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1D, 2D and 3D luminescent zinc(II) coordination polymers assembled from varying flexible thioether ligands.

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TLDR
Using a series flexible thioether ligands, a 1D infinite chain, a 2D interpenetrating sheet, and a chiral 3D framework were obtained and Luminescent properties of these compounds were studied.
Abstract
Using a series flexible thioether ligands, 4-(2-pyridylmethylthio)benzoic acid (HL1), 4-(4-pyridylmethylthio)benzoic acid (HL2) and 4-(3-pyridylmethylthio)benzoic acid (HL3), a 1D infinite chain [Zn3(L1)6]n (1), a 2D interpenetrating sheet [Zn(L2)2]n (2), and a chiral 3D framework [Zn(L3)2H2O]n (3) were obtained Luminescent properties of these compounds were also studied

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Citations
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Journal ArticleDOI

Engineering Metal Organic Frameworks for Heterogeneous Catalysis

TL;DR: In conclusion, MOFs as Host Matrices or Nanometric Reaction Cavities should not be considered as a source of concern in the determination of MOFs’ properties in relation to other materials.
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MOFs, MILs and more: concepts, properties and applications for porous coordination networks (PCNs)

TL;DR: In this paper, a review of metal-organic frameworks (MOFs) and porous coordination polymers (PCPs) with selected examples of their structures, concepts for linkers, syntheses, post-synthesis modifications, metal nanoparticle formations in MOFs, porosity and zeolitic behavior for applications in gas storage for hydrogen, carbon dioxide, methane and applications in conductivity, luminescence and catalysis.
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Lanthanide metal-organic frameworks for luminescent sensing and light-emitting applications

TL;DR: In this paper, the authors summarize the research progress on the design and construction of luminescent lanthanide MOFs, as well as their potential functions and applications on luminecent sensing and light-emitting.
Journal ArticleDOI

Recent advances in crystal engineering

TL;DR: The 10th edition of CrystEngComm as mentioned in this paper highlighted the state-of-the-art of crystal engineering and new trends and developing areas in crystal engineering, such as intermolecular interactions, metal-organic frameworks or coordination polymers; polymorphism and solvates.
Journal ArticleDOI

Syntheses, Structures, and Photoluminescence of Five New Metal−Organic Frameworks Based on Flexible Tetrapyridines and Aromatic Polycarboxylate Acids

TL;DR: In this article, tetrakis(4-pyridyloxymethylene)methane (TPOM) with deprotonated 1,4-benzenedicarboxylate (H2BDc) or 5-hydroxyisophthalic acid (5-OH-H2bdc) were characterized by elemental analysis, IR spectroscopy, and X-ray single-crystal diffraction.
References
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Journal ArticleDOI

Systematic Design of Pore Size and Functionality in Isoreticular MOFs and Their Application in Methane Storage

TL;DR: Metal-organic framework (MOF-5), a prototype of a new class of porous materials and one that is constructed from octahedral Zn-O-C clusters and benzene links, was used to demonstrate that its three-dimensional porous system can be functionalized with the organic groups and can be expanded with the long molecular struts biphenyl, tetrahydropyrene, pyrene, and terphenyl.
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Design and synthesis of an exceptionally stable and highly porous metal-organic framework

TL;DR: In this article, an organic dicarboxylate linker is used in a reaction that gives supertetrahedron clusters when capped with monocarboxyates.
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Hydrogen Storage in Microporous Metal-Organic Frameworks

TL;DR: Inelastic neutron scattering spectroscopy of the rotational transitions of the adsorbed hydrogen molecules indicates the presence of two well-defined binding sites (termed I and II), which are associated with hydrogen binding to zinc and the BDC linker, respectively.
Journal ArticleDOI

A homochiral metal-organic porous material for enantioselective separation and catalysis

TL;DR: The synthesis of a homochiral metal–organic porous material that allows the enantioselective inclusion of metal complexes in its pores and catalyses a transesterification reaction in an enantiOSElective manner is reported.
Journal ArticleDOI

CH/π hydrogen bonds in crystals

Motohiro Nishio
- 11 May 2004 - 
TL;DR: The CH/π interaction is a kind of hydrogen bond operating between a soft acid CH and a soft base π-system (double and triple bonds, C6 and C5 aromatic rings, heteroaromatics, convex surfaces of fullerenes and nanotubes) as discussed by the authors.
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