Aghabozorg Hossein, Kazemi Shokoofeh, Agah Ali Akbar, Mirzaei Masoud, Notash Behrouz
Acta Crystallogr Sect E Struct Rep Online. 2011 Feb 23;67(Pt 3):m360-1. doi: 10.1107/S1600536811005629.
In the centrosymmetric dinuclear complex anion of the title compound, (C(5)H(8)N(3))(2)[Bi(2)(C(7)H(3)NO(4))(4)(H(2)O)(2)]·4H(2)O, the Bi(III) atom is eight-coordinated in an N(2)O(6) environment and has a distorted bicapped trigonal-prismatic coordination environment. Extensive inter-molecular O-H⋯O, N-H⋯O and weak C-H⋯O hydrogen bonds lead to the stability of the crystal structure. Inter-actions between one C-H group of the 2,3-diamino-pyridinium [(2,3-dapyH)(+)] cation and the aromatic ring of the pyridine-2,6-dicarboxyl-ate (pydc) ligand (C-H⋯centroid distance = 2.78 Å) and π-π inter-actions between the (2,3-dapyH)(+) cations and between the (2,3-dapyH)(+) cation and the pydc ligand [centroid-centroid distances = 3.489 (5) and 3.694 (5) Å] are observed.
在标题化合物(C₅H₈N₃)₂[Bi₂(C₇H₃NO₄)₄(H₂O)₂]·4H₂O的中心对称双核络合物阴离子中,Bi(III)原子在N₂O₆环境中呈八配位,具有扭曲的双帽三角棱柱配位环境。广泛的分子间O—H⋯O、N—H⋯O和弱C—H⋯O氢键导致晶体结构的稳定性。2,3 - 二氨基吡啶鎓阳离子[(2,3 - dapyH)⁺]的一个C—H基团与吡啶 - 2,6 - 二羧酸酯(pydc)配体的芳环之间存在相互作用(C—H⋯质心距离 = 2.78 Å),并且观察到(2,3 - dapyH)⁺阳离子之间以及(2,3 - dapyH)⁺阳离子与pydc配体之间存在π - π相互作用(质心 - 质心距离 = 3.489(5)和3.694(5)Å)。