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April 2020 issue
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The report of the crystal structure of a new form of [CoCl2(en)2]Cl is both interesting and important as it allows a reassessment of the early work of Werner and brings an emphasis to the occurrence of cocrystals of complexes.
research papers
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Two CdII coordination polymers have been synthesized from 1,4-bis[(1H-imidazol-1-yl)methyl]benzene and 1,3,5-tris[(1H-imidazol-1-yl)methyl]benzene ligands, forming a distorted seven-coordinated pentagonal bipyramidal geometry and a one-dimensional ladder chain with the former ligand, and a six-coordinated octahedral structure with layers connected by hexafluorosilicate anions with the latter.
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Crystallographic studies demonstrated that two 1,3,5-triazine salts derived from 2,4,6-trichloro-1,3,5-triazine and 2-(aminomethyl)-1H-benzimidazole are electron-deficient aromatic systems and that they can interact with electron-rich chemical species. This property makes them potentially useful in the recognition of anions and neutral molecules, and as synthons in the construction of new supramolecular architectures in crystal engineering.
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This work is the first comprehensive summary of noncovalent interactions combined with a library of the supramolecular synthon patterns in all crystal structures of amino acids with the Fmoc moiety reported so far.
CCDC reference: 1951365
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The replacement of the OH group at the C3′ position of a furanose ring by fluorine changes the N-type furanose ring puckering to S-type in the crystalline state.
CCDC reference: 1988181
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A novel three-dimensional (3D) ZnII coordination polymer exhibits excellent photocatalytic activity on the degradation of the organic dyes Rhodamine B (RhB), Rhodamine 6G (Rh6G) and Methyl Red (MR).
CCDC reference: 1945486
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The introduction of a methoxy subsituent into an aromatic ring of 4-methyl-1,6-diphenylpyrimidine-2(1H)-selenone alters the antimicrobial activities and results in greater selectivity.
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A series of tridentate Schiff base ligands has been structurally characterized in the forms of free bases, hydrates/solvates and mono- and diprotonated cations. The most important contribution to the stabilization energy of the crystal is provided by π–π interactions, especially between charged ligands, while the details of the crystal architectures are influenced by directional interactions, especially relatively strong hydrogen bonds.