jan
    Uppsala University, Disciplinary Domain of Science and Technology, Chemistry, Department of Physical Chemistry.
    Kritikos, Mikael
    Eriksson, Lars
    Norrby, Per-Ola
    Bergquist, Jonas
    Uppsala University, Disciplinary Domain of Science and Technology, Chemistry, Department of Chemistry, Analytical Chemistry.
    Sun, Licheng
    Åkermark, Björn
    Hammarström, Leif
    Uppsala University, Disciplinary Domain of Science and Technology, Chemistry, Department of Physical Chemistry.
    A New Strategy for the Improvement of Photophysical Properties in Ruthenium(II) Polypyridyl Complexes: Synthesis and Photophysical and Electrochemical Characterization of Six Mononuclear Ruthenium(II) Bisterpyridine-Type Complexes2005In: Inorganic Chemistry, ISSN 0020-1669, E-ISSN 1520-510X, Vol. 44, no 9, p. 3215-3225Article in journal (Refereed)
  • 2.
    Aranyos, V
    et al.
    Uppsala University, Disciplinary Domain of Science and Technology, Chemistry, Department of Chemistry.
    Grennberg, Helena
    Uppsala University, Disciplinary Domain of Science and Technology, Chemistry, Department of Physical Chemistry.
    Tingry, S
    Lindquist, Sten-Eric
    Hagfeldt, Anders
    Uppsala University, Disciplinary Domain of Science and Technology, Chemistry, Department of Physical Chemistry.
    Electrochemical and photoelectrochemical investigation of new carboxylatobipyridine (bis-bipyridine)ruthenium(II) complexes for dye-sensitized TiO2 electrodes2000In: SOLAR ENERGY MATERIALS AND SOLAR CELLS, ISSN 0927-0248, Vol. 64, no 2, p. 97-114Article in journal (Refereed)
    Abstract [en]

    Methods for the preparation and purification of new carboxylated 2,2'-bipyridine ligands, two of which contain the new anchoring functionality malonate, and a reliable method for the synthesis of the corresponding [Ru(bpy)(2)(L)](PF6)(2) complexes are des

  • 3.
    Aranyos, Viviane
    et al.
    Uppsala University, Teknisk-naturvetenskapliga vetenskapsområdet, Chemistry, Department of Physical Chemistry. Uppsala University, Teknisk-naturvetenskapliga vetenskapsområdet, Chemistry, Department of Physical and Analytical Chemistry, Physical Chemistry I.
    Hagfeldt, Anders
    Uppsala University, Teknisk-naturvetenskapliga vetenskapsområdet, Chemistry, Department of Physical Chemistry. Uppsala University, Teknisk-naturvetenskapliga vetenskapsområdet, Chemistry, Department of Physical and Analytical Chemistry, Physical Chemistry I.
    Grennberg, Helena
    Uppsala University, Teknisk-naturvetenskapliga vetenskapsområdet, Chemistry, Department of Chemistry. Organisk kemi.
    Figgemeier, Egbert
    Uppsala University, Teknisk-naturvetenskapliga vetenskapsområdet, Chemistry, Department of Physical Chemistry.
    Electropolymerisable bipyridine ruthenium(II) complexes: synthesis, spectroscopic and electrochemical characterisation of 4-((2-thienyl)ethenyl)-and 4,4'-di((2-thienyl) ethenyl)-2,2'-bipyridine ruthenium complexes2004In: Polyhedron, Vol. 23, p. 589-598Article in journal (Refereed)
    Abstract [en]

    Four new ruthenium polypyridyl complexes with mono- or di-((2-thienyl) ethenyl) substituted bipyridines have been synthesized. The complexes were characterized by NMR, elemental analysis, UV-Vis absorption and electrochemistry (differentioal pulse and cyclic voltammetry). Electroactive polymer films of these complexes have been prepared by oxidative electropolymerisation and characterized by UV-Vis absorption spectroscopy and electrochemistry. The electrochemically induced polymerisation of the complexes resulted in a significant shift of the oxidation potential of the Ru(II)-Ru(III) process towards more positive potentials. Also, MLCT absorption band of the polymeric complexes is shifted towards shorter wavelengths. These results are interpreted in terms of an interrupiton of the conjugated system of the (2-thienyl)ethenyl-substituted bipyridine ligands due to a radical polymerisation mechanism affecting rather the ethenyl part of the ligand than the thienyl.

  • 4.
    Aranyos, Viviane
    et al.
    Uppsala University, Disciplinary Domain of Science and Technology, Chemistry, Department of Chemistry.
    Hjelm, Johan
    Uppsala University, Disciplinary Domain of Science and Technology, Chemistry, Department of Physical Chemistry.
    Hagfeldt, Anders
    Uppsala University, Disciplinary Domain of Science and Technology, Chemistry, Department of Physical Chemistry.
    Grennberg, Helena
    Free-base tetra-arylphthalocyanines for dye-sensitised nanostructured solar cell applications2001In: JOURNAL OF PORPHYRINS AND PHTHALOCYANINES, ISSN 1088-4246, Vol. 5, no 8, p. 609-616Article in journal (Refereed)
    Abstract [en]

    Adsorption of phthalocyanines lacking conventional attaching substituents onto nanostructured TiO2 electrodes has been studied, and some of the important factors for sensitisation have been identified. Tetra-dimethoxyphenyl phthalocyanine (2) and tetra-ph

  • 5.
    Aranyos, Viviane
    et al.
    Uppsala University, Disciplinary Domain of Science and Technology, Chemistry, Department of Physical Chemistry.
    Hjelm, Johan
    Uppsala University, Disciplinary Domain of Science and Technology, Chemistry, Department of Physical Chemistry.
    Hagfeldt, Anders
    Uppsala University, Disciplinary Domain of Science and Technology, Chemistry, Department of Physical Chemistry.
    Grennberg, Helena
    Uppsala University, Disciplinary Domain of Science and Technology, Chemistry, Department of Chemistry.
    Tuning the properties of ruthenium bipyridine dyes for solar cells by substitution on the ligands – characterisation of bis[4,4’-di(2-(3-methoxyphenyl)ethenyl)-2,2’-bipyridine][4,4’-dicarboxy-2,2’-bipyridine]ruthenium(II) dihexafluorophosphate2003In: Dalton Transactions, ISSN 1477-9226, E-ISSN 1477-9234, p. 1280-1283Article in journal (Refereed)
  • 6.
    Carlsson, Jörgen
    et al.
    Uppsala University, Medicinska vetenskapsområdet, Faculty of Medicine, Department of Oncology, Radiology and Clinical Immunology.
    Bohl Kullberg, Erika
    Uppsala University, Medicinska vetenskapsområdet, Faculty of Medicine, Department of Oncology, Radiology and Clinical Immunology. Teknisk-naturvetenskapliga vetenskapsområdet, Chemistry, Department of Chemistry.
    Capala, Jacek
    Uppsala University, Medicinska vetenskapsområdet, Faculty of Medicine, Department of Oncology, Radiology and Clinical Immunology.
    Sjöberg, Stefan
    Edwards, Katarina
    Department of Physical Chemistry.
    Gedda, Lars
    Uppsala University, Medicinska vetenskapsområdet, Faculty of Medicine, Department of Oncology, Radiology and Clinical Immunology.
    Ligand liposomes and boron neutron capture therapy2003In: Journal of Neuro-Oncology, Vol. 62, p. 47-Article in journal (Refereed)
  • 7. Johansson, Olof
    et al.
    Wolpher, Henriette
    Borgström, Magnus
    Uppsala University, Disciplinary Domain of Science and Technology, Chemistry, Department of Physical Chemistry.
    Hammarström, L.eif
    Uppsala University, Disciplinary Domain of Science and Technology, Chemistry, Department of Physical Chemistry.
    Bergquist, Jonas
    Uppsala University, Disciplinary Domain of Science and Technology, Chemistry, Department of Chemistry, Analytical Chemistry.
    Sun, Licheng
    Åkermark, Björn
    Intramolecular charge separation in a hydrogen bonded tyrosine-ruthenium(II)-naphthalene diimide triad2004In: Chemical Communications, ISSN 1359-7345, E-ISSN 1364-548X, no 2, p. 194-195Article in journal (Refereed)
    Abstract [en]

    Long-lived charge-separated states in the ns to [micro sign]s range were observed upon laser flash excitation of a donor-chromophore-acceptor triad based on tris(bipyridine) ruthenium(ii) as photo-sensitizer, naphthalene diimide as acceptor, and a hydrogen bonded phenol as donor.

  • 8.
    Ohlsson, Judit
    et al.
    Uppsala University, Teknisk-naturvetenskapliga vetenskapsområdet, Chemistry, Department of Chemistry.
    Wolpher, Henriette
    Uppsala University, Teknisk-naturvetenskapliga vetenskapsområdet, Chemistry, Department of Chemistry.
    Hagfeldt, Anders
    Department of Physical Chemistry.
    Grennberg, Helena
    Uppsala University, Teknisk-naturvetenskapliga vetenskapsområdet, Chemistry, Department of Chemistry.
    New dyes for solar cells based on nanostructured semiconducting metal oxides: Synthesis and characterisation of ruthenium(II) complexes with thiol-substituted ligands2002In: Journal of Photochemistry and Photobiology A: Chemistry, Vol. 148, p. 41-48Article in journal (Refereed)
  • 9. Ott, Sascha
    et al.
    Borgström, Magnus
    Uppsala University, Disciplinary Domain of Science and Technology, Chemistry, Department of Physical Chemistry.
    Kritikos, Mikael
    Lomoth, Reiner
    Uppsala University, Disciplinary Domain of Science and Technology, Chemistry, Department of Physical Chemistry.
    Bergquist, Jonas
    Uppsala University, Disciplinary Domain of Science and Technology, Chemistry, Department of Chemistry, Analytical Chemistry.
    Åkermark, Björn
    Hammarström, Leif
    Uppsala University, Disciplinary Domain of Science and Technology, Chemistry, Department of Physical Chemistry.
    Sun, Licheng
    Model of the iron hydrogenase active site covalently linked to a ruthenium photosensitizer: Synthesis and photophysical properties2004In: Inorganic Chemistry, ISSN 0020-1669, E-ISSN 1520-510X, Vol. 43, no 15, p. 4683-4692Article in journal (Refereed)
    Abstract [en]

    A model of the iron hydrogenase active site with the structure [(mu-ADT)Fe2(CO)6] (ADT = azadithiolate (S-CH2-NR-CH2-S), (2: R = 4-bromophenyl, 3: R = 4-iodophenyl)) has been assembled and covalently linked to a [Ru(terpy)2]2+ photosensitizer. This trinuclear complex 1 represents one synthetic step toward the realization of our concept of light-driven proton reduction. A rigid phenylacetylene tether has been incorporated as the linking unit in 1 in order to prolong the lifetime of the otherwise short-lived [Ru(terpy)2]2+ excited state. The success of this strategy is demonstrated by comparison of the photophysical properties of 1 and of two related ruthenium complexes bearing acetylenic terpyridine ligands, with those of [Ru(terpy)2]2+. IR and electrochemical studies reveal that the nitrogen heteroatom of the ADT bridge has a marked influence on the electronic properties of the [Fe2(CO)6] core. Using the Rehm-Weller equation, the driving force for an electron transfer from the photoexcited *[Ru(terpy)2]2+ to the diiron site in 1 was calculated to be uphill by 0.59 eV. During the construction of the trinuclear complex 1, n-propylamine has been identified as a decarbonylation agent on the [(mu-ADT)Fe2(CO)6] portion of the supermolecule. Following this procedure, the first azadithiolate-bridged dinuclear iron complex coordinated by a phosphine ligand [(mu-ADT)Fe2(CO)5PPh3] (4, R = 4-bromophenyl) was synthesized.

  • 10.
    Wallin, Staffan
    et al.
    Uppsala University, Teknisk-naturvetenskapliga vetenskapsområdet, Chemistry, Department of Physical Chemistry. Department of Biochemistry and Organic Chemistry, Organic Chemistry I. Department of Physical and Analytical Chemistry, Physical Chemistry I. Physics, Department of Physics and Materials Science, Chemical Physics.
    Davidsson, Jan
    Uppsala University, Teknisk-naturvetenskapliga vetenskapsområdet, Chemistry, Department of Physical Chemistry. Department of Biochemistry and Organic Chemistry, Organic Chemistry I. Department of Physical and Analytical Chemistry, Physical Chemistry I. Physics, Department of Physics and Materials Science, Chemical Physics.
    Modin, Judit
    Department of Chemistry. Department of Biochemistry and Organic Chemistry, Organic Chemistry I. Department of Physical and Analytical Chemistry, Physical Chemistry I. Physics, Department of Physics and Materials Science, Chemical Physics. Organisk kemi.
    Hammarström, Leif
    Uppsala University, Teknisk-naturvetenskapliga vetenskapsområdet, Chemistry, Department of Physical Chemistry. Department of Biochemistry and Organic Chemistry, Organic Chemistry I. Department of Physical and Analytical Chemistry, Physical Chemistry I. Physics, Department of Physics and Materials Science, Chemical Physics.
    Femtosecond Transient Absorption Anisotropy Study on [Ru(bpy)3]2+ and [Ru(bpy)(py)4]2+. Ultrafast Interligand Randomization of the MLCT State2005In: J. Phys. Chem. A, no 109, p. 4697-4704Article in journal (Refereed)
    Abstract [en]

    It is known that the relaxed excited state of [Ru(bpy)3]2+ is best described as a metal to ligand charge transfer (MLCT) state having one formally reduced bipyridine and two neutral. Previous reports have suggested [Malone, R. et al. J.Chem. Phys 1991, 95, 8970] that the electron "hops" from ligand to ligand in the MLCT state with a time constant of about 50 ps in acetonitrile. However, we have done transient absorption anisotropy measurements indicating that already after one picosecond the molecule has no memory of which bipyridine was initially photoselected, which suggest an ultrafast interligand randomization of the MLCT state.

  • 11. Wolpher, H.
    et al.
    Huang, P.
    Borgström, Magnus
    Uppsala University, Disciplinary Domain of Science and Technology, Chemistry, Department of Physical Chemistry.
    Bergquist, Jonas
    Uppsala University, Disciplinary Domain of Science and Technology, Chemistry, Department of Chemistry, Analytical Chemistry.
    Styring, S.
    Sun, L.C.
    Åkermark, B.
    Synthesis of a Ru(bpy)(3)-type complex linked to a free terpyridine ligand and its use for preparation of polynuclear bimetallic complexes2004In: Catalysis Today, ISSN 0920-5861, E-ISSN 1873-4308, Vol. 98, no 4, p. 529-536Article in journal (Refereed)
    Abstract [en]

    A terpyridine ligand has been covalently linked to a Ru(bpy)3 complex via an amide bond. By using this functionalized terpyridine ligand, a series of multinuclear bimetallic complexes have been synthesized and characterized. One of these complexes has the structure of di-μ-oxo-bridged Mn dimer. EPR spectra of this complex showed that, depending on the procedure for the preparation, the oxidation states of the Mn dimer is either a Mn2III,IV dimer or a mixture of this and Mn2IV,IV dimer. Water oxidation catalyzed by this complex has been performed.

  • 12.
    Wolpher, Henriette
    et al.
    Uppsala University, Disciplinary Domain of Science and Technology, Chemistry, Department of Physical Chemistry.
    Borgström, Magnus
    Uppsala University, Disciplinary Domain of Science and Technology, Chemistry, Department of Chemistry.
    Hammarström, Leif
    Bergquist, Jonas
    Sundström, Villy
    Styring, Stenbjörn
    Sun, Lichen
    Åkermark, Björn
    Synthesis and properties of an iron hydrogenase active site model linked to a ruthenium tris-bipyridine photosensitizer2003In: Inorganic Chemistry Communications, Vol. 6, p. 989-991Article in journal (Refereed)
  • 13. Yanagisawa, Masaru
    et al.
    Korodi, Ferenc
    Bergquist, Jonas
    Uppsala University, Teknisk-naturvetenskapliga vetenskapsområdet, Chemistry, Department of Chemistry. Department of Physical and Analytical Chemistry, Physical Chemistry. Analytical Chemistry. Analytisk kemi.
    Holmberg, Anna
    Hagfeldt, Anders
    Department of Physical Chemistry. Department of Physical and Analytical Chemistry, Physical Chemistry. Analytical Chemistry.
    Åkermark, Björn
    Sun, Licheng
    Synthesis of phthalocyanines with two carboxylic acid groups and their utilization in solar cells based on nano-structured TiO22004In: Journal of Porphyrins and Phthalocyanines, Vol. 8, no 10, p. 1228-1235Article in journal (Refereed)
  • 14.
    Zettersten, Camilla
    et al.
    Uppsala University, Disciplinary Domain of Science and Technology, Chemistry, Department of Chemistry, Analytical Chemistry.
    Lomoth, Reiner
    Uppsala University, Disciplinary Domain of Science and Technology, Chemistry, Department of Physical Chemistry.
    Hammarström, Leif
    Uppsala University, Disciplinary Domain of Science and Technology, Chemistry, Department of Physical Chemistry.
    Sjöberg, Per
    Uppsala University, Disciplinary Domain of Science and Technology, Chemistry, Department of Chemistry, Analytical Chemistry.
    Nyholm, Leif
    Uppsala University, Disciplinary Domain of Science and Technology, Chemistry, Department of Materials Chemistry.
    The influence of the thin-layer flow cell design on the mass spectra when coupling electrochemistry to electrospray ionisation mass spectrometry2006In: Journal of Electroanalytical Chemistry, ISSN 0022-0728, E-ISSN 1873-2569, Vol. 590, no 1, p. 90-99Article in journal (Refereed)
    Abstract [en]

    The influence of the flow cell configuration on the mass spectra obtained when coupling an electrochemical thin-layer flow cell to electrospray mass spectrometry (ESI-MS) has been investigated. It is shown that interferences due to the electrochemical reaction on the counter electrode and/or the absence of 100% conversion efficiency can alter the mass spectra when conventional thin-layer flow cells are used in conjunction with ESI-MS. The effects, which affect the intensities and distribution of the peaks in the mass spectra, can result in the inability to detect products formed at the working electrode. Comparisons of mass spectra, generated after the electrochemical oxidation of a dinuclear Mn complex (where bpmp = 2,6-bis[bis(2-pyridylmethyl) amino]methyl-4-methylphenol) using two different thin-layer flow cells clearly show that the potential dependence and appearance of the mass spectra depend on the flow cell configuration used. The use of a modified thin-layer flow cell, in which the counter electrode had been separated from the working electrode, gave rise to significantly increased intensities for the oxidised MnIII,IV state of the complex. With the conventional unmodified cell, the corresponding complex was only seen for considerably higher oxidation potentials. The different results can be explained by the reduced risk of redox cycling and interferences due to species generated at the counter electrode with the modified cell. As interferences due to the counter electrode reactions likewise may be expected with many coulometric flow cells, the electrochemical cell design clearly needs to be considered when using electrochemistry coupled to ESI-MS to study electrochemical reactions.

1 - 14 of 14
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