A crucial role of adamantanoid Cu(II) complexes in the redox systems: CuCl–diallylsulfoxide–O2 and CuCl2–diallylsulfide–O2

The hypothetically reversible [Cu(I)(diallylsulfoxide)] ↔O2 [Cu(II)(diallylsulfide)] system was examined by FTIR spectroscopy and X-ray diffraction. It is stated that the Cu4OCl6 body centered adamantanoid cages, appearing at both the substrate and product sites, act as a template to promote the oxidation of diallylsulfide to diallylsulfoxide or Cu(I) to Cu(II), thus making the reaction irreversible. Each of these two adamantanoid cores possesses a different point symmetry as well as self assembly mode to form two polymorphs of the [Cu4OCl6(diallylsulfoxide)4] complex. Their polymorphic relationships based on the symmetry homology S4 ← Td → C3, as well as the distortion in the Cu(II) coordination geometry, are discussed.

The Cu4OCl6 core formation promotes oxidation of Cu(I) and diallylsulfide in the Cu(I) + diallylsulfoxide and Cu(II) + diallylsulfide systems, respectively, leading to the occurrence of different polymorphs in the above reactions. The polymorphic relationship is based on the symmetry homology: S4 ←Td → C3.Figure optionsDownload as PowerPoint slide