Evidence map›Paper›PMID 42175813›Full record

ArticleAngewandte Chemie (International ed. in English)2026

Catalyst Hide-and-Seek Beneath Porous Support Surfaces: Pinpointing Active Site Distribution Through Resonance Energy Transfer.

Buddhima K P Maldeni Kankanamalage, William J Thompson, Danielle N Smith, Grace C Thaggard, Namodhi Wijerathne, Isabella Incognito, Jeffery A Byers, Jia Niu, Natalia B Shustova

Abstract read
In one paragraph

Article in Angewandte Chemie (International ed. in English), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

9 authors.

Buddhima K P Maldeni KankanamalageDepartment of Chemistry and Biochemistry, University of South Carolina, Columbia, South Carolina, USA.
William J ThompsonDepartment of Chemistry, Boston College, Chestnut Hill, Massachusetts, USA.
Danielle N SmithDepartment of Chemistry and Biochemistry, University of South Carolina, Columbia, South Carolina, USA.
Grace C ThaggardDepartment of Chemistry and Biochemistry, University of South Carolina, Columbia, South Carolina, USA.
Namodhi WijerathneDepartment of Chemistry and Center for Catalysis, University of Florida, Gainesville, Florida, USA.
Isabella IncognitoDepartment of Chemistry and Biochemistry, University of South Carolina, Columbia, South Carolina, USA.
Jeffery A ByersDepartment of Chemistry, Boston College, Chestnut Hill, Massachusetts, USA.ORCID https://orcid.org/0000-0002-8109-674X
Jia NiuDepartment of Chemistry, Boston College, Chestnut Hill, Massachusetts, USA.ORCID https://orcid.org/0000-0002-5622-6362
Natalia B ShustovaDepartment of Chemistry and Biochemistry, University of South Carolina, Columbia, South Carolina, USA.ORCID https://orcid.org/0000-0003-3952-1949

Funding

Camille and Henry Dreyfus FoundationUnited States Department of Energy, Camille and Henry Dreyfus Foundation, American Chemical Society, Office of the Vice President for Research at the University of South Carolina, and Office of Undergraduate Research at the University of South Carolina.
6 · The paper itself

Abstract

Merging the high selectivity and efficiency of homogeneous catalysts with the recyclability of heterogeneous systems represents an attractive, industry-driven concept that can be realized through the "heterogenization" of existing molecular catalysts by incorporating them into porous solid-state matrices. The concept proposed herein uses Förster resonance energy transfer analysis to establish the first direct correlations among matrix topology, catalyst integration strategy, and active site positioning in porous materials without employing fluorescent model systems. This catalyst mapping method can be applied to several classes of porous materials, including metal-organic frameworks and mesoporous silica. It addresses the existing challenges in relating the factors that control the spatial surface (re)distribution of molecular catalysts within such matrices before and after catalytic transformations. On the example of a series of six different catalyst-integrated materials, Å-level mapping of active site distribution was correlated with the nature of the porous host and the catalyst integration mechanism, which dictates the loading and accessibility of integrated catalysts. Thus, these studies provide a foundation for developing a framework to guide the design of recyclable heterogeneous catalysts with well-defined active site distributions, both before and after catalytic transformations, which are key fundamental parameters for heterogeneous catalysis.

Indexed as

active sitescatalyst distributionheterogeneous catalysismetal‐organic frameworksphotophysics

Identifiers

PMID42175813
PMCPMC13383038

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.