| Autor: |
Sumrit P; Laboratory of Catalysts and Advanced Polymer Materials, Department of Chemistry and Centre of Excellence for Innovation in Chemistry, Faculty of Science, Kasetsart University, Bangkok 10900, Thailand. fscipph@ku.ac.th.; Centre for Advanced Studies in Nanotechnology for Chemical, Food and Agricultural Industries, Kasetsart University, Bangkok 10900, Thailand., Kamavichanurat S; Laboratory of Catalysts and Advanced Polymer Materials, Department of Chemistry and Centre of Excellence for Innovation in Chemistry, Faculty of Science, Kasetsart University, Bangkok 10900, Thailand. fscipph@ku.ac.th.; Centre for Advanced Studies in Nanotechnology for Chemical, Food and Agricultural Industries, Kasetsart University, Bangkok 10900, Thailand., Joopor W; Laboratory of Catalysts and Advanced Polymer Materials, Department of Chemistry and Centre of Excellence for Innovation in Chemistry, Faculty of Science, Kasetsart University, Bangkok 10900, Thailand. fscipph@ku.ac.th.; Centre for Advanced Studies in Nanotechnology for Chemical, Food and Agricultural Industries, Kasetsart University, Bangkok 10900, Thailand., Wattanathana W; Department of Materials Engineering, Faculty of Engineering, Kasetsart University, Bangkok 10900, Thailand., Nakornkhet C; Laboratory of Catalysts and Advanced Polymer Materials, Department of Chemistry and Centre of Excellence for Innovation in Chemistry, Faculty of Science, Kasetsart University, Bangkok 10900, Thailand. fscipph@ku.ac.th.; Centre for Advanced Studies in Nanotechnology for Chemical, Food and Agricultural Industries, Kasetsart University, Bangkok 10900, Thailand., Hormnirun P; Laboratory of Catalysts and Advanced Polymer Materials, Department of Chemistry and Centre of Excellence for Innovation in Chemistry, Faculty of Science, Kasetsart University, Bangkok 10900, Thailand. fscipph@ku.ac.th.; Centre for Advanced Studies in Nanotechnology for Chemical, Food and Agricultural Industries, Kasetsart University, Bangkok 10900, Thailand. |
| Abstrakt: |
Fourteen new phenoxy-azo aluminium complexes comprising two series, namely, dimethyl{phenoxy-azo}aluminium complexes 1a-7a and monomethyl{phenoxy-azo}aluminium complexes 1b-7b, were successfully synthesised and characterised. The molecular structure of complex 4a, determined using X-ray diffraction analysis, displayed a distorted tetrahedral geometry. The 1 H NMR spectrum of complex 5b revealed fluxional behaviour caused by isomeric transformation that occurs in the solution at room temperature. The activation parameters determined by lineshape analysis of variable-temperature 1 H NMR spectra in toluene-d 8 are as follows: Δ H ‡ = 70.05 ± 1.19 kJ mol -1 , Δ S ‡ = 21.78 ± 3.58 J mol -1 K -1 and Δ G ‡ (298 K) = 63.56 ± 0.11 kJ mol -1 . All aluminium complexes are active initiators for the ring-opening polymerisation of rac -lactide, and the polymerisations proceeded in a controlled manner and were living. In comparison, the catalytic activity of the dimethyl{phenoxy-azo}aluminium complexes was insignificantly different from that of the corresponding monomethyl{phenoxy-azo}aluminium complexes. The steric factor of the ortho -phenoxy substituent was observed to exert a decelerating effect on the catalytic rate. Kinetic investigations revealed first-order dependency on both monomer and initiator concentrations. Comparative catalytic investigations conducted on phenoxy-azo aluminium and phenoxy-imine aluminium complexes revealed that the former complexes exhibited lower catalytic activity. |
