A series of controlled microstructure polybutadiene rubbers (PBs) was synthesized via anionic polymerization. Their structure and properties are analyzed by means of GPC, 13 C NMR, DSC, and DMA, and compared to the behavior of some commercial high cis rubbers. Thermal analyses results indicate the presence of crystalline domains of different nature in PBs with high cis-1,4 and high trans-1,4 isomers content, while rubbers with high content of vinyl-1,2 units do not show evidence of crystals. A shift in T g to higher temperatures as vinyl content increases is observed; an expression was found for predicting T g of rubber from microstructure data.
The ruthenium complex with (N,N,N-tris(benzimidazol-2yl-methyl)amine, L(1)) was prepared, and characterized. Fukui data were used to localize the reactive sites on the ligand. The structural and electronic properties of the complex were analyzed by DFT in different oxidation states in order to evaluate its oxidant properties for phenol oxidation. The results show that the hard Ru(IV) cation bonds preferentially with a hard base (Namine = amine nitrogen, or axial chloride ion), and soft Ru(II) with a soft base (Nbzim = benzimidazole nitrogen or axial triphenyl phosphine). Furthermore, the Jahn-Teller effect causes an elongation of the axial bond in the octahedral structure. The bonding nature and the orbital contribution to the electronic transitions of the complex were studied. The experimental UV-visible bands were interpreted by using TD-DFT studies. The complex oxidizes phenol to benzoquinone in the presence of H2O2 and the intermediate was detected by HPLC and (13)C NMR. A possible mechanism and rate law are proposed for the oxidation. The adduct formation of phenol with [Ru(O)L(1)](2+) or [Ru(OH)L(1)](+) is theoretically analyzed to show that [Ru(OH)L(1)-OPh](+) could produce the phenol radical.
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