Evidence map›Paper›PMID 40903432›Full record

ArticleJournal of the American Chemical Society2025

Controlling Magnetic Anisotropy of Endohedral Lanthanide Ions by Carbene Addition: Paramagnetic NMR, Lanthanide Luminescence, and Single-Molecule Magnetism in Adamantylidene Adducts of MSc

Wei Yang, Matheus Felipe de Souza Barbosa, Noel Israel, Marco Rosenkranz, Fupin Liu, Stanislav M Avdoshenko, Alexey A Popov

Abstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in Journal of the American Chemical Society, 2025. 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. Relaxation of magnetization in DyChemical science · 2026
    Article
  2. 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.

Wei YangLeibniz Institute for Solid State and Materials Research (IFW Dresden), Helmholtzstr. 20, Dresden 01069, Germany.ORCID 0000-0002-0038-0010
Matheus Felipe de Souza BarbosaLeibniz Institute for Solid State and Materials Research (IFW Dresden), Helmholtzstr. 20, Dresden 01069, Germany.
Noel IsraelLeibniz Institute for Solid State and Materials Research (IFW Dresden), Helmholtzstr. 20, Dresden 01069, Germany.
Marco RosenkranzLeibniz Institute for Solid State and Materials Research (IFW Dresden), Helmholtzstr. 20, Dresden 01069, Germany.
Fupin LiuJiangsu Key Laboratory of New Power Batteries, Jiangsu Collaborative Innovation Center of Biomedical Functional Materials, School of Chemistry and Materials Science, Nanjing Normal University, Nanjing 210023, China.ORCID 0000-0002-8454-726X
Stanislav M AvdoshenkoLeibniz Institute for Solid State and Materials Research (IFW Dresden), Helmholtzstr. 20, Dresden 01069, Germany.
Alexey A PopovLeibniz Institute for Solid State and Materials Research (IFW Dresden), Helmholtzstr. 20, Dresden 01069, Germany.ORCID 0000-0002-7596-0378

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Metallofullerenes with endohedral lanthanides have emerged as a versatile class of single-molecule magnets owing to strong single-ion magnetic anisotropy, which can be realized in the interior of the fullerene cage. Since exohedral chemical modification of fullerenes is often used to adjust their properties and processability for prospective practical applications, it is necessary to understand how it can affect their magnetic properties. In this work, we studied how a popular [2 + 1] cycloaddition reaction, photochemical addition of adamantylidene (Ad), affects single-ion magnetic anisotropy and single-molecule magnetism of MSc

Identifiers

PMID40903432
PMCPMC12447498

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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.