三峡工程坝址花岗岩体缓倾角结构面成因综合研究

本文对长江三峡工程坝址花岗岩体中缓倾角结构面成因进行了全面的综合研究。从野外地质调查人手,在大量野外勘测的基础上进行宏观分析,同时辅之以扫描电镜、透射电镜、包体温度测定等方法进行微观构造组构、差异应力等的研究。在地质力学宏观分析的基础上,利用地质力学物理模拟进行相似条件下的反演,并利用非线性有限元数值模拟进行验证。同类研究在国内外均未见先例,可为同类工程研究借鉴。     

结构随机激励的响应灵敏度分析

本文建立了有色噪声随机激励的响应协方差矩阵方程,推导了响应灵敏度的计算式,给出了进行灵敏度计算的方法,并作了实例计算。     

可扩展的冲击—接触并行计算研究

冲击—接触计算模型在汽车碰撞、金属成型等的模拟计算中有着广泛的应用，鉴于冲击—接触计算过程复杂和计算量大，本文在分布式可扩展的并行计算平台上，设计并实现了冲击—接触的并行计算。算例证明，计算平台稳定可靠，算法简单实用，且具有较好的并行效率和可扩展性。     

Delayed Fluorescent Emission from Pyrene Doped Phenanthrene Nanoparticles Based on Triplet-triplet Energy Transfer

Doped nanoparticles were prepared from pyrene and phenanthrene using a facile reprecipitation method. The doped nanoparticles presented unique delayed fluorescent emissions of pyrene under the unprotected condition. The ratio of the intensity of delayed fluorescence (I_DF) to that of phosphorescence (I_P) is about 4:1, which almost keeps unchanged with the decrease of pyrene content at room temperature. The intensity of the delayed fluorescence emissions is dependent on the relative content of pyrene, as well as the aggregation degree of nanoparticles. The delayed emissions are contributed to efficient triplet‐triplet energy transfer from phenanthrene (donor) to pyrene (acceptor). Steady fluorescence measurement have proved that the singlet‐singlet energy transfer process was also existent dominated by the radiation energy transfer mechanism.     

Synthesis and Structural Characterization of Lanthanide Amides Stabilized by an N-Aryloxo Functionalized β-Ketoiminate Ligand

The synthesis and characterization of dimeric lanthanide amides stabilized by a dianionic N‐aryloxo functionalized β‐ketoiminate ligand are described in this paper. Reactions of 4‐(2‐hydroxy‐5‐tert‐butyl‐phenyl)imino‐2‐pentanone (LH₂) with Ln[N(SiMe₃)₂]₃(µ‐Cl)Li(THF)₃ in a 1:1 molar ratio in THF gave the dimeric lanthanide amido complexes [LLn{N(SiMe₃)₂}(THF)]₂ [Ln=Nd ( 1 ), Sm ( 2 ), Yb ( 3 ), Y ( 4 )] in good isolated yields. These complexes were characterized by IR spectroscopy, elemental analysis, and ¹H NMR spectroscopy in the case of complex 4 . The definitive molecular structures of complexes 1 , 3 , and 4 were determined. It was found that complexes 1 to 4 can initiate the ring‐opening polymerization of L‐lactide.     

A new shortcut synthesis route for (±)raphidecursinol

<正>The new shortcut synthesis route of(±)raphidecursinol 1,a racemic 8,4′-oxyneolignan compound,can be more easily achieved by the synthesis route,starting from readily available inexpensive 3,4,5-trimethoxybenzaldehyde and 1,2,3-trihydroxybenzene.All structures were confirmed by ~1H NMR,IR and MS.     

Synthesis and CDK2 kinase inhibitory activity of 7/7′-azaindirubin derivatives

A series of novel 7′-azaindirubin (1a-g) and 7-azaindirubin (2a, 2c, 2e and 2f) derivatives were designed and synthesized. Their structures were characterized by 1H NMR and MS spectroscopy as well as by elemental analysis. Their inhibitory properties against CDK2/cylinA were evaluated in vitro. In contrast to indirubin, some of the described azaindirubins emerged as potent inhibitors of CDK2/cylinA and compound 2b had more potent activity. Biological tests also showed that nitrogen atom at 7-position of azaindirubin was more beneficial to enhance the kinase inhibitory activity.     

Separation of gibberellin A4 from A4 and A7 mixture by selective complex

<正>Gibberellin A4 is effectively separated from mixture of gibberellin A4 and its analogue gibberellin A7,in the form of its crystalline complex with N,N,N',N'-tetramethylethylenediamine.After removing the tetramethylethylenediamine from the crystal by dilute HCl,gibberellin A4 is obtained a purity of 98.1%and a yield of 72.7%.     

The detection of tetrahydrofuran hydrate formation and saturation using magnetic resonance imaging technique

Tetrahydrofuran (THF) hydrate was formed in bulk as well as in glass beads pack with a mean diameter of 3.0 mm by controlling the temperature under ambient pressure. Images of THF hydrate formation procedure were obtained using the magnetic resonance imaging (MRI) technique. The experiment results showed that MRI is an effective method for the detection of hydrate formation. Saturation of hydrate formed both in bulk and glass beads can be confirmed by intensity integration of MRI images.     

检测维生素C的囊泡荧光传感器的制备

利用合成的含有识别基团苯硼酸和荧光读出基团萘的新型双亲化合物(DNMPBA)在THF/水选择性溶剂中自组织成囊泡,囊泡的相变温度为56.8℃;当向囊泡体系加维生素C时,DNMPBA囊泡中的萘生色基在345nm的荧光峰强度急剧减弱.荧光强度减弱归于所形成的硼酸酯增强了DNMPBA双亲化合物中一个氧原子孤对电子对萘生色基的淬灭作用.DNMPBA囊泡与维生素C的相互作用而导致体系荧光强度变化,使该体系有可能应用于检测生物物质如维生素C的化学传感器.