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中性发光金属有机框架:结构多样性、光物理性质及传感应用

Neutral Luminescent Metal-Organic Frameworks: Structural Diversification, Photophysical Properties, and Sensing Applications.

作者信息

Chakraborty Gouri, Mandal Sanjay K

机构信息

Department of Chemical Sciences, Indian Institute of Science Education and Research Mohali , Sector 81, Manauli PO, S.A.S. Nagar, Mohali, Punjab 140306, India.

出版信息

Inorg Chem. 2017 Dec 4;56(23):14556-14566. doi: 10.1021/acs.inorgchem.7b02264. Epub 2017 Nov 17.

Abstract

Utilizing flexible bis(tridentate)polypyridyl ligands, the two new luminescent 2D metal organic frameworks {Zn(tpbn)(2,6-NDC)} (1) and {[Zn(tphn)(2,6-NDC)]·4HO} (2), where tpbn = N,N',N″,N‴-tetrakis(2-pyridylmethyl)-1,4-diaminobutane, tphn = N,N',N″,N‴-tetrakis(2-pyridylmethyl)-1,6-diaminohexane, and 2,6-HNDC = 2,6-naphthalenedicarboxylic acid, have been isolated in good yields under solvothermal conditions. Their solid-state molecular structures have been determined by single-crystal X-ray diffractometry. Both 1 and 2 have pentacoordinated Zn(II) centers with an NO environment from three nitrogen atoms of the tpbn or tphn ligand and two carboxylate oxygen atoms from two different 2,6-NDC linkers. However, the binding modes of the tridentate part of polypyridyl ligands to the Zn(II) center are different in 1 and 2-meridional (tpbn) vs facial (tphn) due to an increase (1.5 times) in the methylene chain length. Thus, the binding mode of 2,6-NDC to the Zn(II) center differs: bis(monodentate) syn-anti in 1 and bis(monodentate) syn-syn in 2. This difference in binding modes of the components has a profound effect on the conformation of the six-membered ring (metal centers are considered as the vertices in it) within the 2D framework: honeycomb vs chair form for 1 and 2, respectively. In addition to further characterization by elemental analysis and UV-vis and FT-IR spectroscopy, their framework stabilities in water and thermal properties have been studied by powder X-ray diffraction and thermogravimetric analysis, respectively. On the basis of thermodiffractometry, 1 and 2 retain their crystallinity and overall structure up to 350 and 325 °C, respectively. Their luminescent properties have been utilized to demonstrate sensing of various solvents as well as nitro-aromatic compounds in water, which correlate well with their structural differences. Through the spectral overlap, lifetime measurements, and nature of the Stern-Volmer plots, the fluorescence quenching pathway for the nitro-analytes, particularly 2,4,6-trinitrophenol (TNP), is established for 1 and 2. Their recyclability and stability after sensing experiments are found to be excellent.

摘要

利用柔性双(三齿)多吡啶配体,在溶剂热条件下高产率地分离出了两种新型发光二维金属有机框架{Zn(tpbn)(2,6 - NDC)} (1) 和{[Zn(tphn)(2,6 - NDC)]·4H₂O} (2),其中tpbn = N,N',N″,N‴ - 四(2 - 吡啶甲基)-1,4 - 二氨基丁烷,tphn = N,N',N″,N‴ - 四(2 - 吡啶甲基)-1,6 - 二氨基己烷,2,6 - HNDC = 2,6 - 萘二甲酸。通过单晶X射线衍射测定了它们的固态分子结构。1和2都具有五配位的Zn(II)中心,其配位环境为来自tpbn或tphn配体的三个氮原子以及来自两个不同的2,6 - NDC连接体的两个羧酸根氧原子。然而,由于亚甲基链长度增加(1.5倍),多吡啶配体的三齿部分与Zn(II)中心的结合模式在1中为经式(tpbn),在2中为面式(tphn),二者不同。因此,2,6 - NDC与Zn(II)中心的结合模式也不同:在1中为双(单齿)顺 - 反式,在2中为双(单齿)顺 - 顺式。这种组分结合模式的差异对二维框架内六元环(金属中心被视为其中的顶点)的构象有深远影响:1和2分别为蜂窝状和椅式。除了通过元素分析、紫外 - 可见光谱和傅里叶变换红外光谱进行进一步表征外,还分别通过粉末X射线衍射和热重分析研究了它们在水中的框架稳定性和热性质。基于热衍射分析,1和2分别在高达350和325 °C时保持其结晶度和整体结构。利用它们的发光性质证明了对水中各种溶剂以及硝基芳烃化合物的传感,这与它们的结构差异密切相关。通过光谱重叠、寿命测量以及斯特恩 - 沃尔默图的性质,确定了1和2中硝基分析物,特别是2,4,6 - 三硝基苯酚(TNP)的荧光猝灭途径。发现它们在传感实验后的可回收性和稳定性都非常好。

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