Evidence map›Paper›PMID 42626518›Full record

ArticleACS omega2026

Kinetic Modeling and Quantification of Pressure-Derived Oxygen Accumulation from Anthracene Endoperoxides under Confined Conditions.

Abhishek Sharma, Vanessa Barth, Chandrika Sethumadhavan, Frank Goldschmidtboeing, Henning J Jessen, Laura M Comella

Abstract read
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Article in ACS omega, 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

6 authors.

Abhishek SharmaCluster of Excellence livMatS at FIT-Freiburg Center for Interactive Materials and Bioinspired Technologies, University of Freiburg, Georges-Köhler-Allee 105, 79110 Freiburg, Germany.ORCID https://orcid.org/0009-0009-0100-690X
Vanessa BarthCluster of Excellence livMatS at FIT-Freiburg Center for Interactive Materials and Bioinspired Technologies, University of Freiburg, Georges-Köhler-Allee 105, 79110 Freiburg, Germany.
Chandrika SethumadhavanLaboratory for the Design of Microsystems, Department of Microsystems Engineering (IMTEK), University of Freiburg, Georges-Köhler-Allee 102, 79110 Freiburg, Germany.
Frank GoldschmidtboeingLaboratory for the Design of Microsystems, Department of Microsystems Engineering (IMTEK), University of Freiburg, Georges-Köhler-Allee 102, 79110 Freiburg, Germany.
Henning J JessenCluster of Excellence livMatS at FIT-Freiburg Center for Interactive Materials and Bioinspired Technologies, University of Freiburg, Georges-Köhler-Allee 105, 79110 Freiburg, Germany.ORCID https://orcid.org/0000-0002-1025-9484
Laura M ComellaCluster of Excellence livMatS at FIT-Freiburg Center for Interactive Materials and Bioinspired Technologies, University of Freiburg, Georges-Köhler-Allee 105, 79110 Freiburg, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The controlled release of gas is central to chemically triggered systems and pressure-driven processes, where both the magnitude and temporal evolution of gas must be predictable. Anthracene-endoperoxides (ANT-EPO) are a class of oxygen-releasing molecules that decompose with well-defined stoichiometry and temperature-dependent kinetics, making them attractive candidates for tunable chemical sources. Prior work has demonstrated optical and pressure-based monitoring of ANT-EPO decomposition, providing valuable insights into its oxygen release behavior. The present work establishes a kinetic model to quantify and estimate oxygen release from ANT-EPO under confined geometries, using pressure as an experimental observable. Pressure-time data acquired using gauge and absolute sensors at ambient room temperature and 37 °C were converted into gas-phase oxygen accumulation using an ideal gas law formulation. The resulting profiles were described by first-order kinetics, yielding temperature-dependent rate constants that were independent of concentration. An apparent gas-phase recovery factor was introduced to account for nonideal conversion between the theoretical oxygen release capacity and the experimentally accessible oxygen amount recovered in the headspace. These parameters were integrated into a compact empirical-mechanistic model that relates concentration and temperature to pressure evolution within the defined chamber geometry. Model performance was evaluated through forward prediction of oxygen release using an independently measured concentration excluded from parameter extraction, demonstrating accurate prediction without refitting. This approach enables quantitative analysis and prediction of confined gas-evolving reactions and provides a basis for translating ANT-EPO reaction kinetics into pressure evolution under defined operating conditions. This work bridges responsive materials, chemical kinetics, and engineering applications, demonstrating ANT-EPO as a potential controllable oxygen source.

Identifiers

PMID42626518
PMCPMC13491977

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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.