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Benzobisoxazole cruciforms: a tunable, cross-conjugated platform for the generation of deep blue OLED materials
Four new cross-conjugated small molecules based on a central benzo[1,2- d :4,5- d ′]bisoxazole moiety possessing semi-independently tunable HOMO and LUMO levels were synthesized and the properties of these materials were evaluated experimentally and theoretically. The molecules were thermally stable...
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Published in: | Journal of materials chemistry. C, Materials for optical and electronic devices Materials for optical and electronic devices, 2016-01, Vol.4 (17), p.3765-3773 |
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container_end_page | 3773 |
container_issue | 17 |
container_start_page | 3765 |
container_title | Journal of materials chemistry. C, Materials for optical and electronic devices |
container_volume | 4 |
creator | Chavez III, Ramiro Cai, Min Tlach, Brian Wheeler, David L Kaudal, Rajiv Tsyrenova, Ayuna Tomlinson, Aimée L Shinar, Ruth Shinar, Joseph Jeffries-EL, Malika |
description | Four new cross-conjugated small molecules based on a central benzo[1,2-
d
:4,5-
d
′]bisoxazole moiety possessing semi-independently tunable HOMO and LUMO levels were synthesized and the properties of these materials were evaluated experimentally and theoretically. The molecules were thermally stable with 5% weight loss occurring well above 350 °C. The cruciforms all exhibited blue emission in solution ranging from 433-450 nm. Host-guest OLEDs fabricated from various concentrations of these materials using the small molecule host 4,4′-bis(9-carbazolyl)-biphenyl (CBP) exhibited deep blue-emission with Commission Internationale de L'Eclairage (CIE) coordinates of (0.15 ≤
x
≤ 0.17, 0.05 ≤
y
≤ 0.11), and maximum luminance efficiencies as high as ∼2 cd A
−1
. These results demonstrate the potential of benzobisoxazole cruciforms as emitters for developing high-performance deep blue OLEDs.
A structure-property investigation of a series of cross-conjugated molecules shows that their performance is dependent on both the nature of the substituents and their conjugation axis. |
doi_str_mv | 10.1039/c5tc03622d |
format | article |
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d
:4,5-
d
′]bisoxazole moiety possessing semi-independently tunable HOMO and LUMO levels were synthesized and the properties of these materials were evaluated experimentally and theoretically. The molecules were thermally stable with 5% weight loss occurring well above 350 °C. The cruciforms all exhibited blue emission in solution ranging from 433-450 nm. Host-guest OLEDs fabricated from various concentrations of these materials using the small molecule host 4,4′-bis(9-carbazolyl)-biphenyl (CBP) exhibited deep blue-emission with Commission Internationale de L'Eclairage (CIE) coordinates of (0.15 ≤
x
≤ 0.17, 0.05 ≤
y
≤ 0.11), and maximum luminance efficiencies as high as ∼2 cd A
−1
. These results demonstrate the potential of benzobisoxazole cruciforms as emitters for developing high-performance deep blue OLEDs.
A structure-property investigation of a series of cross-conjugated molecules shows that their performance is dependent on both the nature of the substituents and their conjugation axis.</description><identifier>ISSN: 2050-7526</identifier><identifier>EISSN: 2050-7534</identifier><identifier>DOI: 10.1039/c5tc03622d</identifier><language>eng</language><publisher>United States: Royal Society of Chemistry</publisher><subject>Electronic devices ; Emission ; Emitters ; Luminance ; MATERIALS SCIENCE ; Molecular orbitals ; Platforms ; Thermal stability ; Weight loss</subject><ispartof>Journal of materials chemistry. C, Materials for optical and electronic devices, 2016-01, Vol.4 (17), p.3765-3773</ispartof><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c349t-7d180847d3ac33c15d3ef5c6e69462ae7c9d0f7d7d11bc984c794e8bf4ec4b273</citedby><cites>FETCH-LOGICAL-c349t-7d180847d3ac33c15d3ef5c6e69462ae7c9d0f7d7d11bc984c794e8bf4ec4b273</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,777,781,882,27905,27906</link.rule.ids><backlink>$$Uhttps://www.osti.gov/servlets/purl/1259481$$D View this record in Osti.gov$$Hfree_for_read</backlink></links><search><creatorcontrib>Chavez III, Ramiro</creatorcontrib><creatorcontrib>Cai, Min</creatorcontrib><creatorcontrib>Tlach, Brian</creatorcontrib><creatorcontrib>Wheeler, David L</creatorcontrib><creatorcontrib>Kaudal, Rajiv</creatorcontrib><creatorcontrib>Tsyrenova, Ayuna</creatorcontrib><creatorcontrib>Tomlinson, Aimée L</creatorcontrib><creatorcontrib>Shinar, Ruth</creatorcontrib><creatorcontrib>Shinar, Joseph</creatorcontrib><creatorcontrib>Jeffries-EL, Malika</creatorcontrib><creatorcontrib>Ames Lab., Ames, IA (United States)</creatorcontrib><title>Benzobisoxazole cruciforms: a tunable, cross-conjugated platform for the generation of deep blue OLED materials</title><title>Journal of materials chemistry. C, Materials for optical and electronic devices</title><description>Four new cross-conjugated small molecules based on a central benzo[1,2-
d
:4,5-
d
′]bisoxazole moiety possessing semi-independently tunable HOMO and LUMO levels were synthesized and the properties of these materials were evaluated experimentally and theoretically. The molecules were thermally stable with 5% weight loss occurring well above 350 °C. The cruciforms all exhibited blue emission in solution ranging from 433-450 nm. Host-guest OLEDs fabricated from various concentrations of these materials using the small molecule host 4,4′-bis(9-carbazolyl)-biphenyl (CBP) exhibited deep blue-emission with Commission Internationale de L'Eclairage (CIE) coordinates of (0.15 ≤
x
≤ 0.17, 0.05 ≤
y
≤ 0.11), and maximum luminance efficiencies as high as ∼2 cd A
−1
. These results demonstrate the potential of benzobisoxazole cruciforms as emitters for developing high-performance deep blue OLEDs.
A structure-property investigation of a series of cross-conjugated molecules shows that their performance is dependent on both the nature of the substituents and their conjugation axis.</description><subject>Electronic devices</subject><subject>Emission</subject><subject>Emitters</subject><subject>Luminance</subject><subject>MATERIALS SCIENCE</subject><subject>Molecular orbitals</subject><subject>Platforms</subject><subject>Thermal stability</subject><subject>Weight loss</subject><issn>2050-7526</issn><issn>2050-7534</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><recordid>eNpF0c9LwzAUB_AiCo65i3cheBKxmjTpL2_azR8w2GWeS_r6unW0TU1S0P31ZqtoDnmPxychfON5l4zeM8rTBwgtUB4FQXniTQIaUj8OuTj964Po3JsZs6NuJSxKonTiqWfs9qqojfqSe9UgAT1AXSndmkciiR06WTR458bKGB9Utxs20mJJ-kbaAyNuI3aLZIMdamlr1RFVkRKxJ0UzIFktF3PSujO6lo258M4qV3D2W6fex8tinb35y9Xre_a09IGL1PpxyRKaiLjkEjgHFpYcqxAijFIRBRJjSEtaxaVzrIA0ERCnApOiEgiiCGI-9a7He5WxdW6gtghb9_wOweYsCFORMIduRtRr9TmgsXlbG8CmkR2qweTMpURDzsWB3o70GITGKu913Ur9nTOaH9LPs3CdHdOfO3w1Ym3gz_3_Dv8BWcCCFw</recordid><startdate>20160101</startdate><enddate>20160101</enddate><creator>Chavez III, Ramiro</creator><creator>Cai, Min</creator><creator>Tlach, Brian</creator><creator>Wheeler, David L</creator><creator>Kaudal, Rajiv</creator><creator>Tsyrenova, Ayuna</creator><creator>Tomlinson, Aimée L</creator><creator>Shinar, Ruth</creator><creator>Shinar, Joseph</creator><creator>Jeffries-EL, Malika</creator><general>Royal Society of Chemistry</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7SP</scope><scope>7SR</scope><scope>7U5</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope><scope>L7M</scope><scope>OIOZB</scope><scope>OTOTI</scope></search><sort><creationdate>20160101</creationdate><title>Benzobisoxazole cruciforms: a tunable, cross-conjugated platform for the generation of deep blue OLED materials</title><author>Chavez III, Ramiro ; Cai, Min ; Tlach, Brian ; Wheeler, David L ; Kaudal, Rajiv ; Tsyrenova, Ayuna ; Tomlinson, Aimée L ; Shinar, Ruth ; Shinar, Joseph ; Jeffries-EL, Malika</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c349t-7d180847d3ac33c15d3ef5c6e69462ae7c9d0f7d7d11bc984c794e8bf4ec4b273</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Electronic devices</topic><topic>Emission</topic><topic>Emitters</topic><topic>Luminance</topic><topic>MATERIALS SCIENCE</topic><topic>Molecular orbitals</topic><topic>Platforms</topic><topic>Thermal stability</topic><topic>Weight loss</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Chavez III, Ramiro</creatorcontrib><creatorcontrib>Cai, Min</creatorcontrib><creatorcontrib>Tlach, Brian</creatorcontrib><creatorcontrib>Wheeler, David L</creatorcontrib><creatorcontrib>Kaudal, Rajiv</creatorcontrib><creatorcontrib>Tsyrenova, Ayuna</creatorcontrib><creatorcontrib>Tomlinson, Aimée L</creatorcontrib><creatorcontrib>Shinar, Ruth</creatorcontrib><creatorcontrib>Shinar, Joseph</creatorcontrib><creatorcontrib>Jeffries-EL, Malika</creatorcontrib><creatorcontrib>Ames Lab., Ames, IA (United States)</creatorcontrib><collection>CrossRef</collection><collection>Electronics & Communications Abstracts</collection><collection>Engineered Materials Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><collection>OSTI.GOV - Hybrid</collection><collection>OSTI.GOV</collection><jtitle>Journal of materials chemistry. C, Materials for optical and electronic devices</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Chavez III, Ramiro</au><au>Cai, Min</au><au>Tlach, Brian</au><au>Wheeler, David L</au><au>Kaudal, Rajiv</au><au>Tsyrenova, Ayuna</au><au>Tomlinson, Aimée L</au><au>Shinar, Ruth</au><au>Shinar, Joseph</au><au>Jeffries-EL, Malika</au><aucorp>Ames Lab., Ames, IA (United States)</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Benzobisoxazole cruciforms: a tunable, cross-conjugated platform for the generation of deep blue OLED materials</atitle><jtitle>Journal of materials chemistry. C, Materials for optical and electronic devices</jtitle><date>2016-01-01</date><risdate>2016</risdate><volume>4</volume><issue>17</issue><spage>3765</spage><epage>3773</epage><pages>3765-3773</pages><issn>2050-7526</issn><eissn>2050-7534</eissn><abstract>Four new cross-conjugated small molecules based on a central benzo[1,2-
d
:4,5-
d
′]bisoxazole moiety possessing semi-independently tunable HOMO and LUMO levels were synthesized and the properties of these materials were evaluated experimentally and theoretically. The molecules were thermally stable with 5% weight loss occurring well above 350 °C. The cruciforms all exhibited blue emission in solution ranging from 433-450 nm. Host-guest OLEDs fabricated from various concentrations of these materials using the small molecule host 4,4′-bis(9-carbazolyl)-biphenyl (CBP) exhibited deep blue-emission with Commission Internationale de L'Eclairage (CIE) coordinates of (0.15 ≤
x
≤ 0.17, 0.05 ≤
y
≤ 0.11), and maximum luminance efficiencies as high as ∼2 cd A
−1
. These results demonstrate the potential of benzobisoxazole cruciforms as emitters for developing high-performance deep blue OLEDs.
A structure-property investigation of a series of cross-conjugated molecules shows that their performance is dependent on both the nature of the substituents and their conjugation axis.</abstract><cop>United States</cop><pub>Royal Society of Chemistry</pub><doi>10.1039/c5tc03622d</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record> |
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source | Royal Society of Chemistry |
subjects | Electronic devices Emission Emitters Luminance MATERIALS SCIENCE Molecular orbitals Platforms Thermal stability Weight loss |
title | Benzobisoxazole cruciforms: a tunable, cross-conjugated platform for the generation of deep blue OLED materials |
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