Cargando…
Bimetallic aluminum complexes bearing novel spiro-phenanthrene-monoketone/OH derivatives: synthesis, characterization and the ring-opening polymerization of ε-caprolactone
A series of spiro-phenanthrene-monoketone/OH derivatives (L1–L6) were synthesized and fully characterized with (1)H/(13)C NMR spectroscopy and elemental analyses. By treating ligands with AlMe(3), oxygen-bridged binuclear aluminum complexes (Al1–Al6) were isolated and characterized by (1)H/(13)C NMR...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8697580/ https://www.ncbi.nlm.nih.gov/pubmed/35423871 http://dx.doi.org/10.1039/d1ra01288f |
Sumario: | A series of spiro-phenanthrene-monoketone/OH derivatives (L1–L6) were synthesized and fully characterized with (1)H/(13)C NMR spectroscopy and elemental analyses. By treating ligands with AlMe(3), oxygen-bridged binuclear aluminum complexes (Al1–Al6) were isolated and characterized by (1)H/(13)C NMR spectroscopy. The molecular structures of ligands (L2, L4 and L5) and complex Al1 were determined by single crystal X-ray diffraction. In the presence of benzyl alcohol (BnOH), these aluminum complexes demonstrated high efficiency towards the ring-opening polymerization of ε-caprolactone (ε-CL), resulting in PCL in a linear manner with the BnO-end group. In addition, complexes Al1 and Al5 exhibited good catalytic activities even without BnOH. Moreover, complexes Al3 and Al6 with the bulkier substituent of (i)Pr at the ortho-position of the arylamines demonstrated better catalytic activities than the analogs. Moreover, substituents on the backbone also affected catalytic behaviors. |
---|