Synthesis, structure and luminescence of novel lanthanide containing coordination polymers

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Exploration of the influence of 5-iodo-2'-deoxyuridine incorporation on the structure of d[CACG(IDU)G]

The first antiviral nucleoside 5-iodo-2'-deoxyuridine (IDU) against herpes simplex virus type 1 and type 2 is a thymidine analogue, i.e. the C5 methyl group is replaced by an I atom. The structure of the self-complementary hexamer d[CACG(IDU)G] was determined by single-crystal X-ray diffraction techniques. The orthorhombic crystals belong to space group P2(1)2(1)2(1), with unit-cell parameters a = 18.16, b = 30.03, c = 41.99 Angstrom. Refinement in the resolution range 20 - 1.3 Angstrom converged with a final R1 = 0.167, including 43 water molecules and two cobalt hexammine complexes. The incorporation of a large I atom has only minor consequences for the overall structure as is noticed in the IDU . A base pairs, which are of the common Watson - Crick type. To contribute to the still puzzling mechanism of this historically important agent, details of base stacking, helical parameters, hydration etc. have been studied. A general scheme of cobalt hexammine-binding modes in Z-DNA is provided, revealing similar binding modes for the reported structure

Holmium, thulium and lutetium-octamolybdate [Mo8O28](8-) 1D chains : luminescence investigation of europium doped lutetium-octamolybdate

In this work we report a novel lanthanide octamolybdate 1D chain type of structure formed with holmium, thulium and lutetium. This is a rare case of compounds built out of [Mo8O28](8-) units. These compounds were prepared in a mild reaction synthesis starting from the commonly used heptamolybdate polyoxometalate (POM) [(NH4)(6)[Mo7O24]. Interestingly, in our previous study we have employed a very similar synthesis route for lanthanides with a larger ionic radius and obtained heptamolybdate clusters. For the lanthanides with a smaller ionic radius (Ho3+, Tm3+ and Lu3+) no crystals could be obtained under those conditions. Only when doubling the amount of the lanthanide salt, single crystals suitable for measurements were obtained. These crystals revealed yet a very different structure from those previously observed. Lanthanide octamolybdate 1D chains were formed. Doubling the amount of the salt for other lanthanide ions still yielded heptamolybdate compounds previously reported by us. The lutetium octamolybdate compound was doped with 1-7.5% of Eu3+ ions yielding emission colors ranging from blue to strong red. Additionally in these materials the excitation wavelength was varied, and it was observed that the materials emission color was excitation-wavelength dependent