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首页> 外文期刊>Journal of Photochemistry and Photobiology, A. Chemistry >A lanthanide doped metal-organic framework demonstrated as naked eye detector of a trace of water in organic solvents including alcohols by monitoring the turn-on of luminescence
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A lanthanide doped metal-organic framework demonstrated as naked eye detector of a trace of water in organic solvents including alcohols by monitoring the turn-on of luminescence

机译:镧系金属 - 有机框架在有机溶剂中作为痕量的水,包括醇通过监测发光的开启

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It is very crucial to have a very simple, instant and low-cost detection and estimation of a trace of water in common organic solvents including alcohols. To obtain the sensor material we have synthesized a metal-organic framework (MOF) {[Y1.0Mn1.5(PDA)(3)(H2O)(3)]center dot 3 center dot 5H(2)O}, 1, (PDA = 2,6-pyridinedicarboxylic acid) through hydrothermal process. A doping of compound 1 by 10 % terbium {[Y0.9Tb0.1Mn1.5(PDA)(3)(H2O)(3)]center dot 3 center dot 5H(2)O}, 1:Tb, was done through an isomorphous substitution technique. The most advantageous point about 1:Tb was the metal centre luminescence, which was largely stokes shifted from the excitation light making possible the naked eye observation. The weak metal centre luminescence intensity of dehydrated 1:Tb (excluding lattice and coordinated water molecules) in organic solvents EtOH, CH3OH, CH3CN, THE and n-heptane showed huge turn-on in presence of trace amounts of H 2 O in the said solvents. The luminescence intensity of Tb3+ centre was enhanced by several folds with a limit of detection 1.12 %(v/v), 0.47 %(v/v), 0.04 %(v/v), 0.13 %(v/v) and 0.53 %(v/v) respectively. The coordinated water molecules as well as the lattice water molecules in 1:Tb play a vital role during sensitization of the Tb3+ centre by enhancing the rigidity of the structure and facilitating the formation of LMCT state which ultimately results in a huge turn-on of metal centre luminescence.
机译:在普通的有机溶剂中具有非常简单,即时和低成本的检测和估算痕量的水,这是非常重要的。为了获得传感器材料,我们合成了金属有机框架(MOF){[Y1.0MN1.5(PDA)(3)(3)(3)(3)]中心点3中心点5H(2)O},1, (PDA = 2,6-吡啶二羧酸)通过水热法。化合物1掺杂化合物1×10%铽{[Y0.9TB0.1MN1.5(PDA)(3)(3)(3)(3))中心点3中心点5H(2)O},1:TB通过同构替代技术。大约1:Tb的最有利点是金属中心发光,这在很大程度上是斯托克斯从激发光线移位,使得肉眼观察可能。在有机溶剂EtOH,CH 3 OH,CH 3 CN,和正庚烷中,在有机溶剂中脱水1:Tb(不包括晶格和配位水分子)的弱金属中心发光强度在所述上述痕量H 2 O存在下显示出巨大的开启溶剂。 TB3 +中心的发光强度由几倍的折叠增强,限制1.12%(v / v),0.47%(v / v),0.04%(v / v),0.13%(v / v)和0.53% (v / v)分别。通过提高结构的刚性并促进LMCT状态的形成最终导致金属突出的敏感性,在1:TB在TB3 +中心的敏感过程中发挥着至关重要的作用。最终导致金属巨大导通的LMCT状态中心发光。

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