Generation of Blue Light-Emitting Zinc Complexes by Band-Gap Control of the Oxazolylphenolate Ligand System: Syntheses, Characterizations, and Organic Light Emitting Device Applications of 4-Coordinated Bis(2-oxazolylphenolate) Zinc(II) Complexes
Color-tunable Zn(II) complexes of the type Zn(N,O-OPhOxZArX)2 (5), where the ligand consists of an oxazolylphenolate ion connected at the 4-position by a 2,4-substituted aryl functional group with X = NMe2 a, OMe b, Ph c, Cl d, F2 e, and CN f, were prepared. X-ray structural studies of 5a, 5b, and 5...
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description | Color-tunable Zn(II) complexes of the type Zn(N,O-OPhOxZArX)2 (5), where the ligand consists of an oxazolylphenolate ion connected at the 4-position by a 2,4-substituted aryl functional group with X = NMe2 a, OMe b, Ph c, Cl d, F2 e, and CN f, were prepared. X-ray structural studies of 5a, 5b, and 5e showed that a zinc atom was positioned in a distorted tetrahedral coordination environment created by two oxazolylphenolate ligands with N,O-chelation. Hammet plots of absorption and emission maxima, respectively, in UV and photoluminescence (PL) spectra with respect to electron-donating and electron-withdrawing groups of the substituents indicate a direct correlation between the highest occupied molecular orbital (HOMO)−lowest unoccupied molecular orbital (LUMO) band gaps and electronic alterations at the ligand sites. A similar correlation was also observed for the reduction and oxidation potentials in cyclic voltammograms (CVs). A gradual increase in the HOMO−LUMO band gap is seen from electron-donating to electron-withdrawing functional groups, NMe2 < OMe < Ph < Cl < F2 < CN. An emission peak with a maximum at 455 nm was achieved when the most electron-withdrawing group (cyano) was applied to the oxazolylphenolate ligand system. Density-functional theory (DFT) calculations on the HOMOs and LUMOs for this series lead to a conclusion similar to that arrived at from a blue-shift trend observed in UV data and trends in the CVs. The 4-coordinated zinc complex (5c) was shown to be a potential blue-emitting material, exhibiting a maximum efficiency of 1720 cd/m2 at 17 V with 0.3 cd/A in a multilayered device structure of ITO/NPB/5c/BCP/Alq3/LiF/Al. On the basis of the low HOMO level of this series, 5a was tested as a hole-transporting material; this resulted in the successful fabrication of a multilayered device of ITO/5a/DPVBI/Alq3/LiF/Al with an efficiency of 7000 cd/m2 at 13 V with 2.0 cd/A. |
doi_str_mv | 10.1021/ic702491j |
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X-ray structural studies of 5a, 5b, and 5e showed that a zinc atom was positioned in a distorted tetrahedral coordination environment created by two oxazolylphenolate ligands with N,O-chelation. Hammet plots of absorption and emission maxima, respectively, in UV and photoluminescence (PL) spectra with respect to electron-donating and electron-withdrawing groups of the substituents indicate a direct correlation between the highest occupied molecular orbital (HOMO)−lowest unoccupied molecular orbital (LUMO) band gaps and electronic alterations at the ligand sites. A similar correlation was also observed for the reduction and oxidation potentials in cyclic voltammograms (CVs). A gradual increase in the HOMO−LUMO band gap is seen from electron-donating to electron-withdrawing functional groups, NMe2 < OMe < Ph < Cl < F2 < CN. An emission peak with a maximum at 455 nm was achieved when the most electron-withdrawing group (cyano) was applied to the oxazolylphenolate ligand system. Density-functional theory (DFT) calculations on the HOMOs and LUMOs for this series lead to a conclusion similar to that arrived at from a blue-shift trend observed in UV data and trends in the CVs. The 4-coordinated zinc complex (5c) was shown to be a potential blue-emitting material, exhibiting a maximum efficiency of 1720 cd/m2 at 17 V with 0.3 cd/A in a multilayered device structure of ITO/NPB/5c/BCP/Alq3/LiF/Al. On the basis of the low HOMO level of this series, 5a was tested as a hole-transporting material; this resulted in the successful fabrication of a multilayered device of ITO/5a/DPVBI/Alq3/LiF/Al with an efficiency of 7000 cd/m2 at 13 V with 2.0 cd/A.</description><identifier>ISSN: 0020-1669</identifier><identifier>EISSN: 1520-510X</identifier><identifier>DOI: 10.1021/ic702491j</identifier><identifier>PMID: 18543905</identifier><language>eng</language><publisher>United States: American Chemical Society</publisher><ispartof>Inorganic chemistry, 2008-07, Vol.47 (13), p.5666-5676</ispartof><rights>Copyright © 2008 American Chemical Society</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a332t-e1dab504cc8937ae6ba8aa0c72e5bac34847ce09b8c9dc48121c8a6d51dcef533</citedby><cites>FETCH-LOGICAL-a332t-e1dab504cc8937ae6ba8aa0c72e5bac34847ce09b8c9dc48121c8a6d51dcef533</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://pubs.acs.org/doi/pdf/10.1021/ic702491j$$EPDF$$P50$$Gacs$$H</linktopdf><linktohtml>$$Uhttps://pubs.acs.org/doi/10.1021/ic702491j$$EHTML$$P50$$Gacs$$H</linktohtml><link.rule.ids>314,776,780,2752,27053,27901,27902,56713,56763</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18543905$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Son, Ho-Jin</creatorcontrib><creatorcontrib>Han, Won-Sik</creatorcontrib><creatorcontrib>Chun, Ji-Yun</creatorcontrib><creatorcontrib>Kang, Byoung-Kook</creatorcontrib><creatorcontrib>Kwon, Soon-Nam</creatorcontrib><creatorcontrib>Ko, Jaejung</creatorcontrib><creatorcontrib>Han, Su Jung</creatorcontrib><creatorcontrib>Lee, Chongmok</creatorcontrib><creatorcontrib>Kim, Sung Joo</creatorcontrib><creatorcontrib>Kang, Sang Ook</creatorcontrib><title>Generation of Blue Light-Emitting Zinc Complexes by Band-Gap Control of the Oxazolylphenolate Ligand System: Syntheses, Characterizations, and Organic Light Emitting Device Applications of 4-Coordinated Bis(2-oxazolylphenolate) Zinc(II) Complexes</title><title>Inorganic chemistry</title><addtitle>Inorg. Chem</addtitle><description>Color-tunable Zn(II) complexes of the type Zn(N,O-OPhOxZArX)2 (5), where the ligand consists of an oxazolylphenolate ion connected at the 4-position by a 2,4-substituted aryl functional group with X = NMe2 a, OMe b, Ph c, Cl d, F2 e, and CN f, were prepared. X-ray structural studies of 5a, 5b, and 5e showed that a zinc atom was positioned in a distorted tetrahedral coordination environment created by two oxazolylphenolate ligands with N,O-chelation. Hammet plots of absorption and emission maxima, respectively, in UV and photoluminescence (PL) spectra with respect to electron-donating and electron-withdrawing groups of the substituents indicate a direct correlation between the highest occupied molecular orbital (HOMO)−lowest unoccupied molecular orbital (LUMO) band gaps and electronic alterations at the ligand sites. A similar correlation was also observed for the reduction and oxidation potentials in cyclic voltammograms (CVs). A gradual increase in the HOMO−LUMO band gap is seen from electron-donating to electron-withdrawing functional groups, NMe2 < OMe < Ph < Cl < F2 < CN. An emission peak with a maximum at 455 nm was achieved when the most electron-withdrawing group (cyano) was applied to the oxazolylphenolate ligand system. Density-functional theory (DFT) calculations on the HOMOs and LUMOs for this series lead to a conclusion similar to that arrived at from a blue-shift trend observed in UV data and trends in the CVs. The 4-coordinated zinc complex (5c) was shown to be a potential blue-emitting material, exhibiting a maximum efficiency of 1720 cd/m2 at 17 V with 0.3 cd/A in a multilayered device structure of ITO/NPB/5c/BCP/Alq3/LiF/Al. On the basis of the low HOMO level of this series, 5a was tested as a hole-transporting material; this resulted in the successful fabrication of a multilayered device of ITO/5a/DPVBI/Alq3/LiF/Al with an efficiency of 7000 cd/m2 at 13 V with 2.0 cd/A.</description><issn>0020-1669</issn><issn>1520-510X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><recordid>eNptkd9v0zAQxyMEYmXwwD-A_AJaJQJ2EucHb2sYpaJSYRto2ovlONfVJbGD7aB2fzjPuE3VSYins86fu-_37oLgJcHvCI7IeykyHCUFWT8KRoRGOKQE3zwORhj7N0nT4iR4Zu0aY1zESfo0OCE5TeIC01HwZwoKDHdSK6SXaNL0gObybuXCi1Y6J9UdupVKoFK3XQMbsKjaoglXdTjlnc8qZ3Szq3QrQIsNv9fNtulWoHTD3b6VZ9HV1jpoP_ioPGfBvkXlihsuHBh5v1f3qR25ML5AisEDOnr4CL-lAHTedY0UA78TTcJSa1NL5bVqNJH2LAr1vybG-wnOZrPxwxTPgydL3lh4cYinwfdPF9fl53C-mM7K83nI4zhyIZCaVxQnQuRFnHFIK55zjkUWAa24iJM8yQTgospFUYskJxEROU9rSmoBSxrHp8GboW9n9K8erGOttAKahivQvWVpEWUZzakHxwMojLbWwJJ1RrbcbBnBbHdkdjyyZ18dmvZVC_UDebiqB8IBkH7tm-M_Nz9ZmsUZZddfr9jll5s8vfx2y354_vXAc2HZWvdG-Z38R_gvAAnDIQ</recordid><startdate>20080707</startdate><enddate>20080707</enddate><creator>Son, Ho-Jin</creator><creator>Han, Won-Sik</creator><creator>Chun, Ji-Yun</creator><creator>Kang, Byoung-Kook</creator><creator>Kwon, Soon-Nam</creator><creator>Ko, Jaejung</creator><creator>Han, Su Jung</creator><creator>Lee, Chongmok</creator><creator>Kim, Sung Joo</creator><creator>Kang, Sang Ook</creator><general>American Chemical Society</general><scope>BSCLL</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20080707</creationdate><title>Generation of Blue Light-Emitting Zinc Complexes by Band-Gap Control of the Oxazolylphenolate Ligand System: Syntheses, Characterizations, and Organic Light Emitting Device Applications of 4-Coordinated Bis(2-oxazolylphenolate) Zinc(II) Complexes</title><author>Son, Ho-Jin ; Han, Won-Sik ; Chun, Ji-Yun ; Kang, Byoung-Kook ; Kwon, Soon-Nam ; Ko, Jaejung ; Han, Su Jung ; Lee, Chongmok ; Kim, Sung Joo ; Kang, Sang Ook</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a332t-e1dab504cc8937ae6ba8aa0c72e5bac34847ce09b8c9dc48121c8a6d51dcef533</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Son, Ho-Jin</creatorcontrib><creatorcontrib>Han, Won-Sik</creatorcontrib><creatorcontrib>Chun, Ji-Yun</creatorcontrib><creatorcontrib>Kang, Byoung-Kook</creatorcontrib><creatorcontrib>Kwon, Soon-Nam</creatorcontrib><creatorcontrib>Ko, Jaejung</creatorcontrib><creatorcontrib>Han, Su Jung</creatorcontrib><creatorcontrib>Lee, Chongmok</creatorcontrib><creatorcontrib>Kim, Sung Joo</creatorcontrib><creatorcontrib>Kang, Sang Ook</creatorcontrib><collection>Istex</collection><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>Son, Ho-Jin</au><au>Han, Won-Sik</au><au>Chun, Ji-Yun</au><au>Kang, Byoung-Kook</au><au>Kwon, Soon-Nam</au><au>Ko, Jaejung</au><au>Han, Su Jung</au><au>Lee, Chongmok</au><au>Kim, Sung Joo</au><au>Kang, Sang Ook</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Generation of Blue Light-Emitting Zinc Complexes by Band-Gap Control of the Oxazolylphenolate Ligand System: Syntheses, Characterizations, and Organic Light Emitting Device Applications of 4-Coordinated Bis(2-oxazolylphenolate) Zinc(II) Complexes</atitle><jtitle>Inorganic chemistry</jtitle><addtitle>Inorg. Chem</addtitle><date>2008-07-07</date><risdate>2008</risdate><volume>47</volume><issue>13</issue><spage>5666</spage><epage>5676</epage><pages>5666-5676</pages><issn>0020-1669</issn><eissn>1520-510X</eissn><abstract>Color-tunable Zn(II) complexes of the type Zn(N,O-OPhOxZArX)2 (5), where the ligand consists of an oxazolylphenolate ion connected at the 4-position by a 2,4-substituted aryl functional group with X = NMe2 a, OMe b, Ph c, Cl d, F2 e, and CN f, were prepared. X-ray structural studies of 5a, 5b, and 5e showed that a zinc atom was positioned in a distorted tetrahedral coordination environment created by two oxazolylphenolate ligands with N,O-chelation. Hammet plots of absorption and emission maxima, respectively, in UV and photoluminescence (PL) spectra with respect to electron-donating and electron-withdrawing groups of the substituents indicate a direct correlation between the highest occupied molecular orbital (HOMO)−lowest unoccupied molecular orbital (LUMO) band gaps and electronic alterations at the ligand sites. A similar correlation was also observed for the reduction and oxidation potentials in cyclic voltammograms (CVs). A gradual increase in the HOMO−LUMO band gap is seen from electron-donating to electron-withdrawing functional groups, NMe2 < OMe < Ph < Cl < F2 < CN. An emission peak with a maximum at 455 nm was achieved when the most electron-withdrawing group (cyano) was applied to the oxazolylphenolate ligand system. Density-functional theory (DFT) calculations on the HOMOs and LUMOs for this series lead to a conclusion similar to that arrived at from a blue-shift trend observed in UV data and trends in the CVs. The 4-coordinated zinc complex (5c) was shown to be a potential blue-emitting material, exhibiting a maximum efficiency of 1720 cd/m2 at 17 V with 0.3 cd/A in a multilayered device structure of ITO/NPB/5c/BCP/Alq3/LiF/Al. On the basis of the low HOMO level of this series, 5a was tested as a hole-transporting material; this resulted in the successful fabrication of a multilayered device of ITO/5a/DPVBI/Alq3/LiF/Al with an efficiency of 7000 cd/m2 at 13 V with 2.0 cd/A.</abstract><cop>United States</cop><pub>American Chemical Society</pub><pmid>18543905</pmid><doi>10.1021/ic702491j</doi><tpages>11</tpages></addata></record> |
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title | Generation of Blue Light-Emitting Zinc Complexes by Band-Gap Control of the Oxazolylphenolate Ligand System: Syntheses, Characterizations, and Organic Light Emitting Device Applications of 4-Coordinated Bis(2-oxazolylphenolate) Zinc(II) Complexes |
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