<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Li G</submitter><funding>Natural Science Foundation of Jiangsu Province</funding><pagination>566</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9864372</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>28(2)</volume><pubmed_abstract>Five novel bis-tridentate Ir(III) complexes (&lt;b>Ir-1&lt;/b>-&lt;b>Ir-5&lt;/b>) incorporating versatile N^N^C ligands and a N^C^N ligand (1,3-di(2-pyridyl)-4,6-dimethylbenzene) were synthesized. With the combination of experimental and theoretical methods, their steady and transient state characteristics were researched scientifically. The UV-visible absorption spectra show that the broadband charge transfer absorbance of those bis-tridentate Ir(III) complexes can reach 550 nm, all of these complexes reveal the long-lasting phosphorescent emission. Because the excited-state absorption is more powerful than the ground-state absorption, a sturdy reverse saturable absorption (RSA) process can ensue in the visible and near-infrared regions when the complexes are exposed to a 532 nm laser. Therefore, the optical power limiting (OPL) effect follows the trend: &lt;b>Ir-5&lt;/b> &amp;gt; &lt;b>Ir-4&lt;/b> ≈ &lt;b>Ir-3&lt;/b> &amp;gt; &lt;b>Ir-2&lt;/b> &amp;gt; &lt;b>Ir-1&lt;/b>. Generally speaking, the expansion of π-conjugation and the introduction of electron donating/withdrawing groups on the N^N^C ligand could effectively elevate the OPL effect. Therefore, these octahedral bis-tridentate Ir(III) complexes might be exploited as potential OPL materials.</pubmed_abstract><journal>Molecules (Basel, Switzerland)</journal><pubmed_title>Synthesis, Photophysics and Tunable Reverse Saturable Absorption of Bis-Tridentate Iridium(III) Complexes via Modification on Diimine Ligand.</pubmed_title><pmcid>PMC9864372</pmcid><funding_grant_id>BK20220351</funding_grant_id><pubmed_authors>Li G</pubmed_authors><pubmed_authors>Jiang Z</pubmed_authors><pubmed_authors>Tang M</pubmed_authors><pubmed_authors>Jiang X</pubmed_authors><pubmed_authors>Liu R</pubmed_authors><pubmed_authors>Zhu H</pubmed_authors><pubmed_authors>Tu H</pubmed_authors><pubmed_authors>Zhu S</pubmed_authors></additional><is_claimable>false</is_claimable><name>Synthesis, Photophysics and Tunable Reverse Saturable Absorption of Bis-Tridentate Iridium(III) Complexes via Modification on Diimine Ligand.</name><description>Five novel bis-tridentate Ir(III) complexes (&lt;b>Ir-1&lt;/b>-&lt;b>Ir-5&lt;/b>) incorporating versatile N^N^C ligands and a N^C^N ligand (1,3-di(2-pyridyl)-4,6-dimethylbenzene) were synthesized. With the combination of experimental and theoretical methods, their steady and transient state characteristics were researched scientifically. The UV-visible absorption spectra show that the broadband charge transfer absorbance of those bis-tridentate Ir(III) complexes can reach 550 nm, all of these complexes reveal the long-lasting phosphorescent emission. Because the excited-state absorption is more powerful than the ground-state absorption, a sturdy reverse saturable absorption (RSA) process can ensue in the visible and near-infrared regions when the complexes are exposed to a 532 nm laser. Therefore, the optical power limiting (OPL) effect follows the trend: &lt;b>Ir-5&lt;/b> &amp;gt; &lt;b>Ir-4&lt;/b> ≈ &lt;b>Ir-3&lt;/b> &amp;gt; &lt;b>Ir-2&lt;/b> &amp;gt; &lt;b>Ir-1&lt;/b>. Generally speaking, the expansion of π-conjugation and the introduction of electron donating/withdrawing groups on the N^N^C ligand could effectively elevate the OPL effect. Therefore, these octahedral bis-tridentate Ir(III) complexes might be exploited as potential OPL materials.</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Jan</publication><modification>2025-04-26T00:41:27.73Z</modification><creation>2025-04-06T09:48:21.734Z</creation></dates><accession>S-EPMC9864372</accession><cross_references><pubmed>36677626</pubmed><doi>10.3390/molecules28020566</doi></cross_references></HashMap>