In this paper we report the temperature and pH dependent syntheses and systematic characterization of four new Co(II)/Co(III) and Ni(II) complexes with a pentadentate Schiff base ligand H(3)L obtained by condensing 1,3,-diaminopropan-2-ol with 2-hydroxyacetophenone in 1:2 molar ratio. The room temperature syntheses involving Co(II) and Ni(II) nitrates and the ligand H(3)L lead to the isolation of the dinuclear species [Co(2)L(2)(H(2)O)] (1), and the mononuclear complex [Ni(LH)] (3), respectively, whereas refluxing at basic pH leads to the tetranuclear complexes, [Co(II)(2)Co(III)(2)L(2)(μ(3)-OMe)(2)(NO(3))(H(2)O)(2)]NO(3)·2(H(2)O) (2), and [Ni(4)L(2)(μ(3)-OMe)(2)(H(2)O)(2)]·2H(2)O (4). 1 is found to be a simple mono alkoxo-bridged Co(III) dinuclear species, whereas 2 and 4 are both rhomb-like tetrameric complexes with double oxo bridges and μ(3)-methoxo bridges, derived from the methanol solvent, in an open dicubane arrangement. Moreover 2 shows six coordinate ordered Co(II) and Co(III) ions and 4 has both six- and five-coordinate Ni(II) centers. Compound 3 is assigned a tentative mononuclear structure based on IR, UV-Vis spectroscopic, (1)H-NMR and ESI mass study results and is supposed to have one Ni(II) center coordinated with a ligand fragment in square planar geometry. The variable temperature magnetic susceptibility study for 2 and 4 is performed which indicate for both 2 and 4 the presence of intracluster dominant ferromagnetic interactions. 相似文献
A new class of bio-based fully degradable block polyesters are pressure-sensitive adhesives. Bio-derived monomers are efficiently polymerized to make block polyesters with controlled compositions. They show moderate to high peel adhesions (4–13 N cm−1) and controllable storage and loss moduli, and they are removed by adhesive failure. Their properties compare favorably with commercial adhesives or bio-based polyester formulations but without the need for tackifier or additives. 相似文献
The sodium salt of the new bis(mesitoyl)phosphinic acid (BAPO‐OH) can be prepared in a very efficient one‐pot synthesis. It is well soluble in water and hydrolytically stable for at least several weeks. Remarkably, it acts as an initiating agent for the surfactant‐free emulsion polymerization (SFEP) of styrene to yield monodisperse, spherical nanoparticles. Time‐resolved electron paramagnetic resonance (TR‐EPR) and chemically induced electron polarisation (CIDEP) indicate preliminary mechanistic insights.
Two new octahedral Cd(II) complexes [Cd(L)2] (1) and {[Cd(LH)2(SCN)2]H2O} (2) [where LH = C14H13N3O] are synthesized using a tridentate hydrazone ligand (LH) and they are characterized by elemental analysis, IR spectra, NMR spectra, thermal studies and finally the structures have
been determined by single crystal X-ray diffraction. Complex 1 crystallizes in monoclinic system, space group C2/c with a = 22.565(6) ?, b = 10.252(3) ?, c = 12.187(4) ?, β = 118.851(2)∘, and Z = 4. Complex 2 also crystallizes in the monoclinic system, space group P21/c with a = 9.257(9)?, b = 17.809(2)?, c = 9.548(9)?, β = 107.439(4)∘, and Z = 2. In 1 the ligand binds the Cd(II) ion in tridentate fashion, whereas in 2 it acts as a bidentate ligand. 相似文献
Symmetric 4,5,2,3-M(2)C(2)B(9) 13-vertex bimetallacarboranes of cobalt and ruthenium with 14 skeletal electron pairs are afforded by reduction and metallation of 3,1,2-MC(2)B(9) icosahedra; the symmetric species can be converted to their asymmetric 4,5,1,6-M(2)C(2)B(9) isomers by heat, but an easier route is by thermolysis of the reduced species before metallation. 相似文献
The equilibrium constants of salicylaldoxime in water at 25 degrees C, 0.5 M of ionic strength with NaCl and concentration of 1x10(-4) M were determined spectrophotometrically. The spectral data were processed using SQUAD program. The salicylaldoxime in acid medium has the value of pKa1=1.224+/-0.027. In alkaline medium the salicylaldoxime has the values of pKa2=8.551+/-0.024 and pKa3=11.728+/-0.016. 相似文献
In the title compound, [Rh(C2H11B9)(NO3)(C18H15P)2]·2.2CH2Cl2, studied as a 2.2‐solvate of what was assumed to be dichloromethane, the nitrate ligand lies cis with respect to both cage C atoms. Accordingly, the compound displays a pronounced preferred exopolyhedral ligand orientation (ELO) which is traced to both the greater trans influence of the cage B over the cage C atoms and the greater trans influence of the triphenylphosphane ligands over the nitrate ligand. The overall molecular architecture therefore agrees with that of a number of similar 3‐L‐3,3‐L′2‐3,1,2‐closo‐MC2B9H11 species in the literature. 相似文献