Hydantoin Derivatives as Spacers for Crystal Engineering in the Chemistry of Heavy Alkali Metal Ions:  Synthesis and Crystal Structure of Layered (CsLOH)∞(L = 5,5-Dimethyl-4-oxoimidazolidine-2-thione)

1998 ◽  
Vol 37 (17) ◽  
pp. 4164-4165 ◽  
Author(s):  
Massimiliano Arca ◽  
Francesco Demartin ◽  
Francesco A. Devillanova ◽  
Alessandra Garau ◽  
Francesco Isaia ◽  
...  
Keyword(s):  
Crystal Structure ◽  
Alkali Metal ◽  
Metal Ions ◽  
Crystal Engineering ◽  
Alkali Metal Ions ◽  
Synthesis And Crystal Structure ◽  
Hydantoin Derivatives

scholarly journals Synthesis and crystal structure of two manganese-based 12-metallacrown-4 complexes: Na2(3-chlorobenzoate)2[12-MCMn(III)N(shi)-4](DMF)6 and MnNa(3-chlorobenzoate)3[12-MCMn(III)N(shi)-4](DMF)(H2O)4·4DMF·0.72H2O

2020 ◽  
Vol 76 (6) ◽  
pp. 848-856
Author(s):  
Curtis M. Zaleski ◽  
Matthias Zeller
Keyword(s):  
Crystal Structure ◽  
Transition Metal ◽  
Alkali Metal ◽  
Metal Ions ◽  
Axial Direction ◽  
Alkali Metal Ions ◽  
Convex Side ◽  
Central Cavity ◽  
Synthesis And Crystal Structure ◽  
Whole Molecule Disorder

Similar synthetic schemes yield two different metallacrown (MC) complexes: bis(μ-3-chlorobenzoato)hexakis(dimethylformamide)tetrakis(μ4-N,2-dioxidobenzene-1-carboximidato)tetramanganese(III)disodium(I), [Mn4Na2(C7H4ClO2)2(C7H4NO3)4(C3H7NO)6] or Na2(3-chlorobenzoate)2[12-MCMn(III)N(shi)-4](DMF)6, 1, and tetra-μ-aqua-tris(μ-3-chlorobenzoato)(dimethylformamide)tetrakis(μ4-N,2-dioxidobenzene-1-carboximidato)pentamanganese(III)sodium(I) dimethylformamide tetrasolvate 0.72-hydrate, [Mn5Na(C7H4ClO2)3(C7H4NO3)4(C3H7NO)(H2O)4]·4C3H7NO·0.718H2O or MnNa(3-chlorobenzoate)3[12-MCMn(III)N(shi)-4](DMF)(H2O)4·4DMF·0.72H2O, 2, where shi3− is salicylhydroximate and DMF is N,N-dimethylformamide. Both complexes have the same framework consisting of four MnIII ions in the MC ring and four shi3− ligands, resulting in an overall square-shaped molecule. The MnIII ions are either five- or six-coordinate with elongated bond lengths in the apical or axial direction, respectively. The structure of 1 is nearly planar, and the MC binds two Na+ ions on opposite faces of the MC central cavity. The 3-chlorobenzoate anions also bind on opposite faces of the MC and form bridges between the central Na+ ions and the ring MnIII ions. For 1 the metallacrown molecule, except for the central Na+ ion, exhibits whole molecule disorder over two sets of sites. Both moieties are centrosymmetric and are related to each other by a pseudo-mirror operation with opposite sense of rotation around the Na...Na axis. The occupancy ratio of the main disorder of the metallacrown molecules and 3-chlorobenzoate anions refined to 0.9276 (9):0.0724 (9). The structure of 2 is slightly domed, and the MC binds both an MnII ion and an Na+ ion in the MC central cavity. The MnII ion is located on the convex side of the MC, while the Na+ ion binds to the concave side. Complex 2 represents the first instance of a [12-MCMn(III)N(shi)-4] molecule binding both 3d transition metal and alkali metal ions in the central cavity. In addition, three 3-chlorobenzoate anions bind on the convex side of the MC and connect the MnII ion to three of the ring MnIII ions.

Ion–peptide interactions between alkali metal ions and a termini-protected dipeptide: modeling a portion of the selectivity filter in K+ channels

2019 ◽  
Vol 21 (2) ◽  
pp. 561-571 ◽  
Author(s):  
Shun-ichi Ishiuchi ◽  
Yuta Sasaki ◽  
James M. Lisy ◽  
Masaaki Fujii
Keyword(s):  
Alkali Metal ◽  
Metal Ions ◽  
Selectivity Filter ◽  
Alkali Metal Ions ◽  
K Channels ◽  
Peptide Interactions

Differentiating K+ and Na+ binding patterns in peptide sequences.

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