唑

The incidence of nausea and vomiting, dizziness in aripiprazole group were significantly different form risperidone group (x2=20.397,P.001; x2=10.557,P.01), but that of menoxenia, EPS and increasing in weight in aripiprazole group were lower than in risperidone (x2=11.81-102.29,P.05), the other side effects were not significantly different.

阿立哌唑组的恶心呕吐、头晕头昏不良反应比利培酮组，差异具有显著性（x2=20.397，P.05；x2=10.557，P.05），利培酮组的月经紊乱、体重增加、锥体外系反应等不良反应均比阿立哌唑组多，差异具有显著性（x2=11.81-102.29， P均。05），其余不良反应均无显著性差异。

The incidence of nausea and vomiting, dizziness in aripiprazole group were significantly different form risperidone group (x2=20.397,P.001; x2=10.557,P.01), but that of menoxenia, EPS and increasing in weight in aripiprazole group were lower than in risperidone (x2=11.81-102.29,P.05), the other side effects were not significantly different.

阿立哌唑组的恶心呕吐、头晕头昏不良反应比利培酮组多，差异具有显著性（x2=20.397，P.05；x2=10.557，P.05），利培酮组的月经紊乱、体重增加、锥体外系反应等不良反应均比阿立哌唑组多，差异具有显著性（x2=11.81-102.29， P均。05），其余不良反应均无显著性差异。

2 mercapto 5 methoxybenzimidazole,a key intermediate for the synthesis of omeperazole,was synthesized in 80% yield over two steps.

目的 合成奥美拉唑中间体2 巯基 5 甲氧基 1H 苯并咪唑。

Kg-1. d-1 was administered in a single daily dose;in the second group,Netilmicin (200 mg/d) was combined with cefazolin (3 g,Q12 h);and in the third control group,the combination of cefazolin and Amikacin was used. Pharmacokinetics were studied in 7 patients using the TDX system, and PAE induced by Netilmicin was determined by the Avantage microbiologic system. Clinical symptoms, laboratory studies, chest X-rays, and side effects were observed.

kg-1。 h-1；（2）合用组16例，使用头孢唑啉每12小时1次投药3 g，奈替米星每天200 mg；（3）对照组18例，使用头胞唑啉每12小时投药3 g，与阿米卡星每天200 mg联合使用，分别观察临床症状、实验室很痛检查及临床疗效；应用荧光偏振分析仪药物浓度自动分析仪研究其药代动力学；应用AVANTAGE微生物分析仪研究奈替米星病痛抗生素后效应，观察了奈替米星的肾、耳毒性。

Under normaltemperature condition,it can retard elongation,Promote tillering,increase leafnitrogen and sheath starch content,increase leaf tissue electric resistance andchlorophyll content,increase free protine content;under low temperature stresscondition,paclobutrazol has the ability to minify the permeability of leaf cellmembrance,maintain leaf tissue electric resista...

在常温条件下，多效唑具有延缓早稻秧苗的伸长生长，促进分蘖，提高叶片含氮量和叶鞘淀粉含量，提高叶片组织电阻和叶绿素含量，提高游离脯氨酸含量等方面的生理效应；在低温胁迫条件下，多效唑能够减小秧苗叶片细胞膜透性，维持叶片组织电阻以及延缓叶绿素含量和净光合速度的下降趋势，提高脯氨酸含量，减轻回暖后秧苗的外部伤害程度。

Bis-imidazoline was prepared from triethylene tetraamine and N,N-dimethylformamide dimethyl acetal at 85℃ for 2 h with toluene as solvent, with a yield of 90.4%. The reaction of bis-imidazoline with 1,2-dibromoethane and potassium carbonate in acetonitrile provided with a monobromide salt yield of 78.7%. Hydrolysis of monobromide salt under aqueous causic solution formed 1,4,7,10-tetraazzcyclododecane in a 74.2% yield.

用甲苯作溶剂，使三乙烯四胺和N，N-二甲基甲酰胺二甲基缩醛在85℃反应2 h，得到中间体双咪唑啉，产率90.4%，在乙腈溶剂中，碳酸钾存在下，双咪唑啉和1，2-二溴乙烷进行扩环反应，得到环状中间体一溴盐，产率78.7%，一溴盐经碱性水解2 h，得到1，4，7，10-四氮杂十二烷，产率74.2%。

The relative stabilities and probable proton transfer in isolated and monohydrated 2-hydroxyimidazole molecules have been studied in gas phase using ab initio (MP2/6-31＋G *) method.

采用从头算方法在MP2/6-31＋G*水平上研究了2-羟基咪唑分子在孤立分子和一水合物的异构体的相对稳定性和可能的质子迁移反应，分析了一个水分子的参与对2-羟基咪唑分子异构体的相对稳定性和质子迁移速率的影响，采用Monte Carlo模拟方法研究了反应体系在水溶液中反应的溶剂化效应。

The second part focus on the synthesis of 4-(benzothiazol-2-yl)naphtho [1,2-d]oxzole derivatives.

第二部分是4-苯并噻唑基-[1，2-d]萘并噁唑衍生物的合成。

The third part is the spectroscopy of the 4-(benzothiazol-2-yl)naphtho[1,2-d]oxzole derivatives.

第三部分是4-苯并噻唑基-[1，2-d]萘并噁唑衍生物光谱性质的研究。

Organic fluorescent compound;(benzothiazol-2-yl)naphtho[1; 2-d]oxzole derivatives; UV spectroscopy; Fluorescent spectroscopy; Quantum yield

工程科技I，化学，有机化学有机荧光化合物；苯并噻唑基-萘并噁唑衍生物；紫外光谱；荧光光谱；量子产率

And Pharaoh spoke to Joseph, saying, Your father and your brothers have come to you.

47：5 法老对约瑟说，你父亲和你弟兄们到你这里来了。

Additionally, the approximate flattening of surface strip using lines linking midpoints on perpendicular lines between geodesic curves and the unconditional extreme value method are discussed.

提出了用测地线方程、曲面上两点间短程线来计算膜结构曲面测地线的方法，同时，采用测地线间垂线的中点连线和用无约束极值法进行空间条状曲面近似展开的分析。