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991.
992.
The new nickel selenite chloride, Ni5(SeO3)4Cl2, was obtained by high-temperature solid state reaction of NiCl2, Ni2O3 and SeO2 in a 1:2:4 molar ratio at 700 °C in an evacuated quartz tube. Its structure was established by single-crystal X-ray diffraction. Ni5(SeO3)4Cl2 crystallizes in the triclinic system, space group P-1 (No. 2) with cell parameters of a=8.076(2), b=9.288(2), c=9.376(2) Å, α=101.97(3), β=105.60(3), γ=91.83(3)° and Z=2. All nickel(II) ions in Ni5(SeO3)4Cl2 are octahedrally coordinated by selenite oxygens or/and chloride anions (([Ni(1)O5Cl], [Ni(2)O4Cl2], [Ni(3)O5Cl], [Ni(4)O6] and [Ni(5)O4Cl]). The structure of the title compound features a condensed three-dimensional (3D) network built by Ni(II) ions interconnected by SeO32− anions as well as Cl− anions. Magnetic property measurements show strong antiferromagnetic interaction between nickel(II) ions. 相似文献
993.
Wei Xiang Qi‐Shi Song Hong‐Jie Zhang Rong‐Tao Li Zhi Na Han‐Dong Sun 《Helvetica chimica acta》2004,87(11):2842-2847
A new ursane‐type nortriterpenoid, adenanthusone (=(11α,12α)‐4‐demethyl‐11,12‐epoxy‐3,13‐dihydroxy‐2‐oxoursa‐3,20(30)‐diene‐28‐oic acid γ‐lactone; 1 ) was isolated from Isodon adenanthus. Its structure was determined by NMR spectra and X‐ray crystallographic diffraction analysis. The biogenetic implication of the nortriterpene is discussed. 相似文献
994.
Tong Lin Michael R. Asam Gary L. Glish 《Journal of the American Society for Mass Spectrometry》1996,7(9):930-937
The major dissociation pathways of the [M-H]+ (loss of NH3 or CH4) and the [M+H]+ (loss of NH3 or CH3) ions from dimethylpyrroles have been determined to occur from isomeric parent ions. For the [M-H]+ ion (formed by loss of a methyl hydrogen), loss of NH3 leads to the formation of the phenylium ion and is preceded by consecutive carbon ring expansions followed by a ring contraction to form protonated aniline. Loss of CH4 occurs after the first carbon ring expansion, which forms protonated picoline. The relative partitioning between the two dissociation paths depends upon the internal energy content of the parent ion; the highest point on the potential energy surface is the second ring expansion step. The [M+H]+ ion reacts through a similar pathway via dihydro analogs of picoline and aniline. The proposed reaction pathways are supported by results of semiempirical molecular orbital calculations. 相似文献
995.
C. N. Pope L. J. Romans E. Sezgin X. Shen 《Communications in Mathematical Physics》1991,140(1):149-157
We study the holomorphic structure of certain complex manifolds associated withW
algebras, namely, the flag manifoldsW
/T
andW
1+/T
1+, and the spacesW
/SL(),R) andW
1+/GL(,R), whereT
andT
1+ are the maximal tori inW
andW
1+. We compute their Ricci curvature and show how the results are related to the anomaly-freedom conditions forW
andW
1+. We discuss the relation of these manifolds with extensions of universal Teichmüller space.Supported in part by the U.S. Department of Energy, under grant DE-AS05-81ER40039Supported in part by the U.S. Department of Energy, under grant DE-FG03-84ER40168 相似文献
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