光致发光
超分子化学
发光
金属有机骨架
结晶学
配体(生物化学)
金属
固态
拓扑(电路)
结构母题
材料科学
化学
粉末衍射
衍射
晶体结构
物理
物理化学
光电子学
光学
有机化学
组合数学
吸附
受体
生物化学
数学
作者
Abdul Malik Puthan Peedikakkal,Mohammad Qamar
标识
DOI:10.1007/s12039-018-1441-4
摘要
Two known Pb(II) metal-organic frameworks (MOFs), pseudo-supramolecular isomeric pairs synthesized namely, [Pb $$_{3}$$ (BDC) $$_{3}$$ (DMF) $$_{3.5}$$ ] (1) and [Pb(BDC)(H $$_{2}$$ O)] (2) (where BDC $$=$$ benzenedicarboxylate) were synthesized and reexamined their structures to determine the topology of the networks. In that 1 displayed a 3D (10,3)-b linked network with having the ths topology whereas 2 shows a (6,3) 2D layers interconnected to a 3D framework structure. Remarkably, the desolvation of both 1 and 2 cause structural transformation to a known 3D network structure of [Pb(BDC)] $$_n$$ (3) as established by X-ray powder diffraction patterns. Photoluminescence studies in the solid-state at room temperature of 1–3 compounds exhibit interesting luminescence close to white light region due to ligand-to-metal charge-transfer (LMCT). Synopsis: Two pseudo-supramolecular isomeric pairs of Pb(II) metal-organic frameworks (MOFs) have been synthesized which show structural transformation to desolvated 3D network structure. All the compounds exhibit interesting solid-state photoluminescence at room temperature which is very close to white light emission.
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