Three new molybdenyl iodates, KMoO3(IO3) (1), RbMoO3(IO3) (2), and CsMoO3(IO3) (3), have been prepared through the hydrothermal reactions of MoO3 with AIO4 (A = K, Rb, or Cs) at 180 C. These compounds are isolated as nearly colorless, air-stable crystals. Single-crystal X-ray diffraction experiments reveal that 1 possesses a corrugated layered structure constructed from molybdenum oxide chains that are bridged by iodate anions. The puckering of the layers is caused by the alignment of bent molybdenyl (MoO2(2+)) groups along one side of the molybdenum oxide chains. The K+ cations separate these layers from one another and serve to balance charge. In contrast, compounds 2 and 3, which are isostructural, form three-dimensional structures with small cavities filled with Rb+ or Cs+ cations. The differences between the structures of 1 and those of 2 and 3 are due to rotation of the molybdenyl units as translation occurs down the molybdenum oxide chains in order to accommodate the increased size of the Rb+ and Cs+ cations. This rotation allows for the iodate anions to bridge the molybdenum oxide chains in an additional dimension, creating a three-dimensional network structure. Furthermore, while 1 crystallizes in a centrosymmetric space group, 2 and 3 crystallize in polar space groups. Second-harmonic generation measurements on 2 and 3 show large responses of 400x alpha-quartz. Differential scanning calorimetry measurements demonstrate that 2 and 3 are thermally stable to 494 and 486 C, respectively. UV-vis diffuse reflectance spectra of these compounds show a high degree of transparency from 1 to 3 eV and a band gap of 3.1 eV.

Vulcanisation is a process of transforming a plastic rubber compound into a highly elastic product by forming a three-dimensional cross-linked network structure in the rubber matrix. Many systems have been developed to vulcanise rubber compounds, among which sulphur and peroxide curing systems remain the most desirable. The application of sulphur systems leads to the forming of sulphidic cross-links between elastomer chains, while carbon–carbon bonds are formed in peroxide-curing. Both vulcanisation systems provide certain benefits to the cross-linked rubber articles, but also some disadvantages. The present work seeks to provide an overview on both vulcanisation systems; their composition, possibilities of their application, reaction mechanisms, structure of the cross-links formed and the main feature of the final cross-linked materials – vulcanisates.

Vulcanization or curing is one of the most important processes in rubber technologies. During this process, plastic rubber compounds by parallel and subsequent physical and mainly chemical reactions change into highly elastic products—vulcanizates. The fundamental goal of curing is forming chemical cross-links between rubber macromolecules, which leads to the formation of a three-dimensional network or rubber matrix. A number of curing systems have been introduced in cross-linking of elastomers; each system has its own characteristics and composition; therefore, vulcanizates with different properties also can be prepared. We characterize organic peroxides as curing agents and their decomposition mechanisms and characteristics and bring a detailed view to understanding mechanisms between peroxides and different types of rubber matrices. Then, we focus on the classification and characterization of co-agents used in peroxide cross-linking and explain the mutual interactions and reaction mechanisms between peroxide, co-agents, and rubber matrices in relation to the properties of prepared materials. Finally, the drawbacks and the main features of final cross-linked materials are outlined.

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Lanthanide‐like: X‐ray diffraction and density functional theory studies show that [An(H2O)9]3+ ions of the actinides U3+–Cf3+ in crystals of their triflate salts have the same structure and electrostatic bonding as their lanthanide counterparts La3+–Eu3+. Moreover, the nine‐coordinate geometry is essentially preserved in solution for the lighter elements (see picture).

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The reactions of RE(IO3)3 [RE = Nd, Sm, Eu] with I2O5 and MoO3 in a 1:2:2 molar ratio at 200 degrees C in aqueous media provide access to RE(MoO2)(IO3)4(OH) [RE = Nd (1), Sm (2), Eu (3)] as pure phases as determined from powder X-ray diffraction data. Single crystal X-ray diffraction experiments demonstrate that these compounds are isostructural and crystallize in the chiral and polar space group P2(1). The structures are composed of three-dimensional networks formed from eight-coordinate, square antiprismatic RE3+ cations and MoO2(OH)+ moieties that are bound by bridging iodate anions. The Mo(VI) centers are present in distorted octahedral environments composed of two cis-oxo atoms, a hydroxo group, and three bridging iodate anions arranged in a fac geometry. There are four crystallographically unique iodate anions in the structures of 1-3, one of these is actually present in the form of a IO3+1 polyhedron where a short interaction of 2.285(4) A is formed between the iodate anion and the hydroxo group bound to the Mo(VI) center. This interaction results in significant distortions of the iodate anion similar to those found in tellurites with TeO3+1 units. Two of the four iodate anions are aligned along the polar b-axis, imparting the required polarity to these compounds. Second-harmonic generation (SHG) measurements on sieved powders of 1 show a response of 350 x alpha-quartz. Crystallographic data: 1, monoclinic, space group P2(1), a = 6.9383(5) A, b = 14.0279(9) A, c = 7.0397(5) A, beta = 114.890(1) degrees, Z = 2; 2, monoclinic, space group P2(1), a = 6.9243(6) A, b = 13.963(1) A, c = 7.0229(6) A, beta = 114.681(1) degrees, Z = 2; 3, monoclinic, space group P2(1), a = 6.9169(6) A, b = 13.943(1) A, c = 7.0170(6) A, beta = 114.542(1) degrees, Z = 2.

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