Evidence map›Paper›PMID 39270030›Full record

ArticleScience advances2024

Supramolecular scaffold-directed two-dimensional assembly of pentacene into a configuration to facilitate singlet fission.

Masato Fukumitsu, Tomoya Fukui, Yoshiaki Shoji, Takashi Kajitani, Ramsha Khan, Nikolai V Tkachenko, Hayato Sakai, Taku Hasobe, Takanori Fukushima

Abstract read
In one paragraph

Article in Science advances, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

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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.

Masato FukumitsuLaboratory for Chemistry and Life Science, Institute of Innovative Research, Tokyo Institute of Technology, 4259 Nagatsuta, Midori-ku, Yokohama 226-8501, Japan.ORCID 0000-0002-5541-5022
Tomoya FukuiLaboratory for Chemistry and Life Science, Institute of Innovative Research, Tokyo Institute of Technology, 4259 Nagatsuta, Midori-ku, Yokohama 226-8501, Japan.ORCID 0000-0003-3339-1178
Yoshiaki ShojiLaboratory for Chemistry and Life Science, Institute of Innovative Research, Tokyo Institute of Technology, 4259 Nagatsuta, Midori-ku, Yokohama 226-8501, Japan.ORCID 0000-0001-8437-1965
Takashi KajitaniOpen Facility Development Office, Open Facility Center, Tokyo Institute of Technology, 4259 Nagatsuta, Midori-ku, Yokohama 226-8501, Japan.
Ramsha KhanChemistry and Advanced Material Group, Faculty of Engineering and Natural Sciences, Tampere University, Korkeakoulunkatu 8, FI33720 Tampere, Finland.
Nikolai V TkachenkoChemistry and Advanced Material Group, Faculty of Engineering and Natural Sciences, Tampere University, Korkeakoulunkatu 8, FI33720 Tampere, Finland.ORCID 0000-0002-8504-2335
Hayato SakaiDepartment of Chemistry, Faculty of Science and Technology, Keio University, 3-14-1 Hiyoshi, Kohoku-ku, Yokohama, Kanagawa 223-8522, Japan.
Taku HasobeDepartment of Chemistry, Faculty of Science and Technology, Keio University, 3-14-1 Hiyoshi, Kohoku-ku, Yokohama, Kanagawa 223-8522, Japan.ORCID 0000-0002-4728-9767
Takanori FukushimaLaboratory for Chemistry and Life Science, Institute of Innovative Research, Tokyo Institute of Technology, 4259 Nagatsuta, Midori-ku, Yokohama 226-8501, Japan.ORCID 0000-0001-5586-9238

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Molecular assemblies featuring two-dimensionality have attracted increasing attention, whereas such structures are difficult to construct simply relying on spontaneous molecular assembly. Here, we present two-dimensional assemblies of acene chromophores achieved using a tripodal triptycene supramolecular scaffold, which have been shown to exhibit a strong ability to assemble molecular and polymer motifs two-dimensionally. We designed pentacene and anthracene derivatives sandwiched by two triptycene units. These compounds assemble into expected two-dimensional structures, with the pentacene chromophores having both sufficient overlap to cause singlet fission and space for conformational change to facilitate the dissociation of a triplet pair into free triplets, which is not the case for the anthracene analog. Detailed spectroscopic analysis revealed that the pentacene chromophore in the assembly undergoes singlet fission with a quantum yield of 88 ± 5%, giving rise to triplet pairs, from which free triplets are efficiently generated (Φ

Identifiers

PMID39270030
PMCPMC11397492

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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.