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Tobias Bäcker, Anja-Verena Mudring

• The first betaine chloride tetrachloroidoferrate(III) double salt, \((Hbet)_{2}Cl[FeCl_{4}]\) = \((Hbet)Cl·(Hbet)[FeCl_{4}]\), was obtained from a solution of betaine hydrochloride (HbetCl) and \(FeCl_{3}∙6\) \(H_{2}O\) in water. The crystal structure (orthorhombic, \(\it Pbcm\), \(\it a\) = 6.2717(13), \(\it b\) = 12.841(3), \(\it c\) = 25.693(5) Å, \(\it Z\) = 4) is characterized by layers of tetrachloridoferrate(III) anions separated by chloride-bridged, H-bond mediated cationic (Hbet) dimers. The hydrogen bonding network in the crystal structure follows the Pearson HSAB (hard acid-soft base) concept: According to the Pearson concept, the chloride anions show high affinity to the carboxyl group (hard acid and base), and the tetrachloroidoferrate(III) anion preferentially interacts with the activated methyl donors (soft acid and base). These interactions between the COOH group, as hard H-bond donor, and chloride as hard acceptor besides those between the soft, activated methyl groups and the soft tetrachloridoferrate(III) anions are the major structure-directing forces in the crystal structure of \((Hbet)_{2}Cl[FeCl_{4}]\).