<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>27(23)</volume><submitter>Lane AM</submitter><pubmed_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.</pubmed_abstract><journal>Molecules (Basel, Switzerland)</journal><pagination>8256</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9737893</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Synthetic Exploration of Bis(phenolate) Aza-BODIPYs and Heavier Group 13 Chelates.</pubmed_title><pmcid>PMC9737893</pmcid><pubmed_authors>Lummis PA</pubmed_authors><pubmed_authors>Luong NTC</pubmed_authors><pubmed_authors>Neal MJ</pubmed_authors><pubmed_authors>Montgomery TD</pubmed_authors><pubmed_authors>Kelly JC</pubmed_authors><pubmed_authors>Jamrom J</pubmed_authors><pubmed_authors>Lane AM</pubmed_authors><pubmed_authors>Chase DT</pubmed_authors><pubmed_authors>Bloomfield AJ</pubmed_authors></additional><is_claimable>false</is_claimable><name>Synthetic Exploration of Bis(phenolate) Aza-BODIPYs and Heavier Group 13 Chelates.</name><description>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.</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Nov</publication><modification>2025-04-20T03:35:19.988Z</modification><creation>2025-04-20T03:35:19.988Z</creation></dates><accession>S-EPMC9737893</accession><cross_references><pubmed>36500349</pubmed><doi>10.3390/molecules27238256</doi></cross_references></HashMap>