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Updated: Feb 20, 2026

X-ray Powder Diffraction in Conservation Science: Towards Routine Crystal Structure Determination of Corrosion Products on Heritage Art Objects
Published on: June 8, 2016
On verdigris, part I: synthesis, crystal structure solution and characterisation of the 1-2-0 phase
Sebastian Bette1, Reinhard K Kremer, Gerhard Eggert
1Max Planck Institute for Solid State Research, Heisenbergstr. 1, 70569 Stuttgart, Germany. S.Bette@fkf.mpg.de.
Abstract:
Known synthesis approaches for basic copper(ii) acetates, the main components of historic verdrigis pigments were reinvestigated and revealed to be partially irreproducible. A modification of the reaction conditions led to the successful and reproducible synthesis of the 1-2-0 phase (Cu3(CH3COO)2(OH)4 = 1Cu(CH3COO)2·2Cu(OH)2·0H2O). The phase composition was derived from elemental and thermal analysis and confirmed by the crystal structure solution using synchrotron X-ray powder diffraction (XRPD) data. The 1-2-0 phase crystallises in space group Pbca with lattice parameters of a = 20.9742(1) Å, b = 7.2076(1) Å, and c = 13.1220(1) Å. The crystal structure consists of Cu2(CH3-COO)2(OH)4/3(OH)2/21/3- dimers, which are interconnected by corner sharing Cu(OH)2/3(OH)2/21/3+ squares forming layers perpendicular to the a-axis. The deep blue color of the solid originates from a reflectance maximum at 472 nm and from an absorbance maximum at 676 nm that is comparable with other historic blue pigments like azurite or Egyptian blue. IR- and Raman-spectroscopic properties of the solid were investigated as well, which demonstrated that the obtained product is identical with a previously synthesised verdigris phase that was obtained by applying historical procedures. Therefore, our reference data for the title compound will help to improve the understanding of the multiphase mixtures occurring in historic verdigris samples. The magnetic properties of the 1-2-0 phase were also investigated. At low temperatures the magnetic susceptibility is well described by a spin-1/2 Heisenberg chain with uniform antiferromagnetic nearest-neighbour spin exchange coupling of only one of three Cu magnetic moments. Due to the very strong antiferromagnetic coupling of the Cu2(CH3-COO)2(OH)4/3(OH)2/21/3- dimers their contribution to magnetism becomes relevant above ∼140 K, which results in the presence of two distinct temperature regions where Curie-Weiss behaviour of the magnetic susceptibility with different Curie constants and Weiss temperatures is found.
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