{"title":"Catalytic Arene-Norbornene Annulation toward All-Hydrocarbon Benzocyclobutene-Based Polymers with Ultralow Dielectric Constants","authors":"Quan Sun*, , , Yan He, , , Meng Xie, , , Wenjie Fan, , , Menglu Li, , , Pingxia Zhang, , , Jingcheng Xu, , , Aijiao Guan, , and , Wenxin Fu*, ","doi":"10.1021/acs.macromol.5c03319","DOIUrl":null,"url":null,"abstract":"<p >The development of ultralow dielectric constant (<i>D</i><sub>k</sub> < 2.5) materials with high thermal stability and mechanical robustness faces a critical bottleneck: traditional strategies relying on fluorination or nanoporosity inevitably compromise processability or environmental compatibility. Here, we report a catalytic arene-norbornene annulation (CANAL) strategy to synthesize all-hydrocarbon benzocyclobutene (BCB)-based polymers with intrinsic microporosity. By leveraging the rigid and twisted norbornene-bridged BCB architecture, the optimized polymer (P-NBD-BCB) achieves an ultralow <i>D</i><sub>k</sub> of 2.37 at 10 GHz. Combined experimental and computational analyses reveal that the synergy between norbornene-induced free volume (22.2%) and suppressed chain polarization underpins the reduced dielectric constants, while Diels–Alder cross-linking stabilizes the network against thermal decomposition (<i>T</i><sub>d5%</sub> = 483 °C). The material further demonstrates 5G-compatible dielectric loss and exceptional mechanical properties. This work establishes a robust strategy for designing sustainable ultralow dielectrics through precise control of hydrocarbon topology, addressing the escalating demands of high-frequency communication and three-dimensional heterogeneous integration.</p>","PeriodicalId":51,"journal":{"name":"Macromolecules","volume":"59 8","pages":"4775–4786"},"PeriodicalIF":5.7000,"publicationDate":"2026-04-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Macromolecules","FirstCategoryId":"92","ListUrlMain":"https://pubs.acs.org/doi/10.1021/acs.macromol.5c03319","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2026/4/13 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"POLYMER SCIENCE","Score":null,"Total":0}
引用次数: 0
Abstract
The development of ultralow dielectric constant (Dk < 2.5) materials with high thermal stability and mechanical robustness faces a critical bottleneck: traditional strategies relying on fluorination or nanoporosity inevitably compromise processability or environmental compatibility. Here, we report a catalytic arene-norbornene annulation (CANAL) strategy to synthesize all-hydrocarbon benzocyclobutene (BCB)-based polymers with intrinsic microporosity. By leveraging the rigid and twisted norbornene-bridged BCB architecture, the optimized polymer (P-NBD-BCB) achieves an ultralow Dk of 2.37 at 10 GHz. Combined experimental and computational analyses reveal that the synergy between norbornene-induced free volume (22.2%) and suppressed chain polarization underpins the reduced dielectric constants, while Diels–Alder cross-linking stabilizes the network against thermal decomposition (Td5% = 483 °C). The material further demonstrates 5G-compatible dielectric loss and exceptional mechanical properties. This work establishes a robust strategy for designing sustainable ultralow dielectrics through precise control of hydrocarbon topology, addressing the escalating demands of high-frequency communication and three-dimensional heterogeneous integration.
期刊介绍:
Macromolecules publishes original, fundamental, and impactful research on all aspects of polymer science. Topics of interest include synthesis (e.g., controlled polymerizations, polymerization catalysis, post polymerization modification, new monomer structures and polymer architectures, and polymerization mechanisms/kinetics analysis); phase behavior, thermodynamics, dynamic, and ordering/disordering phenomena (e.g., self-assembly, gelation, crystallization, solution/melt/solid-state characteristics); structure and properties (e.g., mechanical and rheological properties, surface/interfacial characteristics, electronic and transport properties); new state of the art characterization (e.g., spectroscopy, scattering, microscopy, rheology), simulation (e.g., Monte Carlo, molecular dynamics, multi-scale/coarse-grained modeling), and theoretical methods. Renewable/sustainable polymers, polymer networks, responsive polymers, electro-, magneto- and opto-active macromolecules, inorganic polymers, charge-transporting polymers (ion-containing, semiconducting, and conducting), nanostructured polymers, and polymer composites are also of interest. Typical papers published in Macromolecules showcase important and innovative concepts, experimental methods/observations, and theoretical/computational approaches that demonstrate a fundamental advance in the understanding of polymers.