Evidence map›Paper›PMID 34221324›Full record

ArticleChemical science2021

Cyclophane with eclipsed pyrene units enables construction of spin interfaces with chemical accuracy.

Marvin Metzelaars, Sebastian Schleicher, Takuma Hattori, Bogdana Borca, Frank Matthes, Sergio Sanz, Daniel E Bürgler, Jeff Rawson, Claus M Schneider, Paul Kögerler

Abstract read
In one paragraph

Article in Chemical science, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Side-Chain Type Ferrocene Macrocycles.Precision chemistry · 2024
    Article
  3. Article
  4. 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

10 authors.

Marvin MetzelaarsInstitute of Inorganic Chemistry, RWTH Aachen University 52074 Aachen Germany.ORCID https://orcid.org/0000-0002-3529-557X
Sebastian SchleicherPeter Grünberg Institute (PGI-6), Forschungszentrum Jülich 52428 Jülich Germany d.buergler@fz-juelich.de.
Takuma HattoriPeter Grünberg Institute (PGI-6), Forschungszentrum Jülich 52428 Jülich Germany d.buergler@fz-juelich.de.ORCID https://orcid.org/0000-0003-0339-1847
Bogdana BorcaPeter Grünberg Institute (PGI-6), Forschungszentrum Jülich 52428 Jülich Germany d.buergler@fz-juelich.de.ORCID https://orcid.org/0000-0001-5485-4536
Frank MatthesPeter Grünberg Institute (PGI-6), Forschungszentrum Jülich 52428 Jülich Germany d.buergler@fz-juelich.de.ORCID https://orcid.org/0000-0002-9427-2933
Sergio SanzPeter Grünberg Institute (PGI-6), Forschungszentrum Jülich 52428 Jülich Germany d.buergler@fz-juelich.de.ORCID https://orcid.org/0000-0002-4790-4184
Daniel E BürglerPeter Grünberg Institute (PGI-6), Forschungszentrum Jülich 52428 Jülich Germany d.buergler@fz-juelich.de.ORCID https://orcid.org/0000-0002-5579-4886
Jeff RawsonInstitute of Inorganic Chemistry, RWTH Aachen University 52074 Aachen Germany.ORCID https://orcid.org/0000-0002-8431-0772
Claus M SchneiderPeter Grünberg Institute (PGI-6), Forschungszentrum Jülich 52428 Jülich Germany d.buergler@fz-juelich.de.ORCID https://orcid.org/0000-0002-3920-6255
Paul KögerlerInstitute of Inorganic Chemistry, RWTH Aachen University 52074 Aachen Germany.ORCID https://orcid.org/0000-0001-7831-3953

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Advanced functionality in molecular electronics and spintronics is orchestrated by exact molecular arrangements at metal surfaces, but the strategies for constructing such arrangements remain limited. Here, we report the synthesis and surface hybridization of a cyclophane that comprises two pyrene groups fastened together by two ferrocene pillars. Crystallographic structure analysis revealed pyrene planes separated by ∼352 pm and stacked in an eclipsed geometry that approximates the rare configuration of AA-stacked bilayer graphene. We deposited this cyclophane onto surfaces of Cu(111) and Co(111) at submonolayer coverage and studied the resulting hybrid entities with scanning tunnelling microscopy (STM). We found distinct characteristics of this cyclophane on each metal surface: on non-magnetic Cu(111), physisorption occurred and the two pyrene groups remained electronically coupled to each other; on ferromagnetic Co(111) nanoislands, chemisorption occurred and the two pyrene groups became electronically decoupled. Spin-polarized STM measurements revealed that the ferrocene groups had spin polarization opposite to that of the surrounding Co metal, while the pyrene stack had no spin polarization. Comparisons to the non-stacked analogue comprising only one pyrene group bolster our interpretation of the cyclophane's STM features. The design strategy presented herein can be extended to realize versatile, three-dimensional platforms in single-molecule electronics and spintronics.

Identifiers

PMID34221324
PMCPMC8221062

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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.