设计合成一系列具有不同取代基的苯甲酰萘（苯）胺衍生物，测定它们在非极性溶剂环己烷中的荧光发射光谱。
A series of prar-and meta-substituted benzanilides were synthesized and their fluorescence spectra in nonpolar solvent cyclohexane were investigated.
讨论了烷基化、酰基化和直接提取制备烷基萘的工艺路线。
The process of alkyl naphthalene preparation by alkylation, acylation and direct extraction are also discussed.
介绍了用于纺织品的荧光化合物的发色机理，探索了未来的研究方向。重点介绍了香豆素类、1，8-萘酰亚胺类荧光染料。
The chromogenic mechanism of the fluorescent compds. for textiles were presented with emphasis on coumarin and 1,8- naphthalimide dyes. The future research directions were also probed.
与单独使用反义寡核苷酸相比较，萘二酰亚胺对寡核苷酸的共价修饰显著地提高了反义寡核苷酸对KB-A - 1细胞生长的抑制。
Compared with the unmodified one, the inhibition of antisense oligonucleotides to the growth of KB - a - 1 cell was increased by conjugating with naphthyl imide.
电子级2.1.5 -重氮萘醌磺酰氯的萃取液及其制备方法。
Extraction liquid of electronic grade 2, 1, 5-diazo naphthoquinones sulfonyl chloride and preparation method thereof.
另外这些突变体对生长素极性运输抑制剂1-萘氨甲酰苯甲酸的敏感性提高，说明这些突变影响了生长素的运输。
The mutants also displayed enhanced sensitivity to N-1-naphthylphthalamic acid, an inhibitor of polar auxin transport (PAT), indicating that the mutations affected auxin transport.
本论文由两部分内容组成：新型萘酰亚胺金属离子荧光探针的设计、合成及性能研究和丁二酰亚胺光解的研究。
This dissertation consists of two parts: Study on the naphthlimide fluorescent probes for metal ions and investigation on the photolysis mechanism of succinimides.
本文合成了四支x -型1,8萘酰亚胺类活性荧光染料，并对它们的光谱及染料性能进行了研究。
Four X-reactive fluorescent dyes of 1, 8-naphthalimide were synthesized. Their spectrophotometric and dyeing properties were studied.
烯丙基是这类可聚合色素单体主要的聚合基团，可以在萘酰亚胺分子的不同位置引入，形成多种结构。
Because the molecular structure is easy to be modified, it is a polymerizable fluorescent monomer studied by many researcher.
萘酰亚胺类荧光化合物的应用很广泛，可用于荧光增白剂，荧光染料，荧光化学传感器等。
Naphthalimide fluorescent compounds have broad application. For example it can be used for optical brighteners, fluorescent dyes, fluorescent chemical sensors.
本发明公开了一种通式（1）的具有对称结构的含咔唑和萘酰亚胺基团的化合物及制备方法。
The invention discloses a compound which is as shown in a general formula (1), has a symmetrical structure and contains carbazole and naphthalimide radicals, and a method for preparing the same.
第一部分研究了氨基酸-萘酰亚胺加合物的抗肿瘤性能。
The first section described the antitumor activities of naphthalimide-amino acid conjugates.
用二氯亚砜将萘普生酰氯化，在氮气保护下与脱镁叶绿酸交联，以硅胶柱层析分离产物。
Naproxin was treated by thionyl chloride, then conjugated to Phaeophorbide under protection of N2. The compound was purified by silica gel column.
第三部分研究了二苯基烯丙哌嗪苯甲酸-萘酰亚胺衍生物的抗肿瘤和促凋亡性能。
The third section studied on the alternative modification of naphthalimide scaffold and evaluated their antitumor and apoptosis-inducing function.
在研究中比较了不同识别分子与靶序列DNA结合的强弱，发现双萘酰亚胺衍生物4对此序列DNA具有高亲合性的结合，并分析了识别分子与DNA复合物的碎裂机理以及结合模式。
It revealed that imide derivative 4, a potent binder of HIV-1 DNA, had the higher binding affinity with the duplex DNA among six DNA-recognizing mole-cules.
在研究中比较了不同识别分子与靶序列DNA结合的强弱，发现双萘酰亚胺衍生物4对此序列DNA具有高亲合性的结合，并分析了识别分子与DNA复合物的碎裂机理以及结合模式。
It revealed that imide derivative 4, a potent binder of HIV-1 DNA, had the higher binding affinity with the duplex DNA among six DNA-recognizing mole-cules.
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