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1.
2.
The pentafluorobenzenethiyl radical is an efficient hydrogen abstractor from an activated methylene or methine group and bis(pentafluorophenyl) disulfide is an efficient electron acceptor from the resulting radical intermediate. Thus benzyl-OTBS ether was easily converted into the corresponding pinacol, and 2-phenyl-1,3-dioxanes are converted into the monobenzoates of diols. 相似文献
3.
We study the metrical theory of fibred systems, in particular, in the case of continued fraction mixing systems. We get the
limit distribution of the largest value of a continued fraction mixing stationary stochastic process with infinite expectation
and some related results. These are analogous to J. Galambos, W. Philipp, and H. G. Diamond–J. D. Vaaler theorems for the
regular continued fractions. As an application, we see that these theorems hold for Jacobi-Perron algorithm.
Received September 30, 2001; in revised form January 8, 2002 相似文献
4.
Ciguatoxin C-CTX-1 was isolated as a principal causative toxin of ciguatera seafood poisoning in the Caribbean Sea, and is structurally classified as a ladder-shaped polycyclic ether. In this Letter, we report the synthesis of the tricyclic LMN-ring system of C-CTX-1. SmI2-mediated reductive cyclization efficiently constructed the seven-membered M-ring with the axially oriented 1,3-dimethyl structure. 相似文献
5.
Hynd Remita Prem Felix Siril Israel-Martyr Mbomekalle Bineta Keita Louis Nadjo 《Journal of Solid State Electrochemistry》2006,10(7):506-511
Three Pt-based catalysts prepared in different radiolytic conditions and supported on graphite powder were packed into a carbon paste electrode configuration. They were compared to each other, to the commercial (Pt) deposited on activated carbon powder (Johnson Matthey) and to pure Vulcan XC-72 for their respective abilities toward the hydrogen evolution reaction (HER). The Tafel parameters were determined for all these electrodes. From the I–V curves and their quantitative treatment, the following order of activity emerged unambiguously and reads: (PtCO)2 (fcc structure) > (PtCO)1 (Chini cluster) > (Pt)neat > (Pt)JM (Johnson Matthey) ≫ (Vulcan XC-72). As expected, all the Pt-loaded electrodes were more efficient than Vulcan XC-72. The classification appears to be linked with the mean nanoparticle size, and for comparable sizes, with the surface morphology of the materials. The results and the stability of the electrodes suggest that the small particle sizes and the good dispersity on the carbon support were maintained during the HER. 相似文献
6.
The demetalation process of 10 multi-iron Wells-Dawson polyoxometalates is studied by cyclic voltammetry and controlled potential coulometry. Eight sandwich-type complexes (alphaalphaalphaalpha-Na(16)[(NaOH(2))(2)(Fe(III))(2)(X(2)W(15)O(56))(2)], alphaalphabetaalpha-Na(14)[(NaOH(2))(Fe(III)OH(2))(Fe(III))(2)(X(2)W(15)O(56))(2)], alphabetabetaalpha-Na(12)[(Fe(III)OH(2))(2)(Fe(III))(2)(X(2)W(15)O(56))(2)], and alphabetabetaalpha-Na(14)[(Mn(II)OH(2))(2)(Fe(III))(2)(X(2)W(15)O(56))(2)] (where X = P(V) or As(V))) and two monomeric complexes (alpha-Na(11)[(P(2)(Fe(III)Cl)(2)(Fe(III)OH(2))W(15)O(59))] and alpha-Na(11)[(As(2)(Fe(III)Cl)(2)Fe(III)OH(2))W(15)O(59))]) were selected for this study. All 10 complexes show Fe(III) waves which are well-separated from the redox activity of the W(VI) centers. At room temperature and under mild conditions, iron release from the complexes is observed upon reduction of the Fe(III) centers. This release is controlled by the ionic strength of the medium, the nature and concentration of the anions present in the supporting electrolyte, and by the pH of the solution. This behavior parallels those described for most siderophores which depend on the same parameters. 相似文献
7.
A. Breakstone G. Claesson H. B. Crawley G. M. Dallavalle K. Doroba D. Drijard F. Fabbri A. Firestone M. A. Faessler H. G. Fischer S. Y. Fung S. Garpman W. Geist G. Giacomelli R. Gokieli M. Gorbics C. R. Gruhn P. Hanke M. Heiden W. Herr T. J. Ketel E. E. Kluge J. W. Lamsa T. Lohse I. Lund R. Mankel W. T. Meyer G. Mornacchi T. Nakada I. Otterlund M. Panter H. Pugh A. Putzer K. Rauschnabel B. Rensch F. Rimondi M. Schmelling G. P. Siroli R. Sosnowski E. Stenlund M. Szczekowski R. Szwed O. Ullaland R. Walczak D. Wegener M. Wunsch 《Zeitschrift fur Physik C Particles and Fields》1986,30(4):507-512
The relative yields of kaons and protons compared with the yield of pions at highp T and polar angles θ away from 90° (in the range from 10° to 45°) are presented forpp, dd, and αα interactions at a centre-of-mass energy \(\sqrt {s_{NN} } = 31\) GeV per nucleon-nucleon collision. The measured particle ratios depend on the atomic mass numberA of the beam particles and on θ. TheA dependence of the ratios becomes stronger for largerp T and is more pronounced at smaller polar angles. 相似文献
8.
W. Bell K. Braune G. Claesson D. Drijard M. A. Faessler H. G. Fischer H. Frehse R. W. Frey S. Garpman W. Geist C. Gruhn P. Hanke M. Heiden W. Herr P. G. Innocenti T. J. Ketel E. E. Kluge I. Lund G. Mornacchi T. Nakada I. Otterlund M. Panter B. Povh A. Putzer E. Stenlund T. J. M. Symons R. Szwed O. Ullaland 《Zeitschrift fur Physik C Particles and Fields》1986,30(4):513-520
Properties of secondaries associated with a high-p T charged trigger particle (3<p T <5 GeV/c) were studied for αp and αα interactions at c.m. energies \(\sqrt s = 88\) GeV and 125 GeV, respectively. Thep T distributions of secondaries in the away-jet and trigger-jet regions were compared with those for high-p T pp interactions. No statistically significant differences were seen, except at lowp T . Momentum and angular distributions of spectator and leading protons were studied as a function of charge and rapidity of the trigger hadron. The observed correlations between trigger charge and number of spectator protons provide evidence of valence quark contributions to the trigger jet. 相似文献
9.
M. Saeki M. Nakada T. Kawasaki T. Nishimura T. Kitazawa M. Takeda 《Journal of Radioanalytical and Nuclear Chemistry》2006,270(2):379-384
Summary The correlations of isomer shifts in various neptunyl(V and VI) compounds with crystallographic structures were revaluated.
A linear correlation between the isomer shifts of neptunyl(VI) compounds and Np-O bond lengths of neptunyl group has been
demonstrated. On the other hand, it has been evidenced that the isomer shifts of neptunyl(V) compounds are correlated much
stronger with the mean Np-O distances in the crystals than the lengths in neptunyl(V) group. 相似文献
10.
[reaction: see text] The enantioselective total synthesis of (+)-allocyathin B(2) has been achieved. Our approach features a convergent enantioselective construction of the 5-6-7 tricyclic core system using the originally developed chiral building blocks via asymmetric catalysis, the intramolecular aldol reaction in high yield, successful samarium diiodide-mediated ring expansion, and a newly developed double-bond installation method. 相似文献