Luminescent Metal-Organic Framework for the Selective Detection of Aldehydes

被引:5
|
作者
Velasco, Ever [1 ]
Zhang, Guoyu [1 ]
Teat, Simon J. [2 ]
Tan, Kui [3 ]
Ullah, Saif [4 ,5 ]
Thonhauser, Timo [4 ,5 ]
Li, Jing [1 ]
机构
[1] Rutgers State Univ, Dept Chem & Chem Biol, Piscataway, NJ 08854 USA
[2] Lawrence Berkeley Natl Lab, Adv Light Source, Berkeley, CA 94720 USA
[3] Univ Texas Dallas, Dept Mat Sci & Engn, Richardson, TX 75080 USA
[4] Wake Forest Univ, Dept Phys, Winston Salem, NC 27109 USA
[5] Wake forest Univ, Ctr Funct Mat, Winston Salem, NC 27109 USA
关键词
D O I
10.1021/acs.inorgchem.3c02115
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The detection of toxic, hazardous chemical species is an important task because they pose serious risks to either the environment or human health. Luminescent metal-organic frameworks (LMOFs) as alternative sensors offer rapid and sensitive detection of chemical species. Interactions between chemical species and LMOFs result in changes in the photoluminescence (PL) profile of the LMOFs which can be readily detected using a simple fluorometer. Herein, we report the use of a robust, Zn-based LMOF, [Zn-5(mu(3)-OH)(2)(adtb)(2)(H2O)(5)center dot 5 DMA] (Zn-adtb, LMOF-341), for the selective detection of benzaldehyde. Upon exposure to benzaldehyde, Zn-adtb experiences significant luminescent quenching, as characterized through PL experiments. Photoluminescent titration experiments reveal that LMOF-341 has a detection limit of 64 ppm and a K-sv value of 179 M-1 for benzaldehyde. Furthermore, we study the guest-host interactions that occur between LMOF-341 and benzaldehyde through in situ Fourier transform infrared and computational modeling employing density functional theory. The results show that benzaldehyde interacts more strongly with LMOF-341 compared to formaldehyde and propionaldehyde. Our combined studies also reveal that the mechanism of luminescence quenching originates from an electron-transfer process.
引用
收藏
页码:16435 / 16442
页数:8
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