Evidence map›Paper›PMID 42720345›Full record

ArticleThe journal of physical chemistry letters2026

Triple Phosphorescence and Rapid Spin Flip Mediated by Ultrafast Electron Transfer in a Spirocyclic Molecule.

Jerzy Karpiuk, Elena Karpiuk

Abstract read
In one paragraph

Article in The journal of physical chemistry letters, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0cells of the map it votes in
0citing papers in PubMed
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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

2 authors.

Jerzy KarpiukInstitute of Physics, Polish Academy of Sciences, Al. Lotników 32/46, 02-668Warsaw, Poland.ORCID 0000-0002-4143-6092
Elena KarpiukInstitute of Physics, Polish Academy of Sciences, Al. Lotników 32/46, 02-668Warsaw, Poland.

Funding

Polska Akademia Nauk NA
6 · The paper itself

Abstract

We report triple phosphorescence emitted by sp3-C linked dimethylaniline-phthalide dyads (DMA-PD) and explore its mechanisms. In 77 K organic solvent glasses, ultrafast photoinduced electron transfer populates in DMA-PD a charge-separated state (CSS), with a DMA cation and PD anion. Depending on glass polarity, the anion is produced in one of two forms, with a closed or open lactone ring. The closed ring CSS deactivates to a locally excited or charge transfer triplet, while the open ring form relaxes to the zwitterion triplet state. All three triplets have different electronic configurations and are formed in different, kinetically noncorrelated intersystem crossing (ISC) mechanisms, particularly rapidly in methylcyclohexane glass (kisc ≥ 2.3 × 1011 s-1). Our findings open the way to structural control over ultrafast triplet generation, population of multiple emissive triplet states in a single molecule, and probing heterogeneous structures and dynamics of supercooled liquids and glasses.

Identifiers

PMID42720345
PMCPMC13573604

What OpenQuestion holds

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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.