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The title compound, C16H21BO6, has has approximate C2 symmetry, but no crystallographically imposed mol­ecular symmetry. In the crystal, mol­ecules are packed into parallel columns along the a axis. Short inter­molecular C—H...O contacts stabilize the crystal packing.

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The title compound, [CoNa4(C6H5O7)2]n, was obtained under hydro­thermal conditions as a minor product. The Co2+ cation is located on a crystallographic inversion center and is coordinated by six O atoms from two different citrate units, forming a [Co(C6H5O7)2]4− building unit with Co—O bond lengths between 2.0578 (17) and 2.0813 (16) Å. The structure features two crystallographically independent Na+ ions. The first Na+ cation is five-coordinated by O atoms of five carboxylate groups from four different citrate anions. The second Na+ cation is surrounded by six O atoms of five carboxylate groups from five different citrate anions. The carboxylate groups of the citrate are completely depronona­ted, the hydroxyl group, however, is not. It is coordinated to the Co2+ cation, and through an O—H...O hydrogen bond connected to a neighboring [Co(C6H5O7)2]4− building unit. The coordination modes of the carboxyl­ate O atoms vary, with one O atom being coordinated to three different Na+ cations, three are bridging O atoms bound to two Na+ cations and two are connected to a Co2+ cation and a Na+ cation, respectively. Through these inter­connections, the basic [Co(C6H5O7)2]4− building units are linked with each other through coordination of their carboxyl­ate groups to the Na+ cations, forming a three-dimensional framework.

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The complete mol­ecule of the title compound, C28H28B2Br4O4, is generated by the application of a centre of inversion. In the mol­ecule, the BO2 plane is perpendicular to that through the pyrene ring [dihedral angle = 86.27 (13)°]. In the crystal, mol­ecules stack into columns along the b axis, the closest contact between these being of the type C—Br...π.
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