The reactions of pyrrolidine derived salalen-type {ONNO} ligands (S)-L-H with 1 equiv. M(OPr)(HOPr) (M = Zr or Hf) in diethyl ether yielded complexes [LM(OPr)] (L = L, M = Zr (1); L = L, M = Zr (2), Hf (3); L = L, M = Zr (4), Hf (5)). All of these complexes were well characterized by NMR spectroscopy, elemental analyses and single-crystal X-ray analysis in the case of complexes 1 and 3-5. X-ray structural determination revealed that these complexes were analogous mononuclear species and had a similar structure in which the metal centers were six-coordinated to two oxygen atoms and two nitrogen atoms of one ligand and two oxygen atoms of two isopropoxy groups. All of these complexes efficiently initialized the ring-opening polymerization of lactides to afford polymers with controlled molecular weight and narrow polydispersity. Furthermore, the ring-opening polymerization of rac-lactide catalyzed by complexes 1-5 afforded isotactic-enriched polymers in solution (P = 0.74-0.80) and under melt conditions (P = 0.63-0.72).
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http://dx.doi.org/10.1039/c7dt02113e | DOI Listing |
Adv Mater
January 2025
College of Chemistry and Materials Engineering, Wenzhou University, Wenzhou, 325035, P. R. China.
Layered transition metal oxides (LTMOs) are attractive cathode candidates for rechargeable secondary batteries because of their high theoretical capacity. Unfortunately, LTMOs suffer from severe capacity attenuation, voltage decay, and sluggish kinetics, resulting from irreversible lattice oxygen evolution and unstable cathode-electrolyte interface. Besides, LTMOs accumulate surface residual alkali species, like hydroxides and carbonates, during synthesis, limiting their practical application.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
January 2025
University of Science and Technology of China, Hefei National Research Center for Physical Sciences at the Microscale, Department of Chemistry, and Polymer Science and Engineering, 96 Jinzhai Road, 230026, Hefei, CHINA.
Degradable chalcogenide polyesters, e.g., polythioesters (PTEs), typically exhibit improved thermal, mechanical, and optical properties.
View Article and Find Full Text PDFJ Am Chem Soc
January 2025
Department of Polymer Chemistry and Technology, National Institute of Chemistry, Hajdrihova 19, 1000 Ljubljana, Slovenia.
Polyethers are versatile materials extensively used in advanced as well as everyday applications. The incorporation of primary amine functionality into polyethers is particularly attractive due to its well-established coupling chemistries. However, the inherent nucleophilicity of amine group poses a challenge in the anionic ring-opening polymerization (ROP) of epoxides and requires the use of robust protecting groups that can withstand the harsh conditions of ROP without triggering undesirable side reactions.
View Article and Find Full Text PDFACS Macro Lett
January 2025
Faculty of Materials Science and Engineering, South China University of Technology, Guangzhou 510640, People's Republic of China.
Efficient synthesis of cyclic polymers remains a frontier challenge. We report here that macromolecular transesterification during a pseudoblock copolymerization process can be utilized for such a purpose. Organobase-catalyzed ring-opening alternating copolymerization of 3,4-dihydrocoumarin and epoxide is conducted with four-armed poly(ethylene oxide) (PEO) as a macroinitiator.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
January 2025
Northwestern Polytechnical University, School of Chemistry and Chemical Engineering, CHINA.
The increasing power and integration of electronic devices have intensified serious heat accumulation, driving the demand for higher intrinsic thermal conductivity in thermal interface materials, such as polydimethylsiloxane (PDMS). Grafting mesogens onto PDMS can enhance its intrinsic thermal conductivity. However, the high stability of the PDMS chain limits the grafting density of mesogens, restricting the improvement in thermal conductivity.
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