二苯酰

Their structures were confirmed by elemental analysis, 1H NMR, and IR spectral data. The preliminary bioassay results showed that α-phenyl-sul-fonylcyclododecanone oxime 2,4-dichlorophenoxy acetate (8p) had inhibition ratio 100% and 80.07% against Digitaria sanguinalis Scop., and 100% and 88.70% against Abutilon theophrasti Medic. at concentrations of 100 and 1 mg/L.

初步生物活性测定结果显示，部分化合物具有一定的除草活性，如α-苯磺酰基环十二酮肟-2，4-二氯苯氧乙酸酯(8p)在浓度为100和1 mg/L时对马唐的抑制率分别为100%和80.07%；对苘麻的抑制率分别为100%和88.70%。

The calixarenes used as PTC in the fluorination of tetrachlorophthahaloyl chloride to obtain dimethyl tetrafluoroterephthalate were studied in this paper.

研究了杯芳烃在四氯对苯二甲酰氯氟化制备四氟对苯二甲酸二甲酯反应中的相转移催化作用，发现以杯芳烃作相转移催化剂使产品收率得到了明显提高。

Odoquinazolin-4(3H)-one,7-methyl-4(3H)-quinazolinone,7-bromoquinazolin-4(3H)-one were synthesized by using anthranilic acid、2-amino-5-nitrobenzoic acid、2-amino-4-nitrobenzoic acid,6-nitro--4(3H)-quinazoline-one、o-amino-terephthalic acid, 2-amino-4-hydroxy benzoic acid、2-amino-5-bromo-benzoic acid、2-amino-5-iodine acid,1、4-butynediol、L-glutamine、isatin anhydride、formamide as starting materials and utilizing microwave-assisted synthetic approach.

本文利用微波辅助合成的方法，以邻氨基苯甲酸、2-氨基-5-硝基苯甲酸、2-氨基-4-硝基苯甲酸、邻氨基对苯二甲酸、2-氨基-4-羟基苯甲酸、2-氨基-5-溴苯甲酸、2-氨基-5-碘苯甲酸、5-甲基-2-氨基苯甲酸等为原料与甲酰胺反应，以及以1，4-丁炔二醇、L-谷氨酰胺与靛红酸酐反应，共合成了13个喹唑啉酮衍生。。。

Some research and analysis on the reaction of 2,4-difluoronitrobenzene and nucleophilic reagent alcohol sodium (methyl alcohol ,ethyl alcohol, propyl alcohol, n-butyl alcohol, t-butyl alcohol, et hl) and the reaction choice of opposite -F in different solvent and conditions have done in this paper.

论文以2，4-二氟硝基苯为主要原料，研究了其与亲核试剂醇钠(甲醇、乙醇、丙醇、正丁醇、叔丁醇等)在不同溶剂中的反应情况，讨论了在几种代表性的溶剂——醇、四氢呋喃、苯、N，N-二甲基甲酰胺中亲核取代反应的情况，研究了温度、反应时间、亲核试剂、溶剂等条件对亲核取代反应的影响。

Phthalimide,anthranilic acid,2methyleneglutaronitrile bromina 1bromobutane 1,2benzisothiazole3one.

邻苯二甲酰亚胺，邻氨基苯甲酸，2亚甲基戊二脯，2溴2溴甲基戊二脯，溴代正丁烷，1.2苯并异噻唑3酮。

Bromo-2′,4′-dichloroacetophenone was synthesized in three steps,w hich were bromization ,chlorination and acylation,from glacial acetic acid and m -dichlorobenzene.

以冰乙酸和间二氯苯为原料，经溴化、氯化、酰化三个步骤，制得 2—溴- 2′，4′-二氯苯乙酮，产率达 70 %。

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。

We synthesized a new monomer 1, 4-bis (4-fluorobenzoyl) naphthalene(1, 4-BFN) using the acyl chloride reaction and Friedel-Crafts acylation reaction of 1, 4-Naphthalenedicarboxylic acid with fluorobenzene.

第二部分，我们从1，4-萘二甲酸出发，经过酰氯化反应及付氏酰基化反应，合成了新型单体1，4-二（4-氟苯羰基）萘(1， 4-BFN)。

We researched the high molecular polyether,polyamide hot melt adhesive, 2-phenoxy ethanol phenyl cellosolve,propylene glycol phenylate,etc,which have passed appraisal of the provincial science and technology achievement.the company gains higher economy profit after putting into production.

公司设有专业科研机构从事新产品的开发研制工作。先后研制开发成高分子聚醚，聚酰胺热熔胶，乙二醇苯醚，丙二醇苯醚等十多项新产品，均通过省级科技成果鉴定。

Evaluation of some Mannich bases of conjugated styryl ketones and related compounds versus the WiDr colon cancer in vitro.

朱志宏，徐秀娟。2，4-二羟基-3-芳氨基甲基苯乙酮和8-乙酰基-3-芳基-3，4-二氢-5-羟基-2H-1，3-苯并噁嗪的合成及其相互转化。

I can not make it blossom and suits me

我不能让树为我开花

When temperatures are above approximately 80 °C discolouration of the raceways or rolling elements is a frequent feature.

当温度高于 80 °C 左右时，滚道或滚动元件褪色是很常见的特征。