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一种含席夫碱配体的纳米级锌(II)-钕(III)配合物:近红外发光传感阴离子和硝基炸药

One Nanoscale Zn(II)-Nd(III) Complex With Schiff Base Ligand: NIR Luminescent Sensing of Anions and Nitro Explosives.

作者信息

Liu Xia, Yang Xiaoping, Ma Yanan, Liu Jieni, Shi Dongliang, Niu Mengyu, Schipper Desmond

机构信息

College of Chemistry and Materials Engineering, Wenzhou University, Wenzhou, China.

Department of Chemistry and Biochemistry, The University of Texas at Austin, Austin, TX, United States.

出版信息

Front Chem. 2020 Oct 14;8:536907. doi: 10.3389/fchem.2020.536907. eCollection 2020.

DOI:10.3389/fchem.2020.536907
PMID:33195043
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7591804/
Abstract

One Zn-Nd complex [ZnNdL(OAc)(OH)(CHOH)] () was synthesized from Schiff base ligand bis(3-methoxysalicylidene)ethylene-1,2-phenylenediamine (HL). shows nanoscale rectangular structure with sizes of about 0.8 × 1.1 × 2.8 nm. exhibits typical near-infrared luminescence of Nd(III) under the excitation of UV-visible light. Further study shows that the complex displays luminescent response behavior to anions and nitro explosives, especially with high sensitivity to H and 2,4,6-trinitrophenol.

摘要

一种锌-钕配合物[ZnNdL(OAc)(OH)(CHOH)]()由席夫碱配体双(3-甲氧基水杨醛)乙二胺-1,2-苯二胺(HL)合成。显示出尺寸约为0.8×1.1×2.8纳米的纳米级矩形结构。在紫外-可见光激发下表现出典型的钕(III)近红外发光。进一步研究表明,该配合物对阴离子和硝基炸药表现出发光响应行为,尤其是对H和2,4,6-三硝基苯酚具有高灵敏度。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a244/7591804/197312055739/fchem-08-536907-g0011.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a244/7591804/9dd329c47e6f/fchem-08-536907-g0012.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a244/7591804/28e6b1761b31/fchem-08-536907-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a244/7591804/22165a9509ed/fchem-08-536907-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a244/7591804/8efa9e6c9fd4/fchem-08-536907-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a244/7591804/75f3223235b4/fchem-08-536907-g0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a244/7591804/d68dd3ffbfbf/fchem-08-536907-g0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a244/7591804/353d276488d8/fchem-08-536907-g0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a244/7591804/149a5f65edcb/fchem-08-536907-g0007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a244/7591804/1ac399419fbb/fchem-08-536907-g0008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a244/7591804/831a33bac69c/fchem-08-536907-g0009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a244/7591804/02ec8d269e73/fchem-08-536907-g0010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a244/7591804/94cd423d9772/fchem-08-536907-g0013.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a244/7591804/197312055739/fchem-08-536907-g0011.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a244/7591804/9dd329c47e6f/fchem-08-536907-g0012.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a244/7591804/28e6b1761b31/fchem-08-536907-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a244/7591804/22165a9509ed/fchem-08-536907-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a244/7591804/8efa9e6c9fd4/fchem-08-536907-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a244/7591804/75f3223235b4/fchem-08-536907-g0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a244/7591804/d68dd3ffbfbf/fchem-08-536907-g0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a244/7591804/353d276488d8/fchem-08-536907-g0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a244/7591804/149a5f65edcb/fchem-08-536907-g0007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a244/7591804/1ac399419fbb/fchem-08-536907-g0008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a244/7591804/831a33bac69c/fchem-08-536907-g0009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a244/7591804/02ec8d269e73/fchem-08-536907-g0010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a244/7591804/94cd423d9772/fchem-08-536907-g0013.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a244/7591804/197312055739/fchem-08-536907-g0011.jpg

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本文引用的文献

1
Large Ln coordination nanorings: NIR luminescence sensing of metal ions and nitro explosives.大Ln 配位纳米环:金属离子和硝基炸药的近红外发光传感。
Chem Commun (Camb). 2019 Oct 29;55(87):13116-13119. doi: 10.1039/c9cc07430a.
2
Two novel metal-organic frameworks based on pyridyl-imidazole-carboxyl multifunctional ligand: selective CO capture and multiresponsive luminescence sensor.基于吡啶基-咪唑-羧基多功能配体的两种新型金属有机框架:选择性CO捕获和多响应发光传感器。
Dalton Trans. 2019 Aug 7;48(29):10892-10900. doi: 10.1039/c9dt01430f. Epub 2019 May 21.
3
Highly luminescent, biocompatible ytterbium(iii) complexes as near-infrared fluorophores for living cell imaging.
高发光、生物相容性的镱(III)配合物作为用于活细胞成像的近红外荧光团
Chem Sci. 2018 Mar 19;9(15):3742-3753. doi: 10.1039/c8sc00259b. eCollection 2018 Apr 21.
4
A luminescent heterometallic metal-organic framework for the naked-eye discrimination of nitroaromatic explosives.一种用于裸眼识别硝基芳香族炸药的发光异金属金属有机框架。
Chem Commun (Camb). 2017 Sep 14;53(74):10318-10321. doi: 10.1039/c7cc05345b.
5
Highly near-IR emissive ytterbium(iii) complexes with unprecedented quantum yields.具有前所未有的量子产率的高近红外发射镱(III)配合物。
Chem Sci. 2017 Apr 1;8(4):2702-2709. doi: 10.1039/c6sc05021b. Epub 2017 Jan 13.
6
Self-assembly of stable luminescent lanthanide supramolecular ML cages with sensing properties toward nitroaromatics.具有对硝基芳烃传感特性的稳定发光镧系超分子ML笼的自组装。
Chem Commun (Camb). 2017 Feb 21;53(16):2459-2462. doi: 10.1039/c7cc00189d.
7
Fluorescence based explosive detection: from mechanisms to sensory materials.荧光基爆炸物检测:从机理到传感材料。
Chem Soc Rev. 2015 Nov 21;44(22):8019-61. doi: 10.1039/c5cs00496a. Epub 2015 Sep 3.
8
The exceptionally rich coordination chemistry generated by Schiff-base ligands derived from o-vanillin.由邻香草醛衍生的席夫碱配体产生的异常丰富的配位化学。
Dalton Trans. 2015 Oct 14;44(38):16633-53. doi: 10.1039/c5dt02661j. Epub 2015 Aug 18.
9
Heterometal-organic frameworks as highly sensitive and highly selective luminescent probes to detect I⁻ ions in aqueous solutions.异金属有机框架作为高灵敏度和高选择性的发光探针用于检测水溶液中的I⁻离子。
Chem Commun (Camb). 2015 Mar 7;51(19):3985-8. doi: 10.1039/c4cc09081k.
10
A fluorescent metal-organic framework for highly selective detection of nitro explosives in the aqueous phase.一种用于水相中高选择性检测硝基炸药的荧光金属有机框架材料。
Chem Commun (Camb). 2014 Aug 18;50(64):8915-8. doi: 10.1039/c4cc03053b.