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41.
Helene?Bonkerud?Dugstad Nickolaj?Jacob?PetersenEmail author Henrik?Jensen Charlotte?Gabel-Jensen Steen?Honoré?Hansen Stig?Pedersen-Bjergaard 《Analytical and bioanalytical chemistry》2014,406(2):421-429
A small and very simple electromembrane extraction probe (EME-probe) was developed and coupled directly to electrospray ionization mass spectrometry (ESI-MS), and this system was used to monitor in real time in vitro metabolism by rat liver microsomes of drug substances from a small reaction (incubation) chamber (37 °C). The drug-related substances were continuously extracted from the 1.0 mL metabolic reaction mixture and into the EME-probe by an electrical potential of 2.5 V. The extraction probe consisted of a 1-mm long and 350-μm ID thin supported liquid membrane (SLM) of 2-nitrophenyl octyl ether. The drugs and formed metabolites where extracted through the SLM and directly into a 3 μL min?1 flow of 60 mM HCOOH inside the probe serving as the acceptor solution. The acceptor solution was directed into the ESI-MS-system, and the MS continuously monitored the drug-related substances extracted by the EME-probe. The extraction efficiency of the EME-probe was dependant on the applied electrical potential and the length of the SLM, and these parameters as well as the volume of the reaction chamber were set to the values mentioned above to avoid serious depletion from the reaction chamber (soft extraction). Soft extraction was mandatory in order not to affect the reaction kinetics by sample composition changes induced by the EME-probe. The EME-probe/MS-system was used to establish kinetic profiles for the in vitro metabolism of promethazine, amitriptyline and imipramine as model substances. 相似文献
42.
Kirill Arapov Kaarle Jaakkola Vladimir Ermolov Guy Bex Eric Rubingh Samiul Haque Henrik Sandberg Robert Abbel Gijsbertus de With Heiner Friedrich 《固体物理学:研究快报》2016,10(11):812-818
Despite the great promise of printed flexible electronics from 2D crystals, and especially graphene, few scalable applications have been reported so far that can be termed roll‐to‐roll compatible. Here we combine screen printed graphene with photonic annealing to realize radio‐frequency identification devices with a reading range of up to 4 meters. Most notably our approach leads to fatigue resistant devices showing less than 1% deterioration of electrical properties after 1000 bending cycles. The bending fatigue resistance demonstrated on a variety of technologically relevant plastic and paper substrates renders the material highly suitable for various printable wearable devices, where repeatable dynamic bending stress is expected during usage. All applied printing and post‐processing methods are compatible with roll‐to‐roll manufacturing and temperature sensitive flexible substrates providing a platform for the scalable manufacturing of mechanically stable and environmentally friendly graphene printed electronics.
43.
44.
Eduard Hryha Henrik Borgström Karin Sterky Lars Nyborg 《Journal of Thermal Analysis and Calorimetry》2014,118(2):695-704
Binders present an important part of the powder metallurgy technology as they are vital to provide efficient powder agglomeration and/or lubrication during shaping. At the same time, they have to be easily removed from the compacts during initial stages of sintering without any harmful effect for the base material, as well as for the environment. Therefore, behavior of gelatin as a binder for stainless- and tool-steel gas-atomised powder compacts was studied by thermal analysis and electron microscopy. Thermal analysis showed that peak mass-loss occurred in the range between 340 and 370 °C, depending on the base powder and heating rate. Risk for base powder oxidation at temperatures below 425 °C was detected. Based on the obtained results, it is recommended to perform debinding at ~425 °C after applying a heating rate of around 7.5 °C min?1. Only in this way efficient enough binder removal can be obtained concurrently to avoiding base powder oxidation. 相似文献
45.
Casper Jon Steenbjerg Ibsen Bjørn Fridur Mikladal Uffe Bjørnholt Jensen Assoc. Prof. Henrik Birkedal 《Chemistry (Weinheim an der Bergstrasse, Germany)》2014,20(49):16112-16120
Three dimensional hierarchical materials are widespread in nature but are difficult to synthesize by using self‐assembly/organization. Here, we employ a gel–liquid interface to obtain centimeter‐long ~100 μm diameter tubes with complex mineral wall structures that grow from the interface into solution. The gel, made from gelatin, is loaded with metal chloride salt, whereas the solution is a high pH anion source. Tubes were obtained with a range of cations (Ca2+, Sr2+, Ba2+, Cu2+, and Zn2+) and anions (CO32? and PO43?). The crystalline phases found in the tube walls corresponded to expectations from solution chemistries and phase solubilities. The growth mechanism is found to be akin to that of chemical gardens. The divalent cations modify the strength of the gelatin gel in a manner that involves not only simple electrostatic screening, but also ion‐specific effects. Thus, tubes were not obtained for those ions and/or concentrations that significantly changed the gel’s mechanical structure. At high Cu2+ loading, for example, vertical convection bands, not Liesegang bands, were observed in the gels. 相似文献
46.
Henrik Eickhoff Christian Sedlmeier Wilhelm Klein Gabriele Raudaschl-Sieber Hubert A. Gasteiger Thomas F. Fässler 《无机化学与普通化学杂志》2020,646(3):95-102
Recently fast lithium ion conductors were discovered in compounds containing tetrahedral SiP48– and GeP48– units. In the context of material development for all solid state batteries the ternary Li/Ge/P phase system has been further investigated and two new lithium phosphidogermanates were discovered on the lithium poor side of the ternary composition diagram. Li2GeP2 crystallizes in space group I41/acd with unit cell parameters of a = 12.3069(1) Å and c = 19.0306(4) Å, consists of a framework of Ge4P10 supratetrahedra, and exhibits an ionic conductivity of 1.5(3)×10–7 S · cm–1 at 27 °C. LiGe3P3 crystallizes in Pbam with a = 9.8459(5) Å, b = 15.7489(7) Å, and c = 3.5995(2) Å. In LiGe3P3 Ge and P atoms form a two dimensional polyanion. The slabs consist of five- and six-membered heteroatomic rings comprising GeP4 and Ge(P3Ge) tetrahedra including homoatomic Ge–Ge bonds. A semiconducting behavior with an electronic conductivity of ∼10–4 S · cm–1 and a remarkable stability vs. air and moisture is observed. 相似文献
47.
Hideyuki Tatsuno Kasper S. Kjr Kristjan Kunnus Tobias C. B. Harlang Cornelia Timm Meiyuan Guo Pavel Chbera Lisa A. Fredin Robert W. Hartsock Marco E. Reinhard Sergey Koroidov Lin Li Amy A. Cordones Olga Gordivska Om Prakash Yizhu Liu Mads G. Laursen Elisa Biasin Frederik B. Hansen Peter Vester Morten Christensen Kristoffer Haldrup Zoltn Nmeth Dorottya Srosin Szemes va Bajnczi Gyrgy Vank Tim B. Van Driel Roberto Alonso‐Mori James M. Glownia Silke Nelson Marcin Sikorski Henrik T. Lemke Dimosthenis Sokaras Sophie E. Canton Asmus O. Dohn Klaus B. Mller Martin M. Nielsen Kelly J. Gaffney Kenneth Wrnmark Villy Sundstrm Petter Persson Jens Uhlig 《Angewandte Chemie (International ed. in English)》2020,59(1):364-372
Iron N‐heterocyclic carbene (NHC) complexes have received a great deal of attention recently because of their growing potential as light sensitizers or photocatalysts. We present a sub‐ps X‐ray spectroscopy study of an FeIINHC complex that identifies and quantifies the states involved in the deactivation cascade after light absorption. Excited molecules relax back to the ground state along two pathways: After population of a hot 3MLCT state, from the initially excited 1MLCT state, 30 % of the molecules undergo ultrafast (150 fs) relaxation to the 3MC state, in competition with vibrational relaxation and cooling to the relaxed 3MLCT state. The relaxed 3MLCT state then decays much more slowly (7.6 ps) to the 3MC state. The 3MC state is rapidly (2.2 ps) deactivated to the ground state. The 5MC state is not involved in the deactivation pathway. The ultrafast partial deactivation of the 3MLCT state constitutes a loss channel from the point of view of photochemical efficiency and highlights the necessity to screen transition‐metal complexes for similar ultrafast decays to optimize photochemical performance. 相似文献
48.
In the development of therapeutic proteins, analytical assessment of structural stability and integrity constitutes an important activity, as protein stability and integrity influence drug efficacy, and ultimately patient safety. Existing analytical methodologies solely rely on relative changes in optical properties such as fluorescence or scattering upon thermal or chemical perturbation. Here, we present an absolute analytical method for assessing protein stability, structure, and unfolding utilizing Taylor dispersion analysis (TDA) and LED-UV fluorescence detection. The developed TDA method measures the change in size (hydrodynamic radius) and intrinsic fluorescence of a protein during in-line denaturation with guanidinium hydrochloride (GuHCl). The conformational stability of the therapeutic antibody adalimumab and human serum albumin were characterized as a function of pH. The simple workflow and low sample consumption (40 ng protein per data point) of the methodology make it ideal for assessing protein characteristics related to stability in early drug development or when having a scarce amount of sample available. 相似文献
49.
50.
Córdova A Ibrahem I Casas J Sundén H Engqvist M Reyes E 《Chemistry (Weinheim an der Bergstrasse, Germany)》2005,11(16):4772-4784
Hexose sugars play a fundamental role in vital biochemical processes and their biosynthesis is achieved through enzyme-catalyzed pathways. Herein we disclose the ability of amino acids to catalyze the asymmetric neogenesis of carbohydrates by sequential cross-aldol reactions. The amino acids mediate the asymmetric de novo synthesis of natural L- and D-hexoses and their analogues with excellent stereoselectivity in organic solvents. In some cases, the four new stereocenters are assembled with almost absolute stereocontrol. The unique feature of these results is that, when an amino acid is employed as the catalyst, a single reaction sequence can convert a protected glycol aldehyde into a hexose in one step. For example, proline and its derivatives catalyze the asymmetric neogenesis of allose with >99 % ee in one chemical manipulation. Furthermore, all amino acids tested catalyzed the asymmetric formation of natural sugars under prebiotic conditions, with alanine being the smallest catalyst. The inherent simplicity of this catalytic process suggests that a catalytic prebiotic "gluconeogenesis" may occur, in which amino acids transfer their stereochemical information to sugars. In addition, the amino acid catalyzed stereoselective sequential cross-aldol reactions were performed as a two-step procedure with different aldehydes as acceptors and nucleophiles. The employment of two different amino acids as catalysts for the iterative direct aldol reactions enabled the asymmetric synthesis of deoxysugars with >99 % ee. In addition, the direct amino acid catalyzed C(2)+C(2)+C(2) methodology is a new entry for the short, highly enantioselective de novo synthesis of carbohydrate derivatives, isotope-labeled sugars, and polyketide natural products. The one-pot asymmetric de novo syntheses of deoxy and polyketide carbohydrates involved a novel dynamic kinetic asymmetric transformation (DYKAT) mediated by an amino acid. 相似文献