Search

Direct synthesis of magnesium amidinates of the general formula [RNC(R1)NR]MgR2 has been performed from appropriate carbodimide and Grignard reagents (R = iPr, Cy, pTol; R1 = Me, nBu; R2 = nBu, Cl, I). Magnesium bisamidinates of the composition [RNC(R1)NR]2Mg(solvent)2 are accessible from [RNC(R1)NR]MgR2 and via the Schlenk-like equilibrium in coordinating solvents. The only isolated amidinatomagnesium halide, preserved in the dinuclear form of {[pTolNC(Me)N-pTol]Mg(THF)}2-μ-(THF)-μ-(Cl)2, has been obtained from the reaction of pTol-N=C=N-pTol with MeMgCl(THF)n in hexane. The reaction of pTol-N=C=N-pTol with two equivalents of MeMgI gives an unprecedented dinuclear cyclic adduct {μ-[pTolNC(Me)N-pTol][MgI(OEt2)]2-μ-Me}. The structures of these complexes have been investigated by NMR spectroscopy, sc-XRD and theoretical methods. Selected complexes have been tested as initiators of ring-opening polymerization reactions with various substrates, the copolymerization of oxiranes and CO2 as well as the esterification of lactides. [ABSTRACT FROM AUTHOR]

Novel ionene-type cationic copolyimides based on 4,4'-oxydiphthalic anhydride (ODPA), 4,4'-(1,4-phenylenediisopropylidene)bisaniline (BIS P), and 2,6-diaminopyridine (DAP) were synthesized. The copolyimides were obtained in two stages: first, the copolyimides with the 0/1, 0.2/0.8, 0.3/0.7, 0.5/0.5, 0.6/0.4 and 1/0 DAP/Bis P ratios were obtained through thermal imidization, and then quaternization of soluble copolyimides with methyl iodide was conducted for 24 or 48 h. The samples were characterized via FTIR, NMR and EDX methods to confirm their structure and composition. The cationic copolyimides with a DAP content of less than 0.3 showed initial weight loss (onset) at about 250 °C, according to TGA results and demonstrated solubility in chloroform. The highest ionic conductivity value of 0.234 S cm -1 was showed by the sample with 0.3 DAP content and 0.15 degree of quaternization. The stability of the membranes in alkaline media was evaluated using FTIR and TGA. It was shown that samples with a DAP content of more than 0.3 lost their integrity probably owing to partial hydrolysis of imide rings, while copolyimides with a DAP content of 0.2 and 0.3 remained stable., Competing Interests: There are no conflicts to declare., (This journal is © The Royal Society of Chemistry.)

Direct synthesis of magnesium amidinates of the general formula [RNC(R1)NR]MgR2 has been performed from appropriate carbodimide and Grignard reagents (R = iPr, Cy, pTol; R1 = Me, nBu; R2 = nBu, Cl, I). Magnesium bisamidinates of the composition [RNC(R1)NR]2Mg(solvent)2 are accessible from [RNC(R1)NR]MgR2 and via the Schlenk-like equilibrium in coordinating solvents. The only isolated amidinatomagnesium halide, preserved in the dinuclear form of {[pTolNC(Me)N-pTol]Mg(THF)}2-μ-(THF)-μ-(Cl)2, has been obtained from the reaction of pTol-N[double bond, length as m-dash]C[double bond, length as m-dash]N-pTol with MeMgCl(THF)n in hexane. The reaction of pTol-N[double bond, length as m-dash]C[double bond, length as m-dash]N-pTol with two equivalents of MeMgI gives an unprecedented dinuclear cyclic adduct {μ-[pTolNC(Me)N-pTol][MgI(OEt2)]2-μ-Me}. The structures of these complexes have been investigated by NMR spectroscopy, sc-XRD and theoretical methods. Selected complexes have been tested as initiators of ring-opening polymerization reactions with various substrates, the copolymerization of oxiranes and CO2 as well as the esterification of lactides.