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The title compound, (NH4)2[Zn(NCS)4]·2C12H24O6·H2O, the result of the reaction of ammonium thio­cyanate, 18-crown-6 and zinc(II) chloride in aqueous solution, exhibits an unusual supra­molecular structure. The Zn atom, two of the thio­cyanate chains and a water mol­ecule, disordered over two positions, lie on a mirror plane. The macrocycle adopts a conformation with approximate D3d symmetry. The ammonium mol­ecules are contained within the bowl of the macrocycle via extensive N—H...O hydrogen bonds and the complex mol­ecules are linked via N—H...S hydrogen bonds, forming chains along the c-axis direction. The macrocycle is disordered over two positions [refined occupancy ratio = 0.666 (8):0.334 (8)]. The S atoms of two iso­thio­cyanate ligands are disordered within and about the mirror plane.

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The title compound, C14H20N4O4·0.5H2O [systematic name: (2S)-5-{[amino­(iminium­yl)meth­yl]amino}-2-{[(1Z)-4-meth­oxy-2-oxido­benzyl­idene]aza­nium­yl}penta­noate hemihydrate], has been synthesized by the reaction of L-arginine and 4-meth­oxy­salicyl­aldehyde and crystallizes with two independent substituted L-arginine mol­ecules and one water mol­ecule of solvation in the asymmetric unit. Each mol­ecule exists as a zwitterion and adopts a Z configuration about the central C=N. The mol­ecular conformation is stabilized by strong intra­molecular N—H...O hydrogen bonds that generate S(6) and S(10) ring motifs. Inter­molecular N—H...O and O—H...O hydrogen bonds involving also the water mol­ecule and weak inter­molecular C—H...Owater inter­actions link the mol­ecules into an infinite one-dimensional ribbon structure extending along the b axis. The known (2S) absolute configuration for L-arginine was invoked. Weak intermolecular C—H...π interactions are also present.
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