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Four- and five-coordinate aluminum complexes supported by N,O-bidentate β-pyrazylenolate ligands: synthesis, structure and application in ROP of ε-caprolactone and lactide.
- Source :
-
Dalton Transactions: An International Journal of Inorganic Chemistry . 8/28/2019, Vol. 48 Issue 32, p12315-12325. 11p. - Publication Year :
- 2019
-
Abstract
- In this paper we report a series of Al(III) complexes supported by N,O-bidentate β-pyrazyl functionalized enolate ligands HL1–HL5 (L = (6-Me-2,5-C4H2N2)–CH=C(R)–O–), (R = tBu, Ph, p-tolyl, p-OMePh, o-tolyl) and their exploitation for the ring-opening polymerization of ε-caprolactone (ε-CL) and rac-lactide (rac-LA). The structures of the form LAlMe2 (1a–5a) or L2AlMe (1b–4b) were isolated depending on the ligand or stoichiometry of complexation. The investigation of these complexes toward the ROP of both ε-CL and rac-LA under the same conditions showed that dimethyl-aluminum complexes LAlMe2 (1a–5a) gave a higher activity than monomethyl-aluminum complexes L2AlMe (1b–4b). Meanwhile, monomethyl-aluminum complexes 1b–4b promoted the ring-opening polymerization with a better control over molecular weights and polydispersities than 1a–5a. Moreover, all of the LAlMe2 and L2AlMe produced PLA with strong isotactic bias (Pm up to 0.77) and narrow distributions. Generally, a β-pyrazyl enolate system exhibited significantly higher catalytic activity for the ROP of ε-CL and rac-LA than the analogous β-quinolyl enolate systems reported recently. The results are discussed in terms of electronic and steric properties affected by the substituents on the ligands. [ABSTRACT FROM AUTHOR]
Details
- Language :
- English
- ISSN :
- 14779226
- Volume :
- 48
- Issue :
- 32
- Database :
- Academic Search Index
- Journal :
- Dalton Transactions: An International Journal of Inorganic Chemistry
- Publication Type :
- Academic Journal
- Accession number :
- 138030707
- Full Text :
- https://doi.org/10.1039/c9dt02330e