Issue 22, 2021, Issue in Progress

Bimetallic aluminum complexes bearing novel spiro-phenanthrene-monoketone/OH derivatives: synthesis, characterization and the ring-opening polymerization of ε-caprolactone

Abstract

A series of spiro-phenanthrene-monoketone/OH derivatives (L1–L6) were synthesized and fully characterized with 1H/13C NMR spectroscopy and elemental analyses. By treating ligands with AlMe3, oxygen-bridged binuclear aluminum complexes (Al1–Al6) were isolated and characterized by 1H/13C 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 iPr at the ortho-position of the arylamines demonstrated better catalytic activities than the analogs. Moreover, substituents on the backbone also affected catalytic behaviors.

Graphical abstract: Bimetallic aluminum complexes bearing novel spiro-phenanthrene-monoketone/OH derivatives: synthesis, characterization and the ring-opening polymerization of ε-caprolactone

Supplementary files

Article information

Article type
Paper
Submitted
17 Feb 2021
Accepted
23 Mar 2021
First published
08 Apr 2021
This article is Open Access
Creative Commons BY license

RSC Adv., 2021,11, 13274-13281

Bimetallic aluminum complexes bearing novel spiro-phenanthrene-monoketone/OH derivatives: synthesis, characterization and the ring-opening polymerization of ε-caprolactone

E. Yue, F. Cao, J. Zhang, W. Zhang, Y. Jiang, T. Liang and W. Sun, RSC Adv., 2021, 11, 13274 DOI: 10.1039/D1RA01288F

This article is licensed under a Creative Commons Attribution 3.0 Unported Licence. You can use material from this article in other publications without requesting further permissions from the RSC, provided that the correct acknowledgement is given.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements