Evidence map›Paper›PMID 37649660›Full record

ArticleRSC advances2023

Bis(thienyl)ethenes with α-methoxymethyl groups. Syntheses, spectroscopic Hammett plots, and stabilities in PMMA films.

Thea Weingartz, Sven Nagorny, Jörg Adams, André Eitzeroth, Marvin Schewe, Christian Rembe, Andreas Schmidt

Abstract read
In one paragraph

Article in RSC advances, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. On photokinetics under polychromatic light.Frontiers in chemistry · 2024
    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

7 authors.

Thea WeingartzClausthal University of Technology, Institute of Organic Chemistry Leibnizstrasse 6 D-38678 Clausthal-Zellerfeld Germany schmidt@ioc.tu-clausthal.de.
Sven NagornyClausthal University of Technology, Institute of Organic Chemistry Leibnizstrasse 6 D-38678 Clausthal-Zellerfeld Germany schmidt@ioc.tu-clausthal.de.
Jörg AdamsClausthal University of Technology, Institute of Physical Chemistry Arnold-Sommerfeld-Straße 4 D-38678 Clausthal-Zellerfeld Germany adams@pc.tu-clausthal.de.ORCID https://orcid.org/0000-0001-7878-2952
André EitzerothClausthal University of Technology, Institute of Physical Chemistry Arnold-Sommerfeld-Straße 4 D-38678 Clausthal-Zellerfeld Germany adams@pc.tu-clausthal.de.
Marvin ScheweClausthal University of Technology, Institute for Electrical Information Technology Leibnizstraße 28 D-38678 Clausthal-Zellerfeld Germany.
Christian RembeClausthal University of Technology, Institute for Electrical Information Technology Leibnizstraße 28 D-38678 Clausthal-Zellerfeld Germany.
Andreas SchmidtClausthal University of Technology, Institute of Organic Chemistry Leibnizstrasse 6 D-38678 Clausthal-Zellerfeld Germany schmidt@ioc.tu-clausthal.de.ORCID https://orcid.org/0000-0002-6160-6108

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A series of bis(thienyl)ethenes (BTEs) possessing perfluorocyclopentene backbones and methoxymethyl groups (MOM) in the 2/2'-positions of the thiophenes was prepared and examined. The substitution pattern of the 5/5'-positions was varied, covering the range from electron-donating to electron-withdrawing. The substituent effects of the absorption wavelengths of the ring-opened and the ring-closed isomers, which are interconverted by reversible 6π-electrocyclizations and cycloreversions, are studied by means of the spectroscopic Hammett equation and the Hammett-Brown equation. Excellent correlations of these linear free energy relationships were found, when the

Identifiers

PMID37649660
PMCPMC10462923

What OpenQuestion holds

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Registered trials

None linked

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.