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61.
F. D. Berg M. Pfeiffer O. Schwalb M. Appenheimer W. Döring M. Franke W. Kühn V. Metag W. Niebur R. Novotny J. Ritman M. Röbig H. Ströher A. Boonstra H. Löhner A. Raschke L. Venema H. W. Wilschut N. Brummund W. Henning S. Hlavac R. Holzmann R. S. Simon 《Zeitschrift für Physik A Hadrons and Nuclei》1990,337(3):351-352
π0 -production probability of (9± 2)· 10? 3 per20Ne+Al reaction has been measured at 350 MeV/u using the Two Arm Photon Spectrometer TAPS. This yield is consistent with an interpolation of published π-production rates in heavy ion collisions. 相似文献
62.
Laura Senft Jamonica L. Moore Alicja Franke Katherine R. Fisher Andreas Scheitler Achim Zahl Ralph Puchta Dominik Fehn Sidney Ison Safaa Sader Ivana Ivanovi-Burmazovi Christian R. Goldsmith 《Chemical science》2021,12(31):10483
Reactivity assays previously suggested that two quinol-containing MRI contrast agent sensors for H2O2, [Mn(H2qp1)(MeCN)]2+ and [Mn(H4qp2)Br2], could also catalytically degrade superoxide. Subsequently, [Zn(H2qp1)(OTf)]+ was found to use the redox activity of the H2qp1 ligand to catalyze the conversion of O2˙− to O2 and H2O2, raising the possibility that the organic ligand, rather than the metal, could serve as the redox partner for O2˙− in the manganese chemistry. Here, we use stopped-flow kinetics and cryospray-ionization mass spectrometry (CSI-MS) analysis of the direct reactions between the manganese-containing contrast agents and O2˙− to confirm the activity and elucidate the catalytic mechanism. The obtained data are consistent with the operation of multiple parallel catalytic cycles, with both the quinol groups and manganese cycling through different oxidation states during the reactions with superoxide. The choice of ligand impacts the overall charges of the intermediates and allows us to visualize complementary sets of intermediates within the catalytic cycles using CSI-MS. With the diquinolic H4qp2, we detect Mn(iii)-superoxo intermediates with both reduced and oxidized forms of the ligand, a Mn(iii)-hydroperoxo compound, and what is formally a Mn(iv)-oxo species with the monoquinolate/mono-para-quinone form of H4qp2. With the monoquinolic H2qp1, we observe a Mn(ii)-superoxo ↔ Mn(iii)-peroxo intermediate with the oxidized para-quinone form of the ligand. The observation of these species suggests inner-sphere mechanisms for O2˙− oxidation and reduction that include both the ligand and manganese as redox partners. The higher positive charges of the complexes with the reduced and oxidized forms of H2qp1 compared to those with related forms of H4qp2 result in higher catalytic activity (kcat ∼ 108 M−1 s−1 at pH 7.4) that rivals those of the most active superoxide dismutase (SOD) mimics. The manganese complex with H2qp1 is markedly more stable in water than other highly active non-porphyrin-based and even some Mn(ii) porphyrin-based SOD mimics.Manganese complexes with polydentate quinol-containing ligands are found to catalyze the degradation of superoxide through inner-sphere mechanisms. The redox activity of the ligand stabilizes higher-valent manganese species. 相似文献
63.
The decomposition of chloroform by the combination of hydrodynamic and acoustic cavitation (Hydrodynamic-Acoustic-Cavitation/HAC) has been investigated. The flow rate and the hole diameter of the orifice plate remarkably affect the conversion of chloroform in the combined system. The conversion increases with increasing fluid velocity without any restriction. With a 2.8mm orifice plate the conversion reaches an optimal value. A synergistic effect has been obtained by the hybrid method of acoustic and hydrodynamic cavitation. The total synergistic effect achieves 17% and 73% per pass, respectively. The analysis of the energy efficiencies shows different results. Due to high optimization potential, this hybrid method can be visualized as a new step for wastewater treatment. 相似文献
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Marlene Espinoza-Moraga Tania Petta Marco Vasquez-Vasquez V. Felipe Laurie Luis A.B. Moraes Leonardo Silva Santos 《Tetrahedron: Asymmetry》2010,21(16):1988-1992
β-Carboline imine reductions mediated by Saccharomyces bayanus have been described achieving moderate to good enantiomeric excesses of the amine products. The enantiomeric excesses of the bioreduction showed a dependence on the imine substituents. Compounds presenting C1–C11 aliphatic substituent groups afforded amines with an (S)-configuration, whereas C15 and higher aliphatic- and aromatic-substituted β-carboline imines achieved inversion of the configuration in the final (R)-2 amine products. Based on this data, a model for the Saccharomyces reduction is proposed. 相似文献
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69.
U. Starke J. Schardt M. Franke 《Applied Physics A: Materials Science & Processing》1997,65(6):587-596
Received: 21 March 1997 相似文献
70.
Attenuated total reflection leaky-mode spectroscopy is used for a thermo-optical investigation of a clamped film of the ferroelectric vinylidene fluoridetrifluoroethylene copolymer. A hysteresis loop for the optical parameters refractive index and film thickness is found for a full temperature cycle between 25° C and 60° C. In the vicinity of the ferroelectric/paraelectric phase transition increased optical losses are found. 相似文献