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    <subfield code="2">doi</subfield>
    <subfield code="a">10.1021/acs.inorgchem.9b03509</subfield>
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    <subfield code="2">sideral</subfield>
    <subfield code="a">117390</subfield>
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    <subfield code="a">ART-2020-117390</subfield>
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    <subfield code="a">eng</subfield>
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  <datafield tag="100" ind1=" " ind2=" ">
    <subfield code="a">Boudreault, Pierre-Luc T.</subfield>
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  <datafield tag="245" ind1=" " ind2=" ">
    <subfield code="a">Preparation and Photophysical Properties of Bis(tridentate) Iridium(III) Emitters: Pincer Coordination of 2, 6-Di(2-pyridyl)phenyl</subfield>
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    <subfield code="c">2020</subfield>
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    <subfield code="a">The way to prepare molecular emitters [5t + 4t'] of iridium(III) with a 5t ligand derived from the abstraction of the hydrogen atom at position 2 of the aryl group of 1, 3-di(2-pyridyl)benzene (dpybH) is shown. In addition, the photophysical properties of the new emitters are compared with those of their counterparts resulting from the deprotonation of 1, 3-di(2-pyridyl)-4, 6-dimethylbenzene (dpyMebH), at the same position, which are also synthesized. Treatment of 0.5 equiv of the dimer [Ir(µ-Cl)(¿2-COE)2]2 (COE = cyclooctene) with 1.0 equiv of Hg(dpyb)Cl leads to the iridium(III) derivative IrCl2{¿3-N, C, N-(dpyb)}(¿2-COE) (3), which reacts with 2-(1H-imidazol-2-yl)-6-phenylpyridine (HNImpyC6H5) and 2-(1H-benzimidazol-2-yl)-6-phenylpyridine (HNBzimpyC6H5) in the presence of Na2CO3 to give Ir{¿3-C, N, N-(NImpyC6H4)}{¿3-N, C, N-(dpyb)} (4) and Ir{¿3-C, N, N-(NBzimpyC6H4)}{¿3-N, C, N-(dpyb)} (5), respectively. Similar reactions of the Williams''s dimer [IrCl(µ-Cl){¿3-N, C, N-(dpyMeb)}]2 with HNImpyC6H5 and HNBzimpyC6H5 in the presence of Na2CO3 afford the dimethylated counterparts Ir{¿3-C, N, N-(NImpyC6H4)}{¿3-N, C, N-(dpyMeb)} (6) and Ir{¿3-C, N, N-(NBzimpyC6H4)}{¿3-N, C, N-(dpyMeb)} (7), whereas 2-(6-phenylpyridine-2-yl)-1H-indole (HIndpyC6H5) initially gives IrH{¿2-N, N-(IndpyC6H5)}{¿3-N, C, N-(dpyMeb)} (8) and subsequently Ir{¿3-C, N, N-(IndpyC6H4)}{¿3-N, C, N-(dpyMeb)} (9). Complexes 4-7 are phosphorescent green emitters (¿em 490-550 nm), whereas 9 is greenish yellow emissive (¿em 547-624 nm). They display lifetimes in the range 0.5-9.7 µs and quantum yields in both doped poly(methyl)methacrylate films and in 2-methyltetrahydrofuran at room temperature depending upon the ligands: 0.5-0.7 for 6 and 7, about 0.4 for 4 and 5, and 0.3-0.2 for 9.</subfield>
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    <subfield code="a">Access copy available to the general public</subfield>
    <subfield code="f">Unrestricted</subfield>
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  <datafield tag="536" ind1=" " ind2=" ">
    <subfield code="9">info:eu-repo/grantAgreement/ES/DGA/E06-17R</subfield>
    <subfield code="9">info:eu-repo/grantAgreement/ES/DGA/LMP148-18</subfield>
    <subfield code="9">info:eu-repo/grantAgreement/ES/MINECO-AEI-FEDER/CTQ2017-82935-P</subfield>
    <subfield code="9">info:eu-repo/grantAgreement/ES/MINECO-AEI-FEDER/RED2018-102387-T</subfield>
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    <subfield code="9">info:eu-repo/semantics/openAccess</subfield>
    <subfield code="a">All rights reserved</subfield>
    <subfield code="u">http://www.europeana.eu/rights/rr-f/</subfield>
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    <subfield code="a">5.165</subfield>
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    <subfield code="b">5 / 45 = 0.111</subfield>
    <subfield code="c">2020</subfield>
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    <subfield code="a">1.348</subfield>
    <subfield code="b">2020</subfield>
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  <datafield tag="593" ind1=" " ind2=" ">
    <subfield code="a">Chemistry (miscellaneous)</subfield>
    <subfield code="c">2020</subfield>
    <subfield code="d">Q1</subfield>
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  <datafield tag="593" ind1=" " ind2=" ">
    <subfield code="a">Physical and Theoretical Chemistry</subfield>
    <subfield code="c">2020</subfield>
    <subfield code="d">Q1</subfield>
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  <datafield tag="593" ind1=" " ind2=" ">
    <subfield code="a">Inorganic Chemistry</subfield>
    <subfield code="c">2020</subfield>
    <subfield code="d">Q1</subfield>
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  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Esteruelas, Miguel A.</subfield>
    <subfield code="0">(orcid)0000-0002-4829-7590</subfield>
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    <subfield code="a">Gómez-Bautista, Daniel</subfield>
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    <subfield code="a">Izquierdo, Susana</subfield>
    <subfield code="0">(orcid)0000-0002-6608-1910</subfield>
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  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">López, Ana M.</subfield>
    <subfield code="u">Universidad de Zaragoza</subfield>
    <subfield code="0">(orcid)0000-0001-7183-4975</subfield>
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  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Oñate, Enrique</subfield>
    <subfield code="0">(orcid)0000-0003-2094-719X</subfield>
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    <subfield code="a">Raga, Esther</subfield>
    <subfield code="0">(orcid)0000-0001-8609-7947</subfield>
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    <subfield code="a">Tsai, Jui-Yi</subfield>
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    <subfield code="1">2010</subfield>
    <subfield code="2">760</subfield>
    <subfield code="a">Universidad de Zaragoza</subfield>
    <subfield code="b">Dpto. Química Inorgánica</subfield>
    <subfield code="c">Área Química Inorgánica</subfield>
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    <subfield code="g">59, 6 (2020), 3838-3849</subfield>
    <subfield code="p">Inorg. chem.</subfield>
    <subfield code="t">Inorganic Chemistry</subfield>
    <subfield code="x">0020-1669</subfield>
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