Biomedical subjects

Ghenadie Novitchi

Publications and source records attributed to Ghenadie Novitchi.

4 recordsLinked to original sources

PubMed2004

Synthesis, structure, and magnetic properties of heterometallic dicyanamide-bridged Cu-Na and Cu-Gd one-dimensional polymers.

The monometallic precursors L1Cu and L2Cu (L1H2 standing for 1,3-bis((3-ethoxysalicylidene)amino) propane and L2H2 standing for 1,2-bis((3-methoxysalicylidene)amino) ethane) react with sodium dicyanamide (dca) (NaN3C2), a mixture of gadolinium nitrate, and sodium dicyanamide to yield heterodinuclear L2CuNa(NCNCN) and L1CuGd(NO3)(NCNCN)2 entities. The structural determination shows that two Cu-Na entities are linked by dca with an original mu1,1 coordination mode, evidenced here for the first time, to yield tetranuclear complexes. Two hydrogen bonds operate between the water molecule coordinated to one of the sodium ions and the free nitrogen atoms of two dca ligands, yielding infinite zigzag chains. The structural determination of the Cu-Gd entities indicates that they are held together by two dca ligands, bridging alternately Cu to Gd and Gd to Gd cations, in the more common mu1,5 mode to yield a one-dimensional (1D) network. The dca ligands are not able to transmit interaction between the magnetically active centers in these chains, which are the unique example of structurally characterized Cu-Gd complexes involving dca ligands.

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PubMed2004

Bis-dinuclear (Cu-Gd)2 complexes with a probable helicate structure.

Two ligands have been designed to simultaneously favour complexation of 3d and 4f metal ions and the formation of helical structures. This synthetic strategy has allowed the isolation of two bis-dinuclear (Cu-Gd)(2) complexes [L(i)(2)Cu(2)Gd(2)(NO(3))(6)] derived from 3-alkoxysalicylaldehyde and 4,4'-diaminodiphenylmethane. The magnetic data shows that both bis-dinuclear complexes behave as two practically independent (Cu-Gd) pairs, each presenting a ferromagnetic interaction (J= 4.6 cm(-1)). Very weak additional antiferromagnetic interactions, probably originating from intra- and/or intermolecular [small pi] stackings, are suggested by the decrease in chiMT below 8 K.

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PubMed2004

Hetero di- and trinuclear Cu-Gd complexes with trifluoroacetate bridges: synthesis, structural and magnetic studies.

The synthesis, structural determinations and magnetic properties of an original dinuclear Cu-Gd and two trinuclear Cu-Ln-Cu complexes (Ln = Gd or Dy) made with a Schiff base ligand and carboxylate ligands are reported. In each complex, the copper and gadolinium or dysprosium ions are linked by a double phenoxo bridge and a eta1:eta1:mu trifluoroacetato bridge. The dinuclear Cu-Gd complex exhibits the usual ferromagnetic interaction while the trinuclear (Cu-Gd-Cu) complexes can not be fitted with a simple Hamiltonian that only takes into account the Cu-Gd interaction. Introduction into the Hamiltonian of a Cu-Cu interaction between the terminal copper ions gives a nice fit in the case of a ferromagnetic Cu-Cu interaction (J'(Cu-Cu) = 8.3 and 9.8 cm(-1)). For the first time, the occurrence of a ferromagnetic interaction between the copper ions of the trinuclear entities is evidenced and supported by the field dependence of the magnetization. As there is no direct proof for the existence of an interaction between two centers through a third magnetic center located in between them, we can conclude that the existence of pi-pi stacking interactions through the phenyl rings of the ligands are responsible for the presence of these interactions.

Journal Article↗

PubMed2004

Richness of isomerism in labile octahedral Werner-type cobalt(II) complexes demonstrated by 19F NMR spectroscopy: structure and stability.

The cobalt(II) complexes [CoL2(R2-Py)2] (1-4) where HLA = 1,1,1-trifluoro-5,5-dimethyl-2,4-hexanedione, R2-Py = 4-methylpyridine (1), HLB = 4,4,4-trifluoro-1-(2-thienyl)-1,3-butanedione, R2-Py = 4-methylpyridine (2), 4-phenylpyridine (3) and S-(-)-1-(4-pyridyl)ethanol (4) were prepared by two-step reactions. X-ray structure analysis of [CoLA2(CH3-Py)2] revealed the {trans(N)-trans(CF3)-trans} configuration for the complex obtained by crystallization from ethanol. A dynamic equilibrium between the five possible stereoisomers was observed for each complex 1-4 in solution by 19F NMR spectroscopy. The criteria used for full NMR assignment (180-265 K) include comparison of integral ratios, cis(N) and trans(N) differentiation in presence of the chiral amine [S-(-)-1-(4-pyridyl)ethanol], effect of solvent polarity on the relative stabilities of the five isomers and observation of trans influences in a mixture of complexes. Thermodynamic parameters for the equilibria between the isomers of 2 in CD2Cl2 (DeltaHi,j, DeltaSi,j and Ki,j) were obtained from signal integrals. The two trans(N) isomers are slightly more stable than the three cis(N) isomers at low temperature [DeltaGdegreesi,j (max) = 2.8 kJ mol(-1) at 179.8 K], but this stability difference almost vanishes with increasing temperature [DeltaGdegreesi,j (max) = 1.0 kJ mol(-1) at 265.0 K]. The values found for DeltaHdegreesi,j are relatively small and largely entropy compensated.

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