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Dai-Zheng Liao

Bio: Dai-Zheng Liao is an academic researcher from Chinese Academy of Sciences. The author has contributed to research in topics: Crystal structure & Copper. The author has an hindex of 29, co-authored 97 publications receiving 3979 citations. Previous affiliations of Dai-Zheng Liao include Nanjing University & Dalian University of Technology.

Papers published on a yearly basis

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TL;DR: Two 3d-4f heterometallic coordination polymers synthesized under hydrothermal conditions increased significantly upon addition of Zn2+, while the introduction of other metal ions caused the intensity to be either unchanged or weakened.
Abstract: Two 3d-4f heterometallic coordination polymers {[Ln(PDA)3Mn1.5(H2O)3].3.25H2O}infinity with 1D channels were synthesized under hydrothermal conditions (PDA = pyridine-2,6-dicarboxylic acid; Ln = Eu (1); Ln = Tb (2)). The emission intensities of 1 and 2 increased significantly upon addition of Zn2+, while the introduction of other metal ions caused the intensity to be either unchanged or weakened. The case implies that 1 and 2 may be used as luminescent probes of Zn2+.

818 citations

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TL;DR: A nanotubular 3D heterometallic zeolitic polymer was designed and synthesized by simply tuning the amount of coordinated water on the Mn ion in the molecular ladder polymer.
Abstract: A nanotubular 3D heterometallic zeolitic polymer, {[Yb(PDA)3Mn1.5(H2O)3]·1.5H2O}n (2), was designed and synthesized by simply tuning the amount of coordinated water on the Mn ion in the molecular ladder polymer {[Yb(PDA)3Mn1.5(H2O)6]·6H2O}n (1). 1 and 2 were structurally and magnetically characterized. The water molecules capsulated within the nanotube were arrayed into an unprecedented “water” pipe. The robust 2 retained intact networks after the removal of guest water trapped in the nanotubes and even after methanol replaced guest water.

562 citations

Journal ArticleDOI
Long Yi1, Bin Ding1, Bin Zhao1, Peng Cheng1, Dai-Zheng Liao1, Shi-Ping Yan1, Zong-Hui Jiang1 
TL;DR: Six complexes exhibit six types of bridging modes of N1,N2-triazole in combination with single-atom bridges, whereas 3 is the first example of the micro(3)-Cl bridging mode in triazole-metal complexes.
Abstract: Cadmium salts with different triazole ligands have led to a series of novel triazole−cadmium compounds varying from zero- to three-dimensionality. [Cd2(deatrz)2(H2O)Br4] (1) (deatrz = 3,5-diethyl-4-amino-1,2,4-triazole) is a zero-dimensional complex which uses a triazole ligand together with μ-OH2 as bridges to form a 1D chain via hydrogen-bonding contacts. {[Cd3(deatrz)2Cl6(H2O)2]·2H2O}n (2), {[Cd(dmtrz)Cl2]·1.5H2O}n (3) (dmtrz = 3,5-dimethyl-1,2,4-triazole), and {[Cd3(deatrz)4Cl2(SCN)4]·2H2O}n (4) are polymeric 1D chains. 2 and 4 were constructed via trinuclear cadmium units bridged by triazole ligands and chloride atoms, while 3 consists of μ2-Cl, μ3-Cl, and triazole bridges, cross-linked by hydrogen bonding to give a 3D framework. {[Cd3(dmatrz)4(SCN)6]}n (5) (dmatrz = 3,5-dimethyl-4-amino-1,2,4-triazole) shows a two-dimensional structure whose fundamental units are trinuclear metal cations bridged via triazole ligands. The complex {[Cd(dmtrz)(SCN)2]}n (6) is the first three-dimensional example in N1,N...

202 citations

Journal ArticleDOI
TL;DR: Two novel three-dimensional (3D) 3d-4f mixed complexes, synthesized and characterized by X-ray crystal diffraction and magnetic properties, show that these complexes form a 3D framework, comprised of an unusual infinite one-dimensional chain based on heterometallic Ln2Ni2 rings.
Abstract: Two novel three-dimensional (3D) 3d-4f mixed complexes [Ln(H(2)O)(4)][Ni(2)TTHA(SCN)(2)].H(3)O+ [Ln = Pr (1), Ce (2); H(6)TTHA = triethylenetetraaminehexaacetic acid], based on the building blocks of [Ni(2)TTHA(SCN)(2)](4-), were synthesized and characterized by X-ray crystal diffraction and magnetic properties. The single-crystal structures show that these complexes form a 3D framework, comprised of an unusual infinite one-dimensional chain based on heterometallic Ln2Ni2 rings. The temperature-dependent magnetic susceptibilities were analyzed by an approximate model, leading to g = 2.06. Delta = 2.83, zJ' = -0.6 cm-1 for complex 1 and g = 2.07, Delta = 1.00, zJ' = -0.5 cm(-1) for complex 2.

83 citations


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TL;DR: This critical review starts with a brief introduction to gas separation and purification based on selective adsorption, followed by a review of gas selective adsorbents in rigid and flexible MOFs, and primary relationships between adsorptive properties and framework features are analyzed.
Abstract: Adsorptive separation is very important in industry. Generally, the process uses porous solid materials such as zeolites, activated carbons, or silica gels as adsorbents. With an ever increasing need for a more efficient, energy-saving, and environmentally benign procedure for gas separation, adsorbents with tailored structures and tunable surface properties must be found. Metal–organic frameworks (MOFs), constructed by metal-containing nodes connected by organic bridges, are such a new type of porous materials. They are promising candidates as adsorbents for gas separations due to their large surface areas, adjustable pore sizes and controllable properties, as well as acceptable thermal stability. This critical review starts with a brief introduction to gas separation and purification based on selective adsorption, followed by a review of gas selective adsorption in rigid and flexible MOFs. Based on possible mechanisms, selective adsorptions observed in MOFs are classified, and primary relationships between adsorption properties and framework features are analyzed. As a specific example of tailor-made MOFs, mesh-adjustable molecular sieves are emphasized and the underlying working mechanism elucidated. In addition to the experimental aspect, theoretical investigations from adsorption equilibrium to diffusion dynamics via molecular simulations are also briefly reviewed. Furthermore, gas separations in MOFs, including the molecular sieving effect, kinetic separation, the quantum sieving effect for H2/D2 separation, and MOF-based membranes are also summarized (227 references).

7,186 citations

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TL;DR: This critical review discusses the origins of MOF luminosity, which include the linker, the coordinated metal ions, antenna effects, excimer and exciplex formation, and guest molecules.
Abstract: Metal–organic frameworks (MOFs) display a wide range of luminescent behaviors resulting from the multifaceted nature of their structure. In this critical review we discuss the origins of MOF luminosity, which include the linker, the coordinated metal ions, antenna effects, excimer and exciplex formation, and guest molecules. The literature describing these effects is comprehensively surveyed, including a categorization of each report according to the type of luminescence observed. Finally, we discuss potential applications of luminescent MOFs. This review will be of interest to researchers and synthetic chemists attempting to design luminescent MOFs, and those engaged in the extension of MOFs to applications such as chemical, biological, and radiation detection, medical imaging, and electro-optical devices (141 references).

4,407 citations

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2,877 citations

Journal ArticleDOI
TL;DR: A review on metal ion containing coordination polymer networks is given in this paper, where the authors highlight the current research in the field by giving a short overview on the concept of coordination polymers networks, how and why they are made.

1,361 citations