Evidence map›Paper›PMID 41826237›Full record

ArticleAngewandte Chemie (International ed. in English)2026

Chiral Heptagon-Embedded Double [6]Helicenes via Scholl Reaction.

Dan Wang, Philipp Penert, Lars Schneider, Moritz P Schuldt, Frank Rominger, Felix Deschler, Michael Mastalerz

Abstract read
In one paragraph

Article in Angewandte Chemie (International ed. in English), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. A Chiral Saddle-Shaped Nanographene With Two Heptagon-Embedded [4]Helicenes.Angewandte Chemie (International ed. in English) · 2026
    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.

Dan WangOrganisch-Chemisches Institut, Ruprecht-Karls-Universität Heidelberg, Heidelberg, Germany.
Philipp PenertOrganisch-Chemisches Institut, Ruprecht-Karls-Universität Heidelberg, Heidelberg, Germany.
Lars SchneiderPhysikalisch-Chemisches Institut, Ruprecht-Karls-Universität Heidelberg, Heidelberg, Germany.
Moritz P SchuldtOrganisch-Chemisches Institut, Ruprecht-Karls-Universität Heidelberg, Heidelberg, Germany.
Frank RomingerOrganisch-Chemisches Institut, Ruprecht-Karls-Universität Heidelberg, Heidelberg, Germany.
Felix DeschlerPhysikalisch-Chemisches Institut, Ruprecht-Karls-Universität Heidelberg, Heidelberg, Germany.
Michael MastalerzOrganisch-Chemisches Institut, Ruprecht-Karls-Universität Heidelberg, Heidelberg, Germany.ORCID https://orcid.org/0000-0003-3231-4816

Funding

German Research Foundation (DFG) INST 40/575-1FUGG
6 · The paper itself

Abstract

A series of heptagon-embedded multiple helicenes was synthesized in which the heptagon subunit was fused to the π-framework through Knoevenagel condensation reactions. By controlling the conditions of the cyclodehydrogenation (Scholl) reactions, different fused chiral and twisted PAHs were accessible. The optical and electronic properties of all products were investigated by UV-vis, fluorescence spectroscopy, and cyclic voltammetry. One member of the series displays an unusual anti-Kasha-like fluorescence emission. In addition, all the enantiopure [6]helicenes were separated by chiral HPLC and characterized by circular dichroism spectroscopy.

Indexed as

chiral PAHheptagonsmultiple helicenesScholl reaction

Identifiers

PMID41826237
PMCPMC13080427

What OpenQuestion holds

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Registered trials

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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.