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Fourth new aryl acyl ureas of triazole, tetrazole and thiodiazole have been synthesized.

合成了30个新的含三唑、四唑和噻二唑的芳酰基硫脲类化合物。

The studies segmented polyester polyurethaneurea elastomers based on 4,4'-diphenylmethane diisocyanate, ethylene diamine and polybutylene adipate (M. W. 1975 and M. W. 1228) were studied by means of IR spectrascopy.

用红外光谱法对基於4,4'-二苯基甲烷二异氰酸酯、乙二胺和聚己二酸丁二醇酯(分子量分别为1975和1228)的嵌段聚脲氨酯弹性体进行了研究。

Therewas a significant characteristic of the vertical distribution of soil enzyme activity,the relationship analysis indicated that there was a significant positive relationshipbetween the catalase activity and OM,and total N,and effective P、K,and ex-changible Mg,there was a negative relationship between the catalase activity andBase Situatiou percentage,and Total Contents of Base;the activity of the polyphe-nol oxidase was positively related with OM,and negatively related with total N andexchangible Ca clearly;The urease activity decreased with CPR increasing,and thechange of the former two kinds of soil enzyme actirity was not significantly withCPR increasing,It is possible to be related with maned disturbance frequently.

随着代次增加,有机质和交换性Ca下降明显;土壤的CEC和交换性酸分别下降了8.8—16.1%和6.8—18.5%,因此,其养分总量亦逐代降低,其中有机质下降幅度最大;土壤酶的活性具有明显的垂直分布特征,相关分析表明,过氧化氢酶活性与土壤OM、全N、有效P、K和交换性Mg有极显著的正相关,而与盐基总量、盐基饱和度呈明显的负相关。多酚氧化酶活性与OM呈显著负相关,与全N、交换性Ca有显著相关。脲酶活性则有随连栽代次增加而有下降趋势,前两种酶在代次之间变化不明显,可能与频繁的土壤干扰有关。

In order to find new pyrazole leading compounds, 14 1--4-(pyrazol- 5-ylcarbony)semicarbazide devivatives were synthesized from 4-chloro-3-ethyl-1-methyl-5-pyrazole car-bonydrazide and substituted phenylisocyanate.

为了寻求新的吡唑先导化合物,用4-氯-1-甲基-3-乙基-5-吡唑甲酰肼与取代苯基异氰酸酯反应得到了14个新的1-吡唑酰基-4-芳基氨基脲类化合物。

Two novel pyrazolone derivatives 2-ethylamino-6H-5-(1-phenyl-3-methyl/phenyl-5-pyrazolone-4-ylene)-1,3,4-thiadiazine (PMCP-ETSC/DPCP-ETSC) containing NNS six-membered heterocycles were synthesized by the condensation reaction of 1-phenyl-3-methyl/phenyl-4-chloroacetyl-pyrazolone-5 with 4-ethyithiosemicarbazide. The title compounds were characterized by elemental analysis, IR, 1H NMR, 13C NMR and single-crystal X-ray diffraction.

利用1-苯基-3-甲基/苯基-4-氯乙酰基-吡唑啉酮-5与4-乙基氨基硫脲发生缩合反应,生成了2个新的双杂环化合物2-乙氨基-6H-5-(1-苯基-3-甲基/苯基-5-吡唑啉酮-4-基)-1,3,4-噻二嗪(PMCP-ETSC/DPCP-ETSC),并对其进行元素分析、红外光谱、核磁共振表征和晶体结构分析。

The literature about the synthesis of the ion exchange and chelating adsorbents used in the off-line separation and preconcentration of the noble metals and the development of the on-line microcolumn separation and preconcentration of the noble metals were reviewed. Four silica gel-based adsorbents with rhodanine, 2-mercaptopyrimidine, 2-mercaptothiazoline and isophenylthiourea as the functional groups were first synthesized and applied to the on-line separation and preconcentration of silver, gold, palladium and platinum for their FAAS determination.

本论文在回顾螯合吸附材料的合成及其在贵金属的离线和流动注射在线预浓集分离发展状况的基础上,首次合成了含罗丹宁、2-巯基嘧啶、2-巯基噻唑啉和异二苯基硫脲等四种以硅胶为载体的螯合吸附剂,并用于银、金、钯和铂的流动注射微填充柱在线预浓集分离、火焰原子吸收光谱分析。

Because the limonene does not have a carbonyl group, the small amount of it which remainsin the carvone fraction will not form a semicarbazone derivative.

由于柠檬烯没有羧基,留在香芹酮馏份中少量的柠檬烯将不会产生缩胺基脲的衍生物。

Mercaptopropyl methyldimethoxysilane was synthesized by thiourea in the presence of tetramethylammonium iodine as a catalyst and mixed liquid containing ethylenediamine and trichloroethylene as a neutralizer, without solvent, in which the reaction temperature, catalysts ,neutralizer and their amounts were optimized.

以四甲基碘化铵为催化剂,乙二胺和三氯乙烯的复合液为中和剂,在无溶剂体系中,用硫脲法合成了甲基巯丙基二甲氧基硅烷。

Arylselenoureas with electron donor group on benzene ringreacted with excess sulfinyl chloride to give 2-aminobenzosele-nazoles.

苯环上有给电子基的N-芳基硒脲在过量的氯化亚砜中自动氧化合环生成2-氨基取代笨并硒唑。

The structures were identified by IR, UV,〓 NMR and element analyses. 2. Free radical 4-hydroxy-2,2,6,6-tetramethyl-1-piperidinyloxyl as catalyst, the phase transfer catalyzed method of oxidation eighteen semicarbazides to N-Aryl-2-Phenyl diazenecarboxamide with a solution of potassium ferricyanide in 2N aqueous sodium hydroxide and dichloromethane is described for the first time.

利用2,2,6,6-四甲基-4-羟基-1-哌啶氮氧自由基为相转移催化剂,在饱和铁氰化钾的2N氢氧化钠溶液与二氯甲烷的两相反应液中,催化氧化十八个取代氨基脲得到十八个相应的新型偶氮化合物N,2-二芳基二氮亚烯甲酰胺,均获得了较高的产率。

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