New heterometallic coordination polymers constructed from 3d–3d′ binuclear nodes

Heterobinuclear [CuIIMnII] and [CuIICoII] cationic complexes can efficiently act as nodes for designing coordination polymers. The crystal structures of two binuclear precursors, [LCuCo(NO3)2] (1) and [LCuMn(NO3)2] (2), have been solved (L2− is the dianion of the Schiff base resulting from the 2 : 1 condensation of 3-methoxysalicyladehyde with 1,3-propanediamine). The nitrato ligands, coordinated to CoII and, respectively, the MnII ions from the precursors, are easily replaced by exo-dentate ligands, resulting in 1-D coordination polymers: 1∞[L(H2O)CuCo(oxy-bbz)]·CH3CN·C2H5OH (3), 1∞[L(H2O)CuCo(2,5-dhtp)]·CH3CN (5) and ∞[L(H2O)CuMn(ox)]·3H2O (6) (oxy-bbz2− = the dianion of 4,4′-oxy-bis(benzoic) acid; 2,5-dhtp2− = the dianion of 2,5-dihydroxy-terephthalic acid; ox2− = the dianion of the oxalic acid). In the case of the [CuMn] node, the interaction with oxy-bbz2− affords a binuclear complex, [LCuMn(oxy-bbz)(H2O)2] (4)

Magnetic Anisotropy Trends along a Full 4f-Series: The fn+7Effect

[Image: see text] The combined experimental and computational study of the 13 magnetic complexes belonging to the Na[LnDOTA(H(2)O)] (H(4)DOTA = tetraazacyclododecane-N,N′,N″,N‴-tetraacetic acid and Ln = Ce–Yb) family allowed us to identify a new trend: the orientation of the magnetic anisotropy tensors of derivatives differing by seven f electrons practically coincide. We name this trend the f(n+7) effect. Experiments and theory fully agree on the match between the magnetic reference frames (e.g., the easy, intermediate, and hard direction). The shape of the magnetic anisotropy of some couples of ions differing by seven f electrons might seem instead different at first look, but our analysis explains a hidden similarity. We thus pave the way toward a reliable predictivity of the magnetic anisotropy of lanthanide complexes with a consequent reduced need of computational and synthetical efforts. We also offer a way to gain information on ions with a relatively small total angular momentum (i.e., Sm(3+) and Eu(3+)) and on the radioactive Pm(3+), which are difficult to investigate experimentally

Dialettica riproposta

Il saggio affronta l'arduo e dibattuto tema della relazione Hegel / Marx, soffermandosi in particolo sul modo in cui i due autori impiegano il pensiero dialettico

Carbonic anhydrase inhibitors: X-ray crystallographic structure of the adduct of human isozyme II with the antipsychotic drug sulpiride

The X-ray crystal structure for the adduct of human carbonic anhydrase (hCA) II with sulpiride, a sulfonamide derivative clinically used as antipsychotic drug, has been resolved at a resolution of 1.6 Å. This compound is an effective inhibitor of the physiologically most relevant isozyme hCA II (Ki of 40 nM), being only a moderate or moderate-weak inhibitor of the cytosolic isozyme hCA I (Ki of 1200 nM) and the membrane-bound isozyme hCA IV (Ki of 620 nM). Sulpiride shows CA inhibitory properties of the same magnitude as dichlorophenamide, a clinically used antiglaucoma sulfonamide, or valdecoxib, a COX-2 selective inhibitor recently shown to inhibit CA. The binding of sulpiride to the hCA II active site is similar to that of other sulfonamide inhibitors, considering the interactions of the sulfonamide zinc anchoring group, but differs considerably when the organic scaffold of the molecule is analyzed. Indeed, one unprecedented hydrogen bond involving the imino moiety of the carboxamido group of sulpiride and a water molecule was observed, together with a unique stacking interaction of the N-methyl-pyrrolidine ring of the inhibitor and the aromatic ring of Phe 131 of the enzyme active site, which has been observed only recently in another CA–sulfonamide complex