Preparation of Phosphorescent Iridium(III) Complexes with a Dianionic C,C,C,C-Tetradentate Ligand

The preparation and photophysical properties of heteroleptic iridium­(III) complexes containing a dianionic C,C,C,C-tetradentate ligand and a cyclometalated phenylpyridine group are described. Complex [Ir­(μ-OMe)­(COD)]2 (1, COD = 1,5-cyclooctadiene) reacts with 1,1-diphenyl-3,3-butylenediimidazoliu...

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Veröffentlicht in:Inorganic chemistry 2018-04, Vol.57 (7), p.3720-3730
Hauptverfasser: Esteruelas, Miguel A, López, Ana M, Oñate, Enrique, San-Torcuato, Ainhoa, Tsai, Jui-Yi, Xia, Chuanjun
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container_end_page 3730
container_issue 7
container_start_page 3720
container_title Inorganic chemistry
container_volume 57
creator Esteruelas, Miguel A
López, Ana M
Oñate, Enrique
San-Torcuato, Ainhoa
Tsai, Jui-Yi
Xia, Chuanjun
description The preparation and photophysical properties of heteroleptic iridium­(III) complexes containing a dianionic C,C,C,C-tetradentate ligand and a cyclometalated phenylpyridine group are described. Complex [Ir­(μ-OMe)­(COD)]2 (1, COD = 1,5-cyclooctadiene) reacts with 1,1-diphenyl-3,3-butylenediimidazolium iodide ([PhIm­(CH2)4­ImPh]­I2), in the presence NaOtBu, to give [Ir­(μ-I)­{κ4-C,C,C,C-[C6H4Im­(CH2)4­ImC6H4]}]2 (2), which leads to {[Ir­{κ4-C,C,C,C-[C6H4Im­(CH2)4­ImC6H4]}]2­(μ-OH)­(μ-OMe)} (3) by treatment first with silver trifluoromethanesulfonate (AgOTf) in acetone–dichloromethane and subsequently with KOH in methanol. The reaction of 2 with AgOTf and acetonitrile affords the bis­(solvento) complex [Ir­{κ4-C,C,C,C-[C6H4Im­(CH2)4­ImC6H4]}­(CH3CN)2]­OTf (4). The latter promotes the pyridyl-supported heterolytic ortho-CH bond activation of the phenyl group of 2-phenylpyridine, 2-(2,4-difluorophenyl)­pyridine, 2-(p-tolyl)­pyridine, and 5-methyl-2-phenylpyridine to yield Ir­{κ4-C,C,C,C-[C6H4Im­(CH2)4­ImC6H4]}­{κ2-C,N-[Ar-py]} (Ar-py = C6H4-py (5), C6H2F2-py (6), C6H3Me-py (7), C6H4-Mepy (8)) using (piperidinomethyl)­polystyrene as an external base. Complexes 5–8 are blue-green emitters, which display short lifetimes (0.6–4.8 μs) and quantum yields close to unity in both doped poly­(methyl methacrylate) films at 5 wt % and in 2-methyltetrahydrofuran at room temperature.
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Complex [Ir­(μ-OMe)­(COD)]2 (1, COD = 1,5-cyclooctadiene) reacts with 1,1-diphenyl-3,3-butylenediimidazolium iodide ([PhIm­(CH2)4­ImPh]­I2), in the presence NaOtBu, to give [Ir­(μ-I)­{κ4-C,C,C,C-[C6H4Im­(CH2)4­ImC6H4]}]2 (2), which leads to {[Ir­{κ4-C,C,C,C-[C6H4Im­(CH2)4­ImC6H4]}]2­(μ-OH)­(μ-OMe)} (3) by treatment first with silver trifluoromethanesulfonate (AgOTf) in acetone–dichloromethane and subsequently with KOH in methanol. The reaction of 2 with AgOTf and acetonitrile affords the bis­(solvento) complex [Ir­{κ4-C,C,C,C-[C6H4Im­(CH2)4­ImC6H4]}­(CH3CN)2]­OTf (4). The latter promotes the pyridyl-supported heterolytic ortho-CH bond activation of the phenyl group of 2-phenylpyridine, 2-(2,4-difluorophenyl)­pyridine, 2-(p-tolyl)­pyridine, and 5-methyl-2-phenylpyridine to yield Ir­{κ4-C,C,C,C-[C6H4Im­(CH2)4­ImC6H4]}­{κ2-C,N-[Ar-py]} (Ar-py = C6H4-py (5), C6H2F2-py (6), C6H3Me-py (7), C6H4-Mepy (8)) using (piperidinomethyl)­polystyrene as an external base. Complexes 5–8 are blue-green emitters, which display short lifetimes (0.6–4.8 μs) and quantum yields close to unity in both doped poly­(methyl methacrylate) films at 5 wt % and in 2-methyltetrahydrofuran at room temperature.</description><identifier>ISSN: 0020-1669</identifier><identifier>EISSN: 1520-510X</identifier><identifier>DOI: 10.1021/acs.inorgchem.7b02993</identifier><identifier>PMID: 29537827</identifier><language>eng</language><publisher>United States: American Chemical Society</publisher><ispartof>Inorganic chemistry, 2018-04, Vol.57 (7), p.3720-3730</ispartof><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a398t-a347838699551ee30a7dc638122564b4f7b738bc3e102581c4ba3a1567bd72d33</citedby><cites>FETCH-LOGICAL-a398t-a347838699551ee30a7dc638122564b4f7b738bc3e102581c4ba3a1567bd72d33</cites><orcidid>0000-0002-4829-7590 ; 0000-0002-8516-9985 ; 0000-0003-2094-719X ; 0000-0003-1709-3672 ; 0000-0001-6841-6027 ; 0000-0001-7183-4975</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://pubs.acs.org/doi/pdf/10.1021/acs.inorgchem.7b02993$$EPDF$$P50$$Gacs$$H</linktopdf><linktohtml>$$Uhttps://pubs.acs.org/doi/10.1021/acs.inorgchem.7b02993$$EHTML$$P50$$Gacs$$H</linktohtml><link.rule.ids>314,777,781,2752,27057,27905,27906,56719,56769</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29537827$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Esteruelas, Miguel A</creatorcontrib><creatorcontrib>López, Ana M</creatorcontrib><creatorcontrib>Oñate, Enrique</creatorcontrib><creatorcontrib>San-Torcuato, Ainhoa</creatorcontrib><creatorcontrib>Tsai, Jui-Yi</creatorcontrib><creatorcontrib>Xia, Chuanjun</creatorcontrib><title>Preparation of Phosphorescent Iridium(III) Complexes with a Dianionic C,C,C,C-Tetradentate Ligand</title><title>Inorganic chemistry</title><addtitle>Inorg. Chem</addtitle><description>The preparation and photophysical properties of heteroleptic iridium­(III) complexes containing a dianionic C,C,C,C-tetradentate ligand and a cyclometalated phenylpyridine group are described. Complex [Ir­(μ-OMe)­(COD)]2 (1, COD = 1,5-cyclooctadiene) reacts with 1,1-diphenyl-3,3-butylenediimidazolium iodide ([PhIm­(CH2)4­ImPh]­I2), in the presence NaOtBu, to give [Ir­(μ-I)­{κ4-C,C,C,C-[C6H4Im­(CH2)4­ImC6H4]}]2 (2), which leads to {[Ir­{κ4-C,C,C,C-[C6H4Im­(CH2)4­ImC6H4]}]2­(μ-OH)­(μ-OMe)} (3) by treatment first with silver trifluoromethanesulfonate (AgOTf) in acetone–dichloromethane and subsequently with KOH in methanol. The reaction of 2 with AgOTf and acetonitrile affords the bis­(solvento) complex [Ir­{κ4-C,C,C,C-[C6H4Im­(CH2)4­ImC6H4]}­(CH3CN)2]­OTf (4). The latter promotes the pyridyl-supported heterolytic ortho-CH bond activation of the phenyl group of 2-phenylpyridine, 2-(2,4-difluorophenyl)­pyridine, 2-(p-tolyl)­pyridine, and 5-methyl-2-phenylpyridine to yield Ir­{κ4-C,C,C,C-[C6H4Im­(CH2)4­ImC6H4]}­{κ2-C,N-[Ar-py]} (Ar-py = C6H4-py (5), C6H2F2-py (6), C6H3Me-py (7), C6H4-Mepy (8)) using (piperidinomethyl)­polystyrene as an external base. Complexes 5–8 are blue-green emitters, which display short lifetimes (0.6–4.8 μs) and quantum yields close to unity in both doped poly­(methyl methacrylate) films at 5 wt % and in 2-methyltetrahydrofuran at room temperature.</description><issn>0020-1669</issn><issn>1520-510X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><recordid>eNqFkFtLwzAYhoMobk5_gpJLBTtzaJr2UuqpMHAXE7wLaZuuGW1Tkxb135u5uVv5IMnF-3zhfQC4xGiOEcF3snBz3Rm7LmrVznmOSJLQIzDFjKCAYfR-DKYI-TeOomQCzpzbIIQSGkanYEISRnlM-BTIpVW9tHLQpoOmgsvauL42VrlCdQPMrC712F5nWXYDU9P2jfpSDn7qoYYSPmjZeU4XML39nWClBitLT8pBwYVey648ByeVbJy62N8z8Pb0uEpfgsXrc5beLwJJk3jwZ8hjGkdJwhhWiiLJyyKiMSaERWEeVjznNM4Lqnx9FuMizCWVmEU8LzkpKZ2B693e3pqPUblBtNqXaBrZKTM6QRAO_cSc-yjbRQtrnLOqEr3VrbTfAiOxtSu8XXGwK_Z2PXe1_2LMW1UeqD-dPoB3gS2_MaPtfON_lv4AiCKJLg</recordid><startdate>20180402</startdate><enddate>20180402</enddate><creator>Esteruelas, Miguel A</creator><creator>López, Ana M</creator><creator>Oñate, Enrique</creator><creator>San-Torcuato, Ainhoa</creator><creator>Tsai, Jui-Yi</creator><creator>Xia, Chuanjun</creator><general>American Chemical Society</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-4829-7590</orcidid><orcidid>https://orcid.org/0000-0002-8516-9985</orcidid><orcidid>https://orcid.org/0000-0003-2094-719X</orcidid><orcidid>https://orcid.org/0000-0003-1709-3672</orcidid><orcidid>https://orcid.org/0000-0001-6841-6027</orcidid><orcidid>https://orcid.org/0000-0001-7183-4975</orcidid></search><sort><creationdate>20180402</creationdate><title>Preparation of Phosphorescent Iridium(III) Complexes with a Dianionic C,C,C,C-Tetradentate Ligand</title><author>Esteruelas, Miguel A ; López, Ana M ; Oñate, Enrique ; San-Torcuato, Ainhoa ; Tsai, Jui-Yi ; Xia, Chuanjun</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a398t-a347838699551ee30a7dc638122564b4f7b738bc3e102581c4ba3a1567bd72d33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Esteruelas, Miguel A</creatorcontrib><creatorcontrib>López, Ana M</creatorcontrib><creatorcontrib>Oñate, Enrique</creatorcontrib><creatorcontrib>San-Torcuato, Ainhoa</creatorcontrib><creatorcontrib>Tsai, Jui-Yi</creatorcontrib><creatorcontrib>Xia, Chuanjun</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Inorganic chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Esteruelas, Miguel A</au><au>López, Ana M</au><au>Oñate, Enrique</au><au>San-Torcuato, Ainhoa</au><au>Tsai, Jui-Yi</au><au>Xia, Chuanjun</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Preparation of Phosphorescent Iridium(III) Complexes with a Dianionic C,C,C,C-Tetradentate Ligand</atitle><jtitle>Inorganic chemistry</jtitle><addtitle>Inorg. Chem</addtitle><date>2018-04-02</date><risdate>2018</risdate><volume>57</volume><issue>7</issue><spage>3720</spage><epage>3730</epage><pages>3720-3730</pages><issn>0020-1669</issn><eissn>1520-510X</eissn><abstract>The preparation and photophysical properties of heteroleptic iridium­(III) complexes containing a dianionic C,C,C,C-tetradentate ligand and a cyclometalated phenylpyridine group are described. Complex [Ir­(μ-OMe)­(COD)]2 (1, COD = 1,5-cyclooctadiene) reacts with 1,1-diphenyl-3,3-butylenediimidazolium iodide ([PhIm­(CH2)4­ImPh]­I2), in the presence NaOtBu, to give [Ir­(μ-I)­{κ4-C,C,C,C-[C6H4Im­(CH2)4­ImC6H4]}]2 (2), which leads to {[Ir­{κ4-C,C,C,C-[C6H4Im­(CH2)4­ImC6H4]}]2­(μ-OH)­(μ-OMe)} (3) by treatment first with silver trifluoromethanesulfonate (AgOTf) in acetone–dichloromethane and subsequently with KOH in methanol. The reaction of 2 with AgOTf and acetonitrile affords the bis­(solvento) complex [Ir­{κ4-C,C,C,C-[C6H4Im­(CH2)4­ImC6H4]}­(CH3CN)2]­OTf (4). The latter promotes the pyridyl-supported heterolytic ortho-CH bond activation of the phenyl group of 2-phenylpyridine, 2-(2,4-difluorophenyl)­pyridine, 2-(p-tolyl)­pyridine, and 5-methyl-2-phenylpyridine to yield Ir­{κ4-C,C,C,C-[C6H4Im­(CH2)4­ImC6H4]}­{κ2-C,N-[Ar-py]} (Ar-py = C6H4-py (5), C6H2F2-py (6), C6H3Me-py (7), C6H4-Mepy (8)) using (piperidinomethyl)­polystyrene as an external base. Complexes 5–8 are blue-green emitters, which display short lifetimes (0.6–4.8 μs) and quantum yields close to unity in both doped poly­(methyl methacrylate) films at 5 wt % and in 2-methyltetrahydrofuran at room temperature.</abstract><cop>United States</cop><pub>American Chemical Society</pub><pmid>29537827</pmid><doi>10.1021/acs.inorgchem.7b02993</doi><tpages>11</tpages><orcidid>https://orcid.org/0000-0002-4829-7590</orcidid><orcidid>https://orcid.org/0000-0002-8516-9985</orcidid><orcidid>https://orcid.org/0000-0003-2094-719X</orcidid><orcidid>https://orcid.org/0000-0003-1709-3672</orcidid><orcidid>https://orcid.org/0000-0001-6841-6027</orcidid><orcidid>https://orcid.org/0000-0001-7183-4975</orcidid><oa>free_for_read</oa></addata></record>
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title Preparation of Phosphorescent Iridium(III) Complexes with a Dianionic C,C,C,C-Tetradentate Ligand
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