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991.
LI Ying 《中国科学:物理学 力学 天文学(英文版)》2015,(3):22-30
Motivated by the recent LHCb collaboration measurements of charmless three-body decays of ■s meson, we calculate the branching fractions of ■ s →K0π+π-, ■s→K0K+K-, ■s→K0π+K- and ■s→K0K+π- decay modes using the factorization approach.Both the resonant and nonresonant contributions are studied in detail. For the decays ■s→K0π+π- and ■s→K0K+K-, our results agree well with experimental data, and the former is dominated by the K*, while the latter one is dominated by the nonresonant contribution. Considering the flavor S U(3) symmetry violation, the sum of branching fractions of ■s→K0π+K- and ■s→K0K+π-could accommodate the data well too. It should be noted that both branching fractions are sensitive to the scalar density Kπ|ˉsq|0.Furthermore, the resonant contributions are dominated by the scalar K*0(1430). We hope that these branching fractions could be measured individually in the experiments so as to test the factorization approach and the flavor S U(3) asymmetry. Moreover, the direct C P asymmetries of these decays are also investigated, which could be measured in the running LHCb experiment and Super-b factory in the future. 相似文献
992.
993.
主要研究一类耦合的Benjamin-Bona-Mahony型方程组的显式行波解.应用(G′/G)-展开法,Jacobi椭圆函数展开法以及详细的计算,得到了方程组的多个精确行波解.所得结果推广了方程组的sechξ型孤立波解的存在性结果. 相似文献
994.
Interactions of delta shock waves for the relativistic Chaplygin Euler equations with split delta functions
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In this article, we are concerned with the interactions of delta shock waves with contact discontinuities for the relativistic Euler equations for Chaplygin gas by using split delta functions method. The solutions are obtained constructively and globally when the initial data consists of three piecewise constant states. The global structure and large time‐asymptotic behaviors of the solutions are analyzed case by case. During the process of the interaction, the strengths of delta shock waves are computed completely. Moreover, it can be found that the Riemann solutions are stable for such small perturbations with special initial data by letting perturbed parameter ε tends to zero. Copyright © 2014 John Wiley & Sons, Ltd. 相似文献
995.
Suppose A is a unital C*-algebra and r 1.In this paper,we define a unital C*-algebra C_(cb)*(A,r) and a completely bounded unital homomorphism α_r:A → C_(cb)*(A,r)with the property that C_(cb)*(A,r)=C*(α_r(A))and,for every unital C*-algebra B and every unital completely bounded homomorphism φ:A→ B,there is a(unique)unital *-homomorphism π:C_(cb)*(A,r)→B such thatφ=πoα_r.We prove that,if A is generated by a normal set {t_λ:λ∈Λ},then C_(cb)*(A,r)is generated by the set {α_r(t_λ):λ∈Λ}.By proving an equation of the norms of elements in a dense subset of C_(cb)*(A,r)we obtain that,if Β is a unital C*-algebra that can be embedded into A,then C_(cb)*(B,r)can be naturally embedded into C(cb)*(A,r).We give characterizations of C_(cb)*(A,r)for some special situations and we conclude that C_(cb)*(A,r)will be "nice" when dim(A)≤ 2 and "quite complicated" when dim(A)≥ 3.We give a characterization of the relation between K-groups of A and K-groups of C_(cb)*(A,r).We also define and study some analogous of C_(cb)*(A,r). 相似文献
996.
Ying Dong Bangyu Liu Peng Chen Qun Liu Mang Wang 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2014,126(13):3510-3514
The insertion of an aryne into a C S bond can suppress the addition of an S nucleophile to the aryne in the presence of palladium. Catalyzed by Pd(OAc)2, a wide range of α‐carbamoyl ketene dithioacetals readily react with arynes to selectively afford functionalized 2‐quinolinones in high yields under neutral reaction conditions by a C S activation/aryne insertion/intramolecular coupling sequence. The attractive feature of the new strategy also lies in the versatile transformations of the alkythio‐substituted quinolinone products. 相似文献
997.
Shao‐Jie Lou Dan‐Qian Xu Zhen‐Yuan Xu 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2014,126(39):10498-10503
A novel and facile C H bond fluorination proceeds under remarkably mild conditions (close to room temperature in most cases). Both aromatic and olefinic C(sp2) H bonds with a wide range of electronic properties are selectively fluorinated in the presence of a catalytic amount of simple, cheap, and nontoxic nitrate as the promoter. A PdII/PdIV catalytic cycle that is initiated by an in situ generated cationic [Pd(NO3)]+ species was proposed based on preliminary mechanistic studies. 相似文献
998.
Chao Wang Changpeng Chen Jingyu Zhang Jian Han Qian Wang Kun Guo Pei Liu Mingyu Guan Yingming Yao Yingsheng Zhao 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2014,126(37):10042-10046
An easily synthesized and accessible N,O‐bidentate auxiliary has been developed for selective C H activation under palladium catalysis. The novel auxiliary showed its first powerful application in C H functionalization of remote positions. Both C(sp2) H and C(sp3) H bonds at δ‐ and ε‐positions were effectively activated, thus giving tetrahydroquinolines, benzomorpholines, pyrrolidines, and indolines in moderate to excellent yields by palladium‐catalyzed intramolecular C H amination. 相似文献
999.
Qian Li Matthias Driess John F. Hartwig 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2014,126(32):8611-8614
Reported herein is an iridium‐catalyzed, regioselective silylation of the aromatic C H bonds of benzylamines and the benzylic C H bonds of 2,N‐dialkylanilines. In this process, (hydrido)silyl amines, generated in situ by dehydrogenative coupling of benzylamine or aniline with diethylsilane, undergo selective silylation at the C H bond γ to the amino group. The products of this silylation are suitable for subsequent oxidation, halogenation, and cross‐coupling reactions to deliver benzylamine and arylamine derivatives. 相似文献
1000.
Thirteen new glucosides (1–13) of magnolol and honokiol were obtained from specific O-glycosylation by two filamentous fungi, Cunninghamella echinulata AS 3.3400 and Rhizopus japonicus ZW-4. The glucosides' structures were determined on the basis of extensive spectroscopic (HRESIMS, 1D and 2D NMR, and CD) analyses and a chemical method. C. echinulata appeared to transfer a glucosyl moiety to 2-OH of magnolol and honokiol, whereas R. japonicus preferred to regio-specifically transfer a glucosyl moiety to 4′-OH when honokiol was as the substrate. In addition, hydroxylation by C. echinulata and specific 6″-O-acylation of the introduced glucosyl moiety by R. japonicus were observed as minor reactions. Bioassay results indicated that glucosides 1–12 together with magnolol and honokiol at 10 μM attenuated the glutamate-induced toxicity in SK-N-SH cells to levels comparable to the results for MK-801, a positive control. However, the water-solubility of major glucosylated products (1, 8, and 11) increased greatly. 相似文献