Editorial: Advanced Catalysts in Ring-Opening Polymerization of Cyclic Esters
نویسندگان
چکیده
منابع مشابه
Use of Metal Catalysts Bearing Schiff Base Macrocycles for the Ring Opening Polymerization (ROP) of Cyclic Esters
Schiff base macrocycles are emerging as useful scaffolds for binding two or more catalytic metals in close proximity. Such coordination chemistry allows for the evaluation of potentially beneficial catalytic cooperative effects. In the field of ring opening polymerization (ROP) of cyclic esters, only a handful of metal systems bound by Schiff base [2 + 2] type macrocycles have been studied. Nev...
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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 be...
متن کاملIntroduction of abnormal N-heterocyclic carbene as an efficient organocatalyst: ring opening polymerization of cyclic esters.
The recently isolated abnormal N-heterocyclic carbene (aNHC) has been established as an efficient organocatalyst in ring opening polymerization of three different cyclic esters rac-lactide (rac-LA), ε-caprolactone (ε-CL), and δ-valerolactone (δ-VL). Preliminary DFT calculations indicate that aNHC can be a better organocatalyst than the corresponding nNHC counterpart.
متن کاملHeteroscorpionate rare-earth initiators for the controlled ring-opening polymerization of cyclic esters.
A series of neutral rare-earth metal amides containing different achiral and chiral heteroscorpionate ligands was synthesized and characterized and these compounds were employed in the polymerization of cyclic esters. Thus, treatment of [Ln{N(SiHMe(2))(2)}(3)(thf)(2)] (Ln = Nd, Sm) with acetamide or thioacetamide heteroscorpionate ligands for 2 h at 0 °C afforded the α-agostic silylamido dimeri...
متن کاملZinc calixarene complexes for the ring opening polymerization of cyclic esters.
Reaction of Zn(C6F5)2·toluene (two equivalents) with 1,3-dipropoxy-p-tert-butyl-calix[4]arene (L(1)H2) led to the isolation of the complex [{Zn(C6F5)}2L(1)] (1), whilst similar use of Zn(Me)2 resulted in the known complex [{Zn(Me)}2L(1)] (2). Treatment of L(1)H2 with in situ prepared Zn{N(SiMe3)2}2 in refluxing toluene led to the isolation of the compound [(Na)ZnN(SiMe3)2L(1)] (3). The stepwise...
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ژورنال
عنوان ژورنال: Frontiers in Chemistry
سال: 2019
ISSN: 2296-2646
DOI: 10.3389/fchem.2019.00404