Evidence map›Paper›PMID 34250327›Full record

ArticleACS omega2021

Design and Synthesis of Fluorescent 1,3-Diaryl-β-carbolines and 1,3-Diaryl-3,4-dihydro-β-carbolines.

JiYang Pu, Biao Chen, Wanhua Wu, Cheng Yang, Guoqing Zhang, Jason J Chruma

Abstract read
In one paragraph

Article in ACS omega, 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

6 authors.

JiYang PuKey Laboratory of Green Chemistry & Technology, College of Chemistry, State Key Laboratory of Biotherapy and Healthy Food Evaluation Research Center, and Sino-British Materials Research Institute, College of Physical Sciences & Technology, Sichuan University, Chengdu, Sichuan 610064, P. R. China.
Biao ChenHefei National Laboratory for Physical Science at the Microscale, University of Science and Technology of China, 96 Jinzhai Rd, Hefei, Anhui 230026, P. R. China.
Wanhua WuKey Laboratory of Green Chemistry & Technology, College of Chemistry, State Key Laboratory of Biotherapy and Healthy Food Evaluation Research Center, and Sino-British Materials Research Institute, College of Physical Sciences & Technology, Sichuan University, Chengdu, Sichuan 610064, P. R. China.ORCID https://orcid.org/0000-0002-8969-1148
Cheng YangKey Laboratory of Green Chemistry & Technology, College of Chemistry, State Key Laboratory of Biotherapy and Healthy Food Evaluation Research Center, and Sino-British Materials Research Institute, College of Physical Sciences & Technology, Sichuan University, Chengdu, Sichuan 610064, P. R. China.ORCID https://orcid.org/0000-0002-2049-1324
Guoqing ZhangHefei National Laboratory for Physical Science at the Microscale, University of Science and Technology of China, 96 Jinzhai Rd, Hefei, Anhui 230026, P. R. China.ORCID https://orcid.org/0000-0003-3155-8915
Jason J ChrumaKey Laboratory of Green Chemistry & Technology, College of Chemistry, State Key Laboratory of Biotherapy and Healthy Food Evaluation Research Center, and Sino-British Materials Research Institute, College of Physical Sciences & Technology, Sichuan University, Chengdu, Sichuan 610064, P. R. China.ORCID https://orcid.org/0000-0002-3669-4863

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The 1,3-diaryl-β-carboline derivatives, including 3,4-dihydro variants, were synthesized via a multiple-step approach. These compounds possess rigid and twisted configurations, which are expected to exhibit unique optical properties. The absorption and fluorescence properties of the newly synthesized compounds were investigated. These synthetic 1,3-diaryl-β-carbolines displayed strong emission in the range of 387-409 nm and exhibited absolute photoluminescence quantum yields of up to 74%. Density functional theory calculations were performed to better elucidate the geometric, electronic, and optical properties of these novel 1,3-diaryl-β-carbolines.

Identifiers

PMID34250327
PMCPMC8260278

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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.