Cu(II) 4-phenoxybenzoate dimers and monomer coordinated by pyridines: synthesis and crystal structures

The complexes [Cu(PhOBz)2(dPy)]2 (PhOBz = 4-phenoxybenzoate; dPy = pyridine (1), 3-phenylpyridine (2), 4-benzylpyridine (3) and 4-phenylpyridine (4) and the complex [Cu(PhOBz)2(4-Phpy)2(H2O)] (5) were prepared and fully characterized. X-ray crystal structures of the five complexes have been determined. Complexes 1-4 consist of binuclear units where both Cu(II) are linked by four syn-syn carboxylate bridges, showing a paddle-wheel unit. The compound 5 is mononuclear and the metal center is coordinated to two PhOBz in monodentate form, two 4-Phpy ligands and one H2O molecule with slightly distorted square pyramidal geometry. Finally, the magnetic properties of compounds 3 and 5 have also been studied, confirming the different strength interactions between Cu(II) cations

Investigations on the weak interactions assembling the crystal structure of Betti bases.

The crystal structures of (S, S)-aminobenzylnaphthols, easily produced by a chromatography-free highly stereoselective Betti reaction, were investigated by means of single crystal X-ray diffraction analysis, and the main intra- and intermolecular interactions were described. The presence of a strong intramolecular hydrogen bond was confirmed, whereas the whole crystal building was found to be due mainly to other bondings, such as CH…O and CH…p interactions. As far as the last interactions were concerned, we observed many short distances from one hydrogen atom to an aryl plane, together with the appropriate geometric requirements for the assemblies. The observations suggest that these interactions can play a relevant role in the crystal building. The absence of similar short distance CH…p interactions in the crystal of a diastereomeric (R, S)-aminobenzylnaphthol could be a suggestion of the preferential crystallisation of the (S, S)-stereoisomer and, consequently, its prevalence as a product of the Betti reaction

Behavior of thiosemicarbazones derived from some terpenones under acetylation conditions. Part II

Preparation of chiral heterocyclic compounds of the thiadiazoline types, starting from natural α,β-unsaturated and bicyclic terpenones is described. Stereochemical assignment of the compounds synthesized was performed by NMR spectroscopy and X-ray analysis. ©ARKAT.Fil:D'Accorso, N. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina.Fil:Moltrasio, G.Y. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina