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Aluminum Alkyl Complexes Bearing Salicylaldiminato Ligands: Versatile Initiators in the Ring-Opening Polymerization of Cyclic Esters
KTH, Skolan för kemivetenskap (CHE), Fiber- och polymerteknologi.
KTH, Skolan för kemivetenskap (CHE), Fiber- och polymerteknologi.ORCID-id: 0000-0001-9699-9151
2017 (engelsk)Inngår i: CATALYSTS, ISSN 2073-4344, Vol. 7, nr 2, artikkel-id 64Artikkel, forskningsoversikt (Fagfellevurdert) Published
Abstract [en]

Linear aliphatic polyesters are degradable thermoplastic polymers, which can be obtained by ring-opening polymerization (ROP) of cyclic esters through a coordination-insertion mechanism. Aluminum based organometallic complexes have a leading position as efficient catalysts for this polymerization process. Aluminumalkyl complexes bearing salicylaldiminato ligands, although less explored, have been shown to be efficient and versatile catalysts for the ROP of various cyclic esters. These species have the potential to function as active catalysts in the ROP because of their less coordinatively saturated nature with respect to analogous SALEN-type complexes. They have been used as efficient catalysts in the ROP of commercially available cyclic esters, such as epsilon-caprolactone, L-lactide, rac-lactide, and glycolide. Moreover, they resulted in efficient catalysts for the ROP of cyclic esters with large ring-size and for the ROP of functionalized lactide. Furthermore, they have been used in the co- and ter-polymerization of various cyclic esters affording well controlled polymerization and a plethora of microstructural architectures, ranging from random to block to multiblock.

sted, utgiver, år, opplag, sider
MDPI AG , 2017. Vol. 7, nr 2, artikkel-id 64
Emneord [en]
aluminum, ring-opening polymerization, aliphatic poly(esters), poly(lactide), poly(caprolactone), poly(glycolide)
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Identifikatorer
URN: urn:nbn:se:kth:diva-205128DOI: 10.3390/catal7020064ISI: 000395436800029Scopus ID: 2-s2.0-85013216673OAI: oai:DiVA.org:kth-205128DiVA, id: diva2:1096393
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QC 20170517

Tilgjengelig fra: 2017-05-17 Laget: 2017-05-17 Sist oppdatert: 2017-05-17bibliografisk kontrollert

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