Crystal structures of two new divalent transition-metal salts of carboxybenzenesulfonate anions

Reuben T. Bettinger, Philip J. Squattrito, Darpandeep Aulakh, Christopher G. Gianopoulos, J. T. Mague

Research output: Contribution to journalArticlepeer-review

Abstract

Hexaaquanickel(II) bis(3-carboxy-4-hydroxybenzenesulfonate) dihydrate, [Ni(H2O)6][C6H3(CO2H)(OH)SO3]2·2H2O, (I), crystallizes in the triclinic space group P with the nickel(II) aqua complexes on centers of inversion. The carboxylate group is protonated and neither it nor the sulfonate group is involved in direct coordination to the metal ions. The structure consists of alternating layers of inorganic cations and organic anions linked by O-HO hydrogen bonds that also include non-coordinated water molecules of crystallization. The first-row divalent transition-metal salts of this anion are reported as both dihydrates and tetrahydrates, with two distinct structures for the dihydrates that are both layered but differ in the hydrogen-bonding pattern. Compound (I) represents the second known example of one of these structures. Hexaaquacobalt(II) bis(3-carboxybenzenesulfonate) dihydrate, [Co(H2O)6][C6H4(CO2H)SO3]2·2H2O, (II), also crystallizes in triclinic P with the cobalt(II) aqua complexes on centers of inversion. The structure is also built of alternating layers of complex cations and organic anions without direct coordination to the metal by the protonated carboxylate or unprotonated sulfonate groups. A robust O-HO hydrogen-bonding network involving primarily the coordinated and non-coordinated water molecules and sulfonate groups directs the packing. This is the first reported example of a divalent transition-metal salt of the 3-carboxybenzenesulfonate anion.

Original languageEnglish
Pages (from-to)961-965
Number of pages5
JournalActa Crystallographica Section E: Crystallographic Communications
Volume78
Issue numberPt 9
DOIs
StatePublished - Sep 1 2022

Keywords

  • carboxybenzenesulfonate
  • crystal structure
  • transition-metal salts

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