复动量表象方法对奇特核中晕现象的研究

晕现象的研究使人们对核结构有了新的认识。连续谱,尤其是连续谱中的共振态在其中扮演着重要角色。复动量表象(CMR)方法不仅能够统一描述束缚态、共振态和连续谱,而且能够很好地描述窄共振和宽共振。本文介绍了CMR方法对原子核共振态的研究。给出了31Ne和19C等核的束缚态和共振态的单粒子能量随形变参数β₂的变化规律,分析了19C和31Ne中单中子晕形成的物理机制和在中子数N=20附近能级反转的原因,并预测了比37Mg重的核中的单中子晕现象,这一预测结果对在实验中寻找较重的晕核具有一定的参考价值。这些研究表明CMR 方法不仅适用于描述稳定核,也适用于描述具有弥散物质分布的奇特核。     

原子核单粒子共振态的研究进展

共振是自然界普遍存在的有趣现象。在核物理领域,存在许多奇特现象,共振在其中扮演着重要角色。介绍了近期发展的RMF-CSM、RMF-CGF和RMF-CMR方法及其对原子核单粒子共振态的研究。给出了120Sn,31Ne等核的单粒子共振态的能量和宽度及其随质量数、形变的变化规律,分析了19C,31Ne和39Mg等核的晕形成的物理机制和在N=20附近能级反转的原因。特别是新发展的RMF-CMR方法,在描述稳定核和奇特核方面都取得了成功,支持Zr同位素存在巨晕的预言。Resonance is an interesting phenomenon in nature. In nuclear physics, resonance plays an important role in the formation of many exotic phenomena. This paper introduces the recently developed RMF-CSM, RMFCGF, and RMF-CMR methods and their researches on nuclear single-particle resonances. The energies and widths of the single-particle resonant states in 120Sn and 31Ne and their evolution to mass number and deformation are given. In addition, the physical mechanism of the halo formation in 19C, 31Ne and 39Mg and the cause of energy level inversion near N=20 are analyzed. In particular, the newly developed RMF-CMR approach has been successful in describing stable and exotic nuclei and supports the prediction that Zr isotopes exist in a giant halo.     

Synthesis of Indoles through Domino Reactions of 2‐Fluorotoluenes and Nitriles

Indoles are essential heterocycles in medicinal chemistry, and therefore, novel and efficient approaches to their synthesis are in high demand. Among indoles, 2‐aryl indoles have been described as privileged scaffolds. Advanced herein is a straightforward, practical, and transition‐metal‐free assembly of 2‐aryl indoles. Simply combining readily available 2‐fluorotoluenes, nitriles, LiN(SiMe₃)₂, and CsF enables the generation of a diverse array of indoles (38 examples, 48–92 % yield). A range of substituents can be introduced into each position of the indole backbone (C4 to C7, and aryl groups at C2), providing handles for further elaboration.     

Preparative isolation and purification of three rotenoids and one isoflavone from the seeds of Millettia pachycarpa Benth by high-speed counter-current chromatography

Both analytical and preparative high-speed counter-current chromatography (HSCCC) were used to isolate and separate chemical bioactive constituents from the seeds of Millettia pachycarpa Benth, a famous traditional Chinese medicine. Three rotenoids and one isoflavone were successfully purified for the first time by HSCCC with a two-phase solvent system composed of n-hexane-ethyl acetate-methanol-water (HEMWat) (1:0.8:1:0.6, v/v/v/v). The separation parameters were first performed on the analytical HSCCC and optimized conditions were then scaled up to preparative HSCCC. The separation produced 160.2 mg tephrosin, 14.6 mg 4',5'-dimethoxy-6,6-dimethylpyranoisoflavone, 109.4 mg deguelin, 6.7 mg 6a,12a-dehydrodeguelin with respective purities of 95, 93, 95, 95%, in one single run from 400 mg crude extract of the seeds of M. pachycarpa Benth. The purity of the isolated compounds was analyzed by high-performance liquid chromatography (HPLC) and their structures were identified by electrospray ionization mass spectrometry (ESI-MS); (1)H nuclear magnetic resonance ((1)H NMR) and (13)C nuclear magnetic resonance ((13)C NMR) analysis. This paper is an excellent example of the role that CCC is playing in isolating active compounds for pre-clinical trials of new chemical entities, even when scaling up between centrifuges from different manufacturers.     

Synergistic N-Heterocyclic Carbene/Palladium-Catalyzed Umpolung 1,4-Addition of Aryl Iodides to Enals

An umpolung 1,4-addition of aryl iodides to enals promoted by cooperative (terpy)Pd/NHC catalysis was developed that generates various bioactive β,β-diaryl propanoate derivatives. This system is not only the first reported palladium-catalyzed arylation of NHC-bound homoenolates but also expands the scope of NHC-induced umpolung transformations. A diverse array of functional groups such as esters, nitriles, alcohols, and heterocycles are tolerated under the mild conditions. This method also circumvents the use of moisture-sensitive organometallic reagents.     

Nickel/Photoredox-Catalyzed Asymmetric Reductive Cross-Coupling of Racemic α-Chloro Esters with Aryl Iodides

A unique nickel/organic photoredox co-catalyzed asymmetric reductive cross-coupling between α-chloro esters and aryl iodides is developed. This cross-electrophile coupling reaction employs an organic reductant (Hantzsch ester), whereas most reductive cross-coupling reactions use stoichiometric metals. A diverse array of valuable α-aryl esters is formed under these conditions with high enantioselectivities (up to 94 %) and good yields (up to 88 %). α-Aryl esters represent an important family of nonsteroidal anti-inflammatory drugs. This novel synergistic strategy expands the scope of Ni-catalyzed reductive asymmetric cross-coupling reactions.     

Synergistic N‐Heterocyclic Carbene/Palladium‐Catalyzed Umpolung 1,4‐Addition of Aryl Iodides to Enals

An umpolung 1,4‐addition of aryl iodides to enals promoted by cooperative (terpy)Pd/NHC catalysis was developed that generates various bioactive β,β‐diaryl propanoate derivatives. This system is not only the first reported palladium‐catalyzed arylation of NHC‐bound homoenolates but also expands the scope of NHC‐induced umpolung transformations. A diverse array of functional groups such as esters, nitriles, alcohols, and heterocycles are tolerated under the mild conditions. This method also circumvents the use of moisture‐sensitive organometallic reagents.     

块体理论赤平解析法在锦屏二级水电站皮带机隧洞稳定分析中的应用

在小子样结构响应试验数据样本的基础上,利用支持向量机回归的方法模拟了圆柱壳体动态 极限应变峰值同壳体几何尺寸和外加脉冲载荷大小的非线性函数关系,同时通过改进的模拟 退火单纯形混合算法优化了支持向量机的性能参数,并将支持向量机回归分析的预测性能同 BP人工神经网络方法做了比较,验证了具有优化性能参数组合的支持向量机在小样本条件下 更好的预测和推广能力. 最后,从支持向量机回归模型导出了大尺寸圆柱壳体抗脉冲载荷的 强度极限同自身几何尺寸的多元函数关系,从而为该类型壳体设备抗脉冲载荷的强度分析提 供了一个可借鉴的预估模型. 研究结果表明了支持向量机在机械结构的强度预估和可靠性分 析等力学领域具有广泛的应用前景.