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  • 51.
    Lee, Bao-Lin
    et al.
    Stockholm University, Faculty of Science, Department of Organic Chemistry.
    Karlsson, Erik A.
    Kärkäs, Markus D.
    Stockholm University, Faculty of Science, Department of Organic Chemistry.
    Åkermark, Torbjörn
    Stockholm University, Faculty of Science, Department of Materials and Environmental Chemistry (MMK).
    Johnston, Eric
    Stockholm University, Faculty of Science, Department of Organic Chemistry.
    Das, Biswanath
    Nordlander, Ebbe
    Åkermark, Björn
    Stockholm University, Faculty of Science, Department of Organic Chemistry.
    Light-induced water oxidation by a dinuclear iron-based molecular catalystManuscript (preprint) (Other academic)
  • 52.
    Lind, Maria E. S.
    et al.
    Stockholm University, Faculty of Science, Department of Organic Chemistry.
    Himo, Fahmi
    Stockholm University, Faculty of Science, Department of Organic Chemistry.
    Quantum Chemical Modeling of Enantioconvergency in Soluble Epoxide HydrolaseManuscript (preprint) (Other academic)
  • 53.
    Lindén, Auri
    et al.
    Stockholm University, Faculty of Science, Department of Organic Chemistry.
    Johansson, Mikael
    Hermanns, Nina
    Bäckvall, Jan-Erling
    Efficient and Selective Sulfoxidation by Hydrogen Peroxide Using Recyclable Flavin-Catalyst-[BMIm]PF6 SystemManuscript (Other academic)
  • 54.
    Liu, Jianguo
    et al.
    Stockholm University, Faculty of Science, Department of Organic Chemistry.
    Krajangsri, Suppachai
    Stockholm University, Faculty of Science, Department of Organic Chemistry.
    Li, Jiaqi
    Andersson, Pher G.
    Stockholm University, Faculty of Science, Department of Organic Chemistry.
    Iridium-catalyzed Asymmetric Hydrogenation of Allylic Alcohols via Dynamic Kinetic ResolutionManuscript (preprint) (Other academic)
  • 55.
    Lundborg, Magnus
    et al.
    Stockholm University, Faculty of Science, Department of Organic Chemistry.
    Eunus, Ali
    Stockholm University, Faculty of Science, Department of Organic Chemistry.
    Widmalm, Göran
    Stockholm University, Faculty of Science, Department of Organic Chemistry.
    Fragment-based design of norovirus inhibitors by molecular docking and LIE binding free energy calculationsManuscript (preprint) (Other academic)
  • 56.
    Malmgren, Joel
    Stockholm University, Faculty of Science, Department of Organic Chemistry.
    Synthesis of Alkynyl(aryl)iodonium salts from TMS-alkynesManuscript (preprint) (Other academic)
  • 57.
    Mannerstedt, Karin
    et al.
    Stockholm University, Faculty of Science, Department of Organic Chemistry.
    Oscarson, Stefan
    Synthesis of Phosphoethanolamine-substituted Trisaccharides Corresponding to Neisseria meningitidis and Haemophilus influenzae LPS StructuresManuscript (Other academic)
  • 58.
    Mannerstedt, Karin
    et al.
    Stockholm University, Faculty of Science, Department of Organic Chemistry.
    Oscarson, Stefan
    Synthesis ofHaemophilus influenzae LPSManuscript (Other academic)
  • 59.
    Manta, Bianca
    et al.
    Stockholm University, Faculty of Science, Department of Organic Chemistry.
    Himo, Fahmi
    Stockholm University, Faculty of Science, Department of Organic Chemistry.
    Insights from Quantum Chemical Calculations into Active Site Structure and Reaction Mechanism of Manganese-Dependent Dinitrogenase Reductase-Activating GlycohydrolaseManuscript (preprint) (Other academic)
  • 60. Nilsson, Magnus
    et al.
    Belfrage, Anna Karin
    Lindström, Stefan
    Wähling, Horst
    Lindquist, Charlotta
    Stockholm University, Faculty of Science, Department of Organic Chemistry.
    Ayesa Alvarez, Susana
    Kahnberg, Pia
    Pelcman, Mikael
    Vrang, Lotta
    Terselius, Ylva
    Wikström, Kristina
    Hamelink, Elizabeth
    Rydergård, Christina
    Edlund, Michael
    Eneroth, Anders
    Raboisson, Pierre
    Lin, Tse-I.
    de Kock, Herman
    Wigerinck, Piet
    Simmen, Kenneth
    Samuelsson, Bertil
    Rosenquist, Åsa
    Synthesis and SAR of potent inhibitors of the Hepatitis C virus NS3/4A protease: exploration of P2 quinazoline substituents.Manuscript (preprint) (Other academic)
    Abstract [en]

    Novel NS3/4A protease inhibitors comprising quinazoline derivatives as P2 substituent were synthesized. High potency inhibitors displaying advantageous PK properties have been obtained through the optimization of quinazoline P2 substituents in three series of macrocyclic P2 cyclopentane dicarboxylic acid and P2 proline urea motifs. For the quinazoline moiety it was found that 8-methyl substitution for the P2 cyclopentane dicarboxylic acid series improved on the stability in human liver microsomes. By comparison, the proline urea series displayed advantageous Caco-2 permeability over the cyclopentane series. properties were assessed in rat on selected compounds. Excellent exposure and liver–to-plasma ratios were demonstrated for a member of the 14-membered quinazoline substituted P2 proline urea series. In vivo pharmacokinetic properties were assessed in rat on selected compounds. Excellent exposure and liver–to-plasma ratios were demonstrated for a member of the 14-membered quinazoline substituted P2 proline urea series.

  • 61.
    Nordmark, Eva-Lisa
    et al.
    Stockholm University, Faculty of Science, Department of Organic Chemistry.
    Eklund, Robert
    Weintraub, Andrej
    Seckler, Robert
    Widmalm, Göran
    Interaction studies of a Salmonella enteritidis O-antigen octasaccharide to phage P22 tail spike protein by NMR spectroscopy and molecular modelingManuscript (Other academic)
  • 62. Nordmark, Eva-Lisa
    et al.
    Eklund, Robert
    Stockholm University, Faculty of Science, Department of Organic Chemistry.
    Weintraub, Andrej
    Seckler, Robert
    Widmalm, Göran
    Interaction studies of a Salmonella enteritidis O-antigen octasaccharide to Phage P22 tail spike protein by NMR spectroscopy and molecular modellingManuscript (Other academic)
  • 63.
    Nordmark, Eva-Lisa
    et al.
    Stockholm University, Faculty of Science, Department of Organic Chemistry.
    Perepelov, Andrei
    Shashkov, Alexander S.
    Nazarenko, Evgeny L.
    Widmalm, Göran
    Structure of an acidic polysaccharide from the Marine Bacterium Pseudoalteromonas aliena type strain KMM 3562T containing two residues of L-serine in the repeating unitManuscript (Other academic)
  • 64. Närhi, Katja
    et al.
    Franzén, Johan
    Stockholm University, Faculty of Science, Department of Organic Chemistry.
    Bäckvall, Jan-E
    Palladium(0)-Catalyzed Cycloisomerization of Enallenes.Manuscript (Other academic)
  • 65.
    Olsson, Johan
    et al.
    Stockholm University, Faculty of Science, Department of Organic Chemistry.
    Lahmann, Martina
    Oscarson, Stefan
    Stockholm University, Faculty of Science, Department of Organic Chemistry.
    Synthesis of serine substituted 2-N-acetyl 2N,3O-oxazolidinone galactosamine, a key building block for O-glycan synthesisManuscript (preprint) (Other academic)
  • 66.
    Olsson, Johan
    et al.
    Stockholm University, Faculty of Science, Department of Organic Chemistry.
    Oscarson, Stefan
    Stockholm University, Faculty of Science, Department of Organic Chemistry.
    Synthesis of 3,4-branched phosphorylated trisaccharides corresponding to LPS inner core structure of Neisseria meningitidis and Haemophilius influenzaeManuscript (preprint) (Other academic)
  • 67.
    Olsson, Ulrika
    et al.
    Stockholm University, Faculty of Science, Department of Organic Chemistry.
    Säwén, Elin
    Stenutz, Roland
    Widmalm, Göran
    Conformational flexibility and dynamics of a (1-6)-linked disaccharide related to an oligosaccharide epitope expressed on malignant tumor cellsManuscript (Other academic)
  • 68.
    Olsson, Vilhelm
    Stockholm University, Faculty of Science, Department of Organic Chemistry.
    Functionalization of Unactivated Alkenes trough Iridium-Catalyzed Borylation of Carbon-Hydrogen Bonds. Mechanism and Synthetic ApplicationsManuscript (Other academic)
  • 69.
    Pathipati, Stalin R.
    et al.
    Stockholm University, Faculty of Science, Department of Organic Chemistry.
    van der Werf, Angela
    Stockholm University, Faculty of Science, Department of Organic Chemistry.
    Selander, Nicklas
    Stockholm University, Faculty of Science, Department of Organic Chemistry.
    Diastereoselective Synthesis of Polycyclic Indolizines with 2‑(2‑Enynyl)pyridines and EnaminesManuscript (preprint) (Other academic)
  • 70.
    Peters, Byron K.
    et al.
    Stockholm University, Faculty of Science, Department of Organic Chemistry.
    Liu, Jianguo
    Stockholm University, Faculty of Science, Department of Organic Chemistry.
    Margarita, Cristiana
    Stockholm University, Faculty of Science, Department of Organic Chemistry.
    Rabten, Wangchuk
    Stockholm University, Faculty of Science, Department of Organic Chemistry.
    Kerdphon, Sutthichat
    Stockholm University, Faculty of Science, Department of Organic Chemistry.
    Paptchikhine, Alexander
    Stockholm University, Faculty of Science, Department of Organic Chemistry.
    Andersson, Pher
    Stockholm University, Faculty of Science, Department of Organic Chemistry.
    Enantio- and Regioselective Hydrogenation of Minimally and Densely Decorated Unsaturated CarbocyclesManuscript (preprint) (Other academic)
    Abstract [en]

    Several cyclic prochiral olefins were successfully hydrogenated (>99 conv.,up to >99 % ee) using N,P-ligated iridium catalysts. Minimally functionalisedsubstrates (Class 1) were hydrogenated rapidly and in high ee, whichwas consistent with earlier reports. Substrates having functional groups(Class 2) and heterocycles (Class 3) attached to the unsaturated cycle, were43hydrogenated gradually over a period of time, however, high enantioselectivitywas still maintained (up to >99 % ee). This methodology is a highly practical,general and selective means of preparing chiral cyclohexanes.

  • 71. Piera, Julio
    et al.
    Närhi, Katja
    Stockholm University, Faculty of Science, Department of Organic Chemistry.
    Bäckvall, Jan-E.
    Palladium(II)-Catalyzed Aerobic Allylic Oxidative Carbocyclization of Allene-Substituted Olefins. Immobilization of Oxygen-Activating Catalyst.Manuscript (Other academic)
  • 72.
    Rabten, Wangchuk
    et al.
    Stockholm University, Faculty of Science, Department of Organic Chemistry.
    Ponra, Sudipta
    Stockholm University, Faculty of Science, Department of Organic Chemistry.
    Kerdphon, Sutthichat
    Stockholm University, Faculty of Science, Department of Organic Chemistry.
    Wu, Haibo
    Stockholm University, Faculty of Science, Department of Organic Chemistry.
    Andersson, Pher G.
    Stockholm University, Faculty of Science, Department of Organic Chemistry.
    N,P-Iridium Catalyzed Asymmetric Hydrogenation of Vinyl FluoridesManuscript (preprint) (Other academic)
  • 73.
    Ramstadius, Clinton
    et al.
    Stockholm University, Faculty of Science, Department of Organic Chemistry.
    Boklund, Mikael
    Stockholm University, Faculty of Science, Department of Organic Chemistry.
    Cumpstey, Ian
    Stockholm University, Faculty of Science, Department of Organic Chemistry.
    Conversion of fructose into a building block for the synthesis of carbocyclic mannose mimicsManuscript (preprint) (Other academic)
  • 74.
    Ramstadius, Clinton
    et al.
    Stockholm University, Faculty of Science, Department of Organic Chemistry.
    Träff, Annika
    Stockholm University, Faculty of Science, Department of Organic Chemistry.
    Krumlinde, Patrik
    Stockholm University, Faculty of Science, Department of Organic Chemistry.
    Bäcklund, Jan-Erling
    Cumpstey, Ian
    Stockholm University, Faculty of Science, Department of Organic Chemistry.
    Experimental determination of the relative stability of hexopyranoside derivativesManuscript (preprint) (Other academic)
  • 75.
    Rydner, Lina
    et al.
    Stockholm University, Faculty of Science, Department of Organic Chemistry.
    Oscarson, Stefan
    Centre for Synthesis and Chemical biology, University College, Dublin.
    A synthetic strategy to xylose-containing thioglycoside tri- and tetrasaccharide building blocks corresponding to Cryptococcus neoformans capsular polysaccharide structuresManuscript (preprint) (Other academic)
  • 76.
    Rydner, Lina
    et al.
    Stockholm University, Faculty of Science, Department of Organic Chemistry.
    Ulc, Rebecca
    Centre for Synthesis and Chemical Biology, University College, Dublin.
    Oscarson, Stefan
    Centre for Synthesis and Chemical Biology, University College, Dublin.
    Construction of a hexasaccharide thioglycoside building block corresponding to the Cryptococcus neoformans CPS type A triadManuscript (preprint) (Other academic)
  • 77.
    Sandström, Anders G.
    Stockholm University, Faculty of Science, Department of Organic Chemistry.
    Highly Combinatorial Reshaping of the Candida antarctica lipase A Substrate Pocket Using an Extremely Condensed LibraryManuscript (preprint) (Other academic)
    Abstract [en]

    A highly combinatorial structure based protein engineering method is demonstrated resulting in a thorough modification of the binding pocket of Candida antarctica lipase A (CALA). Nine amino acid sites surrounding the entire pocket were simultaneously mutated, contributing to a sculpting of the substrate pocket toward a sterically demanding substrate, an ibuprofen ester. The best variant was highly active and displayed remarkable increase in enantioselectivity toward the substrate, with an E-value of 101, compared to the wild type CALA that poor activity and possesses an E-value of 3.4. The potential mutations introduced were a highly reduced set of amino acids, containing only the wild type residue and an alternative residue, preferably a smaller one with similar properties. These minimal ‘binary’ sets allow for extremely condensed protein libraries. The choice of amino acid sites were based on a computer model, with the substrate forcibly bound in the active site. This highly combinatorial method can be used to obtain tailor-made enzymes that are active toward substrates that are not normally accepted by the enzyme. When multiple sites are altered simultaneously, there is a higher possibility of obtaining positive synergistic effects, and the protein fitness landscape is explored efficiently.

  • 78.
    Sheng, Xiang
    et al.
    Stockholm University, Faculty of Science, Department of Organic Chemistry.
    Lind, Maria E. S.
    Stockholm University, Faculty of Science, Department of Organic Chemistry.
    Himo, Fahmi
    Stockholm University, Faculty of Science, Department of Organic Chemistry.
    Theoretical Study of the Reaction Mechanism of Phenolic Acid DecarboxylaseManuscript (preprint) (Other academic)
  • 79.
    Skantz, Linnéa
    et al.
    Stockholm University, Faculty of Science, Department of Organic Chemistry.
    Oscarson, Stefan
    Stockholm University, Faculty of Science, Department of Organic Chemistry.
    Lahmann, Martina
    Stockholm University, Faculty of Science, Department of Organic Chemistry.
    Synthesis of the B-Lewis b heptasaccharide using a versatile lacto-N-tetraose intermediateManuscript (Other academic)
  • 80.
    Skantz, Linnéa
    et al.
    Stockholm University, Faculty of Science, Department of Organic Chemistry.
    Sajtos, Ferenc
    Stockholm University, Faculty of Science, Department of Organic Chemistry.
    Oscarson, Stefan
    University College Dublin, Centre of synthesis and chemical biology.
    Lahmann, Martina
    University of Bangor, The school of chemistry.
    Synthesis of the Lewis b pentasaccharide and HSA-conjugates thereofManuscript (Other academic)
  • 81.
    Slättegård, Rikard
    et al.
    Stockholm University, Faculty of Science, Department of Organic Chemistry.
    Gammon, David W
    Oscarson, Stefan
    Synthesis of 1-S-(2-amino-2-deoxy-a-D-glucopyranosyl)-1-deoxy-1-thio-D-myo-inositol, a precursor to the thioglycoside analogue of mycothiolManuscript (Other academic)
  • 82.
    Ståhle, Jonas
    et al.
    Stockholm University, Faculty of Science, Department of Organic Chemistry.
    Widmalm, Göran
    Stockholm University, Faculty of Science, Department of Organic Chemistry.
    Structural studies of the O-antigen polysaccharide from Escherichia coli O63 and biosynthetic aspects thereofManuscript (preprint) (Other academic)
  • 83.
    Teodorović, Peter
    et al.
    Stockholm University, Faculty of Science, Department of Organic Chemistry.
    Oscarson, Stefan
    Synthesis of C-Phosphonate Analogues of Neisseria meningitidis group A Capsular Polysaccharide StructuresManuscript (Other academic)
  • 84.
    Thalén, Lisa
    et al.
    Stockholm University, Faculty of Science, Department of Organic Chemistry.
    Hoben, Christine
    Stockholm University, Faculty of Science, Department of Organic Chemistry.
    Bäckvall, Jan-Erling
    Stockholm University, Faculty of Science, Department of Organic Chemistry.
    Synthesis of (R)-2-methoxy-N-(1-phenylethyl)acetamide via Dynamic Kinetic ResolutionManuscript (preprint) (Other academic)
  • 85.
    Tinnis, Fredrik
    et al.
    Stockholm University, Faculty of Science, Department of Organic Chemistry.
    Lundberg, Helena
    Stockholm University, Faculty of Science, Department of Organic Chemistry.
    Kivijärvi, Tove
    Adolfsson, Hans
    Stockholm University, Faculty of Science, Department of Organic Chemistry.
    Zirconium(IV) Chloride Catalyzed Amide Formation from Carboxylic Acids and Amines: N-Benzyl-2-(phenylthio)acetamide and (S)-tert-butyl-2-(benzylcarbamoyl)pyrrolidine-1-carboxylateManuscript (preprint) (Other academic)
  • 86.
    Utas, Josefin
    et al.
    Stockholm University, Faculty of Science, Department of Organic Chemistry.
    Irebo, Tania
    Lomoth, Reiner
    Sjodin, Martin
    Sun, Licheng
    Tommos, Cecilia
    Blomberg, Margareta
    Hammarström, Leif
    Åkermark, Björn
    The Effect of Imidazole on Phenol Oxidation – Models for TyrZ and His190 in Photosystem IIManuscript (Other academic)
  • 87.
    van der Werf, Angela
    et al.
    Stockholm University, Faculty of Science, Department of Organic Chemistry.
    Zheng, Zhiyao
    Stockholm University, Faculty of Science, Department of Organic Chemistry.
    Selander, Nicklas
    Stockholm University, Faculty of Science, Department of Organic Chemistry.
    N-Perfluoroalkylation of Nitrosoarenes with PerfluoroalkanesulfinatesManuscript (preprint) (Other academic)
  • 88.
    Verho, Oscar
    et al.
    Stockholm University, Faculty of Science, Department of Organic Chemistry.
    Kärkäs, Markus
    Åkermark, Torbjörn
    Stockholm University, Faculty of Science, Department of Materials and Environmental Chemistry (MMK), Materials Chemistry.
    Johnston, Eric V.
    Stockholm University, Faculty of Science, Department of Organic Chemistry.
    Gustafson, Karl
    Stockholm University, Faculty of Science, Department of Organic Chemistry.
    Tai, Cheuk-Wai
    Stockholm University, Faculty of Science, Department of Materials and Environmental Chemistry (MMK), Inorganic and Structural Chemistry.
    Svengren, Henrik
    Stockholm University, Faculty of Science, Department of Materials and Environmental Chemistry (MMK), Inorganic and Structural Chemistry.
    Bäckvall, Jan-Erling
    Stockholm University, Faculty of Science, Department of Organic Chemistry.
    Åkermark, Björn
    Stockholm University, Faculty of Science, Department of Organic Chemistry.
    Well-Defined Palladium Nanoparticles Supported on Amino-Functionalized Siliceous Mesocellular Foam: An Efficient Heterogeneous Catalyst for Chemically-Induced H2O OxidationManuscript (preprint) (Other academic)
  • 89.
    Västilä, Patrik
    et al.
    Stockholm University, Faculty of Science, Department of Organic Chemistry.
    Wettergren, Jenny
    Adolfsson, Hans
    Ruthenium-catalyzed enantioselective reduction of ketones - in situ formation of ligand and catalystManuscript (Other academic)
  • 90.
    Västilä, Patrik
    et al.
    Stockholm University, Faculty of Science, Department of Organic Chemistry.
    Zaitsev, Alexey
    Wettergren, Jenny
    Adolfsson, Hans
    The importance of alkali cations in the ruthenium-catalyzed enantioselective transfer-hydrogenation of ketones - novel mechanistic implicationsManuscript (Other academic)
  • 91.
    Warner, Madeleine
    Stockholm University, Faculty of Science, Department of Organic Chemistry.
    Racemization of Olefinic Alcohols by a Cyclopentadienyl Ruthenium Carbonyl Complex: Study of the Inhibiting Effect of the Carbon-Carbon Double BondManuscript (preprint) (Other academic)
  • 92. Wieczorek, Birgit
    et al.
    Träff, Annika
    Stockholm University, Faculty of Science, Department of Organic Chemistry.
    Krumlinde, Patrik
    Stockholm University, Faculty of Science, Department of Organic Chemistry.
    Dijkstra, Harm P.
    Egmond, Maarten R.
    van Koten, Gerard
    Bäckvall, Jan-Erling
    Stockholm University, Faculty of Science, Department of Organic Chemistry.
    Klein Gebbink, Robertus J.M.
    Site-Specific Covalent Immobilization of a Racemization Catalyst onto Lipase-containing BeadsManuscript (preprint) (Other academic)
    Abstract [en]

    The synthesis and application of the novel heterogeneous bifunctional catalyst CALB-5 as a racemization and resolution catalyst for the dynamic kinetic resolution is described. The semisynthetic ruthenium lipase hybrid CALB-5 was obtained by inhibiting CALB beads with the novel ruthenium phosphonate complex 5 possessing a lipase active site-directed phosphonate group. By partially inhibiting the lipase beads with 5, a bifunctional catalytic system was obtained. Racemization, by the Ru-catalytic site, gave 0% ee after 24 h, and the kinetic resolution, enzymatic acylation by the uninhibited CALB sites, gave 28% conversion of 1-phenylethanol after 3 h with >99% ee of the acetylated product. A dynamic kinetic resolution experiment of (S)-1-phenylethanol with CALB-5 gave the acylated (R)-product in 18% yield and with >99% ee.

  • 93.
    Wolpher, Henriette
    et al.
    Stockholm University, Faculty of Science, Department of Organic Chemistry.
    Abrahamsson, Maria
    Eriksson, Lars
    Norrby, Per-Ola
    Johansson, Olof
    Bergquist, Jonas
    Hammarström, Leif
    Åkermark, Björn
    Ruthenium complexes of a bipyridyl(pyridyl)methane ligand: Effect of substituents at the methylene group on structure and photophysicsManuscript (Other academic)
  • 94.
    Wolpher, Henriette
    et al.
    Stockholm University, Faculty of Science, Department of Organic Chemistry.
    Pan, Jingxi
    Johansson, Anh
    Lundqvist, Maria
    Persson, Petter
    Bergquist, Jonas
    Polivka, Tomas
    Sun, Licheng
    Åkermark, Björn
    Electron transfer studies of terpyridine based ruthenium(II)-donor dyads attached to nanostructured TiO2Manuscript (Other academic)
  • 95.
    Xu, Quan
    et al.
    Stockholm University, Faculty of Science, Department of Organic Chemistry.
    Kerdphon, Sutthichat
    Stockholm University, Faculty of Science, Department of Organic Chemistry.
    Rujirawanich, Janjira
    Stockholm University, Faculty of Science, Department of Organic Chemistry.
    Krajangsri, Suppachai
    Stockholm University, Faculty of Science, Department of Organic Chemistry.
    Andersson, Pher
    Stockholm University, Faculty of Science, Department of Organic Chemistry.
    Highly Active Cationic NHC, Phosphine Iridium Catalysts for Base Free Asymmetric Hydrogenation of KetonesManuscript (preprint) (Other academic)
  • 96.
    Xu, Yunhua
    et al.
    Stockholm University, Faculty of Science, Department of Organic Chemistry.
    Eilers, Gerriet
    Borgström, Magnus
    Pan, Jingxi
    Abrahamsson, Maria
    Magnuson, Ann
    Lomoth, Reiner
    Bergquist, Jonas
    Polivka, Tomas
    Sun, Licheng
    Sundström, Villy
    Styring, Stenbjörn
    Hammarström, Leif
    Åkermark, Björn
    Synthesis and Characterization of Novel Dinuclear Ruthenium Complexes Covalently Linked to Ru(II) Trisbipyridine: an Approach to Mimics of the Donor Side of PS IIManuscript (Other academic)
  • 97.
    Xu, Yunhua
    et al.
    Stockholm University, Faculty of Science, Department of Organic Chemistry.
    Pan, Jie
    Huang, Ping
    Feyziyev, Yashar
    Lomoth, Reiner
    Hammarström, Leif
    Styring, Stenbjörn
    Polivka, Tomas
    Sundström, Villy
    Åkermark, Björn
    Sun, Licheng
    Synthesis and Photoinduced Electron Transfer Study of a Substituted Phenol Covalently Linked to Ruthenium Trisbipyridine with or without Four Ester GroupsManuscript (Other academic)
  • 98.
    Yao, Qingxia
    et al.
    Stockholm University, Faculty of Science, Department of Materials and Environmental Chemistry (MMK), Inorganic and Structural Chemistry.
    Bermejo Gómez, Antonio
    Stockholm University, Faculty of Science, Department of Organic Chemistry.
    Su, Jie
    Stockholm University, Faculty of Science, Department of Materials and Environmental Chemistry (MMK), Inorganic and Structural Chemistry.
    Pascanu, Vlad
    Stockholm University, Faculty of Science, Department of Organic Chemistry.
    Yun, Yifeng
    Stockholm University, Faculty of Science, Department of Materials and Environmental Chemistry (MMK).
    Zheng, Haoquan
    Stockholm University, Faculty of Science, Department of Materials and Environmental Chemistry (MMK), Inorganic and Structural Chemistry.
    Chen, Hong
    Stockholm University, Faculty of Science, Department of Materials and Environmental Chemistry (MMK), Inorganic and Structural Chemistry.
    Liu, Leifeng
    Stockholm University, Faculty of Science, Department of Materials and Environmental Chemistry (MMK), Inorganic and Structural Chemistry.
    Martín-Matute, Belén
    Stockholm University, Faculty of Science, Department of Organic Chemistry.
    Zou, Xiaodong
    Stockholm University, Faculty of Science, Department of Materials and Environmental Chemistry (MMK).
    Highly porous isoreticular lanthanide metal-organic frameworksManuscript (preprint) (Other academic)
    Abstract [en]

    As an emerging type of porous materials, metal–organic frameworks (MOFs) have the advantages over conventional inorganic porous materials in that their structures and functions are systematically and predictably designable. Isoreticular expansion is an efficient way for systematic design and control of pore size and shape for MOFs. By using our proposed strategy, a series of highly porous isoreticular lanthanide-based metal-organic frameworks with systematic pore apertures has been obtained, which afford an isoreticular series of MIL-103 structures (termed SUMOF-7I to IV) with pore apertures ranging from 7.2 Å to 23 Å. These materials demonstrated exhibit robust architectures with permanent porosity, and exceptional thermal stability and chemical stability in various solvents. The combination of luminescence property and significant porosity of these MOFs enable them as a potential platform for multifunctional purpose.

  • 99.
    Östervall, Jennie
    et al.
    Stockholm University, Faculty of Science, Department of Organic Chemistry.
    Maliniak, Arnold
    Widmalm, Göran
    Conformational dynamics of the pentasaccharide LNF-1 from NMR spectroscopy and molecular dynamics simulationsManuscript (Other academic)
  • 100.
    Östervall, Jennie
    et al.
    Stockholm University, Faculty of Science, Department of Organic Chemistry.
    Naidoo, Kevin J.
    Chen, Jeff Yu-Jen
    Widmalm, Göran
    Maliniak, Arnold
    Molecular structure and dynamics of α, β and γ-cyclodextrinsManuscript (Other academic)
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