Evidence map›Paper›PMID 39362864›Full record

ArticleNature communications2024

Synthesis of quadruply boron-doped acenes with stimuli-responsive multicolor emission.

Cheng Chen, Yongkang Guo, Zhidong Chang, Klaus Müllen, Xiao-Ye Wang

Abstract read
In one paragraph

Article in Nature communications, 2024. 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
–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

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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.

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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

5 authors.

Cheng ChenState Key Laboratory of Elemento-Organic Chemistry, Frontiers Science Center for New Organic Matter, College of Chemistry, Nankai University, 300071, Tianjin, China.
Yongkang GuoState Key Laboratory of Elemento-Organic Chemistry, Frontiers Science Center for New Organic Matter, College of Chemistry, Nankai University, 300071, Tianjin, China.
Zhidong ChangState Key Laboratory of Elemento-Organic Chemistry, Frontiers Science Center for New Organic Matter, College of Chemistry, Nankai University, 300071, Tianjin, China.
Klaus MüllenMax Planck Institute for Polymer Research, Ackermannweg 10, 55128, Mainz, Germany.ORCID http://orcid.org/0000-0001-6630-8786
Xiao-Ye WangState Key Laboratory of Elemento-Organic Chemistry, Frontiers Science Center for New Organic Matter, College of Chemistry, Nankai University, 300071, Tianjin, China. xiaoye.wang@nankai.edu.cn.ORCID http://orcid.org/0000-0003-3540-0277

Funding

Ministry of Science and Technology of the People's Republic of China (Chinese Ministry of Science and Technology) 2020YFA0711500National Natural Science Foundation of China (National Science Foundation of China) 22071120National Natural Science Foundation of China (National Science Foundation of China) 22221002National Natural Science Foundation of China (National Science Foundation of China) 92256304
6 · The paper itself

Abstract

Boron-doped acenes have attracted attention due to their unique structures and intriguing luminescent properties. However, the hitherto known boron-doped acenes have only one or two boron atoms, limiting the chemical space of this unique family of compounds and the capability to tune their optical properties. Herein, we report the synthesis of quadruply boron-doped acenes, including pentacene, heptacene, and nonacene. The importance of the boron doping level on the luminescent properties of acenes is demonstrated. The title compounds manifest enhanced Lewis acidity as compared with dihydrodiboraacenes, leading to Lewis-base-responsive emission in the solid state. Moreover, quadruply boron-doped nonacene displays mechanochromic luminescence in addition to Lewis-base-responsive properties, realizing high-contrast solid-state multicolor emission. This work greatly expands the chemistry of boron-doped acenes and offers opportunities for developing boron-based luminescent materials.

Identifiers

PMID39362864
PMCPMC11450196

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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.