Evidence map›Paper›PMID 41104884›Full record

ArticleChemistry (Weinheim an der Bergstrasse, Germany)2026

Synthesis of Dithienylcycloalkene Molecular Switches Enabled by a Bench-Stable Ti-Complex.

Marcell M Bogner, Márton Hegedűs, Péter P Kalapos, Attila Kunfi, Gábor London

Abstract read
In one paragraph

Article in Chemistry (Weinheim an der Bergstrasse, Germany), 2026. 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

5 authors.

Marcell M BognerInstitute of Organic Chemistry, HUN-REN Research Centre for Natural Sciences, Budapest, 1117, Hungary.ORCID https://orcid.org/0009-0007-1397-4575
Márton HegedűsInstitute of Organic Chemistry, HUN-REN Research Centre for Natural Sciences, Budapest, 1117, Hungary.
Péter P KalaposInstitute of Organic Chemistry, HUN-REN Research Centre for Natural Sciences, Budapest, 1117, Hungary.
Attila KunfiInstitute of Organic Chemistry, HUN-REN Research Centre for Natural Sciences, Budapest, 1117, Hungary.
Gábor LondonInstitute of Organic Chemistry, HUN-REN Research Centre for Natural Sciences, Budapest, 1117, Hungary.ORCID https://orcid.org/0000-0001-6078-3180

Funding

Magyar Tudományos Akadémia JánosBolyaiScholarshipNational Research, Development and Innovation Office, Hungary FK142622National Research, Development and Innovation Office, Hungary STARTING150352Nemzeti Kutatási Fejlesztési és Innovációs Hivatal FK142622Nemzeti Kutatási Fejlesztési és Innovációs Hivatal STARTING150352
6 · The paper itself

Abstract

Herein, we report a set of cycloalkene-bridged dithienylethene (DTE) molecular switches with ring sizes ranging from 4- to 7-membered rings. These analogs were accessed via McMurry carbonyl coupling using a bench-stable Ti(IV)-complex reagent instead of the generally applied fuming, liquid TiCl

Indexed as

cyclobutenesdithienylethenesfatigue resistanceMcMurry couplingphotoswitch

Identifiers

PMID41104884
PMCPMC13451566

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.