异构的

The influence of solvent and medium on the absorption spectrum and the equilibrium between azo tautomerism and hydrazone tautomerism was discussed.

讨论了溶剂和介质对各个染料紫外可见吸收光谱及偶氮式异构体与腙式异构体互变平衡的影响。

In like wise, the acidic matrixes can prevent transforming from deltamethrin to its isomer.

溴氰菊酯两个异构体峰的比值在不同基质中存在显著差异，橙子、番茄、葡萄等酸性基质和甘蓝中异构体1所占比重最小，溴氰-1：溴氰-2≈1：4；而在洋葱、蒜、黄瓜中两者比例几乎达到1：1。

Complex 4 exists as a mixture of two isomers. The interconversion between the two isomers was studied by variable-temperature 1H NMR.

化合物4存在两种异构体，通过变温核磁研究了这两种异构体的相互转化。

The effects of nature of catalyst, temperature, amount of catalyst, and time on isomerization rate and product compositon were also studied.

同时研究了异构化反应中不同催化剂、反应温度、催化剂用量和时间对异构化速率及产品组成的影响。

The difference of NDP kinase activity and DNase activity among NDPK-A wild type and NDPK-A isomers were analyzed.

通过本文研究：(1)成功构建并制备了大量NDPK-A异构体，为NDPK-A结构异构与生物活性关系的后续研究做好了准备。

The excited-state intramolecular proton transfer tautomerism reaction of 6-methyl-4-hydroxy pyri-midine monomers and dimmers was investigated by the ab initio method with the self-consistent reaction field with Tomas's polarized continuum mode and CIS theories at HF level on the basis of 6-311+G* and 6-31G basis set. By studying the potential energy surface, it was found that the monomer's ground-state proton transfer process together with the excited-state proton transfer process is a molecular system of four energy level, but dimmers were not, which can be used to explain the fact that UV-visible absorption and fluorescence spectra of monomer and dimers all corresponded to quinoid.

采用 ab initio HF理论的组态相关CIS方法和连续溶剂模型PCM，分别在6-311+G*和6-31G水平上研究了6-甲基-4-羟基嘧啶单体及二聚体激发态质子转移的异构化反应；对其反应势能面的研究发现，单体基态和激发态的异构化反应一起可以形成四能级的分子电子体系，而二聚体的却不能，由此解释了单体和二聚体的紫外吸收光谱和荧光发射光谱均对应于酮式构型的原因。

The structure and stability of all possible isomers of C50X(X=SiH2, PH, S) were investigated by ab initio HF/3-21G calculations. The calculation results indicate that the preferred position for cycloaddition of SiH2, PH, and S on C50 is consistent, i.e. on the C3-C4 and C4-C4 sites of C50, and the resultant most stable cycloaddition isomers are [5,6]-closed and [5,5]-closed structures. The main driving force governing the stability of the C50X(X=SiH2, PH, S) isomers is the strain, or the conjugative effect, or the combination of strain and conjugative effect, depending on the addition positions and the types of the attacked C-C bonds.

用从头算HF/3-21G方法研究了C50的环加成衍生物C50X(X=SiH2， PH， S)所有可能的异构体的结构与稳定性，计算结果表明，SiH2基团、PH基团与S原子在C50上环加成的优先加成位置相同，都为C3-C4类键和C4-C4类键，并且相应形成[5，6]-闭环和[5，5]-闭环结构的最稳定异构体；决定C50X(X=SiH2，PH，S)各异构体稳定性的主要因素，因加成位置以及发生加成反应的C-C键的单双键类型的不同，可能是张力、共轭效应或者二者的共同作用。

The generating results of our system were compared with the published,results of DENDRAL and SEMAMI systems, and they were consistent with eachother.

目前本系统对于含C、N、P、S与Si等元素由于不对称中心、不对称轴引起的立体异构和几何异构均能进行穷举生成。

In the catalytic tranformation of n-butane, Pd modified silicoaluminate molecular sieves were tested for n-butane's isomerization and dehydroismerization.

考察了硅铝分子筛为基质的双功能催化剂催化丁烷异构化的反应性能及催化丁烷一步异构脱氢反应的可能性，发现丁烷到异丁烯的一步转化无法在这一反应体系十有效实现。

In the catalytic tranformation of n-butane, Pd modified silicoaluminate molecular sieves were tested for n-butane's isomerization and dehydroismerization.

考察了硅铝分子筛为基质的双功能催化剂催化丁烷异构化的反应性能及催化丁烷一步异构脱氢反应的可能性，发现丁烷到异丁烯的一步转化无法在这一反应体系中有效实现。

This one mode pays close attention to network credence foundation of the businessman very much.

这一模式非常关注商人的网络信用基础。

Cell morphology of bacterial ghost of Pasteurella multocida was observed by scanning electron microscopy and inactivation ratio was estimated by CFU analysi.

扫描电镜观察多杀性巴氏杆菌细菌幽灵和菌落形成单位评价遗传灭活率。