Evidence map›Paper›PMID 41515299›Full record

ArticleMolecules (Basel, Switzerland)2025

Connectivity Effect on Electronic Properties of Azulene-Tetraazapyrene Triads.

Xinyi Liu, Souren Majani, Jian Zhang, Simon M Langenegger, Silvio Decurtins, Ulrich Aschauer, Shi-Xia Liu

Abstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2025. 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
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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

7 authors.

Xinyi LiuDepartment of Chemistry, Biochemistry and Pharmaceutical Sciences, W. Inäbnit Laboratory for Molecular Quantum Materials, WSS-Research Center for Molecular Quantum Systems, University of Bern, Freiestrasse 3, 3012 Bern, Switzerland.ORCID 0009-0004-3539-4852
Souren MajaniDepartment of Chemistry and Physics of Materials, University of Salzburg, Jakob-Haringer-Str. 2A, 5020 Salzburg, Austria.ORCID 0009-0005-6336-8536
Jian ZhangDepartment of Chemistry, Biochemistry and Pharmaceutical Sciences, W. Inäbnit Laboratory for Molecular Quantum Materials, WSS-Research Center for Molecular Quantum Systems, University of Bern, Freiestrasse 3, 3012 Bern, Switzerland.ORCID 0000-0002-4559-1348
Simon M LangeneggerDepartment of Chemistry, Biochemistry and Pharmaceutical Sciences, W. Inäbnit Laboratory for Molecular Quantum Materials, WSS-Research Center for Molecular Quantum Systems, University of Bern, Freiestrasse 3, 3012 Bern, Switzerland.ORCID 0009-0004-6280-1855
Silvio DecurtinsDepartment of Chemistry, Biochemistry and Pharmaceutical Sciences, W. Inäbnit Laboratory for Molecular Quantum Materials, WSS-Research Center for Molecular Quantum Systems, University of Bern, Freiestrasse 3, 3012 Bern, Switzerland.ORCID 0000-0002-1624-8217
Ulrich AschauerDepartment of Chemistry and Physics of Materials, University of Salzburg, Jakob-Haringer-Str. 2A, 5020 Salzburg, Austria.
Shi-Xia LiuDepartment of Chemistry, Biochemistry and Pharmaceutical Sciences, W. Inäbnit Laboratory for Molecular Quantum Materials, WSS-Research Center for Molecular Quantum Systems, University of Bern, Freiestrasse 3, 3012 Bern, Switzerland.ORCID 0000-0001-6104-4320

Funding

Swiss National Science Foundation 200021_204053Swiss National Science Foundation CRSII5_213533
6 · The paper itself

Abstract

Azulene-based chromophores are of growing interest due to their unique electronic structures and potential applications as pH-responsive optical materials. In this study, a series of azulene-1,3,6,8-tetraazapyrene (TAP) triads were successfully synthesized and characterized to systematically explore how connectivity between the TAP and azulene units influences their optical and redox properties. UV-Vis absorption spectroscopy and cyclic voltammetry measurements clearly show that the electronic properties depend heavily on the connectivity pattern, as the effective π-conjugation and molecular planarity vary considerably in triads. Remarkably, triads

Indexed as

azulenecyclic voltammetryintramolecular charge transferoptical pH sensorsTD-DFT calculationstetraazapyreneUV-Vis spectroscopy

Identifiers

PMID41515299
PMCPMC12786884

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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.