环胺

Computationalresults indicate that the no-planar trans-benzanilide is the most stable structure. The spectra indicate that the Franck Condon region photodissociation dynamics have multidimensional character withnine activemodes. The intensity of υ24 mode in methanol is much stronger than that in acetonitrile. Compared with fatty amides and benzamide, phenyl substitution for H atom on-NH2 group makes C=O solvent effects disappear.

结果表明，苯甲酰苯胺的非平面反式结构为最稳定结构；在Frank-Condon区域内，苯甲酰苯胺主要由9个活性振动模组成；其中ν24（苯环上C＝C不对称伸缩振动和CCH的面内弯曲振动，NH面内弯曲振动）振动模在甲醇溶剂中的强度远远大于其在乙腈的强度；与脂肪酰胺类化合物和苯甲酰胺的研究结果比较发现，苯基取代－NH2上的H原子使得C＝O不再具有明显的溶剂效应。

The results of bioassay suggest that 2-methylthio-6-methyl-4-substituted pyrimidine and 4, 6-dimethoxy-2-substituted pyrimidine derivatives show herbicidal activity. In these target compounds, 4, 6-dimethoxy-2-substituted pyrimidine benzylamine and 4, 6-dimethoxy-2-Substituted pyrimidine benzylidene amine exhibit good herbicidal activity, and the herbicidal will be affected by the substituents in the benzene ring.

对分子库中的目标分子进行了生物活性筛选研究，发现其中的2-甲硫基-6-甲基-4-取代嘧啶衍生物和4，6-二甲氧基-2-取代嘧啶类化合物显示出除草活性，其中4，6-二甲氧基-2-取代嘧啶苄胺类化合物和4，6-二甲氧基-2-取代嘧啶亚苄胺类化合物具有较好的除草活性，而且其活性和苯环上的取代基有关。

Methods:The target compound was synthesized using 4-hydrazino-N-methyl-benzyl-sulphonamide hydrochloride and 4,4-dimethoxy-N,N-dimethyl butylamine as the starting materials,PPA and sodium dihydrogen phosphate instead as catalysts and isopropyl ether and acetone as solvents for recrylstallization,via 4-step reactions:condensation,rearrangement,cyclization and salt formtion.

以4-肼基-N-甲基-苄基磺酰胺盐酸盐与4，4-二甲氧基-N，N-二甲基-丁胺为起始原料，改用多聚磷酸和磷酸二氢钠作为催化剂，后处理采用异丙醚和丙酮作为重结晶溶剂，经缩合、重排、环合、成盐的4步反应合成琥珀酸舒马曲坦。

Two kinds of tough curing agents were respectively prepared by using epoxy-oleic methyl ester and epoxy-oleic capryl ester as termination agents of epoxy-amine adduct.

本文选择环氧油酸甲酯和辛酯，分别对环氧树脂—多胺加成物的端胺基进行封端改性，得到了封端改性固化剂G-甲酯和G-辛酯。

The synthesis of the intermediate amidetriazinone was a crucial step in the synthesis of triazinone. Ethyl acetate was used as the initial material then was carried out for five steps hydrazine hydrate, triphosgene, chloroacetone, hydrazine hydrate respectively with the yield of 59.8%.

三嗪酮类化合物的合成关键是中间体氨基三嗪酮，本文以乙酸乙酯为起始原料，经过酯的肼解、成环反应、胺的烷基化、酮和肼的缩合、酰胺的水解五步反应合成中间体氨基三嗪酮，其收率达59.8%。

Methods The target compounds were synthesized from cyclopentanone via Stork reaction, Mannich condensation, amine exchange and selective reduction. Xylene-induced mice ear edema assay was used to evaluate their anti-inflammatory activity.

以环戊酮为起始原料，通过Stork烯胺反应、Mannich缩合反应、胺交换反应和选择性还原制备目标化合物；以二甲苯致小鼠耳肿胀模型测试目标化合物的抗炎活性。

Methods The target compounds were synthesized from cyclopentanone via Stork reaction, Mannich condensation , amine exchange and selective reduction. Xylene-induced mice ear edema assay was used to evaluate their anti-inflammatory activity.

以环戊酮为起始原料，通过Stork烯胺反应、Mannich缩合反应、胺交换反应和选择性还原制备目标化合物；并以二甲苯致小鼠耳肿胀模型测试目标化合物的抗炎活性。

And the epoxy acrylic cationic resin applicable to cathodic electrodeposition coating was synthesized by using aminating agent of diethanolamine and neutralizing agent of acetic acid.

并以二乙醇胺为胺化剂、冰醋酸为中和剂合成了可用于阴极电沉积涂料的环氧丙烯酸阳离子树脂。

The aminolignin flocculant was prepared based on calcium lignosulfonate, diethylamine and epichlorohydrin by amino grafting.

摘要以木质素磺酸钙、二乙胺和环氧氯丙烷为原料，通过接枝氨基，合成了木质素胺脱色絮凝剂。

An organic cationic flocculant containing quaternary ammonium ion was synthesized using epichlorohydrin, diethylamine and 1, 2-diaminoethane as raw materials. The intrinsic viscosity, charge density and turbidity removal rate of PEFD were determined and its structure was characterized by FT-IR.

以环氧氯丙烷、二乙胺和乙二胺为原料合成了有机阳离子絮凝剂PEFD，对其电荷密度、特性粘度以及絮凝性能进行了测试，并采用红外光谱对其结构进行了表征。

James, son of Zebedee, and John the brother of James, whom he named Boanerges, that is, sons of thunder

载伯德的儿子雅各伯和雅各伯的弟弟若望，并为他们起名叫"波纳尔革"，就是"雷霆之子"

The southern Hungarian university city of Szeged will host part of the project, amounting to 40 percent of the total investment, which will mostly be paid for through Hungary's EU structural funds.

位于塞格德南部的匈牙利大学将负责部分项目，总计占总投入资金的40%。大部分资金将由匈牙利的欧盟结构基金会支付。