Evidence map›Paper›PMID 41292261›Full record

ArticleInorganic chemistry2025

Secondary Phosphines Bearing N-Heterocyclic Imine Groups: Polarity Umpolung of Highly Electron-Rich P-H Bonds.

Maike B Röthel, Tobias Eder, Franka Brylak, Michael Seidl, Pawel Löwe, Fabian Dielmann

Abstract read
In one paragraph

Article in Inorganic chemistry, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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.

Maike B RöthelInstitute of General, Inorganic and Theoretical Chemistry, Universität Innsbruck, Innsbruck 6020, Austria.
Tobias EderInstitute of General, Inorganic and Theoretical Chemistry, Universität Innsbruck, Innsbruck 6020, Austria.
Franka BrylakInstitute of General, Inorganic and Theoretical Chemistry, Universität Innsbruck, Innsbruck 6020, Austria.ORCID 0000-0003-1590-9324
Michael SeidlInstitute of General, Inorganic and Theoretical Chemistry, Universität Innsbruck, Innsbruck 6020, Austria.
Pawel LöweInstitute of Inorganic and Analytical Chemistry, Universität Münster, Münster 48149, Germany.ORCID 0000-0003-2275-552X
Fabian DielmannInstitute of General, Inorganic and Theoretical Chemistry, Universität Innsbruck, Innsbruck 6020, Austria.ORCID 0000-0002-7025-5450

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The synthesis and reactivity of secondary phosphines carrying two N-heterocyclic imine substituents are reported. These highly electron-rich phosphines feature a polarized P-H bond, with computational studies revealing their dual nature as excellent hydride donors and superbasic phosphorus nucleophiles. Experimental investigations demonstrated their ability to transfer a hydride, proton, or hydrogen atom, depending on the reaction partner, as well as their reactivity in hydrophosphination reactions. The hydrophosphination of nonactivated alkynes proceeded under mild, metal-free conditions, yielding alkenylphosphine intermediates that partly rearranged into azaphosphole heterocycles.

Identifiers

PMID41292261
PMCPMC12709569

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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.