Evidence map›Paper›PMID 40312778›Full record

ArticleChemphyschem : a European journal of chemical physics and physical chemistry2025

Molecular Fragmentation as a Strategy to Access Hyperpolarized Compounds from Para-Hydrogen.

Philip L Norcott

Abstract read
In one paragraph

Article in Chemphyschem : a European journal of chemical physics and physical chemistry, 2025. 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

1 author.

Philip L NorcottCollege of Science and Engineering, Flinders University, Sturt Road, Bedford Park, South Australia, 5042, Australia.ORCID https://orcid.org/0000-0003-4082-2079

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hyperpolarization significantly increases the detectability of molecules in magnetic resonance spectroscopy and imaging. Beyond recent advancements in hardware and catalyst design, this article discusses harnessing the inherent chemical reactivity of hyperpolarization target molecules as a strategy to expand the scope and versatility of para-hydrogen-based methods. Various fragmentation reactions are considered for their potential to generate otherwise inaccessible hyperpolarized species, thereby broadening potential applications.

Indexed as

fragmentationhyperpolarizationnuclear magnetic resonancepara‐hydrogen‐induced polarizationsignal amplification by reversible exchange

Identifiers

PMID40312778
PMCPMC12276030

What OpenQuestion holds

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LicenceCC BY-NC
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Registered trials

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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.