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Helical motifs are common in nature, for example, the DNA double or the collagen triple helix. In the latter proteins, the helical motif originates from glycine, the smallest amino acid, whose molecular confirmation is closely related to acetic acid. The combination of acetic acid with calcium and water, which are also omnipresent in nature, materializing as calcium acetate hemihydrate, was now revealed to exhibit a collagen‐like triple helix structure. This calcium salt is observed as efflorescence phase on calcareous heritage objects, like historic Mollusca shells, pottery or marble reliefs. In a model experiment pure calcium acetate hemihydrate was crystallized on the surface of a terracotta vessel. Calcium acetate hemihydrate crystallizes in a surprisingly large unit cell with a volume of 11,794.5(3) Å3 at ambient conditions. Acetate ions bridge neighboring calcium cations forming spiral chains, which are arranged in a triple helix motif. [ABSTRACT FROM AUTHOR]

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Pure anhydrous Cu(CH3COO)2 was obtained both, by thermal dehydration of Cu(CH3COO)2·H2O and by drying a commercially purchased mixture of Cu(CH3COO)2·H2O and Cu(CH3COO)2 in a nitrogen atmosphere using P2O5 as drying agent. The crystal structure was solved ab initio from synchrotron X‐ray powder diffraction (XRPD) data at 150 °C and from laboratory XRPD data at ambient conditions and found to be isotypic to anhydrous chromium(II), molybdenum(II) and rhodium(II) acetate. Cu(CH3COO)2 crystallizes in space group P1 (no. 2) with lattice parameters of a = 5.1486(3) Å, b = 7.5856(6) Å, c = 8.2832(6) Å, α = 77.984(4)°, β = 75.911(8)°, γ = 84.256(6)° at ambient conditions. Cu2(CH3COO)4 paddle wheels with short (2.6 Å) Cu–Cu distances form chains in a direction, which is the main motif in the crystal structure. Due to their identical structural main motif Cu(CH3COO)2·H2O and Cu(CH3COO)2 exhibit a similar bluish‐green color, almost identical UV/Vis spectra and comparable magnetic properties. The temperature dependent magnetic susceptibility also indicates only weak inter‐dimer spin exchange between neighbouring Cu2(CH3COO)4 paddle wheels. [ABSTRACT FROM AUTHOR]

The title compound, Zn4Cu3(Zn1–xCux)6(HCOO)8(OH)18·6(H2O), also denoted as "Zinc C", a previously unknown corrosion phase of brass in contact with glass, was found on four different historic objects stored in three different collections. Model experiments demonstrated that formaldehyde emitted e.g. from wooden cabinets undergoes a Cannizarro reaction in the alkaline surface film on the historic glass making formate available for the formation of this corrosion phase. The crystal structure of "Zinc C" was solved ab initio from X‐ray powder diffraction data. From the crystal structure and EDX analyses, a phase composition of Zn4Cu3(Zn1–xCux)6(HCOO)8(OH)18·6(H2O) was derived. Zinc C crystallizes in a trigonal unit cell in space group R3(148) with lattice parameters of a = 10.9185(1) Å, c = 27.5058(4) Å, and V = 2839.74(6) Å3. Layers of edge sharing MO6/3 octahedra with voids capped by Zn(HCOO) forming Zn(HCOO)(OH)3/3 tetrahedra are the main motif in the structure. The zinc/copper ratio of the corrosion phase "Zinc C" can vary between 10:3 and 4:9, due to a partial occupational disorder between copper and zinc in the crystal structure. A corrosion phase found on historic brass objects was characterized and identified as Zn4Cu3(Zn1–xCux)6(HCOO)8(OH)18·6(H2O). The crystal structure exhibits a layered motif with a partial occupational disorder between copper and zinc. Model experiments demonstrate that the corrosion was induced by partial hydrolysis of the historic glass. [ABSTRACT FROM AUTHOR]

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The Front Cover shows historic glass earrings with brass mountings from the Hamburg Museum in the background. The metal parts exhibit severe corrosion, especially where they are in contact with glass. The partial dissolution of the historic glass by moisture leads to a surface film containing formates produced by a Canizzaro reaction of formaldehyde, emitted by, e.g., wooden furniture, with the alkaline components of the film. An excerpt of the crystal structure of a new corrosion phase, Zn4Cu3(Zn1–xCux)6(HCOO)8(OH)18·6(H2O) ("Zinc C"), is presented. More information can be found in the Full Paper by S. Bette et al. For more on the story behind the cover research, see the Cover Profile. [ABSTRACT FROM AUTHOR]