Linear and nonlinear luminescence properties of thiophene based materials

Three new thiophene based organic luminescence compounds, i.e., 2,5-bis(4-N,N-dimethylaminostyryl) thiophene (BMST), 2,5-bis(4-N,N-diethylaminostyryl)thiophene (BEST) and 2,5-bis(4-N-cyclobutylaminostyryl)thiophene (BBST), were synthesized. All of their measured single-photon excited fluorescence (S...

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Main Authors: PING LU, GUANG MING XIA
Format: Article
Language:English
Published: Serbian Chemical Society 2005-02-01
Series:Journal of the Serbian Chemical Society
Subjects:
Online Access:http://www.shd.org.yu/HtDocs/SHD/vol70/No2/JSCS_V70_No2-07.pdf
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author PING LU
GUANG MING XIA
author_facet PING LU
GUANG MING XIA
author_sort PING LU
collection DOAJ
description Three new thiophene based organic luminescence compounds, i.e., 2,5-bis(4-N,N-dimethylaminostyryl) thiophene (BMST), 2,5-bis(4-N,N-diethylaminostyryl)thiophene (BEST) and 2,5-bis(4-N-cyclobutylaminostyryl)thiophene (BBST), were synthesized. All of their measured single-photon excited fluorescence (SP F) are located in the range of ~ 530 nm with quantum yields of around 40 %, and the corresponding lifetime was 1 ns. The examined compounds show strong solvatochromism in their SPEF spectra. Excited by a fs laser at 800 nm, a strong up-converted fluorescence of the examined compounds was detected. The profile of two-proton excited fluorescence (TPEF) was similar to that of SPEF. The two-photon absorption (TPA) cross sections of the compounds were determined by the TPEF method. All the compounds showed large TPA cross sections. Hence these thiophene derivatives may have good TPA properties.
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spelling doaj.art-a08180e5c09245bfa05644fb567edfa72022-12-22T01:07:33ZengSerbian Chemical SocietyJournal of the Serbian Chemical Society0352-51392005-02-01702201208Linear and nonlinear luminescence properties of thiophene based materialsPING LUGUANG MING XIAThree new thiophene based organic luminescence compounds, i.e., 2,5-bis(4-N,N-dimethylaminostyryl) thiophene (BMST), 2,5-bis(4-N,N-diethylaminostyryl)thiophene (BEST) and 2,5-bis(4-N-cyclobutylaminostyryl)thiophene (BBST), were synthesized. All of their measured single-photon excited fluorescence (SP F) are located in the range of ~ 530 nm with quantum yields of around 40 %, and the corresponding lifetime was 1 ns. The examined compounds show strong solvatochromism in their SPEF spectra. Excited by a fs laser at 800 nm, a strong up-converted fluorescence of the examined compounds was detected. The profile of two-proton excited fluorescence (TPEF) was similar to that of SPEF. The two-photon absorption (TPA) cross sections of the compounds were determined by the TPEF method. All the compounds showed large TPA cross sections. Hence these thiophene derivatives may have good TPA properties.http://www.shd.org.yu/HtDocs/SHD/vol70/No2/JSCS_V70_No2-07.pdftwo-photon absorptionup-converted fluorescencethiophene derivatives.
spellingShingle PING LU
GUANG MING XIA
Linear and nonlinear luminescence properties of thiophene based materials
Journal of the Serbian Chemical Society
two-photon absorption
up-converted fluorescence
thiophene derivatives.
title Linear and nonlinear luminescence properties of thiophene based materials
title_full Linear and nonlinear luminescence properties of thiophene based materials
title_fullStr Linear and nonlinear luminescence properties of thiophene based materials
title_full_unstemmed Linear and nonlinear luminescence properties of thiophene based materials
title_short Linear and nonlinear luminescence properties of thiophene based materials
title_sort linear and nonlinear luminescence properties of thiophene based materials
topic two-photon absorption
up-converted fluorescence
thiophene derivatives.
url http://www.shd.org.yu/HtDocs/SHD/vol70/No2/JSCS_V70_No2-07.pdf
work_keys_str_mv AT pinglu linearandnonlinearluminescencepropertiesofthiophenebasedmaterials
AT guangmingxia linearandnonlinearluminescencepropertiesofthiophenebasedmaterials