个人信息Personal Information
副教授
博士生导师
硕士生导师
性别:男
毕业院校:大连化物所
学位:博士
所在单位:化学学院
学科:分析化学
办公地点:大连理工大学西部校区化工综合楼D313
联系方式:+86-411-84986042
电子邮箱:bo.song@dlut.edu.cn
Ratiometric Time-Gated Luminescence Probe for Hydrogen Sulfide Based on Lanthanide Complexes
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论文类型:期刊论文
发表时间:2014-12-02
发表刊物:ANALYTICAL CHEMISTRY
收录刊物:SCIE、PubMed、Scopus
卷号:86
期号:23
页面范围:11883-11889
ISSN号:0003-2700
摘要:Developments of ratiometric bioprobes are highly appealing due to the superiority of their self-calibration capability for the quantitative biotracking. In this work, we designed and synthesized a novel lanthanide complex-based ratiometric luminescence probe, [4'-(2,4-dinitrophenyloxy)-2,2':6',2"-terpyridine-6,6"-diyl]bis(methylenenitrilo) tetrakis(acetate)-Eu3+/Tb3+ (NPTTA-Eu3+/Tb3+), for the specific recognition and quantitative time-gated luminescence detection of hydrogen sulfide (H2S) in aqueous and living cell samples. Due to the presence of the photoinduced electron transfer (PET) process from the terpyridine-Eu3+/Tb3+ moiety to 2,4-dinitrophenyl (DNP), the probe itself is weakly luminescent. In physiological pH aqueous media, the reaction of NPTTA-Eu3+/Tb3+ with H2S leads to the cleavage of DNP moiety from the probe molecule, which affords the deprotonated (4'-hydroxy-2,2':6',2"-terpyridine-6,6"-diyl)bis(methylenenitrilo) tetrakis(acetate)-Eu3+/Tb3+ and terminates the PET process. Meanwhile, the intensity of Tb3+ emission at 540 nm is remarkably increased, while that of the Eu3+ emission at 610 nm is slightly decreased. After the reaction, the intensity ratio of Tb3+ emission to Eu3+ emission, I-540/I-610, was similar to 220-fold increased, and the dose-dependent enhancement of I-540/I-610 showed a good linearity upon the increase of H2S concentration with a detection limit of 3.5 nM. This unique luminescence response allowed NPTTA-Eu3+/Tb3+ to be conveniently used as a ratiometric probe for the time-gated luminescence detection of H2S with I540/I610 as a signal. In addition, the applicability of the probe for the quantitative time-gated luminescence imaging of intracellular H2S in living cells was investigated. The results demonstrated the efficacy and advantage of the new probe for the time-gated luminescence cell imaging application.