Myoung Soo Lah 교수

In this review, we describe two recently implemented conceptual approaches facilitating the design and deliberate construction of metal–organic frameworks (MOFs), namely supermolecular building block (SBB) and supermolecular building layer (SBL) approaches. Our main objective is to offer an appropriate means to assist/aid chemists and material designers alike to rationally construct desired functional MOF materials, made-to-order MOFs. We introduce the concept of net-coded building units (net-cB

The crystal structure of dimeric Fe(III) superoxide dismutase (SOD) from Escherichia coli (3006 protein atoms, 2 irons, and 281 solvents) has been refined to an R of 0.184 using all observed data between 40.0 and 1.85 A (34,879 reflections). Features of this structure are compared with the refined structure of MnSOD from Thermus thermophilus. The coordination geometry at the Fe site is distorted trigonal bipyramidal, with axial ligands His26 and solvent (proposed to be OH-), and in-plane ligands

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Metal-organic polyhedra are a member of metal-organic materials, and are together with metal-organic frameworks utilized as emerging porous platforms for numerous applications in energy- and bio-related sciences. However, metal-organic polyhedra have been significantly underexplored, unlike their metal-organic framework counterparts. In this review, we will cover the topologies and the classification of metal-organic polyhedra and share several suggestions, which might be useful to synthetic che

Metal-organic macrocycles (MOMs), metal-organic polyhedra (MOPs) and metal-organic frameworks (MOFs) are metal-organic systems (MOSs) developed from appropriately designed ligands and selected metal ions. Metalladiazamacrocycles, a class of MOMs, are finite 2D MOSs formed from tricationic hexacoordinate metal ions and ditopic bridging ligands, N-acylsalicylhydrazide, containing diaza residues, where the size and shape of the systems have been modulated by controlling the steric repulsions betwee

A C(3) symmetric ligand with three 1,3-benzenedicarboxylate units has been used to construct a metal-organic framework with a (3,24)-connected network topology, where the nanometre-sized metal-organic cuboctahedra (MOCs) have been incorporated solely into a cubic close packing (CCP) arrangement, which led to superoctahedral and supertetrahedral cavities.

While only a partially transmetalated network was observed in a rigid metal–organic framework (MOF), not only a completely transmetalated isostructural network but also a partially transmetalated core–shell heterostructural network could be obtained in a flexible MOF by controlling the reaction conditions.

The first example of transition metal co-ordination to ethereal like oxygens of a 9-metallocrown-3 ether is seen in FeIII[FeIII(salicylhydroximato)(MeOH)(acetate)]3 and leads to an unusual tetranuclear cluster which exhibits both inter- and intra-cluster antiferromagnetic interactions and an S= 5 ground state.

Two metal–organic frameworks (MOFs) based on metal–organic cuboctahedra were prepared using a rigid C3 symmetric ligand, where Zn polyhedron-based MOF (PMOF-2(Zn)) did not show any significant gas sorption behavior, whereas the isostructural Cu polyhedron-based MOF (PMOF-2(Cu)) showed a large surface area of ∼4180 m2 g−1, high hydrothermal stability, and very promising H2 sorption properties.

ADVERTISEMENT RETURN TO ISSUEPREVArticleNEXTThe fused metallacrown anion Na2{[Na0.5[Ga(salicylhydroximate)]4]2(.mu.2-OH)4}- is an inorganic analog of a cryptateMyoung Soo Lah, Brian R. Gibney, David L. Tierney, James E. Penner-Hahn, and Vincent L. PecoraroCite this: J. Am. Chem. Soc. 1993, 115, 13, 5857–5858Publication Date (Print):June 1, 1993Publication History Published online1 May 2002Published inissue 1 June 1993https://pubs.acs.org/doi/10.1021/ja00066a077https://doi.org/10.1021/ja00066a077

Hydrogen bonding to anions drives the helical folding of an indolocarbazole oligomer, thus resulting in an internal cavity with six NHs and two OHs for binding sulfate with high selectivity.

Various fabrication strategies for hollow metal-organic framework (MOF) superstructures are reviewed and classified using various types of external templates and their properties. Hollow MOF superstructures have also been prepared without external templates, wherein unstable intermediates obtained during reactions convert to the final hollow MOF superstructures. Many hollow MOF superstructures have been fabricated using hard templates. After the core-shell core@MOF structure was prepared using a

An interdigitated 3-D metal-organic framework, [Cd(3)(OH)(2)L(4)(H(2)O)(2)], with 1-D channels was prepared using 4-aminophenyl-1H-tetrazole (HL) and Cd(II) ions, where the host framework shows selective gas sorption behavior that is based on the different nature of the interactions between the gas and the framework rather than on the size-exclusion effect of the micropores.

MOFs of complicated topologies can be analyzed as networks having simple underlying topologies when the MOPs are considered as TBUs.

Abstract Crown ethers have been used for over twenty years as selective binding agents for alkali metal and alkaline earth ions. Although there have been many modifications to the crown ether core, none is so dramatic as to substitute heteroatoms into the positions normally occupied by carbon atoms. In this article we describe a new class of metal clusters which incorporate trivalent metal ions and nitrogen atoms into molecules that structurally and functionally mimic the behavior of crown ether