Cu(OAc)2-catalyzed direct radical C2 arylation of quinoline N-oxide with arylamines

A Cu(OAc)₂-catalyzed synthesis of 2-arylquinoline N-oxides with easily available arylamines is described. The main features of this reaction are mild reaction conditions, high functional-group tolerance, excellent regioselectivity, and good to excellent yields. This procedure is mild, operationally simple, and constitutes a greener approach to the arylation of quinoline N-oxides.     

重元素多重金属-金属键的新发现:U≡Fe三重键

正自1964年Cotton等人发现[Re_2Cl_8]~(2-)化合物中存在Re―Re四重键以来~1,金属―金属多重键的研究在无机化学、金属有机化学、结构化学和理论化学等领域引起了广泛关注~(2,3),其中包含锕系元素的金属-金属键尤为引人关注。锕系元素的5f、6d、7s和7p轨道能量相差不大,在适当条件下均可以参与化学成键,这使得锕系元素的成键情况比过渡金属要复杂得多。然而涉及锕系元素的实验研究非常困难,到目前为止只有少数实验合成     

Interfacial passivation mechanism of sulfide towards quantum dot-sensitized nanocrystalline thin films

Journal of Solid State Electrochemistry - We report on the interfacial passivation mechanism in CdSe quantum dot-sensitized ZnO nanocrystalline thin film, where different sulfide semiconductors...     

Fermion Tunnels of Cylindrical Symmetric Black Hole and?the?Corrected Entropy

Using the method proposed by Banerjee and Majhi, we researched fermion tunneling from cylindrical symmetric black hole, and obtained the correctional entropy. In our work, we first prove that the ratios of the wave function’s components are constants near the horizon, so the reasonable action form of the Dirac equation can then be gotten. From the method beyond semiclassical approximation, we finally calculate the Hawking temperature and correctional entropy.     

Interpolation of Morrey-Campanato and related smoothness spaces

We study the interpolation of Morrey-Campanato spaces and some smoothness spaces based on Morrey spaces, e. g., Besov-type and Triebel-Lizorkin-type spaces. Various interpolation methods, including the complex method, the ±-method and the Peetre-Gagliardo method, are studied in such a framework. Special emphasis is given to the quasi-Banach case and to the interpolation property.     

在模情况时二面体群$D_{2p}$作用下的transfer理想

In this paper, we determine the structures of the transfer ideal and its radical ideal for the ring of polynomials F p[x, y] under the action of dihedral group D2 p in the modular case. We mainly use Transfer variety, p order elements, and Hilbert’s Nullstellensatz Theorem.     

Studies on the Thermodynamic and Kinetic Properties of the Reactions of Ti+ with Sulfur Transfer Reagent SCO Along the C═S Bond Activation Branch at 200–1200K

Theoretical studies on the thermodynamic and kinetic properties of the reactions of Ti⁺ with sulfur transfer reagent SCO via the C═S bond activation pathway have been carried on using DFT/B3LYP method, general statistical thermodynamics, and Eyring transition state theory with Wigner correction. The relevant reactions include reaction 1 ⁴ Ti⁺+¹SCO → ⁴ IM ₁ → ⁴ TS ₁ → ⁴ IM ₂ → ⁴ TiS⁺+ ¹ CO, and reaction 2 ⁴Ti⁺+¹SCO →⁴IM₁→ CP →²IM₂→²TiS⁺+¹CO in which the spin multiplicity changes from the quartet state to the doublet state in the crossing region. It is concluded that the increase of the temperature is favored to the reaction 1 process, since the equilibrium constants (K) rises from 0.566 × 10[P]-9 at 200 K to 0.109 × 10⁰ at 1200 K, and the reaction rate constant (k) from 0.222 × 10⁰ s[P]-1 at 200 K to 0.540 × 10 ¹¹ s[P]-1 at 1200 K. Moreover, reaction 1 is endothermic, and non-spontaneous in the way the entropy increases, while reaction 2 is exothermic and spontaneous in the way their entropy decreases. The reaction path 2 is the energetically favorable channel, and its thermodynamic data change not largely with the rise of temperature.     

Stereoselective Synthesis of Phosphorus Analogs of (R)-Carnitine and (R)-Gabob

Bioreduction of 3-substituted-2-oxoalkanephosphonates by baker's yeast afforded corresponding 2-hydroxy-alkanephosphonates in good yields and ee value. These compounds ( 2a,b ) could serve as useful chirons for the stereoselective synthesis of phosphorus analogs of (R)-Carnitine and (R)-GABOB.