Coordination of ε-Caprolactone to a Cationic Niobium(V) Alkoxide Complex: Fundamental Insight into Ring-Opening Polymerization via Coordination-Insertion.
Coordination of ε-Caprolactone to a Cationic Niobium(V) Alkoxide Complex: Fundamental Insight into Ring-Opening Polymerization via Coordination-Insertion.
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DOI:
10.1021/acs.inorgchem.3c02491
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发表时间:
2023-09-25
影响因子:
4.6
通讯作者:
Mckeown, Paul
中科院分区:
文献类型:
--
作者:
Buchard, Antoine;Davidson, Matthew G.;du Sart, Gerrit Gobius;Jones, Matthew D.;Kociok-Kohn, Gabriele;Mccormick, Strachan N.;Mckeown, Paul
We report three niobium-based initiators for the catalytic ring-opening polymerization (ROP) of ε-caprolactone, exhibiting good activity and molecular weight control. In particular, we have prepared on the gram-scale and fully characterized a monometallic cationic alkoxo-Nb(V) ε-caprolactone adduct representing, to the best of our knowledge, an unprecedented example of a metal complex with an intact lactone monomer and a functional ROP-initiating group simultaneously coordinated at the metal center. At 80 °C, all three systems initiate the immortal solution-state ROP of ε-caprolactone via a coordination–insertion mechanism, which has been confirmed through experimental studies, and is supported by computational data. Natural bond orbital calculations further indicate that polymerization may necessitate isomerization about the metal center between the alkoxide chain and the coordinated monomer. The observations made in this work are expected to inform mechanistic understanding both of amine tris(phenolate)-supported metal alkoxide ROP initiators, including various highly stereoselective systems for the polymerization of lactides and of coordination–insertion-type ROP protocols more broadly. Cationic niobium(V) complexes are reported as catalysts for the controlled, immortal ring-opening polymerization of ε-caprolactone. In particular, gram-scale isolation of an unprecedented stable metal complex, simultaneously bearing a coordinated monomer molecule and an alkoxide initiating group, is facile at ambient temperature. Catalytic studies and mechanistic interrogation of this species and others have been undertaken.
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