Evidence map›Paper›PMID 34084431›Full record

ArticleChemical science2021

Donor-acceptor-acceptor-type near-infrared fluorophores that contain dithienophosphole oxide and boryl groups: effect of the boryl group on the nonradiative decay.

Yoshiaki Sugihara, Naoto Inai, Masayasu Taki, Thomas Baumgartner, Ryosuke Kawakami, Takashi Saitou, Takeshi Imamura, Takeshi Yanai, Shigehiro Yamaguchi

Open access · diamondAbstract read
In one paragraph

Article in Chemical science, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
2.9field-weighted citation impact, top 9% of its field
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

9 citing papers in PubMed, 45 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Luminescent 1RSC advances · 2022
    Article
  8. Article
  9. 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

9 authors at 3 institutions in 3 countries.

Yoshiaki SugiharaDepartment of Chemistry, Graduate School of Science, Integrated Research Consortium on Chemical Sciences (IRCCS), Nagoya University Furo, Chikusa Nagoya 464-8602 Japan yanait@chem.nagoya-u.ac.jp yamaguchi@chem.nagoya-u.ac.jp.
Naoto InaiDepartment of Chemistry, Graduate School of Science, Integrated Research Consortium on Chemical Sciences (IRCCS), Nagoya University Furo, Chikusa Nagoya 464-8602 Japan yanait@chem.nagoya-u.ac.jp yamaguchi@chem.nagoya-u.ac.jp.
Masayasu TakiInstitute of Transformative Bio-Molecules (WPI-ITbM), Nagoya University Furo, Chikusa Nagoya 464-8602 Japan.ORCID https://orcid.org/0000-0003-2185-4593
Thomas BaumgartnerDepartment of Chemistry, York University 4700 Keele St. Toronto ON M3J 1P3 Canada.ORCID https://orcid.org/0000-0001-8066-0559
Ryosuke KawakamiDepartment of Molecular Medicine for Pathogenesis, Graduate School of Medicine, Ehime University Shitsukawa Toon City Ehime 791-0295 Japan.
Takashi SaitouDepartment of Molecular Medicine for Pathogenesis, Graduate School of Medicine, Ehime University Shitsukawa Toon City Ehime 791-0295 Japan.
Takeshi ImamuraDepartment of Molecular Medicine for Pathogenesis, Graduate School of Medicine, Ehime University Shitsukawa Toon City Ehime 791-0295 Japan.
Takeshi YanaiDepartment of Chemistry, Graduate School of Science, Integrated Research Consortium on Chemical Sciences (IRCCS), Nagoya University Furo, Chikusa Nagoya 464-8602 Japan yanait@chem.nagoya-u.ac.jp yamaguchi@chem.nagoya-u.ac.jp.ORCID https://orcid.org/0000-0003-3933-8546
Shigehiro YamaguchiDepartment of Chemistry, Graduate School of Science, Integrated Research Consortium on Chemical Sciences (IRCCS), Nagoya University Furo, Chikusa Nagoya 464-8602 Japan yanait@chem.nagoya-u.ac.jp yamaguchi@chem.nagoya-u.ac.jp.ORCID https://orcid.org/0000-0003-0072-8969
Nagoya University · JPOrganogenesis (United States) · USToronto Public Health · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The use of donor-π-acceptor (D-π-A) skeletons is an effective strategy for the design of fluorophores with red-shifted emission. In particular, the use of amino and boryl moieties as the electron-donating and -accepting groups, respectively, can produce dyes that exhibit high fluorescence and solvatochromism. Herein, we introduce a dithienophosphole

Identifiers

PMID34084431
PMCPMC8115064
OpenAlexW3139307709

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

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.