化学合成

The Knoevenagel condensation reactions between aromatic and α,β-unsaturated aromatic aldehydes with barbituric acid can effectively be performed in ionic liquid without additional acid or base catalyst, it is a simple efficient method for the synthesis of benzylidene barbituric acids, which have been widely used in pharmaceutical chemistry as well as in organic synthesis.

芳醛、α，β-不饱和芳醛和巴比妥酸间的Knoevenagel缩合反应能在离子液体中没有酸碱催化剂的条件下顺利进行，是合成在药物化学和有机合成中有广泛用途的苯亚甲基巴比妥酸类化合物的简单有效的方法。

Name of appearance of the chemical composition that determined all sorts of synthesis outcome according to chemical analysis and XRD analysis data, substance, lens of report of use emissive scanning is calcic to 6 kinds of boric acid microscopical form appearance, grain size undertook token, those who discover them is microscopical form appearance, grain size has very big different.

根据化学分析和XRD分析数据确定了各种合成产物的化学组成、物相名称，用场发射扫描电镜对六种硼酸钙的显微形貌、颗粒大小进行了表征，发现它们的显微形貌、颗粒大小有很大的不同。

In this thesis, we did modifications of alkyl groups upon benzyl fluorophosphonate. In order to study the influence of alkyl length and steric effect on activity and selectivity of probes, we synthesized benzyl fluorophosphonate recognition heads with modifications including ethyl, butyl, octyl and cyclohexyl. By way of connecting different kinds of tag like azido group, biotin and rhodamine with recognition heads separately through a higher hydrophilic ethylene glycol derived linker, a series of benzyl fluorophosphonate probes were made up. And they will apply to various biological testing strategies.

在本论文中，我们以苯甲基氟化磷酸酯为基础，於其上进行一系列烷基之修饰，为了探讨烷基长度与空间立体性质对於探针活性及选择性的影响，我们合成了包含乙烷基、丁烷基、辛烷基以及环己烷基修饰的苯甲基氟化磷酸酯辨识端，并藉由具较高亲水性的聚乙二醇衍生连接桥结合三种不同的发报端，分别有叠氮基团、生物素及萤光基团来构成不同的化学探针组合，这一系列苯甲基氟化磷酸酯类化学探针将可被应用於不同的生物测试策略。

Aluminum phosphate (AlPO 4) can be prepared by solid state synthesis with different templates, aluminum chloride and ammonium diacid phosphate at low temperature (180℃) within a short time (2 h).

以氯化铝和磷酸二氢铵为原料，在模板剂存在下用固相合成方法合成了磷酸铝类化合物，合成的化合物通过化学分析、ICP测定、XRD和 IR图谱对其进行了表征，研究了化合物对铬离子吸附性能，实验表明这类化合物对铬离子有较好的吸附能

Production technology of synthesis of allantoin are reviewed, including glyoxal oxidation, electrochemical synthesis, calcium glyoxylate synthesis, dichloroacetic acid synthesis, ace-tochloral method, and oxidative decarboxylation.

评述了乙二醛氧化法、化学法、醛酸钙法、素三氯乙醛合成法、酸二氯乙酸法和尿酸氧化脱羧法等合成尿囊素的各种工艺。

The new synthetic technology of some important anthraquinone intermediates derived from 1-amino- anthraquinone, l-amino-4-hydroxy-anthraquinone, l-amino-4-bromo- anthraquinone-2-sulfonic acid, 1,5- and 1,8 dinitro- anthraquinone, have been studied.

本文研究了几种重要的由1-氨基蒽醌衍生的蒽醌型中间体：1-氨基-4-羟基蒽醌、1-氨基-4-溴蒽醌-2-磺酸和1，5-及1，8-二硝基蒽醌的合成化学，在此基础上开发了上述中间体的合成新技术。

The new synthetic technology of some important anthraquinone intermediates derived from 1-amino- anthraquinone, l-amino-4-hydroxy-anthraquinone, l-amino-4-bromo- anthraquinone-2-sulfonic acid, 1,5- and 1,8 dinitro- anthraquinone, have been studied.

本文研究了几种重要的由1-氨基蒽醌衍生的蒽醌型中间体：1-氨基-4-羟基蒽醌、1-氨基-4-溴蒽醌-2-磺酸和1，5-及1，8-二硝基蒽醌的合成化学，在此基础上开发了上述中间体的合成新技术。现行1-氨基-4-羟基蒽醌的生产技术是从1-氨基蒽醌出发，经二溴化再水解制得，溴的耗量在1.5mol以上。

Methodologies for stereoselective synthesis of alkenes are of great interest in synthetic organic chemistry since many biologically active compounds occuring in nature possess the structural skeleton of disubstituted or trisubstituted alkenes.

烯烃的立体选择合成方法学研究是有机合成化学中的重要课题，因为许多重要的天然产物中均含有双取代或三取代烯烃的结构单元。

At first, Polyaniline was synthesized by the improved chemical oxidation technique, then, PANI/HCl, PANI/TSA and PANI/DBSA were obtained by doping emeraldine with HCl, 4-methyl benzene sulfonic acid and dodecylbenzene sulfonate acid, separately. Leucoemeraldine was obtained in the N-dimethylformamide by using phenylhydrazine deoxidizing emeraldine in N_2 atmosphere.

本文首先通过改进合成条件的化学氧化法合成了聚苯胺，经氨水脱掺杂获得本征态聚苯胺，再经盐酸、对甲苯磺酸、和十二烷基苯磺酸掺杂，分别获得到质子酸掺杂的聚苯胺样品，然后在N，N-二甲基甲酰胺中，利用苯肼，在N_2氛围下还原本征态聚苯胺得到还原态的聚苯胺。

These compounds are of substantial interest both inviewpoints of theory and practical applications, mainlyunder the stimulus to achieve synthetic models either foractive sites of iron-sulfur proteins or for transitionmetal catalysts. This thesis describes the synthesis, structures andconformations of 51 new iron-sulfur cluster complexes,which have been characterized by elemental analysis andstandard spectroscopic methods. In addition, single-crystalX-ray diffraction analyses were performed for 4 representa-tive new compounds. Reactivities of μ-〓 with mono- and di- Grig-nard reagents derived intermediates toward various organicelectrophilic substrates were studied, along with complexa-tion of arynyl-containing iron-sulfur clusters by 〓Thus, several bridged, non-bridged, monomeric, dimeric,homonuclear, heteronuclear iron-sullfur and iron-sulfur co-balt-carbon cluster complexes were synthesized. A novelreaction and convenient route for the synthesis in highyield of tetranuclear iron complexes 〓 containing atetracoordinated sulfur atom was discovered, whereas aplausible mechanism based on experimental results was propo-sed for the formation of the new cluster type.

鉴于有机铁硫原子簇化学在基础理论发展和应用方面的重要意义，因此我们开展了这一课题的研究，并取得以下主要成果： 1、本文共合成了51个新有机铁硫及含钴碳簇基的有机铁硫原子簇配合物，除用元素分析，NMR，IR，MS法表征其结构和构象外，还用X-光衍射技术测得四个代表性配合物的单晶结构和构象； 2、我们业已发现炔基Grignard试剂同〓可形成一种&开环&与&闭环&中间物的平衡混合物，研究该平衡混合物同各种亲电试剂的反应； 3、研究发现了一种可高产率地形成〓含〓四配位硫挛合簇的新化学反应并对此反应提出了—种有趣的反应机理； 4、首次由1，4-二溴丁烷双Grignard试剂与〓制得一种新型铁硫簇双硫阴离子活性中间体，并进而研究了它的亲核反应性能； 5、找到了通过〓的光化学反应来合成簇合物〓-〓的一条有实用价值的新路线。

This paper discusses design and realizable methods of remote test output interface from logical design angle.

本文从逻辑设计的角度讨论遥测输出接口的设计及实现方法。

This also 星体投射plies to buildings, structures and geological features.

这也适用于建筑物和地质特征。