Evidence map›Paper›PMID 37127975›Full record

ReviewNature reviews. Chemistry2020

Bimetallic cooperation across the periodic table.

Jesús Campos

Abstract readReview
PubMed Publisher
In one paragraph

Review in Nature reviews. Chemistry, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 69 papers.

0numbers the graph read from it
0cells of the map it votes in
69citing 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

69 citing papers in PubMed.

  1. Article
  2. Lewis Acid/Base Au-Mn Pairs in Metal Nanoclusters for Enhanced Photocatalytic C(spAngewandte Chemie (International ed. in English) · 2026
    Article
  3. Formation of Gallium Monofluoride in the Coordination Sphere of Nickel.Angewandte Chemie (International ed. in English) · 2026
    Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Snapshots of Cooperative Trimetallic Alkene Hydrogenation.Journal of the American Chemical Society · 2025
    Article
  12. Review
  13. Article
  14. Alkyne Dihydroboration viaJournal of the American Chemical Society · 2025
    Article
  15. Sequential one-potChemical science · 2025
    Article
  16. Review
  17. Article
  18. Article
  19. Article
  20. A non-metal-to-metal INature communications · 2025
    Article

9 more citing papers are in PubMed but not listed here.

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

1 author.

Jesús CamposInstituto de Investigaciones Químicas (IIQ), Consejo Superior de Investigaciones Científicas (CSIC) and University of Seville, Seville, Spain. jesus.campos@iiq.csic.es.ORCID http://orcid.org/0000-0002-5155-1262

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Organometallic chemistry and its applications in homogeneous catalysis have been dominated by mononuclear transition-metal complexes. The catalytic performance and physico-chemical properties of these mononuclear complexes can be rationally tuned by ligand modification, which has also led to the discovery of new reactions. There is a growing body of evidence implicating the participation of two metals in catalytic processes originally believed to follow monometallic mechanisms. Moreover, the deliberate preparation of bimetallic structures has proven popular because these preorganized structures have many tunable features, such as metal-metal bond order and polarity. These structures can exhibit metal-metal complementarity and allow for multisite activation - reactivity unattainable with truly mononuclear species. This Perspective summarizes the features that are exclusive to bimetallic systems and their roles in substrate activation.

Identifiers

What OpenQuestion holds

Textmetadata
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.