Evidence map›Paper›PMID 34956406›Full record

ArticleBeilstein journal of organic chemistry2021

Synthesis of a novel aminobenzene-containing hemicucurbituril and its fluorescence spectral properties with ions.

Qingkai Zeng, Qiumeng Long, Jihong Lu, Li Wang, Yuting You, Xiaoting Yuan, Qianjun Zhang, Qingmei Ge, Hang Cong, Mao Liu

Abstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in Beilstein journal of organic chemistry, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

10 authors.

Qingkai ZengDepartment of Chemistry, College of Chemistry and Chemical Engineering, Guizhou University, Guiyang, Guizhou Province 550025, PR China.
Qiumeng LongDepartment of Chemistry, College of Chemistry and Chemical Engineering, Guizhou University, Guiyang, Guizhou Province 550025, PR China.
Jihong LuDepartment of Chemistry, College of Chemistry and Chemical Engineering, Guizhou University, Guiyang, Guizhou Province 550025, PR China.
Li WangDepartment of Chemistry, College of Chemistry and Chemical Engineering, Guizhou University, Guiyang, Guizhou Province 550025, PR China.
Yuting YouDepartment of Chemistry, College of Chemistry and Chemical Engineering, Guizhou University, Guiyang, Guizhou Province 550025, PR China.
Xiaoting YuanDepartment of Chemistry, College of Chemistry and Chemical Engineering, Guizhou University, Guiyang, Guizhou Province 550025, PR China.
Qianjun ZhangDepartment of Chemistry, College of Chemistry and Chemical Engineering, Guizhou University, Guiyang, Guizhou Province 550025, PR China.
Qingmei GeDepartment of Chemistry, College of Chemistry and Chemical Engineering, Guizhou University, Guiyang, Guizhou Province 550025, PR China.
Hang CongDepartment of Chemistry, College of Chemistry and Chemical Engineering, Guizhou University, Guiyang, Guizhou Province 550025, PR China.
Mao LiuDepartment of Chemistry, College of Chemistry and Chemical Engineering, Guizhou University, Guiyang, Guizhou Province 550025, PR China.ORCID https://orcid.org/0000-0002-2935-1117

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A novel hemicucurbituril-based macrocycle, alternately consisting of amidobenzene and 2-imidazolidione moieties was designed and synthesized. Based on the fragment coupling strategy, nitrobenzene-containing hemicucurbituril was firstly prepared facilely under alkaline environment, and reduction of the nitro groups produced the desired amidobenzene-containing hemicucurbituril. As an original fluorescent chemosensor, it exhibited strong interactions with Fe

Indexed as

amidobenzene-containing macrocyclehemicucurbiturilhost–guest interactionmacrocyclemodification

Identifiers

PMID34956406
PMCPMC8685562

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