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Journal logoIUCrDATA
ISSN: 2414-3146

September 2026 issue

Early view articles

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metal-organic compounds


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The title complex exhibits a half-sandwich structure with a tripodal piano stool-like arrangement consolidated by non-classical intra- and inter­molecular inter­actions.

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The propeller-like title complex packs with overlapping carbonitrile groups to form a grid with a significant void volume.

organic compounds


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The title Schiff base was prepared by condensation of 2-quinoline­carboxaldehyde with 4-bromo­aniline, is reported. Inter­molecular C—H⋯π inter­actions between quinolinyl and bromo­phenyl rings form a three-dimensional supra­molecular network in the crystal packing.

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The title compound was synthesized using the acid catalyst NH4HF2 in a water/methanol solution. The extended structure features offset stacked quinoxalines along the [100] direction.

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The title salt comprises a N-protonated PTA cation with a nitrate counter-ion.

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The crystal structure of 5-cyclo­propyl-1-tosyl-1H-indole-2-carbaldehyde shows a nearly planar indole core, with slipped π–π stacking inter­actions contributing to the crystal packing. Hirshfeld surface analysis indicates that H⋯H, O⋯H/H⋯O and C⋯H/H⋯C contacts make the major contributions to the crystal packing.

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The crystal structure of a β-carboline, C26H20N2O4S, synthesized via 2 + 2+2-cyclo­addition to an alkynylynamide, is presented.

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The complete mol­ecule of the title compound, which was prepared via a Horner olefination, is generated by a crystallographic centre of symmetry. Whereas the terminal cyano­stilbene units are almost planar, the central dioctoxybenzene unit is substanti­ally tilted, which limits conjugation. van der Waals forces between the alkyl chains connect the mol­ecules, arranged in layers lying parallel to the ac plane.