The relation between the structure of nitrobenzene derivatives and fluorescence quenching efficiency to the poly(2,5 dipentyloxy-para-phenylene ethynylene)

Hongli Xu; Bin Tong; Jianbing Shi; Yang Liu; Xuling Tian; Junge Zhi; Yuping Dong; Jacky Wing Yip Lam; Benzhong Tang

doi:10.3724/sp.j.1105.2007.00293

The relation between the structure of nitrobenzene derivatives and fluorescence quenching efficiency to the poly(2,5 dipentyloxy-para-phenylene ethynylene)

Hongli Xu^*, Bin Tong, Jianbing Shi, Yang Liu, Xuling Tian, Junge Zhi, Yuping Dong, Jacky Wing Yip Lam, Benzhong Tang

^*Corresponding author for this work

Research output: Contribution to journal › Article › peer-review

7 Citations (Scopus)

Abstract

The poly(2,5-dipentyloxy-para-phenylene ethynylene) (P) was synthesized by Pd-catalyzed Sonogashira coupling reaction. Due to causing energy transfer between the nitrobenzene's quenchers and the polymer chains through the charge-transfer interaction, the fluorescence quenched properties of P varied obviously with the parasubstituting group's structure in the nitrobenzene derivatives. The fluorescence quenching efficiency of quenchers improved with increasing of electron repulsion capability of the para-substituting group. The fluorescence quenching efficiency increased nonlinearly with the concentration of the quenchers and had, however, no relation with the quenching time.

Original language	English
Pages (from-to)	293-296
Number of pages	4
Journal	Acta Polymerica Sinica
Issue number	3
DOIs	https://doi.org/10.3724/sp.j.1105.2007.00293
Publication status	Published - Mar 2007

Keywords

Fluorescence quenching
Nitrobenzene derivative
Polyphenylene ethynylene

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10.3724/sp.j.1105.2007.00293

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abstract = "The poly(2,5-dipentyloxy-para-phenylene ethynylene) (P) was synthesized by Pd-catalyzed Sonogashira coupling reaction. Due to causing energy transfer between the nitrobenzene's quenchers and the polymer chains through the charge-transfer interaction, the fluorescence quenched properties of P varied obviously with the parasubstituting group's structure in the nitrobenzene derivatives. The fluorescence quenching efficiency of quenchers improved with increasing of electron repulsion capability of the para-substituting group. The fluorescence quenching efficiency increased nonlinearly with the concentration of the quenchers and had, however, no relation with the quenching time.",

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author = "Hongli Xu and Bin Tong and Jianbing Shi and Yang Liu and Xuling Tian and Junge Zhi and Yuping Dong and Lam, {Jacky Wing Yip} and Benzhong Tang",

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T1 - The relation between the structure of nitrobenzene derivatives and fluorescence quenching efficiency to the poly(2,5 dipentyloxy-para-phenylene ethynylene)

AU - Xu, Hongli

AU - Tong, Bin

AU - Shi, Jianbing

AU - Liu, Yang

AU - Tian, Xuling

AU - Zhi, Junge

AU - Dong, Yuping

AU - Lam, Jacky Wing Yip

AU - Tang, Benzhong

PY - 2007/3

Y1 - 2007/3

N2 - The poly(2,5-dipentyloxy-para-phenylene ethynylene) (P) was synthesized by Pd-catalyzed Sonogashira coupling reaction. Due to causing energy transfer between the nitrobenzene's quenchers and the polymer chains through the charge-transfer interaction, the fluorescence quenched properties of P varied obviously with the parasubstituting group's structure in the nitrobenzene derivatives. The fluorescence quenching efficiency of quenchers improved with increasing of electron repulsion capability of the para-substituting group. The fluorescence quenching efficiency increased nonlinearly with the concentration of the quenchers and had, however, no relation with the quenching time.

AB - The poly(2,5-dipentyloxy-para-phenylene ethynylene) (P) was synthesized by Pd-catalyzed Sonogashira coupling reaction. Due to causing energy transfer between the nitrobenzene's quenchers and the polymer chains through the charge-transfer interaction, the fluorescence quenched properties of P varied obviously with the parasubstituting group's structure in the nitrobenzene derivatives. The fluorescence quenching efficiency of quenchers improved with increasing of electron repulsion capability of the para-substituting group. The fluorescence quenching efficiency increased nonlinearly with the concentration of the quenchers and had, however, no relation with the quenching time.

KW - Fluorescence quenching

KW - Nitrobenzene derivative

KW - Polyphenylene ethynylene

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DO - 10.3724/sp.j.1105.2007.00293

M3 - Article

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JO - Acta Polymerica Sinica

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The relation between the structure of nitrobenzene derivatives and fluorescence quenching efficiency to the poly(2,5 dipentyloxy-para-phenylene ethynylene)

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Keywords

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