查询词典 fluorescence

The initial interaction modes of pyreno[2,1-b]pyrrole and its dimeric derivative with F in MeCN can be understood as hydrogen-bonded complexes. Excess F ions promotes deprotonation of N-protons and results in the bathochromic changes in both absorption and fluorescence spectra.

实验过程中发现，在初始模式中，芘骈吡咯及双芘骈吡咯与氟离子形成氢键附合物；之后加入的氟离子，因其带有极强的碱性，将促使吡咯官能基中氮上氢进行去质子化，而造成吸收及萤光光谱的红位移现象。

The bay area has no substituent and has electron-withdrawing groups,such as bromine atom,cyano-group and 4-formyl phenoxy group compounds have strong absorption in 525 nm,when excitated them,they have strong yellow and salmon pink luminescence bettwen 538 and 566 nm.When introduce electron-donating substituents,such as phenoxy group,morpholinyl,piperidinyl and n-butylamino group,the absorption bathochromic shift while the electron-donating ability is improved,bettwen 536 and 692 nm have strong absorption,reach to the near-infrared region. When excitated them,only the phenoxy group compound has strong salmon pink luminescence in 572 nm,the others have no fluorescence.

其中，港湾位无取代的以及含吸电基团(—Br、—CN、对甲酰基苯氧基)化合物在525 nm左右处均有很强的吸收ε＞10~4M~(-1cm~(-1)，当光激发时，港湾位无取代、溴代和氰基取代物发出538～547 nm的强烈黄色荧光，对甲酰基苯氧基取代物则发出566 nm的强烈橙红色荧光；含供电基团(苯氧基、吗啉基、哌啶基、正丁氨基)化合物随着供电子能力的增强，吸收发生红移，在536～692 nm处均有很强的吸收ε＞10~4M~(-1cm~(-1)，达到了近红外区，当光激发时，只有苯氧基取代物发出572 nm的强烈橙红色荧光，而含氮供电基取代物均发生了荧光淬灭。

The major contents in this thesis are described as follows:(1) Seven new thiol fluorescence reagents containing 2-phenylbenzoxazole (or 2-phenylbenzothiazole) derivatives or benzanthrone as fluorphore and iodinacetylamine or maleimide as reaction groups have been synthesized.

本论文的研究工作主要分为以下几个方面：(1)以碘乙酰胺或马来酰亚胺为反应基团和以2-芳基苯并噁唑类化合物或苯并蒽酮为荧光团，首次合成了七种新的碘乙酰胺类和马来酰亚胺类巯基荧光试剂。

NO content and NOS activity were assayed with benzidine fluorescence spectrophotometry.

NO含量和NOS活性采用联苯胺荧光分光光度法测定。

We firstly introduced benzoazole (including benzimidazole, benzoxazole and benzothiazole) into the meso-positions of porphines and obtained five new porphyrins 36a-e. Their structures were characterized by 1H NMR, MS, UV-vis spectra and fluorescence emission spectra.

将苯并唑类基团(苯并咪唑、苯并噁唑和苯并噻唑)引入到卟吩中位，得到5个新型卟啉36a-e衍生物，并经核磁氢谱、质谱、紫外吸收光谱和荧光发射光谱表征了化合物的结构。

Bimolecular fluorescence complementation; protein interactions ; cellular localization

双分子荧光互补；蛋白质相互作用；亚细胞定位

The chiral polymer P-1 shows strong blue fluorescence due to the extended π-electronic structure between the chiral repeating unit-6,6'-di(4-trifluoromethyl-phenyl)-2,2'-bisoctoxy-1,1'-binaphthyl and the conjugated linker 2,2'-bipyridyl group via vinylene bridge.

手性高分子P-1能发射强的蓝色荧光，这是由于手性重复单元-6，6′-二(4-三氟甲基苯基)-2，2′-二正辛氧基-1，1′-联萘和单元2，2′-联吡啶通过亚乙烯基桥连形成共轭高分子结构造成的。

Otherwise,the fluorescence emission intensity of ternary complexes have been enhanced strongly by 2,2'-bipyridine in mixing.

另外，三元配合物中，2，2'-联吡啶的掺入可大大提高配合物的荧光强度。

A series of fluorene and 2,2'-bipyridine or 1,10-phenanthroline alternate and random copolymers(P1 or P2) have been designed and synthsized, and their interaction with transition metal ions were investigated.The some accomplishments were achieved as follows:(1) It is found that the absorption red shift and fluorescence quench strongly in the presence of transition metal ions.

设计合成了一系列芴与联吡啶、菲洛啉的交替和无规共轭聚合物（P1、P2），通过研究它们与不同过渡金属离子相互作用，获得如下主要成果：（1）由于过渡金属离子的作用，吸收光谱发生不同程度的红移，以及强烈的荧光猝灭现象。

It was found that when the 2,2'-bipyridyl was used as a ligand for metal complex formation,an abnormal new peak was observed obviously whether in fluorescence or absorption spectrum.It indicated that a new species was formed owing to the reaction between them.

发现当以联吡啶为络合物配体时，无论荧光和吸收光谱中均出现反常的新峰，这和 1-溴乙基苯与吡啶间发生了成盐反应有关。

The split between the two groups can hardly be papered over.

这两个团体间的分歧难以掩饰。

This approach not only encourages a greater number of responses, but minimizes the likelihood of stale groupthink.

这种做法不仅鼓励了更多的反应，而且减少跟风的可能性。