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In the sugar mol­ecule of the title compound, C104H94O11·CH4O·0.75C4H8O, the pyran­ose ring adopts the expected chair conformation. Weak intra- and inter­molecular C—H⋯O hydrogen bonds, in part, control the mol­ecular conformation and stabilize the crystal structure. [ABSTRACT FROM AUTHOR]

In the title compound, [Cd(C6H7N2O5)2], the Cd atom lies on an inversion center and has a slightly distorted octa­hedral geometry. The equatorial plane contains two bidentate 5-carb­oxy-2-methyl-1 H-imidazole-4-carboxyl­ate monoanionic ligands. Two coordinated water mol­ecules occupy the axial sites. Inter­molecular N—H⋯O hydrogen bonds link the mol­ecules into chains, which are further connected by inter­molecular O—H⋯O hydrogen bonds, resulting in a three-dimensional supra­molecular framework. [ABSTRACT FROM AUTHOR]

In the title compound, C12H14ClN5O4, the dihedral angles between the purine plane and two methoxy­carbonyl planes are 15.806 (19) and 68.818 (18)°. Inter­molecular N—H⋯O and N—H⋯N hydrogen bonds link mol­ecules into bands along the b axis; they are further aggregated via C—H⋯O inter­actions into layers parallel to the ab plane. [ABSTRACT FROM AUTHOR]

The structure of the title compound, [Cu2Cl2(C10H8N2)] n, consists of a two-dimensional layer. Each Cl atom bridges three Cu atoms to form a ladder-like structure, whereas the 4,4′-bipyridine ligands form a link between Cu atoms of adjacent ladders, thus building a two-dimensional layer structure. [ABSTRACT FROM AUTHOR]

In sugar molecule of the title compound, C22H29Cl3O13·C7H8, the pyran­ose ring adopts the expected chair conformation. The acetoxy­methyl and two acet­oxy substituents are in the equatorial positions of this ring. In the crystal structure, there is a single weak C—H⋯O inter­molecular inter­action (H⋯O = 2.46 Å), which links mol­ecules into chains in the a-axis dirextion. [ABSTRACT FROM AUTHOR]