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  • 1.
    Abbrent, Sabina
    Uppsala University, Teknisk-naturvetenskapliga vetenskapsområdet, Chemistry, Department of Chemistry.
    Lithium ion interactions in polymer gel electrolytes: Effect on structure, dynamics and morphology2000Doctoral thesis, comprehensive summary (Other academic)
    Abstract [en]

    Polymer electrolytes are an essential part of the modern all-solid lithium battery. Several properties, such as mechanical and thermal stability, good ionic conductivity and compatibility with other materials used in the battery are necessary for a successful material.

    This thesis is focused on the ionic interactions in two electrolyte systems, based on a cross-linked polyethylene oxide (nona(ethylene oxide)dimethacrylate) or a fluorinated copolymer (polyvinylidene fluoride-hexafluoropropylene). Changes of thermal properties and morphology of and coordination in the electrolyte on addition of a lithium salt (LiTFSI) and different types and concentrations of solvents are studied. These properties are shown to control the ionic conductivity of the resulting material, influencing the conductivity mechanism.

    The presumably inert polyvinylidene fluoride is shown to undergo large structural changes, where polar conformations of the polymer backbone appear on salt addition, inducing a different crystalline phase. The lithium cation in the polyethylene oxide based electrolyte can coordinate either to the polymer chain or to the solvent. In for example systems containing propylene carbonate, the lithium ion binds more strongly to the polymer than to the solvent. This is in contrast to the systems with dimethyl sulphoxide where the ion prefers the solvent. This variation in coordination also strongly affects the mobility of the cation, reflected both in diffusion constants and in conductivity data.

    A combination of techniques was necessary to use for a deeper understanding of these complex materials. Coordination has been studied by FTIR and high resolution NMR, dynamics by NMR diffusion measurements and impedance spectroscopy, and morphology by diffraction techniques and DSC.

  • 2.
    Abbrent, Sabina
    et al.
    Uppsala University, Disciplinary Domain of Science and Technology, Chemistry, Department of Chemistry.
    Lindgren, J
    Uppsala University, Disciplinary Domain of Science and Technology, Chemistry, Department of Chemistry.
    Tegenfeldt, J
    Uppsala University, Disciplinary Domain of Science and Technology, Chemistry, Department of Chemistry.
    Wendsjö, Å
    Gel electrolytes prepared from oligo(ethylene glycol)dimethacrylate: glass transition, conductivity and Li+-coordination1998In: Electrochimica Acta, ISSN 0013-4686, E-ISSN 1873-3859, Vol. 43, no 10-11, p. 1185-1191p. 1185-1191Article in journal (Refereed)
    Abstract [en]

    The influence of two plasticizers, propylene carbonate and dimethyl sulphoxide, as well as different salt concentrations of Li(TFSI), on properties of a polymer gel electrolyte material has been studied using differential scanning calorimetry (DSC) and ac impedance and FTIR spectroscopy. Variations of glass transition temperature and the conductivity behaviours of the systems were examined, and found to be highly dependent on the amount and type of the plasticizer used. Characteristic band-shifts in FTIR spectra, indicating coordination of lithium ions, have been found for the polymer and both the plasticizers in the corresponding binary solutions. These shifts were used to study the coordination preferences in the complete ternary electrolyte system. The combined results from the three experimental techniques have been discussed.

  • 3.
    Agback, M
    et al.
    Uppsala University, Teknisk-naturvetenskapliga vetenskapsområdet, Physics, Department of Quantum Chemistry. Chemistry, Department of Physical and Analytical Chemistry, Quantum Chemistry. Kvantkemi.
    Lunell, S
    Uppsala University, Teknisk-naturvetenskapliga vetenskapsområdet, Physics, Department of Quantum Chemistry. Chemistry, Department of Physical and Analytical Chemistry, Quantum Chemistry.
    Hussenius, A
    Department of Chemistry. Chemistry, Department of Physical and Analytical Chemistry, Quantum Chemistry.
    Matsson, O
    Department of Chemistry. Chemistry, Department of Physical and Analytical Chemistry, Quantum Chemistry.
    Theoretical studies of proton transfer reactions in 1-methylindene1998In: ACTA CHEMICA SCANDINAVICA, ISSN 0904-213X, Vol. 52, no 5, p. 541-548Article in journal (Refereed)
    Abstract [en]

    The base-catalysed 1,3-proton transfer reactions in 1-methylindene have been studied theoretically in polar (water) and unpolar (cyclohexane) solvents, respectively, for two different choices of bases, namely ammonia and trimethylamine (TMA), using the SM

  • 4.
    Aggeryd, Ingrid
    Uppsala University, Disciplinary Domain of Science and Technology, Chemistry, Department of Chemistry.
    Bestämning av Substitutionsgraden hos Natrium-karboxymetylcellulosa, CMC: En tillämpning av den utvidgade Henderson-Hasselbalchs ekvation och simplex-optimering för bestämning av ekvivalensvolymer vid potentiometrisk titrering1984Licentiate thesis, monograph (Other academic)
  • 5. Aili, Daniel
    et al.
    Enander, Karin
    Baltzer, Lars
    Uppsala University, Disciplinary Domain of Science and Technology, Chemistry, Department of Chemistry.
    Liedberg, Bo
    Synthetic de novo designed polypeptides for control of nanoparticle assembly and biosensing2007In: Biochemical Society Transactions, ISSN 0300-5127, E-ISSN 1470-8752, Vol. 35, no 3, p. 532-534Article in journal (Refereed)
    Abstract [en]

    This contribution describes how de novo designed synthetic helix–loop–helix polypeptides are utilized tocontrol the assembly of gold nanoparticles and as scaffolds for biosensing. The synthetic polypeptides aredesigned to fold into a four-helix bundle upon dimerization. When immobilized on gold nanoparticles,dimerization and folding occur between peptides on neighbouring particles as an effect of particleaggregation and the folded polypeptides are rigid enough to keep the particles separated at a distancecorresponding to the size of the four-helix bundle. Moreover, peptide dimerization offers a convenientroute to assemble nanoparticles into hybrid multilayers on planar substrates. The drastic change in theresonance conditions of the localized nanoparticle surface plasmon upon particle aggregation is shown tobe useful for optical detection of biomolecular interactions.

  • 6.
    Alexander, James N.
    Uppsala University, Teknisk-naturvetenskapliga vetenskapsområdet, Chemistry, Department of Chemistry.
    Novel detection schemes and high resolution separations in microcolumn liquid separations1999Doctoral thesis, comprehensive summary (Other academic)
    Abstract [en]

    Three micro detectors were developed and studied using micro-liquidchromatography (micro-LC). An evaporative light scattering detector (ELSD) nebulizer was developed for use with flow rates ranging from 0.5 to 10 µL/min. The parameters that affect analyte response were investigated and the most influential were capillary tip position and nebulization gas flow rate. One unique advantage of thismicro detector is that it can be operated at ambient conditions which allows for the analysis of semi-volatile compounds.

    A radio activity monitor (RAM) flow cell was developed for use at 3 µL/min and was designed for coupling to mass spectrometry (MS). The parameters that affect analyte response and band broadening were studied. Reducing the solid scintillant particle size to 9 µm and efficiently packing the solid cells allowed for direct coupling to MS without compromising the chromatographic separation.

    A nano-electrospray ionization (BSI) source for MS was developed and coupled to nano-LC and capillary electrophoresis (CE). This source incorporated a 50 µm i.d. stainless steel tip that was coupled to the separation capillary. At flow rates of 100 nL/min a stable electrospray was achieved.

    A multi-use separations system was developed for isocratic and gradient elution micro-LC, capillary electrochromatography (CEC), and pressure CEC (PEC). The details of the system and studies on peak area and retention time repeatability are reported. Comparisons are made between nano-LC and CEC. On average, column efficiency is 57% greater for CEC compared to nano-LC using the same nanocolumn.

  • 7.
    Alexander, JN
    et al.
    Uppsala University, Teknisk-naturvetenskapliga vetenskapsområdet, Chemistry, Department of Chemistry.
    Poli, JB
    Markides, KE
    Evaluation of automated isocratic and gradient nano-liquid chromatography and capillary electrochromatography1999In: ANALYTICAL CHEMISTRY, ISSN 0003-2700, Vol. 71, no 13, p. 2398-2409Article in journal (Refereed)
    Abstract [en]

    An automated liquid nano-separation system has been developed for nano-liquid chromatography (nano-LC) and capillary electrochromatography (CEC) using both isocratic and gradient elution, One fused-silica nanocolumn, typically 75 mu m i x 39 cm (25 cm ef

  • 8.
    Alfredsson, Maria
    Uppsala University, Teknisk-naturvetenskapliga vetenskapsområdet, Chemistry, Department of Chemistry.
    Polar molecules in crystalline and surface environments: From first principles1999Doctoral thesis, comprehensive summary (Other academic)
    Abstract [en]

    With the knowledge of the composition and structure of a chemical system, be it a molecule, a two-dimensional surface or a three-dimensional crystal, it is now possible to predict the specific properties of the compound under consideration via computational studies. Molecular and periodic Hartree-Fock and DFT calculations have been used as a tool to study polar molecules and how their properties respond to the molecular environment in a crystal or on an ionic surface. The investigation covers a range of molecules (HF, HC1, HCN, H2O, OH-, OH., N2, CO and LiF) with different net charges, dipole moments and polarisibility, and a range of crystals and crystalline surfaces: hydrogen-bonded, ionic and ferroelectric.

    The step-wise build up of the molecular properties (geometries, energies, dipole moments, vibrational frequencies etc.) has been investigated. It was found that sorne molecular properties converge quickly towards the crystal value, others more slowly. Molecules adsorbed on a solid surface were studied as a function of adsorptionenergy, substrate and surface coverage. For the ionic surfaces studied here it was found that the properties of the chemi- and physisorbed molecules are as sensitive to the surface coverage as to the adsorption of the ad-molecule to the surface. The vibrational frequency shift of the ad-molecule has been given special attention.

    Finally the spontaneous polarisation in two ferroelectric crystals was calculated within the Berry-phase approach.

  • 9.
    Al-Maharik, N
    et al.
    Uppsala University, Teknisk-naturvetenskapliga vetenskapsområdet, Chemistry, Department of Chemistry.
    Engman, L
    Malmstrom, J
    Schiesser, CH
    Intramolecular homolytic substitution at selenium: Synthesis of novel selenium-containing vitamin E analogues2001In: JOURNAL OF ORGANIC CHEMISTRY, ISSN 0022-3263, Vol. 66, no 19, p. 6286-6290Article in journal (Refereed)
    Abstract [en]

    Treatment of 1-(benzylselenenyl)-5-butyl-5-nonanoI (10) with oxalyl chloride followed by the sodium salt of N-hydroxypyridine-2-thione afforded the corresponding pyridine-2-thione-N-oxycarbonyI (PTOC) oxalate ester which was not isolated but immediately h

  • 10.
    Alonso, DA
    et al.
    Uppsala University, Teknisk-naturvetenskapliga vetenskapsområdet, Chemistry, Department of Chemistry.
    Nordin, SJM
    Andersson, PG
    Highly diastereoselective reaction of 2-azanorbornyl enolates with electrophiles1999In: ORGANIC LETTERS, ISSN 1523-7060, Vol. 1, no 10, p. 1595-1597Article in journal (Refereed)
    Abstract [en]

    A highly diastereoselective reaction of 2-azanorbornyl enolates with electrophiles has been studied. Deprotonation of 4 with LDA at low temperature affords the corresponding exocyclic lithium enolate 5, which reacts with different electrophiles such as al

  • 11.
    Alonso, DA
    et al.
    Uppsala University, Teknisk-naturvetenskapliga vetenskapsområdet, Chemistry, Department of Chemistry.
    Nordin, SJM
    Roth, P
    Tarnai, T
    Andersson, PG
    Thommen, M
    Pittelkow, U
    2-azanorbornyl alcohols: Very efficient ligands for ruthenium-catalyzed asymmetric transfer hydrogenation of aromatic ketones2000In: JOURNAL OF ORGANIC CHEMISTRY, ISSN 0022-3263, Vol. 65, no 10, p. 3116-3122Article in journal (Refereed)
    Abstract [en]

    2-Azanorbornyl-derived amino alcohols were prepared and evaluated as ligands in the Ru(II)-catalyzed asymmetric transfer hydrogenation of aromatic ketones. To improve selectivity and rate, the structure of the ligand was optimized, Acetophenone was reduce

  • 12. Alonso, Diego
    et al.
    Andersson, Pher
    Uppsala University, Teknisk-naturvetenskapliga vetenskapsområdet, Chemistry, Department of Chemistry. Department of Biochemistry and Organic Chemistry, Organic Chemistry I.
    Deprotection of Sulfonyl Aziridines1998In: J. Org. Chem., no 63, p. 9455-9461Article in journal (Refereed)
  • 13. Alonso, Diego
    et al.
    Bertilsson, Sophie
    Uppsala University, Teknisk-naturvetenskapliga vetenskapsområdet, Chemistry, Department of Chemistry. Department of Biochemistry and Organic Chemistry, Organic Chemistry I.
    Johnsson, Sandra
    Nordin, Sofia
    Uppsala University, Teknisk-naturvetenskapliga vetenskapsområdet, Chemistry, Department of Chemistry. Department of Biochemistry and Organic Chemistry, Organic Chemistry I.
    Södergren, Mikael
    Andersson, Pher
    Uppsala University, Teknisk-naturvetenskapliga vetenskapsområdet, Chemistry, Department of Chemistry. Department of Biochemistry and Organic Chemistry, Organic Chemistry I.
    New Expedient Route to Both Enantiomers of Nonproteinogenic a-Amino Acid Derivatives from the Unsaturated 2-Aza-Bicyclo Moiety1999In: J. Org. Chem., no 64, p. 2276-2280Article in journal (Refereed)
  • 14. Alonso, Diego
    et al.
    Brandt, Peter
    Nordin, Sofia
    Uppsala University, Disciplinary Domain of Science and Technology, Chemistry, Department of Chemistry. Uppsala University, Disciplinary Domain of Science and Technology, Chemistry, Department of Biochemistry and Organic Chemistry, Organic Chemistry I.
    Andersson, Pher
    Uppsala University, Disciplinary Domain of Science and Technology, Chemistry, Department of Chemistry. Uppsala University, Disciplinary Domain of Science and Technology, Chemistry, Department of Biochemistry and Organic Chemistry, Organic Chemistry I.
    Ru(arene)(amino alcohol)-Catalyzed Transfer Hydrogenation of Ketones: Mechanism and Origin of Enantioselectivity1999In: J. Am. Chem. Soc., no 121, p. 9580-9588Article in journal (Refereed)
    Abstract
  • 15. Alonso, Diego
    et al.
    Guijarro, David
    Pinho, Pedro
    Uppsala University, Teknisk-naturvetenskapliga vetenskapsområdet, Chemistry, Department of Chemistry. Department of Biochemistry and Organic Chemistry, Organic Chemistry I.
    Temme, Oliver
    Andersson, Pher
    Uppsala University, Teknisk-naturvetenskapliga vetenskapsområdet, Chemistry, Department of Chemistry. Department of Biochemistry and Organic Chemistry, Organic Chemistry I.
    (1S,3R,4R)-2-Azanorbornylmethanol, an Efficient Ligand for Ruthenium-Catalyzed Asymmetric Transfer Hydrogenation of Ketones1998In: J. Org. Chem., no 63, p. 2749-2751Article in journal (Refereed)
  • 16.
    Amirkhani, A.
    et al.
    Uppsala University, Disciplinary Domain of Science and Technology, Chemistry, Department of Chemistry.
    Heldin, E.
    Markides, K.E.
    Bergquist, J.
    Quantitation of tryptophan, kynurenine and kynurenic acid in human plasma by capillary liquid chromatography - electrospray ionization tandem mass spectrometry2002In: J. of Chromatography B, no 780, p. 381-387Article in journal (Refereed)
  • 17.
    Andersson, Anna S.
    Uppsala University, Teknisk-naturvetenskapliga vetenskapsområdet, Chemistry, Department of Chemistry.
    Lithium iron phosphates as cathode materials in lithium batteries2000Doctoral thesis, comprehensive summary (Other academic)
    Abstract [en]

    Iron-based oxides are perhaps the only realistic cathode materials for electric and electric-hybrid vehicle applications. Two types of lithium iron phosphate, LiFePO4 andR-Li3Fe2(PO4)3, have been investigated for use within the lithium/lithium-ion polymer batteryconcept. The main techniques exploited have been: electrochemical cycling; X-ray andneutron diffraction - to study structural changes of the host material during lithiuminsertion/extraction; Mössbauer spectroscopy - to probe changes in the local structure of theFe atoms.

    Lithium extraction/insertion for LiFePO4, (olivine-type structure) has been followed by acombination of in situ X-ray diffraction and in situ Mössbauer spectroscopy. QuantitativeRietveld analysis of diffraction data has given good agreement with electrochemical andMössbauer spectroscopy data: ca. 20% of the LiFePO4 phase remains after charging. Possiblemechanisms to describe the capacity loss are proposed. High-temperature cycling (at 40oC and60oC) has shown the specific capacity to be markedly enhanced at higher temperatures.

    In situ Mössbauer spectroscopy has also been used to study the insertion of lithium into R-Li3Fe2(PO4)3. The two non-equivalent Fe3+ ions cannot be distinguished, whereas two typesof Fe2+ site appear on lithium insertion. Lithium appears to enter a site closer to one of theFe atoms. Elevated-temperature cycling shows the temperature dependence of R-Li3Fe2(PO4)3to be less marked than for the LiFePO4 system.

    The magnetic properties of R-Li3Fe2(PO4)3 have been investigated for the first time: a para- to antiferromagnetic transition is seen at 28 ~ K. Neutron powder diffraction shows that the Fe magnetic dipoles lie close to the ab-plane and are ferromagnetically aligned within an Fesheet perpendicular to the c-axis, but are antiferromagnetically coupled to adjacent sheets.

  • 18.
    Andersson, AS
    et al.
    Uppsala University, Disciplinary Domain of Science and Technology, Chemistry, Department of Chemistry.
    Kalska, B
    Uppsala University, Disciplinary Domain of Science and Technology, Physics, Department of Physics.
    Jonsson, P
    Uppsala University, Disciplinary Domain of Science and Technology, Technology, Department of Materials Science.
    Haggstrom, L
    Nordblad, P
    Tellgren, R
    Thomas, JO
    The magnetic structure and properties of rhombohedral Li3Fe2(PO4)(3)2000In: JOURNAL OF MATERIALS CHEMISTRY, ISSN 0959-9428, Vol. 10, no 11, p. 2542-2547Article in journal (Refereed)
    Abstract [en]

    Magnetic susceptibility measurements indicate that rhombohedral Li3Fe2(PO4)(3), obtained by ion exchange of monoclinic Na3Fe2(PO4)(3), exhibits a paramagnetic to antiferromagnetic transition at T-N approximate to 27 K. Curie-Weiss-like behaviour is observ

  • 19.
    Andersson, AS
    et al.
    Uppsala University, Teknisk-naturvetenskapliga vetenskapsområdet, Chemistry, Department of Chemistry.
    Thomas, JO
    Physics, Department of Physics.
    Kalska, B
    Haggstrom, L
    Thermal stability of LiFePO4-based cathodes2000In: ELECTROCHEMICAL AND SOLID STATE LETTERS, ISSN 1099-0062, Vol. 3, no 2, p. 66-68Article in journal (Refereed)
    Abstract [en]

    The capacity and cyclability of solid-state synthesized LiFePO4-based laminate cells of type <Li \ liq. el. \ LiFePO4> have been studied at 23, 40, and 60 degrees C. Larger capacities were obtained for cells cycled at the elevated temperatures. No evidenc

  • 20. Andersson, Lars I.
    et al.
    Hardenborg, Emilia
    Uppsala University, Teknisk-naturvetenskapliga vetenskapsområdet, Chemistry, Department of Chemistry. Department of Physical and Analytical Chemistry, Analytical Chemistry. Analytisk kemi.
    Sandberg-Ställ, Maria
    Möller, Kristina
    Henriksson, Johan
    Bramsby-Sjöström, Inger
    Olsson, Lars-Inge
    Abdel-Rehim, Mohamed
    Development of a molecularly imprinted polymer based solid-phase extraction of local anaesthetics from human plasma2004In: Analytica Chimica Acta, no 526, p. 147-154Article in journal (Refereed)
  • 21.
    Andersson, Mikael
    Uppsala University, Teknisk-naturvetenskapliga vetenskapsområdet, Chemistry, Department of Chemistry. Analytisk kemi.
    Characterisation of the chemical and functional stability of chromatography media2000Licentiate thesis, monograph (Other scientific)
  • 22.
    Andersson, P.G.
    Uppsala University, Teknisk-naturvetenskapliga vetenskapsområdet, Chemistry, Department of Chemistry.
    Development of New Methodology for th Preparation of Optically Active Alcohols2004In: Pure Appl. Chem., no 76, p. 547-Article in journal (Refereed)
  • 23.
    Andersson, Pher
    Uppsala University, Teknisk-naturvetenskapliga vetenskapsområdet, Chemistry, Department of Chemistry. Department of Biochemistry and Organic Chemistry, Organic Chemistry I.
    On the Stereochemical Outcome of the McMurry Coupling of Acetophenone. A Reinvestigation1994In: Tetrahedron Letters, Vol. 35, no 16, p. 2609-2610Article in journal (Refereed)
  • 24.
    Andersson, Pher
    Uppsala University, Teknisk-naturvetenskapliga vetenskapsområdet, Chemistry, Department of Chemistry. Department of Biochemistry and Organic Chemistry, Organic Chemistry I.
    Regio- and Stereoselective Deuteration of Allylic Chlorides Controlled by Neighboring Alcohol or Ether Groups1996In: J. Org. Chem., no 61, p. 4154-4156Article in journal (Refereed)
  • 25.
    Andersson, Pher
    et al.
    Uppsala University, Teknisk-naturvetenskapliga vetenskapsområdet, Chemistry, Department of Chemistry. Department of Biochemistry and Organic Chemistry, Organic Chemistry I.
    Aranyos, Attila
    Palladium-Mediated Stereo- and Regioselective Tandem-Cyclization-Carbonylations of 1,3-dienes1994In: Tetrahedron Letters, Vol. 35, no 25, p. 4441-4444Article in journal (Refereed)
  • 26.
    Andersson, Pher
    et al.
    Uppsala University, Teknisk-naturvetenskapliga vetenskapsområdet, Chemistry, Department of Chemistry. Department of Biochemistry and Organic Chemistry, Organic Chemistry I.
    Bäckvall, Jan-E.
    Palladium-Catalyzed Tandem Cyclization of 4,6- and 5,7-Diene Amides. A New Route towards the Pyrrolizidine and Indolizidine Alkaloids1992In: J. Am. Chem. Soc., Vol. 114, no 22, p. 8696-8698Article in journal (Refereed)
  • 27.
    Andersson, Pher
    et al.
    Uppsala University, Teknisk-naturvetenskapliga vetenskapsområdet, Chemistry, Department of Chemistry. Department of Biochemistry and Organic Chemistry, Organic Chemistry I.
    Bäckvall, Jan-E.
    Synthesis of Furanoid Terpenes via an Efficient Palladium-Catalyzed Cyclization of 4,6-Dienols1991In: J. Org. Chem., Vol. 56, no 18, p. 5349-5353Article in journal (Refereed)
  • 28.
    Andersson, Pher
    et al.
    Uppsala University, Teknisk-naturvetenskapliga vetenskapsområdet, Chemistry, Department of Chemistry. Department of Biochemistry and Organic Chemistry, Organic Chemistry I.
    Bäckvall, Jan-E.
    Synthesis of Heterocyclic Natural Products via Regio- and Stereocontrolled Palladium-Catalyzed Reactions1996In: Advances in Heterocyclic Natural Product Synthesis, JAI Press Inc, Greenwich , 1996, p. 179-215Chapter in book (Refereed)
  • 29.
    Andersson, Pher
    et al.
    Uppsala University, Teknisk-naturvetenskapliga vetenskapsområdet, Chemistry, Department of Chemistry. Department of Biochemistry and Organic Chemistry, Organic Chemistry I.
    Guijarro, David
    Tanner, David
    Preparation and Use of Aziridino Alcohols as Promoters for the Enantioselective Addition of Dialkylzinc Reagents to N-(Diphenylphosphinoyl) Imines1997In: J. Org. Chem., no 62, p. 7364-7375Article in journal (Refereed)
  • 30.
    Andersson, Pher
    et al.
    Uppsala University, Teknisk-naturvetenskapliga vetenskapsområdet, Chemistry, Department of Chemistry. Department of Biochemistry and Organic Chemistry, Organic Chemistry I.
    Guijarro, David
    Tanner, David
    Simple Aziridino Alcohols as Chiral Ligands. Enantioselective Additions of Diethylzinc to N-Diphenylphosphinoylimines1996In: Synlett, no 8, p. 727-728Article in journal (Refereed)
  • 31.
    Andersson, Pher
    et al.
    Uppsala University, Teknisk-naturvetenskapliga vetenskapsområdet, Chemistry, Department of Chemistry. Department of Biochemistry and Organic Chemistry, Organic Chemistry I.
    Harden, Adrian
    Tanner, David
    Norrby, Per-Ola
    Studies of Allylic Substitution Catalysed by a Palladium Complex of a C2-Symmetric Bis(aziridine): Preparation and NMR Spectroscopic Investigation of a Chiral n-Allyl Species1995In: Chem. Eur. J., no 1, p. 12-16Article in journal (Refereed)
  • 32.
    Andersson, Pher
    et al.
    Uppsala University, Teknisk-naturvetenskapliga vetenskapsområdet, Chemistry, Department of Chemistry. Department of Biochemistry and Organic Chemistry, Organic Chemistry I.
    Johansson, Fredrik
    Tanner, David
    Enantioselective Addition of Organolithium Reagents to Imines Mediated by C2-Symmetric Bis(aziridine) Ligands1998In: Tetrahedron, no 54, p. 11549-11566Article in journal (Refereed)
  • 33.
    Andersson, Pher
    et al.
    Uppsala University, Teknisk-naturvetenskapliga vetenskapsområdet, Chemistry, Department of Chemistry. Department of Biochemistry and Organic Chemistry, Organic Chemistry I.
    Nilsson, Ylva
    Bäckvall, Jan-E.
    Palladium-Catalyzed Oxaspirocyclizations1994In: Tetrahedron, Vol. 50, no 2, p. 559-572Article in journal (Refereed)
  • 34.
    Andersson, Pher
    et al.
    Uppsala University, Teknisk-naturvetenskapliga vetenskapsområdet, Chemistry, Department of Chemistry. Department of Biochemistry and Organic Chemistry, Organic Chemistry I.
    Schab, Szymon
    Mechanism of the Palladium-Catalyzed Elimination of Acetic Acid from Allylic Acetates1995In: Organometallics, Vol. 14, no 1, p. 1-Article in journal (Refereed)
  • 35.
    Andersson, Pher
    et al.
    Uppsala University, Teknisk-naturvetenskapliga vetenskapsområdet, Chemistry, Department of Chemistry. Department of Biochemistry and Organic Chemistry, Organic Chemistry I.
    Schink, Hans
    Österlund, Krister
    Asymmetric Total Synthesis of (+)-Tolterodine, a New Muscarinic Receptor Antagonist, via Copper-Assisted Asymmetric Conjugate Addition of Aryl Grignard Reagents to 3-Phenyl-prop-2-enoyl-oxazolidinones1998In: J. Org. Chem., no 63, p. 8067-8070Article in journal (Refereed)
  • 36.
    Andersson, Pher
    et al.
    Uppsala University, Teknisk-naturvetenskapliga vetenskapsområdet, Chemistry, Department of Chemistry. Department of Biochemistry and Organic Chemistry, Organic Chemistry I.
    Sharpless, K. Barry
    A Dramatic Ligand Effect on the Relative Reactive Reactivites of Substituted Alkenes with Osmium Tetroxide1993In: J. Am. Chem. Soc., no 115, p. 7047-7048Article in journal (Refereed)
  • 37.
    Andersson, Y
    et al.
    Uppsala University, Teknisk-naturvetenskapliga vetenskapsområdet, Chemistry, Department of Chemistry.
    Larsson, T
    Nolang, B
    Rundqvist, S
    Neutron powder diffraction investigations of Nb-3(Al0.84Nb0.16) and Nb-3(Al0.84Nb0.16)H-2(2.52)2000In: JOURNAL OF ALLOYS AND COMPOUNDS, ISSN 0925-8388, Vol. 306, no 1-2, p. 193-196Article in journal (Refereed)
    Abstract [en]

    The crystal structures of Nb-3(Al0.84Nb0.16) and Nb-3(Al0.84Nb0.16)H-2(2.52) have been refined from neutron powder diffraction data using the Rietveld method. Nb-3(Al0.84Nb0.16) crystallizes in the cubic Cr3Si-type structure, space group Pm3n, with the un

  • 38.
    Antoni G., Amschler H., Zech K., Långström B.
    Uppsala University, Teknisk-naturvetenskapliga vetenskapsområdet, Chemistry, Department of Chemistry.
    Synthesis of [18F]labelled roflumilast using difluoro[18F]bromo methane as alkylating agent2001In: Synthesis and Applications of Isotopically LabelledArticle in journal (Refereed)
  • 39.
    Antoni G., Ögren M., Långström B.
    Uppsala University, Teknisk-naturvetenskapliga vetenskapsområdet, Chemistry, Department of Chemistry.
    Enzymes as catalysts in labelling synthesis using short-lived radionuclides2001In: Synthesis and Applications of Isotopically LabelledArticle in journal (Refereed)
  • 40.
    Antoni, Gunnar
    et al.
    Uppsala University, Disciplinary Domain of Science and Technology, Chemistry, Department of Chemistry.
    Kihlberg, T.
    Långström, B.
    11C: Labelling chemistry and labelled compounds2003In: Handbook Chem03_0302, 2003, no 332, p. 119-165Chapter in book (Refereed)
  • 41.
    Antoni, Gunnar
    et al.
    Uppsala University, Disciplinary Domain of Science and Technology, Chemistry, Department of Chemistry.
    Långström, Bengt
    Asymmetric synthesis of L-2-amino[3-11C]butyric acid, L-[3-11C]norvaline and L-[3-11C]valine.1987In: Acta Chemica Scandinavica, ISSN 0904-213X, E-ISSN 1902-3103, Vol. B41, p. 511-Article in journal (Refereed)
  • 42.
    Antoni, Gunnar
    et al.
    Uppsala University, Disciplinary Domain of Science and Technology, Chemistry, Department of Chemistry.
    Långström, Bengt
    Synthesis of DL-11C-labelled alanine, 2-aminobutyric acid, norvaline, leucine and phenylalanine and preparation of L-[3-11C]alanine and L-[3-11C]phenylalanine.1987In: Journal of labelled compounds & radiopharmaceuticals, ISSN ISSN 0362-4803, EISSN 1099-1344, Vol. 24, p. 125-Article in journal (Refereed)
  • 43.
    Antoni, Gunnar
    et al.
    Uppsala University, Disciplinary Domain of Science and Technology, Chemistry, Department of Chemistry.
    Långström, Bengt
    Synthesis of DL-[3-11C]valine using [2-11C]isopropyl iodide and preparation of L-[3-11C]valine by treatment with D-amino acid oxidase.1987In: Int. J. Appl. Radiat. Isot., Vol. 38, p. 655-Article in journal (Refereed)
  • 44.
    Antoni, Gunnar
    et al.
    Uppsala University, Disciplinary Domain of Science and Technology, Chemistry, Department of Chemistry.
    Långström, Bengt
    Synthesis of gamma-amino[4-11C]butyric acid.1989In: Journal of labelled compounds & radiopharmaceuticals, ISSN 0362-4803, E-ISSN 1099-1344, Vol. 27, p. 571-Article in journal (Refereed)
  • 45.
    Antoni, Gunnar
    et al.
    Uppsala University, Disciplinary Domain of Science and Technology, Chemistry, Department of Chemistry.
    Omura, H
    Ikemoto, M
    Moulder, R
    Watanabe, Y
    Långström, B
    Uppsala University, Disciplinary Domain of Science and Technology, Chemistry, Department of Biochemistry and Organic Chemistry.
    Enzyme catalysed synthesis of L-(4-11C) aspartate and L-(5-11C) glutamate2001In: J. Labbelled Compd. Radiopharm.Article in journal (Other academic)
  • 46.
    Antoni, Gunnar
    et al.
    Uppsala University, Disciplinary Domain of Science and Technology, Chemistry, Department of Chemistry.
    Ulin, Johan
    Långström, Bengt
    Synthesis of the 11C-labelled b-adrenargic receptor ligands atenolol, metoprolol and propranol.1989In: The international journal of applied radiation and isotopes, ISSN 0020-708X, E-ISSN 1878-1284, Vol. 40, p. 561-Article in journal (Refereed)
  • 47. Aquilonius, Sten-Magnus
    et al.
    Bergström, Kjell
    Eckernäs, S.A
    Hartvig, Per
    Leenders, K.L.
    Lundkvist, Hans
    Antoni, Gunnar
    Uppsala University, Disciplinary Domain of Science and Technology, Chemistry, Department of Chemistry.
    Rimland, Annika
    Ulin, Johan
    Långström, Bengt
    In vivo visualization of striatal dopamine reuptake sites using [11C]nomifensine and       positron emission tomography.,1987In: Acta Neurol. Scand., Vol. 76, p. 283-287Article in journal (Refereed)
  • 48.
    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

  • 49.
    Aranyos, Viviane
    Uppsala University, Teknisk-naturvetenskapliga vetenskapsområdet, Chemistry, Department of Chemistry.
    Dyes and their adsorption onto nanocrystalline TiO2 electrodes: Synthesis, characterisation and applications2000Doctoral thesis, comprehensive summary (Other academic)
    Abstract [en]

    The syntheses of two type of dyes (phthalocyanine and ruthenium tris-bipyridyl) are presented here. Their characterisation involves the use of cyclic voltammetry, NMR- and UV-visible spectroscopy. Once adsorbed on nanocrystalline TiO2 electrodes, their electrochemical, spectroelectrochemical and photoelectrochemical properties were investigated.

    In the first part, the syntheses of aryl-substituted phthalocyanines are described. The key intermediate, an aryl-substituted phthalonitrile, was prepared by a Pd(0)-catalysed Stille-coupling. The physical properties of tetra-(2,5-dirnetoxyphenyl)phthalocyanine (1a), tetraphenylphthalocyanine (1b) are discussed, An interesting display behaviour was characterised by spectroelectrochemistry in the case of 1b. Considering the system, unexpectedly high efficiencies of the resulting solar cells are observed for both dyes.

    The second part deals with two types of ruthenium tris-bipyridyl complexes. Syntheses of three carboxylated heteroleptic ruthenium complexes [Ru(bpy)2(bpy-R)](PF6)2 (bpy-R, R= (COOLi)n, n= 1, 2, 4) were synthesised for a study of the influence of the number of carboxylic groups on solar cell efficiencies. A lateral electron transfer mechanism for the dyes adsorbed on TiO2, is observed. Homoleptic and heteroleptic ruthenium complexes possessing the polymerisable groups vinyl, methoxyphenyl or thiophene were prepared for an investigation of the substituent effect on the dye-monolayer in the solar cell, both by electrochemistry and absorption spectroscopy. The methoxyphenyl-substituted complexes showed good polymerisation behaviour both at negative and at positive potentials. They also showed good resistance towards water when adsorbed onto TiO2 electrodes.

  • 50.
    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.

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