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61.
Junya Takashima Kazumasa Sugiyama Tokuhei Tagai Osamu Terasaki Jihong Yu 《Acta Crystallographica. Section C, Structural Chemistry》2004,60(7):m333-m334
The title compound, (C4H7N2)2[AlP2O7(OH)], is a one‐dimensional extended‐chain aluminophosphate prepared by a solvothermal synthesis from an alcohol system. The infinite [AlP2O7(OH)]2− chains composed of AlO4, PO2(=O)2 and PO2(=O)(OH) tetrahedra are linked via hydrogen bonds to the 2‐methylimidazolium cations. 相似文献
62.
Masaki Matsui Rie Ikeda Yasuhiro Kubota Kazumasa Funabiki 《Tetrahedron letters》2009,50(35):5047-6547
The solid-state fluorescence of 2-amino-, 2-ethylamino, 2-diethylamino-, and 2,7-bis(diethylamino)perfluorophenazines was examined. They showed their fluorescence maxima in the range of 584-637 nm. The solid-state fluorescence quantum yield of 2-diethylamino derivative was highest among these derivatives, there being 0.22. X-ray crystallographic analysis suggests that the 2-diethylamino derivative has no strong intermolecular interactions among adjacent molecules to show intense fluorescence, whereas the other derivatives have network NH/F hydrogen, π-π, and CH/F interactions to reduce solid-state fluorescence intensity. 相似文献
63.
This paper describes the synthesis and some reactions of potassium, rubidium, cesium and trimethylsilyl carbamoselenothioates. The potassium salts were synthesized in 70–80 % yields by reacting the corresponding thiocarbamoyl chlorides with potassium selenide in acetonitrile. Furthermore, the rubidium and cesium salts were obtained in good yields by treating the trimethylsilyl esters with the corresponding metal fluorides. The crystal structure of acetonitrile‐solvated potassium N,N‐dimethylcarbamoselenothioate consisted of dimeric units, featuring μ‐carbamoselenothioate anions associated with potassium cations that are located on the upper and lower sides of a plane involving two opposing carbamoselenothioate groups. These heavier alkali metal salts readily reacted with alkyl halides to give both S‐ and Se‐alkyl esters. The reaction of the potassium salts with trimethylsilyl chlorides forms S‐ and Se‐trimethylsilyl carbamoselenothioates which are in equilibrium. The reaction of the salts and silyl esters with organo Group‐14 and ‐15 elements halides gave exclusively the corresponding Se‐substituted products in good yields. 相似文献
64.
Tsuzuki S Honda K Uchimaru T Mikami M Fujii A 《The journal of physical chemistry. A》2006,110(33):10163-10168
The CCSD(T) level interaction energies of CH/pi complexes at the basis set limit were estimated. The estimated interaction energies of the benzene complexes with CH(4), CH(3)CH(3), CH(2)CH(2), CHCH, CH(3)NH(2), CH(3)OH, CH(3)OCH(3), CH(3)F, CH(3)Cl, CH(3)ClNH(2), CH(3)ClOH, CH(2)Cl(2), CH(2)FCl, CH(2)F(2), CHCl(3), and CH(3)F(3) are -1.45, -1.82, -2.06, -2.83, -1.94, -1.98, -2.06, -2.31, -2.99, -3.57, -3.71, -4.54, -3.88, -3.22, -5.64, and -4.18 kcal/mol, respectively. Dispersion is the major source of attraction, even if substituents are attached to the carbon atom of the C-H bond. The dispersion interaction between benzene and chlorine atoms, which is not the CH/pi interaction, is the cause of the very large interaction energy of the CHCl(3) complex. Activated CH/pi interaction (acetylene and substituted methanes with two or three electron-withdrawing groups) is not very weak. The nature of the activated CH/pi interaction may be similar to the hydrogen bond. On the other hand, the nature of other typical (nonactivated) CH/pi interactions is completely different from that of the hydrogen bond. The typical CH/pi interaction is significantly weaker than the hydrogen bond. Dispersion interaction is mainly responsible for the attraction in the CH/pi interaction, whereas electrostatic interaction is the major source of attraction in the hydrogen bond. The orientation dependence of the interaction energy of the typical CH/pi interaction energy is very small, whereas the hydrogen bond has strong directionality. The weak directionality suggests that the hydrogen atom of the interacting C-H bond is not essential for the attraction and that the typical CH/pi interaction does not play critical roles in determining the molecular orientation in molecular assemblies. 相似文献
65.
In nuclear industry, removal of nitric acid from solutions is required in the course of chemical separation and waste treatment procedure as well as in chemical conversion steps. The reduction of HNO3 by HCOOH to gaseous products such as nitrogen, nitrogen oxides, and carbon dioxide is an attractive way to accomplish the denitration. A typical problem for the denitration is the existence of the induction period. The induction period has been explained as the time necessary to increase the concentration of HNO2, which is an important reaction intermediate, above a threshold value. In this study, adsorption sites on the surface of active carbon were found to promote HNO2 formation and efficiently suppress the induction period. Induction time was shortened by increasing the amount of active carbon in the solution. When the solution contains 3 M HNO3 and 1 M HCOOH, 10 g/L of active carbon was enough to eliminate the induction period at 50 degrees C. The catalytic effect exhibited by active carbon was similar to that reported for Pt/SiO2. Therefore, on the surface of active carbon, there is a redox cycle, where HNO3 is reduced to HNO2 and then the oxidized surface site will be reduced by HCOOH. 相似文献
66.
Shirahama T Kohno T Kaijima T Nagaoka Y Morimoto D Hirata K Uesato S 《Chemical & pharmaceutical bulletin》2006,54(5):665-668
Dimeric indole alkaloid, anhydrovinblastine, which can be obtained from catharanthine and vindoline in a high yield, was converted stereoselectively into vinblastine through alternating oxidation-reduction with oxygen and NaBH(3)CN in the presence of anti-vinblastine monoclonal antibody. 相似文献
67.
Let K denote a field, and let V denote a vector space over K with finite positive dimension. We consider a pair of linear transformations A : V → V and A∗ : V → V that satisfy (i) and (ii) below:
- (i)
- There exists a basis for V with respect to which the matrix representing A is irreducible tridiagonal and the matrix representing A∗ is diagonal.
- (ii)
- There exists a basis for V with respect to which the matrix representing A∗ is irreducible tridiagonal and the matrix representing A is diagonal.
68.
Fujihisa H Akahama Y Kawamura H Ohishi Y Shimomura O Yamawaki H Sakashita M Gotoh Y Takeya S Honda K 《Physical review letters》2006,97(8):085503
Despite many experimental and theoretical studies, the crystal structure of the epsilon phase of solid oxygen has not been determined. We performed powder x-ray diffraction experiments and the Rietveld analyses in this study to show that a new arrangement of the monoclinic space group C2/m could fit the diffraction patterns of the epsilon phase and obtained a structure that consisted of an O8 cluster with 4 molecules. The dependence of the lattice parameters, the molar volume, and the intermolecular distances on the pressure was investigated. 相似文献
69.
70.
Shigeo Kusuoka Kazumasa Kuwada Yozo Tamura 《Probability Theory and Related Fields》2010,147(3-4):649-674
The large deviation principle for stochastic line integrals along Brownian paths on a compact Riemannian manifold is studied. We regard them as a random map on a Sobolev space of 1-forms. We show that the differentiability order of the Sobolev space can be chosen to be almost independent of the dimension of the underlying space by assigning higher integrability on 1-forms. The large deviation is formulated for the joint distribution of stochastic line integrals and the empirical distribution of a Brownian path. As the result, the rate function is given explicitly. 相似文献