苯并咪唑盐是本课题组提出的四氢叶酸辅酶的新模型。
Benzimidazolium salt as a new tetrahydrofolate coenzyme model was introduced.
而硫代水杨酸与6硝基苯并咪唑配合使用时，得到了超高反差效果。
And a super high contrast was obtained when 6 nitro benzimidazole and thiosalicylic acid were used together.
每种膜吸附水的绝对量顺序为芳香聚酰胺>聚砜酰胺>聚苯并咪唑酮。
The amount of absorbed water per amide group varied in the order. polysulfone amide (PSA)> poly(benzimidazolone) (PBIL) > aromatic polyamid…
优选的过渡金属化合物基于钴和铬，尤其是其具有苯并咪唑配位体的络合物。
Preferred transition metal compounds are based on cobalt and chromium, especially complexes thereof having benzimidazole ligands.
报道了几种由5-氨基苯并咪唑酮为原料与酚偶联形成的偶氮化合物的合成。
In this paper, the synthesis of several azo compounds from diazotized 5 - aminobenzimidazolone and several phenols are studied.
本发明包括含有具有抗溃疡活性的苯并咪唑化合物和水溶性酰胺的药用组合物。
The present invention consists of ulcer activeness resisting benzimidazole compound and water soluble amide medicinal composite.
最近的研究表明苯并咪唑及其衍生物在人体的抗菌消炎过程中具有高效低毒等特点。
Recent observations suggest that the substituted benzimidazoles and their derivatives possess potential activity with lower toxicities in the chemotherapeutic approach in man.
通过3d - QSAR等势图设计出了几种具有较好缓蚀性能的苯并咪唑化合物。
New benzimidazole molecules with excellent corrosion inhibition properties were designed by 3d-qsar contour maps.
利用二苯并咪唑盐与格利雅试剂的加成-水解反应，提出了长链二酮的新合成方法。
Novel synthetic methods for alkyl methyl ketone, symmetric diketone , long-chain diketone and macrocyclic ketone were provided.
本发明公开了2-苯并咪唑-1，10-菲咯啉过渡金属配合物及其制备方法与应用。
The invention discloses a 2-benzimidazole1, 10-phenanthrolines transition metal complex and a preparation method thereof and an application thereof.
结论氯化钕苯并咪唑配合物具有优良的光致发光特性并具有优异的升频转换荧光性质。
Conclusion the complex has the superior photoluminescence fluorescence character and superior up conversion fluorescence character.
结果表明：立体场、静电场和氢键供体场是影响苯并咪唑缓蚀剂缓蚀性能的主要因素；
The results indicated that steric, electrostatic and hydrogen-bond donor fields were main factors to inhibition performance.
本发明提供一种三联苯桥联双苯并咪唑季铵盐类化合物有机发光材料、制备方法及应用。
The invention provides an organic luminescent material, i. e. a terphenyl bridged-bis-benzimidazole quaternary ammonium compound, a preparation method and application thereof.
目的设计合成新型苯胺类苯并咪唑衍生物，并评价其对大白鼠胃液分泌和胃酸分泌的作用。
Aim to design and synthesize the novel aniline-type derivatives of benzimidazole, and to assay their activities of inhibiting secretion of gastric juice and gastric acids.
本发明涉及药物制剂领域，具体涉及含取代苯并咪唑质子泵抑制剂的组合物及其制备方法。
The present invention belongs to the field of medicine preparation, in the concrete, it relates to a composition of substituted benzimidazole proton pump inhibitor and its preparation method.
苯并咪唑衍生物取代的苯并吡喃衍生物，其药用盐，它们的制备方法和含有它们的药物组合物。
Benzopyran derivatives substituted with a benzimidazole derivative, pharmaceutically acceptable salts thereof, their preparations and pharmaceutical compositions containing them.
按照本发明，可将具有抗溃疡活性的水不溶性苯并咪唑化合物增溶，并能提供稳定的药用组合物。
In accordance with said invention, the ulcer activeness resisting water non-soluble benzimidazole compound can be solubilized and the stable medicinal composite can be provided.
苯并咪唑及其衍生物是有机合成中重要的原料和中间体，是一种存在于多种药物中的重要结构单元。
Benzimidazole and their derivatives are important material and intermediate product, it is a important structure cell which consist in many medicines.
介绍了聚苯并咪唑树脂的性能、用途及合成工艺。并详细论述了不同种类聚苯并咪唑树脂的研究状况。
The property , application , synthetic technology and main monomers of the poly(benzimidazoles) were viewed. The kinds of poly(benzimidazoles) resin were also introduced.
这类聚苯并咪唑树脂可用于耐高温纤维、漆、涂料、粘合剂、膜和复合材料等领域，有着广阔的应用前景。
The polybenzimidazole resin can be used in the fields such as high temperature resistant fiber, paint, coatings, adhesives, films, composite materials and the like, and has broad application prospect.
本发明披露作为VR1拮抗剂的苯并咪唑衍生物，制备它们的方法，含有它们的组合物和它们在治疗中的用途。
The claimed invention provides benzimidazole derivatives antagonists of VR1, processes for their preparation, pharmaceutical compositions containing them and their use in therapy.
苯并咪唑及其衍生物的开发，尤其是二取代化合物越来越受到重视，被认为是一类具有多种生物生理活性的杂环。
The development of the benzimidazole and it's derivatives, especially two replacements of benzimidazole, is regarded as a category with a variety bioactivities of heterocyclic.
本论文主要研究了稀土氯化物催化的合成氮杂环化合物的反应，得到了新型的七元氮杂环膦酸酯和苯并咪唑衍生物。
The reactions towards synthesis of novel azaheterocyclic phosphonates and benzimidazoles using lanthanide chlorides as catalyst were studied in this thesis:1.
对2-H苯并咪唑盐与烃基为不饱和取代基的格利雅试剂的加成-水解反应进行了研究，将此反应应用到不饱和醛的制备。
The addition-hydrolysis reaction was applied to the synthesis of unsaturated aldehyde by the -reaction of 2-H benzimidazolium iodide with alkenyl magnesium bromide.
在3-（2＇-苯并咪唑基）-3-羟基丙酸乙酯水解过程中，苯并咪唑基以分子内一般碱催化方式参与催化酯的水解反应。
Benzimidazolyl group exhibits catalytic activity in the way as intramolecular general-base catalysis in the hydrolysis of 3-(2'-benzimidazolyl)-3-hydroxy propionate.
本文比较全面的论述了酰基脲化合物的作用机制、构效关系、合成方法和安全性以及苯并咪唑类化合物作用机制、安全性和应用情况。
In the article, we dissertated comprehensively the functional mechanism, the relationship of structure, the synthetical methods and the safety of acylureas and the benzimidazole.
对甲苯磺酰基酰胺和2-苯基-N，N'-二甲基苯并咪唑啉（PDMBI）之间的光诱导电子转移反应，为酰胺的保护基——对甲苯磺酰基的脱除反应，提供了一条有效途径。
The photoinduced electron transfer reaction between N-tosyl amides and 2-phenyl-N, N'-dimethyl benzimidazoline (PDMBI) provides an efficient approach for the deprotection of N-tosyl amides.
对甲苯磺酰基酰胺和2-苯基-N，N'-二甲基苯并咪唑啉（PDMBI）之间的光诱导电子转移反应，为酰胺的保护基——对甲苯磺酰基的脱除反应，提供了一条有效途径。
The photoinduced electron transfer reaction between N-tosyl amides and 2-phenyl-N, N'-dimethyl benzimidazoline (PDMBI) provides an efficient approach for the deprotection of N-tosyl amides.
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