Loading…
Rational Synthesis of Tetrahydrodibenzophenanthridine and Phenanthroimidazole as Efficient Blue Emitters and their Applications
Ten luminophores based on tetrahydrodibenzophenanthridine (THDP) and phenanthroimidazole (PI) were designed, synthesized and characterized for their thermal, electrochemical, electro‐optical, charge‐transporting characteristics and electroluminescent properties. The blue luminophores exhibited high...
Saved in:
Published in: | European journal of organic chemistry 2020-02, Vol.2020 (7), p.834-844 |
---|---|
Main Authors: | , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | cdi_FETCH-LOGICAL-c3171-3602bee9aefbc3eb8175c9188fd0462733d981bb40aa9082f88546527d3e2afe3 |
---|---|
cites | cdi_FETCH-LOGICAL-c3171-3602bee9aefbc3eb8175c9188fd0462733d981bb40aa9082f88546527d3e2afe3 |
container_end_page | 844 |
container_issue | 7 |
container_start_page | 834 |
container_title | European journal of organic chemistry |
container_volume | 2020 |
creator | Thiyagarajan, Manojkumar Dhanthala Balijapalli, Umamahesh Nasiri, Sohrab Volyniuk, Dmytro Simokaitienec, Jurate Pathak, Madhvesh Iyer, Sathiyanarayanan Kulathu Gražulevičius, Juozas Vidas |
description | Ten luminophores based on tetrahydrodibenzophenanthridine (THDP) and phenanthroimidazole (PI) were designed, synthesized and characterized for their thermal, electrochemical, electro‐optical, charge‐transporting characteristics and electroluminescent properties. The blue luminophores exhibited high photoluminescence quantum yields of 66–93 % in toluene solutions and of 5–59 % in solid films. The highest values were observed for the derivative of THDP and PI containing methoxy group. The compounds showed close values of ionization potentials (5.74–6.11 eV) and electron affinities (2.71–3.06 eV). The selected compounds were tested in electroluminescent devices for the preparation of non‐doped light‐emitting layers. The best device fabricated using derivative of THDP and PI with methoxy groups showed blue electroluminescence with brightness of 10000 cd/m2 at high applied voltages. We performed DFT calculations and observed lowest singlet–triplet gap (ΔEST) values of 0.33 and 0.03 eV, oscillator strength (f) values of 0.034 and 0.008 for CN and NO2 derivatives. Interestingly, we also observed that compounds 3g and 3i showed HOMO and LUMO levels with similar energy gap (Eg) of 3.60 eV and deeper HOMO values of –5.30, –5.33 eV and LUMO values of –1.94, –2.77 eV.
Tetrahydrodibenzo[a,i]phenanthridine (THDP) and phenanthroimidazoles (PI) coupled bipolar THDP‐PI derivatives exhibited deep blue emission in the range of 425–435 nm. The highest PLQY value up to 93 % with displaying positive solvatochromic behaviour proving CT character of their emission. Charge mobility of all the derivatives except compound 3a showed hole mobility of 1.3 × 10–4 cm2/V at electric fields higher than 106 V/cm. |
doi_str_mv | 10.1002/ejoc.201901711 |
format | article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_journals_2359205078</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2359205078</sourcerecordid><originalsourceid>FETCH-LOGICAL-c3171-3602bee9aefbc3eb8175c9188fd0462733d981bb40aa9082f88546527d3e2afe3</originalsourceid><addsrcrecordid>eNqFkEtPwzAQhC0EEqVw5WyJc8razsvHUpWXKhVBkbhFTrJWXaVxsFOh9MJfJ215HDntajTfrmYIuWQwYgD8Gle2GHFgEljC2BEZMJAygFjCcb-HIgyYFG-n5Mz7FQDIOGYD8vmsWmNrVdGXrm6X6I2nVtMFtk4tu9LZ0uRYb22zxFr1BmdKUyNVdUmffiRr1qZUW1v1uqdTrU1hsG7pTbVBOl2btkXn90j_wDg6bprKFPu__pycaFV5vPieQ_J6O11M7oPZ_O5hMp4FhejTBCIGniNKhTovBOYpS6JCsjTVJYQxT4QoZcryPASlJKRcp2kUxhFPSoFcaRRDcnW42zj7vkHfZiu7cX1un3ERSQ4RJGnvGh1chbPeO9RZ48xauS5jkO1KznYlZ78l94A8AB-mwu4fdzZ9nE_-2C8T0oPk</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2359205078</pqid></control><display><type>article</type><title>Rational Synthesis of Tetrahydrodibenzophenanthridine and Phenanthroimidazole as Efficient Blue Emitters and their Applications</title><source>Wiley-Blackwell Read & Publish Collection</source><creator>Thiyagarajan, Manojkumar Dhanthala ; Balijapalli, Umamahesh ; Nasiri, Sohrab ; Volyniuk, Dmytro ; Simokaitienec, Jurate ; Pathak, Madhvesh ; Iyer, Sathiyanarayanan Kulathu ; Gražulevičius, Juozas Vidas</creator><creatorcontrib>Thiyagarajan, Manojkumar Dhanthala ; Balijapalli, Umamahesh ; Nasiri, Sohrab ; Volyniuk, Dmytro ; Simokaitienec, Jurate ; Pathak, Madhvesh ; Iyer, Sathiyanarayanan Kulathu ; Gražulevičius, Juozas Vidas</creatorcontrib><description>Ten luminophores based on tetrahydrodibenzophenanthridine (THDP) and phenanthroimidazole (PI) were designed, synthesized and characterized for their thermal, electrochemical, electro‐optical, charge‐transporting characteristics and electroluminescent properties. The blue luminophores exhibited high photoluminescence quantum yields of 66–93 % in toluene solutions and of 5–59 % in solid films. The highest values were observed for the derivative of THDP and PI containing methoxy group. The compounds showed close values of ionization potentials (5.74–6.11 eV) and electron affinities (2.71–3.06 eV). The selected compounds were tested in electroluminescent devices for the preparation of non‐doped light‐emitting layers. The best device fabricated using derivative of THDP and PI with methoxy groups showed blue electroluminescence with brightness of 10000 cd/m2 at high applied voltages. We performed DFT calculations and observed lowest singlet–triplet gap (ΔEST) values of 0.33 and 0.03 eV, oscillator strength (f) values of 0.034 and 0.008 for CN and NO2 derivatives. Interestingly, we also observed that compounds 3g and 3i showed HOMO and LUMO levels with similar energy gap (Eg) of 3.60 eV and deeper HOMO values of –5.30, –5.33 eV and LUMO values of –1.94, –2.77 eV.
Tetrahydrodibenzo[a,i]phenanthridine (THDP) and phenanthroimidazoles (PI) coupled bipolar THDP‐PI derivatives exhibited deep blue emission in the range of 425–435 nm. The highest PLQY value up to 93 % with displaying positive solvatochromic behaviour proving CT character of their emission. Charge mobility of all the derivatives except compound 3a showed hole mobility of 1.3 × 10–4 cm2/V at electric fields higher than 106 V/cm.</description><identifier>ISSN: 1434-193X</identifier><identifier>EISSN: 1099-0690</identifier><identifier>DOI: 10.1002/ejoc.201901711</identifier><language>eng</language><publisher>Weinheim: Wiley Subscription Services, Inc</publisher><subject>Blue luminophore ; Electrochemistry ; Electroluminescence ; Emitters ; Emitters (electron) ; Energy gap ; Ionization potentials ; Mathematical analysis ; Molecular orbitals ; Nitrogen dioxide ; Optical properties ; Phenananthridines ; Phenanthroimidazoles ; Photoluminescence ; Solvatochromism ; Toluene</subject><ispartof>European journal of organic chemistry, 2020-02, Vol.2020 (7), p.834-844</ispartof><rights>2020 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3171-3602bee9aefbc3eb8175c9188fd0462733d981bb40aa9082f88546527d3e2afe3</citedby><cites>FETCH-LOGICAL-c3171-3602bee9aefbc3eb8175c9188fd0462733d981bb40aa9082f88546527d3e2afe3</cites><orcidid>0000-0003-3865-4088 ; 0000-0002-4408-9727</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Thiyagarajan, Manojkumar Dhanthala</creatorcontrib><creatorcontrib>Balijapalli, Umamahesh</creatorcontrib><creatorcontrib>Nasiri, Sohrab</creatorcontrib><creatorcontrib>Volyniuk, Dmytro</creatorcontrib><creatorcontrib>Simokaitienec, Jurate</creatorcontrib><creatorcontrib>Pathak, Madhvesh</creatorcontrib><creatorcontrib>Iyer, Sathiyanarayanan Kulathu</creatorcontrib><creatorcontrib>Gražulevičius, Juozas Vidas</creatorcontrib><title>Rational Synthesis of Tetrahydrodibenzophenanthridine and Phenanthroimidazole as Efficient Blue Emitters and their Applications</title><title>European journal of organic chemistry</title><description>Ten luminophores based on tetrahydrodibenzophenanthridine (THDP) and phenanthroimidazole (PI) were designed, synthesized and characterized for their thermal, electrochemical, electro‐optical, charge‐transporting characteristics and electroluminescent properties. The blue luminophores exhibited high photoluminescence quantum yields of 66–93 % in toluene solutions and of 5–59 % in solid films. The highest values were observed for the derivative of THDP and PI containing methoxy group. The compounds showed close values of ionization potentials (5.74–6.11 eV) and electron affinities (2.71–3.06 eV). The selected compounds were tested in electroluminescent devices for the preparation of non‐doped light‐emitting layers. The best device fabricated using derivative of THDP and PI with methoxy groups showed blue electroluminescence with brightness of 10000 cd/m2 at high applied voltages. We performed DFT calculations and observed lowest singlet–triplet gap (ΔEST) values of 0.33 and 0.03 eV, oscillator strength (f) values of 0.034 and 0.008 for CN and NO2 derivatives. Interestingly, we also observed that compounds 3g and 3i showed HOMO and LUMO levels with similar energy gap (Eg) of 3.60 eV and deeper HOMO values of –5.30, –5.33 eV and LUMO values of –1.94, –2.77 eV.
Tetrahydrodibenzo[a,i]phenanthridine (THDP) and phenanthroimidazoles (PI) coupled bipolar THDP‐PI derivatives exhibited deep blue emission in the range of 425–435 nm. The highest PLQY value up to 93 % with displaying positive solvatochromic behaviour proving CT character of their emission. Charge mobility of all the derivatives except compound 3a showed hole mobility of 1.3 × 10–4 cm2/V at electric fields higher than 106 V/cm.</description><subject>Blue luminophore</subject><subject>Electrochemistry</subject><subject>Electroluminescence</subject><subject>Emitters</subject><subject>Emitters (electron)</subject><subject>Energy gap</subject><subject>Ionization potentials</subject><subject>Mathematical analysis</subject><subject>Molecular orbitals</subject><subject>Nitrogen dioxide</subject><subject>Optical properties</subject><subject>Phenananthridines</subject><subject>Phenanthroimidazoles</subject><subject>Photoluminescence</subject><subject>Solvatochromism</subject><subject>Toluene</subject><issn>1434-193X</issn><issn>1099-0690</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><recordid>eNqFkEtPwzAQhC0EEqVw5WyJc8razsvHUpWXKhVBkbhFTrJWXaVxsFOh9MJfJ215HDntajTfrmYIuWQwYgD8Gle2GHFgEljC2BEZMJAygFjCcb-HIgyYFG-n5Mz7FQDIOGYD8vmsWmNrVdGXrm6X6I2nVtMFtk4tu9LZ0uRYb22zxFr1BmdKUyNVdUmffiRr1qZUW1v1uqdTrU1hsG7pTbVBOl2btkXn90j_wDg6bprKFPu__pycaFV5vPieQ_J6O11M7oPZ_O5hMp4FhejTBCIGniNKhTovBOYpS6JCsjTVJYQxT4QoZcryPASlJKRcp2kUxhFPSoFcaRRDcnW42zj7vkHfZiu7cX1un3ERSQ4RJGnvGh1chbPeO9RZ48xauS5jkO1KznYlZ78l94A8AB-mwu4fdzZ9nE_-2C8T0oPk</recordid><startdate>20200221</startdate><enddate>20200221</enddate><creator>Thiyagarajan, Manojkumar Dhanthala</creator><creator>Balijapalli, Umamahesh</creator><creator>Nasiri, Sohrab</creator><creator>Volyniuk, Dmytro</creator><creator>Simokaitienec, Jurate</creator><creator>Pathak, Madhvesh</creator><creator>Iyer, Sathiyanarayanan Kulathu</creator><creator>Gražulevičius, Juozas Vidas</creator><general>Wiley Subscription Services, Inc</general><scope>AAYXX</scope><scope>CITATION</scope><orcidid>https://orcid.org/0000-0003-3865-4088</orcidid><orcidid>https://orcid.org/0000-0002-4408-9727</orcidid></search><sort><creationdate>20200221</creationdate><title>Rational Synthesis of Tetrahydrodibenzophenanthridine and Phenanthroimidazole as Efficient Blue Emitters and their Applications</title><author>Thiyagarajan, Manojkumar Dhanthala ; Balijapalli, Umamahesh ; Nasiri, Sohrab ; Volyniuk, Dmytro ; Simokaitienec, Jurate ; Pathak, Madhvesh ; Iyer, Sathiyanarayanan Kulathu ; Gražulevičius, Juozas Vidas</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3171-3602bee9aefbc3eb8175c9188fd0462733d981bb40aa9082f88546527d3e2afe3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Blue luminophore</topic><topic>Electrochemistry</topic><topic>Electroluminescence</topic><topic>Emitters</topic><topic>Emitters (electron)</topic><topic>Energy gap</topic><topic>Ionization potentials</topic><topic>Mathematical analysis</topic><topic>Molecular orbitals</topic><topic>Nitrogen dioxide</topic><topic>Optical properties</topic><topic>Phenananthridines</topic><topic>Phenanthroimidazoles</topic><topic>Photoluminescence</topic><topic>Solvatochromism</topic><topic>Toluene</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Thiyagarajan, Manojkumar Dhanthala</creatorcontrib><creatorcontrib>Balijapalli, Umamahesh</creatorcontrib><creatorcontrib>Nasiri, Sohrab</creatorcontrib><creatorcontrib>Volyniuk, Dmytro</creatorcontrib><creatorcontrib>Simokaitienec, Jurate</creatorcontrib><creatorcontrib>Pathak, Madhvesh</creatorcontrib><creatorcontrib>Iyer, Sathiyanarayanan Kulathu</creatorcontrib><creatorcontrib>Gražulevičius, Juozas Vidas</creatorcontrib><collection>CrossRef</collection><jtitle>European journal of organic chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Thiyagarajan, Manojkumar Dhanthala</au><au>Balijapalli, Umamahesh</au><au>Nasiri, Sohrab</au><au>Volyniuk, Dmytro</au><au>Simokaitienec, Jurate</au><au>Pathak, Madhvesh</au><au>Iyer, Sathiyanarayanan Kulathu</au><au>Gražulevičius, Juozas Vidas</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Rational Synthesis of Tetrahydrodibenzophenanthridine and Phenanthroimidazole as Efficient Blue Emitters and their Applications</atitle><jtitle>European journal of organic chemistry</jtitle><date>2020-02-21</date><risdate>2020</risdate><volume>2020</volume><issue>7</issue><spage>834</spage><epage>844</epage><pages>834-844</pages><issn>1434-193X</issn><eissn>1099-0690</eissn><abstract>Ten luminophores based on tetrahydrodibenzophenanthridine (THDP) and phenanthroimidazole (PI) were designed, synthesized and characterized for their thermal, electrochemical, electro‐optical, charge‐transporting characteristics and electroluminescent properties. The blue luminophores exhibited high photoluminescence quantum yields of 66–93 % in toluene solutions and of 5–59 % in solid films. The highest values were observed for the derivative of THDP and PI containing methoxy group. The compounds showed close values of ionization potentials (5.74–6.11 eV) and electron affinities (2.71–3.06 eV). The selected compounds were tested in electroluminescent devices for the preparation of non‐doped light‐emitting layers. The best device fabricated using derivative of THDP and PI with methoxy groups showed blue electroluminescence with brightness of 10000 cd/m2 at high applied voltages. We performed DFT calculations and observed lowest singlet–triplet gap (ΔEST) values of 0.33 and 0.03 eV, oscillator strength (f) values of 0.034 and 0.008 for CN and NO2 derivatives. Interestingly, we also observed that compounds 3g and 3i showed HOMO and LUMO levels with similar energy gap (Eg) of 3.60 eV and deeper HOMO values of –5.30, –5.33 eV and LUMO values of –1.94, –2.77 eV.
Tetrahydrodibenzo[a,i]phenanthridine (THDP) and phenanthroimidazoles (PI) coupled bipolar THDP‐PI derivatives exhibited deep blue emission in the range of 425–435 nm. The highest PLQY value up to 93 % with displaying positive solvatochromic behaviour proving CT character of their emission. Charge mobility of all the derivatives except compound 3a showed hole mobility of 1.3 × 10–4 cm2/V at electric fields higher than 106 V/cm.</abstract><cop>Weinheim</cop><pub>Wiley Subscription Services, Inc</pub><doi>10.1002/ejoc.201901711</doi><tpages>11</tpages><orcidid>https://orcid.org/0000-0003-3865-4088</orcidid><orcidid>https://orcid.org/0000-0002-4408-9727</orcidid></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1434-193X |
ispartof | European journal of organic chemistry, 2020-02, Vol.2020 (7), p.834-844 |
issn | 1434-193X 1099-0690 |
language | eng |
recordid | cdi_proquest_journals_2359205078 |
source | Wiley-Blackwell Read & Publish Collection |
subjects | Blue luminophore Electrochemistry Electroluminescence Emitters Emitters (electron) Energy gap Ionization potentials Mathematical analysis Molecular orbitals Nitrogen dioxide Optical properties Phenananthridines Phenanthroimidazoles Photoluminescence Solvatochromism Toluene |
title | Rational Synthesis of Tetrahydrodibenzophenanthridine and Phenanthroimidazole as Efficient Blue Emitters and their Applications |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-29T13%3A14%3A25IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Rational%20Synthesis%20of%20Tetrahydrodibenzophenanthridine%20and%20Phenanthroimidazole%20as%20Efficient%20Blue%20Emitters%20and%20their%20Applications&rft.jtitle=European%20journal%20of%20organic%20chemistry&rft.au=Thiyagarajan,%20Manojkumar%20Dhanthala&rft.date=2020-02-21&rft.volume=2020&rft.issue=7&rft.spage=834&rft.epage=844&rft.pages=834-844&rft.issn=1434-193X&rft.eissn=1099-0690&rft_id=info:doi/10.1002/ejoc.201901711&rft_dat=%3Cproquest_cross%3E2359205078%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c3171-3602bee9aefbc3eb8175c9188fd0462733d981bb40aa9082f88546527d3e2afe3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2359205078&rft_id=info:pmid/&rfr_iscdi=true |