Evidence map›Paper›PMID 18679776›Full record

ArticleJournal of fluorescence2009

Rational design of novel benzimidazole-based sensor molecules that display positive and negative fluorescence responses to anions.

Jie Shao, Yanhong Qiao, Hai Lin, Huakuan Lin

Abstract read
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In one paragraph

Article in Journal of fluorescence, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.3field-weighted citation impact, top 22% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed, 26 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. An anthracene-based tripodal chemosensor for anion sensing.International journal of environmental research and public health · 2010
    Article
  5. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors at 1 institution in 1 country.

Jie ShaoDepartment of Chemistry, Nankai University, Tianjin, 300071, People's Republic of China.
Yanhong Qiao
Hai Lin
Huakuan Lin
Nankai University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Two novel and neutral benzimidazole derivatives-based anion receptors bearing a 1,10-phenanthroline fluorophore, N,N'-di-(2'-benzimidazolyl-methylene)-1, 10-phenanthroline-2,9-diamide (1) and N,N'-di-[2'-(benzimidazolyl-2'-) ethyl-]-1,10-phenanthroline-2,9-diamide (2), which exhibited turn-on and turn-off fluorescence responses to various anions, were rationally designed and synthesized and their fluorescent response toward anions was investigated in DMSO solution. In the process of anions binding, there were two different fluorescent responses in presence of anions: a quenching of the fluorescence emission for F- and AcO- and an enhancement of the fluorescence emission for Cl-, Br- and I-. Two different luminescent mechanisms of the receptors 1 and 2 resulting from various anions were exploited to rationalize quenching and enhancement of the fluorescence emission: a photo-induced electronic transfer mechanism (PET) and the increase of the rigidity of the host molecules, respectively. In particular, chloride could be recognized selectively from the anions tested according to changes of fluorescence spectrum.

Indexed as

FluorescenceAnionsBenzimidazolesFluorescent DyesMagnetic Resonance SpectroscopyMolecular StructurePhenanthrolinesAnionsBenzimidazolesFluorescent DyesN,N'-di-(2'-(benzimidazol-2'-yl)ethyl)-1,10-phenanthroline-2,9-diamideN,N'-di-(2'-benzimidazolylmethylene)-1,10-phenanthroline-2,9-diamidePhenanthrolines

Identifiers

PMID18679776
OpenAlexW2049533058

What OpenQuestion holds

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Read underepoch 390

Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.