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首页> 外文期刊>Inorganic Chemistry: A Research Journal that Includes Bioinorganic, Catalytic, Organometallic, Solid-State, and Synthetic Chemistry and Reaction Dynamics >Thermochromic and Mechanochromic Luminescence Umpolung in Isostructural Metal-Organic Frameworks Based on Cu6I6 Clusters
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Thermochromic and Mechanochromic Luminescence Umpolung in Isostructural Metal-Organic Frameworks Based on Cu6I6 Clusters

机译:基于Cu6I6团簇的等构金属有机骨架中的热致变色和机械致变色发光体

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Two isostructural metalorganic framework (MOF) materials, namely, {[MeSi(Py-3)(3)](6)(Cu6I6)}(n) (1) and {[ MeSi((3)Qy)(3)](6)(Cu6I6)}(n) (2), featuring Cu6I6 clusters were synthesized from tridentate arylsilane ligands of the type MeSi(Py-3)(3) (Py-3 = 3-pyridyl) and MeSi(3Qy)(3) ((3)Qy = 3-quinolyl), respectively. While the MOF 1 displays the usual thermochromism associated with traditional Cu4I4Py4 clusters, the MOF 2 shows (XLCT)-X-3/(MLCT)-M-3 emission due to the Cu6I6 cluster core at both 298 and 77 K, albeit with some marginal variations in its emission wavelengths. Interestingly, an unusual reversal in the mechanochromic luminescent behavior was observed for these isostructural MOFs at 298 K wherein a pronounced blue-shifted high energy emission for 1 (from orange to yellowish-orange) and a red-shifted low-energy emission for 2 (from green to orange) were obtained upon grinding these samples. This is primarily due to the variations in their cuprophilic interactions as 1 displays shorter Cu Cu distances (2.745(1) angstrom) in comparison with those present in 2 (3.148(0) angstrom). As a result, the ground sample of 2 exhibits a prominent red shift in luminescence owing to the reduction of its Cu Cu distances to an unknown value closer to the sum of van der Waals radii between two Cu(I) atoms (2.80 angstrom). However, the blue-shifted emission in 1 is presumably attributed to the rise in its lowest unoccupied molecular orbital energy levels caused by changes in the secondary packing forces. Furthermore, the absorption and emission characteristics of 1 and 2 were substantiated by time-dependent density functional theory calculations on their discrete-model compounds. In addition, the syntheses, reactivity studies, and photophysical properties of two one-dimensional MOFs, namely, {[MeSi((3)Qy)(3)](2)(Cu2I2)}(n) (3) and {[MeSi((3)Qy)(3)](CuI)}(n) (4), having dimeric Cu2I2 and monomeric CuI moieties, respectively, were examined.
机译:两种同构的金属有机骨架(MOF)材料,即{[MeSi(Py-3)(3)](6)(Cu6I6)}(n)( 1 )和{[MeSi((3 )Qy)(3)](6)(Cu6I6)}(n)( 2 ),其特征是由MeSi(Py-3)(3)型三齿芳基硅烷配体合成Cu6I6簇Py-3 = 3-吡啶基)和MeSi(3Qy)(3)((3)Qy = 3-喹啉基)。 MOF 1 显示与传统Cu4I4Py4团簇相关的通常的热致变色现象,而MOF 2 显示由于(XLCT)-X-3 /(MLCT)-M-3发射Cu6I6团簇核在298 K和77 K时,尽管其发射波长略有变化。有趣的是,在298 K时,观察到这些同构MOF的机械变色发光行为发生了异常的反转,其中 1 的蓝光高能发射(从橙色变为橙黄色)和红移研磨这些样品后,获得了 2 的低能量发射(从绿色到橙色)。这主要是由于与 2 (3.148(0)相比, 1 显示出更短的Cu Cu距离(2.745(1)埃)导致其嗜铜相互作用的变化。 )埃。结果, 2 的地面样本由于其Cu Cu距离减小到更接近两个Cu(I)之间的范德华半径之和的未知值而在发光中表现出显着的红移。 )原子(2.80埃)。然而, 1 中发生蓝移的发射可能是由于次级堆积力的变化导致其最低的未占据分子轨道能级增加。此外, 1 2 的吸收和发射特性通过时变密度泛函理论对它们的离散模型化合物的证实。另外,两个{{MeSi((3)Qy)(3)](2)(Cu2I2)}(n)一维MOF的合成,反应性研究和光物理性质( 3 < / bold>)和{[MeSi((3)Qy)(3)](CuI)}(n)( 4 )分别具有二聚Cu2I2和单体CuI部分。

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