Synthesis of potential selective cox‐2 enzyme inhibitors derived from ethyl ester of 2‐isothiocyanato‐5‐phenyl‐3‐thiophenecarboxylic acid

Derivatives containing the thieno[2,3‐d]pyrimidin‐4‐one system, potential selective COX‐2 inhibitors, were prepared starting from ethyl ester of 2‐isothiocyanato‐5‐phenyl‐3‐thiophenecarboxylic acid ( 2 ); their structural elucidation is also reported.     

Difference Families in Z2d+1⊕Z2d+1 and Infinite Translation Designs in Z⊕Z

We analyse 3-subset difference families of Z_2d+1⊕Z_2d+1 arising as reductions (mod 2d+1) of particular families of 3-subsets of Z⊕Z. The latter structures, namely perfect d-families, can be viewed as 2-dimensional analogues of difference triangle sets having the least scope. Indeed, every perfect d-family is a set of base blocks which, under the natural action of the translation group Z⊕Z, cover all edges {(x,y),(x′,y′)} such that |x−x′|, |y−y′|≤d. In particular, such a family realises a translation invariant (G,K₃)-design, where V(G)=Z⊕Z and the edges satisfy the above constraint. For that reason, we regard perfect families as part of the hereby defined translation designs, which comprise and slightly generalise many structures already existing in the literature. The geometric context allows some suggestive additional definitions. The main result of the paper is the construction of two infinite classes of d-families. Furthermore, we provide two sporadic examples and show that a d-family may exist only if d≡0,3,8,11 (mod 12).     

Packing into the smallest square: Worst-case analysis of lower bounds

We address the problem of packing a given set of rectangles into the minimum size square. We consider three versions of the problem, arising when the rectangles (i) are squares; (ii) have a fixed orientation; (iii) can be rotated by 90. For each case we study lower bounds, and analyze their worst-case performance ratio. In addition, we evaluate through computational experiments their average performance on instances from the literature.     

Calabi's diastasis function for Hermitian symmetric spaces

In this paper we study the Calabi diastasis function of Hermitian symmetric spaces. This allows us to prove that if a complete Hermitian locally symmetric space (M,g) admits a Kähler immersion into a globally symmetric space (S,G) then it is globally symmetric and the immersion is injective. Moreover, if (S,G) is symmetric of a specified type (Euclidean, noncompact, compact), then (M,g) is of the same type. We also give a characterization of Hermitian globally symmetric spaces in terms of their diastasis function. Finally, we apply our analysis to study the balanced metrics, introduced by Donaldson, in the case of locally Hermitian symmetric spaces.     

The ternary system CsCl−NaCl−LaCl3

The ternary system CsCl?NaCl?LaCl₃ was investigated by means of differential thermal analysis and X-ray powder diffraction analysis. There exists one congruently melting compound, Cs₂NaLaCl₆, crystallizing with the cubic elpasolite structure. No quasi-binary section exists for the whole system, however three binaries range from the ternary compound Cs₂NaLaCl₆ to NaCl, CsLa₂Cl₇ and Cs₃LaCl₆ resp., dividing the system in three areas of composition: one triangle, Cs₃LaCl₆?Cs₂NaLaCl₆?CsLa₂Cl₇, containing additionally a compound Cs₂LaCl₅ below 510°C, and the two areas CsCl?NaCl?Cs₂NaLaCl₆?Cs₃LaCl₆ and Cs₂NaLaCl₆?NaCl?LaCl₃?CsLa₂Cl₇, containing a mixed crystal range between LaCl₃ and Na₃La₅Cl₁₈. These areas could be further divided in five triangles, so that the whole system contains six Alkemade triangles.     

Novel ethero atoms containing polyesters based on 2,6‐naphthalendicarboxylic acid: A comparative study with poly(butylene naphthalate)

Poly(butylene naphthalate) (PBN), poly(diethylene naphthalate) (PDEN), and poly(thiodiethylene naphthalate) (PTDEN) were synthesized and characterized in terms of chemical structure and molecular weight. The polyesters were examined by TGA, DSC, and DMTA. All the polymers showed a good thermal stability, even though depending on chemical structure. At room temperature they appeared as semicrystalline materials; the effect of the introduction along the PBN polymer chain of ether oxygen atoms or sulfur ones was a lowering in the T_g value, a decrement of T_m, and a decrease of the crystallization rate. Changing in chemical structure also affects the main α absorption associated with the glass transition which moves to lower temperature and whose energetic requirements decrease. The results were explained as due to the presence of highly flexible C? S? C or C? O? C bonds in the polymeric chain. © 2007 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 45: 1694–1703, 2007