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重氮化反应

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A series of diazonium salts of 4-(N-methyl-N-phenylamino)-3-amino-1,8-naphthalic anhydride 5a, its naphthalimide derivative 5b, and 5e were designed and synthesized,and it was the first time to discover that aromatic radical-induced intramolecular aromatic 1, 5-hydrogen transfer was also involved in the nitrogen-contianed system during Pschorr cyclization.

实验设计合成了4--3-氨基-1,8-萘酐的重氮盐5a、其衍生物N-丁基-4--3-氨基-1,8-萘酰亚胺的重氮盐5b和N--4--3-氨基-1,8-萘酰亚胺的重氮盐5c,并首次发现了通过普朔尔环化反应以氮甲基化的氮为桥原子的体系存在着芳香自由基诱导的芳香1,5-氢转移。

The surface morphology visualized by AFM as well as the regularity of the films studied by XRD was also reported.We found that the diazonium group can form H-bond with phenolic hydroxy and the multilayered film from DR and phenol-formaldehyde resin was first fabricated.

并且利用重氮树脂的光反应这一独特性质,发展了组装纳米粒子及羧基功能化纳米管的方法,这将会在制备胶体晶体(胶体粒子规整排列,具有似晶体的结构)和固定纳米管上有所应用。

The resultant was hydrogenised to remove protective group of amino group, then the product was reacted with NaNO2 to give diazonium salt, which was conjugated with salicylic acid, hydroxybenzene, N-salicyloyl glycine acid to get azo derivatives of 4-ASA.

本文首先对4-ASA的氨基和羟基进行了选择性保护,通过氢化还原法选择性脱除氨基的保护基,然后将氢化产物制成重氮盐,通过与水杨酸、苯酚和水杨酰甘氨酸发生反应生成4-ASA的偶氮衍生物,最后在碱性条件下水解得到最终产物。

The reaction mechanism for the formation of ultimate carcinogens diazohydroxide, diazonium and oxoniumions by α-hydroxylation-NPYR and the alkylation process of C and guanine were investigated including solvent effects at the B3LYP/6-31G(superscript **) level.

采用密度泛函理论,在B3LYP/6-31G水平上,研究了气相和水溶剂中,α-羟基化吡咯烷亚硝胺(-αhydroxylation-NPYR, A)代谢为终致癌物重氮氢氧化物、重氮烷阳离子和氧离子,以及C与鸟嘌呤碱基相互作用的反应机理。

H-acid is proposed as a self-coupling diazotizing reagent for the determination of nitrite and nitrate.

本文研究了NO_2~-与 H-酸的重氮盐自偶联反应,提出了一个灵敏的分光光度法,用于测定钢件磷化液中的NO_3,结果满意。

Chiral ligands mentioned above and their complexes with acetate copper were used as enantio-selective catalysts in asymmetric cyclopropanation reactions of diazoacetate and 1,1-diphenyl ethylene. Investigations indicate that all of them reveal certain optical-selective capability, but chiral C2-symmetric 2,6-bispyridine ligands show better catalytic capability than chiral asymmetric schifF-base ligands.

选择了2个手性2,6-吡啶双噁唑啉配体和6个手性不对称席夫碱配体与醋酸铜形成的配合物作为催化剂,对重氮乙酸乙酯与1,1-二苯乙烯不对称环加成进行催化反应,发现这8个催化剂对1,1-二苯乙烯的不对称环丙烷化反应都表现出了一定的光学活性诱导能力,手性2,6-吡啶双噁唑啉-铜类具有比手性Schiff碱-铜类更好的催化性能。

A new convenient synthesis of a series of 1-aryl-2-propanones using aromatic amine s as precursors, via diazo reaction and improved Meerwein arylation reaction under mild conditions, was achieved.

以芳香胺为原料,经重氮化和改进的Meerwein芳基取代反应,合成了一系列的1-芳基-2-丙酮,其中1-(3,5-二三氟甲基苯基)-2-丙酮是一个新化合物。

A new convenient synthesis of a series of 1-aryl-2-propanones using aromatic amines as precursors, via diazo reaction and improved Meerwein arylation reaction under mild conditions, was achieved. In addition, 1-[3,5-bisphenyl]-2-propanone is a new compound among the synthesized compounds. This approach is an efficient synthetic method for the aryl-propanones with the different substituting groups.

以芳香胺为原料,经重氮化和改进的Meerwein芳基取代反应,合成了一系列的1-芳基-2-丙酮,其中1-(3,5-二三氟甲基苯基)2-丙酮是一个新化合物改进后的方法简化了合成步骤,提高了收率,可方便地用于在苯环上具有不同取代基的芳基丙酮的合成。

To dye the different types of fibers by the same dye, universal dyes based on naphthalene ring system are prepared by the diazo coupling reaction of 7-acetamide-4-hydroxy-2-oaphtialene-β-(N,N-dimethylaminoethyl)solfonamide and m-aminobenzene-β-hydroxyethyl sulfone sulfunate.

为了实现用同一支染料对不同类型的纤维进行染色的目的,通过间氨基苯基-β-羟乙基砜硫酸酯与7-乙酰氨基-4-羟基-2-萘-β磺酰胺的重氮化偶合反应合成了含萘环的通用染料,其结构通过质谱分析进行了表征。

Improved yield and selectivity are observed while applying this technology on diazo- coupling reactions.

该技术在重氮化、偶合反应中的应用,取得了高于常规反应器的收率和纯度。

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