Evidence map›Paper›PMID 33502818›Full record

ArticleChemistry (Weinheim an der Bergstrasse, Germany)2021

Directed Design of a Au

Julia Beerhues, Maren Neubrand, Sebastian Sobottka, Nicolás I Neuman, Hannes Aberhan, Shubhadeep Chandra, Biprajit Sarkar

Open access · hybridAbstract read
In one paragraph

Article in Chemistry (Weinheim an der Bergstrasse, Germany), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.3field-weighted citation impact, top 12% of its field
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

13 citing papers in PubMed, 26 citations in OpenAlex.

  1. Article
  2. AuInternational journal of molecular sciences · 2025
    Article
  3. Review
  4. Article
  5. Article
  6. Gauging Radical Stabilization with Carbenes.Angewandte Chemie (International ed. in English) · 2022
    Article
  7. Article
  8. A Mesoionic Diselenolene Anion and the Corresponding Radical Dianion.Chemistry (Weinheim an der Bergstrasse, Germany) · 2022
    Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. Directed Design of a AuChemistry (Weinheim an der Bergstrasse, Germany) · 2021
    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 at 2 institutions in 1 country.

Julia BeerhuesLehrstuhl für Anorganische Koordinationschemie, Institut für Anorganische Chemie, Universität Stuttgart, Pfaffenwaldring 55, 70569, Stuttgart, Germany.
Maren NeubrandLehrstuhl für Anorganische Koordinationschemie, Institut für Anorganische Chemie, Universität Stuttgart, Pfaffenwaldring 55, 70569, Stuttgart, Germany.
Sebastian SobottkaInstitut für Chemie und Biochemie, Freie Universität Berlin, Fabeckstraße 34-36, 14195, Berlin, Germany.
Nicolás I NeumanLehrstuhl für Anorganische Koordinationschemie, Institut für Anorganische Chemie, Universität Stuttgart, Pfaffenwaldring 55, 70569, Stuttgart, Germany.ORCID http://orcid.org/0000-0003-3368-0228
Hannes AberhanInstitut für Chemie und Biochemie, Freie Universität Berlin, Fabeckstraße 34-36, 14195, Berlin, Germany.
Shubhadeep ChandraLehrstuhl für Anorganische Koordinationschemie, Institut für Anorganische Chemie, Universität Stuttgart, Pfaffenwaldring 55, 70569, Stuttgart, Germany.
Biprajit SarkarLehrstuhl für Anorganische Koordinationschemie, Institut für Anorganische Chemie, Universität Stuttgart, Pfaffenwaldring 55, 70569, Stuttgart, Germany.ORCID http://orcid.org/0000-0003-4887-7277
University of Stuttgart · DEFreie Universität Berlin · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Carbene-based radicals are important for both fundamental and applied chemical research. Herein, extensive electrochemical investigations of nine different 1,2,3-triazolylidene selenium adducts are reported. It is found that the half-wave potentials of the first reduction of the selones correlate with their calculated LUMO levels and the LUMO levels of the corresponding triazolylidene-based mesoionic carbenes (MICs). Furthermore, unexpected quasi-reversibility of the reduction of two triazoline selones, exhibiting comparable reduction potentials, was discovered. Through UV/Vis/NIR and EPR spectroelectrochemical investigations supported by DFT calculations, the radical anion was unambiguously assigned to be triazoline centered. This electrochemical behavior was transferred to a triazolylidene-type MIC-gold phenyl complex resulting in a MIC-radical coordinated Au

Indexed as

carbene-selenium adductscyclic voltammetrymesoionic carbenesradicalsspectroelectrochemistry

Identifiers

PMID33502818
PMCPMC8252451
OpenAlexW3121438936

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.