YaMei Guo

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Name: 郭亚梅
Organization: Tianjin University , China
Department: Department of Chemistry and Biochemistry
Title: Associate Professor(PhD)

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Co-reporter:Xiao-Xiao He ;Ya-Mei Guo
Acta Crystallographica Section C 2014 Volume 70( Issue 8) pp:764-769
Publication Date(Web):
DOI:10.1107/S2053229614014260

The dipyridyl-type building blocks 4-amino-3,5-bis(pyridin-3-yl)-1,2,4-triazole (3-bpt) and 4,4′-bipyridine (bpy) have been used to assemble with ZnII in the presence of trithiocyanuric acid (ttcH3) to afford two coordination compounds, namely bis[4-amino-3,5-bis(pyridin-3-yl)-1,2,4-triazole-κN3]bis(trithiocyanurato-κ2N,S)zinc(II), [Zn(C3H2N3S3)2(C12H10N6)2]·2H2O, (1), and catena-poly[[[bis(trithiocyanurato-κ2N,S)zinc(II)]-μ-4,4′-bipyridine-κ2N:N′] 4,4′-bipyridine monosolvate], {[Zn2(C3H2N3S3)4(C10H8N2)3]·C10H8N2}n, (2). Single-crystal X-ray analysis indicates that complex (1) is a mononuclear structure, while complex (2) presents a one-dimensional chain coordination motif. In both complexes, the central ZnII cation adopts an octahedral geometry, coordinated by four N- and two S-donor atoms. Notably, trithiocyanurate (ttcH2) adopts the same bidentate chelating coordination mode in each complex and exists in the thione tautomeric form. The 3-bpt co-ligand in (1) adopts a monodentate coordination mode and serves as a terminal pendant ligand, whereas the 4,4′-bipyridine (bpy) ligand in (2) adopts a bidentate–bridging coordination mode. The different coordination characters of the different N-donor auxiliary ligands lead to structural diversity for complexes (1) and (2). Further analysis indicates that the resultant three-dimensional supramolecular networks for (1) and (2) arise through intermolecular N—H...S and N—H...N hydrogen bonds. Both complexes have been further characterized by FT–IR spectroscopy and elemental analyses.

Co-reporter:Wei Guo, Cheng-Hui Jiang, Ya-Mei Guo
Inorganica Chimica Acta 2013 Volume 405() pp:128-133
Publication Date(Web):24 August 2013
DOI:10.1016/j.ica.2013.05.013
•Four Cd(II)–dicyanamide coordination polymers based on a multidentate tripyridyltriazole ligand have been synthesized.•These complexes exhibit a variety of infinite structures such as 1-D chain, 2-D layer, and 3-D homochiral networks.•The structural diversity can be well regulated by the counter anions of Cd(II) salts.•Dinuclear and 1-D helical subunits are observed in different structures, by virtue of the distinct ligand conformations.Assemblies of a tripyridyltriazole ligand, 3,4-bis(2-pyridyl)-5-(3-pyridyl)-1,2,4-triazole (L223) with dicyanamide (dca) anion and different Cd(II) salts in CH3OH–H2O media afford four coordination polymers, namely {[Cd2(L223)2(dca)4(H2O)](H2O)4}n (1), {[Cd(L223)(dca)(ClO4)](H2O)0.25}n (2), and [Cd(L223)(dca)X]n (X− = Cl− for 3 and Br− for 4). All complexes were structurally determined by single-crystal X-ray diffraction. In 1 and 2, the Cd(II) centers are combined by L223 spacers to form [Cd2(L223)2] bimetallic subunits, which are bridged by dca anions to result in the 1D motif and 2D layer, respectively. Complexes 3 and 4 display isostructural 3D homochiral coordination networks that are constructed by 1D [Cd(L223)]n helical subunits and dca bridges. These results indicate that the counter anions of Cd(II) salts will be responsible for the diverse structures of coordination polymers 1–4. Their solid state properties such as thermal stability and fluorescence will also be presented.Four cadmium–dicyanamide coordination polymers with a multidentate tripyridyltriazole ligand have been synthesized and characterized, which display diverse 1D, 2D, and 3D coordination motifs regulated by the counter anions of Cd(II) salts. Their thermal and fluorescent properties have also been studied.
Co-reporter:Cheng-Hui Jiang, Yan-Mei Qi, Yu Sun, Qin Chi, Ya-Mei Guo
Journal of Molecular Structure 2012 1017() pp: 65-71
Publication Date(Web):
DOI:10.1016/j.molstruc.2012.02.050
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