issue contents
April 2021 issue
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Cover illustration: In the crystal of 3,5-dibromo-4-carbamoylbenzoic acid 2-propanol monosolvate, the acid molecules form inversion dimers by pairwise N—H⋯O hydrogen bonds between carbamoyl groups and the carboxyl and carbamoyl groups link to form head-to-tail inversion dimers. The 2-propanol hydroxyl group interposes between adjacent head–tail pairs, resulting in C33(10) chains of hydrogen bonds propagating along [100]. The best-fit planes of the carbamoyl group and benzene ring are inclined by 88.26 (11)°. This is a greater inclination than was previously reported with CH3, Cl, F or H in place of the Br atoms, although those analogues did not have a para carboxyl group. See: Noland, Herzig, Fox & Tritch [IUCrData (2021). 6, x210391].
metal-organic compounds
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organic compounds
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5-[(1,3-Dimethyl-5-oxo-2-sulfanylideneimidazolidin-4-ylidene)amino]-2-methylisoindoline-1,3-dione
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