Evidence map›Paper›PMID 36500349›Full record

ArticleMolecules (Basel, Switzerland)2022

Synthetic Exploration of Bis(phenolate) Aza-BODIPYs and Heavier Group 13 Chelates.

Aiden M Lane, Ny T C Luong, Jordan C Kelly, Martin J Neal, Jeremiah Jamrom, Aaron J Bloomfield, Paul A Lummis, Thomas D Montgomery, Daniel T Chase

Abstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2022. 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. Beyond BODIPY: dipyrrin complexes of P-block elements.Journal of coordination chemistry · 2025
    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.

Aiden M LaneDepartment of Chemistry and Biochemistry, St. Mary's College of Maryland, St. Mary's City, MD 20686, USA.
Ny T C LuongDepartment of Chemistry and Biochemistry, St. Mary's College of Maryland, St. Mary's City, MD 20686, USA.
Jordan C KellyDepartment of Chemistry and Biochemistry, Duquesne University, Pittsburg, PA 15282, USA.ORCID 0000-0002-6539-9169
Martin J NealDepartment of Chemistry and Biochemistry, Duquesne University, Pittsburg, PA 15282, USA.
Jeremiah JamromDepartment of Chemistry and Biochemistry, Duquesne University, Pittsburg, PA 15282, USA.
Aaron J BloomfieldDepartment of Chemistry and Biochemistry, Duquesne University, Pittsburg, PA 15282, USA.
Paul A LummisDepartment of Chemistry and Biochemistry, Duquesne University, Pittsburg, PA 15282, USA.
Thomas D MontgomeryDepartment of Chemistry and Biochemistry, Duquesne University, Pittsburg, PA 15282, USA.ORCID 0000-0002-6526-8564
Daniel T ChaseDepartment of Chemistry and Biochemistry, St. Mary's College of Maryland, St. Mary's City, MD 20686, USA.ORCID 0000-0002-4957-0261

Funding

American Chemical Society Petroleum Research Fund ACS-PRF 61563-UR3National Science Foundation CHE-1726824, CHE-1950585
6 · The paper itself

Abstract

A series of boron, aluminum, gallium, and indium chelates containing the underexplored bis(phenolate) aza-dipyrromethene (aza-DIPY) core were prepared. These compounds were found to possess near-infrared absorption and emission profiles in the 710 to 770 nm domain and exhibit quantum yield values up to 14%. X-ray diffraction analysis revealed that heavier group 13 bis(phenolate) aza-DIPY chelates possessed octahedral geometries with either THF or pyridine groups occupying the axial positions as opposed to the tetrahedral geometry of the boron chelate.

Indexed as

Boron CompoundsFluorescent DyesChelating AgentsCrystallography, X-RayPhenolsazaBDPBA compoundBoron CompoundsChelating AgentsFluorescent DyesPhenolsaza-ALDIPYaza-BODIPYaza-DIPYaza-GADIPYaza-INDIPY

Identifiers

PMID36500349
PMCPMC9737893

What OpenQuestion holds

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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.