Ring opening metathesis polymerization (ROMP) of bicyclo[2.2.1]hept-2-ene (norbornene) is carried out over silica-supported catalysts based on tungsten complexes bearing an oxo ligand (1: [(SiO)W(O)(CH SiMe ) , 2: [(SiO)W(O)(CHCMe Ph)(dAdPO)], dAdPO 2,6 diadamantyl-4-methylphenoxide, 3: [(SiO) W(O)(CH SiMe ) ]). The evaluation of the catalytic activities of the aforementioned materials in ROMP indicates that at low reaction time (0.5 min), the highest polymer yield is obtained with catalyst 2. However, for longer reaction time (>2 min), complex 3, a model of the industrial catalyst, exhibits a better monomer conversion. The polymers obtained are characterized. Moreover, these catalysts are shown to be rather preferentially selective to give the cis polynorbornene (>65%), characterized by high melting points (≈300 °C). The experimental values of the average molecular weight (M ) of polynorbornenes are found to be close to the theoretical ones for the polymers prepared using catalyst 2 and higher for those originated from catalyst 3.
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http://dx.doi.org/10.1002/marc.201600419 | DOI Listing |
J Am Chem Soc
January 2025
Department of Chemistry, Pohang University of Science and Technology, Pohang 37673, Republic of Korea.
Ring expansion metathesis polymerization (REMP) has emerged as a potent strategy for obtaining cyclic polymers over the past two decades. The scope of monomers, however, remains limited due to the poor functional group tolerance and stability of the catalyst, necessitating a rational catalyst design to address this constraint. Here, we present ruthenium complexes featuring tethered cyclic (alkyl)(amino)carbene ligands for REMP, aiming to deepen our understanding of the structure-property relationship in newly designed catalysts.
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January 2025
Department of Chemistry, University of Minnesota, Minneapolis, Minnesota 55455, United States.
Langmuir
December 2024
Department of Chemistry, Carnegie Mellon University, 4400 Avenue, Pittsburgh, Pennsylvania 15213, United States.
Structurally tailored and engineered macromolecular (STEM) networks are attractive materials for soft robotics, stretchable electronics, tissue engineering, and 3D printing due to their tunable properties. To date, STEM networks have been synthesized by atom transfer radical polymerization (ATRP) or the combination of reversible addition-fragmentation chain-transfer (RAFT) polymerization and ATRP. RAFT polymerization could have limited selectivity with ATRP inimer sites that can participate in radical-transfer processes.
View Article and Find Full Text PDFAdv Sci (Weinh)
December 2024
Institute for Nanoscale Science and Technology, College of Science and Engineering, Flinders University, Bedford Park, South Australia, 5042, Australia.
Big data and artificial intelligence are driving increasing demand for high-density data storage. Probe-based data storage, such as mechanical storage using an atomic force microscope tip, is a potential solution with storage densities exceeding hard disks. However, the storage medium must be modifiable on the nanoscale.
View Article and Find Full Text PDFMacromolecules
November 2024
Materials Department, University of California, Santa Barbara, Santa Barbara, California 93106, United States.
Silicone bottlebrush copolymers and networks derived from cyclic carbosiloxanes are reported and shown to have enhanced properties and recyclability compared with traditional dimethylsiloxane-based materials. The preparation of these materials is enabled by the synthesis of well-defined heterotelechelic macromonomers with Si-H and norbornene chain ends via anionic ring-opening polymerization of the hybrid carbosiloxane monomer 2,2,5,5-tetramethyl-2,5-disila-1-oxacyclopentane. These novel heterotelechelic α-Si-H/ω-norbornene macromonomers undergo efficient ring-opening metathesis copolymerization to yield functional bottlebrush polymers with accurate control over molecular weight and functional-group density.
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