Evidence map›Paper›PMID 37377676›Full record

ArticleACS catalysis2023

Tuning Copper Active Site Composition in Cu-MOR through Co-Cation Modification for Methane Activation.

Dieter Plessers, Alexander J Heyer, Hannah M Rhoda, Max L Bols, Edward I Solomon, Robert A Schoonheydt, Bert F Sels

Open access · greenAbstract read
In one paragraph

Article in ACS catalysis, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.5field-weighted citation impact, top 10% 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

15 citing papers in PubMed, 26 citations in OpenAlex.

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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 3 institutions in 2 countries.

Dieter PlessersDepartment of Microbial and Molecular Systems, Center for Sustainable Catalysis and Engineering, KU Leuven-University of Leuven, B-3001 Leuven, Belgium.ORCID 0000-0001-8906-8447
Alexander J HeyerDepartment of Chemistry, Stanford University, Stanford CA 94305, USA.ORCID 0000-0003-4362-8191
Hannah M RhodaDepartment of Chemistry, Stanford University, Stanford CA 94305, USA.ORCID 0000-0001-5730-5209
Max L BolsDepartment of Microbial and Molecular Systems, Center for Sustainable Catalysis and Engineering, KU Leuven-University of Leuven, B-3001 Leuven, Belgium.ORCID 0000-0002-4576-5969
Edward I SolomonDepartment of Chemistry, Stanford University, Stanford CA 94305, USA.ORCID 0000-0003-0291-3199
Robert A SchoonheydtDepartment of Microbial and Molecular Systems, Center for Sustainable Catalysis and Engineering, KU Leuven-University of Leuven, B-3001 Leuven, Belgium.ORCID 0000-0003-0891-773X
Bert F SelsDepartment of Microbial and Molecular Systems, Center for Sustainable Catalysis and Engineering, KU Leuven-University of Leuven, B-3001 Leuven, Belgium.ORCID 0000-0001-9657-1710
KU Leuven · BEStanford University · USSLAC National Accelerator Laboratory · US

Funding

Structure/Function Correlations Over Copper EnzymesR01DK031450 · NIDDK · STANFORD UNIVERSITY · PI EDWARD I SOLOMON · 1986 to 2026
$8.7M
NIDDK NIH HHS R01 DK031450
6 · The paper itself

Abstract

The industrial implementation of a direct methane to methanol process would lead to environmental and economic benefits. Copper zeolites successfully execute this reaction at relatively low temperatures, and mordenite zeolites in particular enable high methanol production. When loaded to a Cu/Al ratio of 0.45, mordenite (Si/Al 5 to 9) has been shown to host three active sites: two [CuOCu]

Indexed as

co-cationscopper mordenitecopper speciationmethane to methanolsingle-site spectroscopy

Identifiers

PMID37377676
PMCPMC10299574
OpenAlexW4317356881

What OpenQuestion holds

Textmetadata
LicenceTDM
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.