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Introducing ethylene units into polybutadiene backbones is an approach to synthesize advanced rubber materials, which has been a research challenge because of distinct polymerization mechanisms of the two monomers. To date, only trans ‐1,4‐ and 1,2‐regulated copolymers have been obtained. Herein, we reported the unprecedented cis ‐1,4 selective copolymerization of ethylene and butadiene by using the thiophene‐fused cyclopentadienyl‐ligated scandium complexes. The effects of the sterics and electronics of the catalytic precursors as well as the monomer loading mode on the activity and selectivity as well as the sequence lengths were investigated, and the mechanism was elucidated. Thus a novel ethylene‐based rubber material possessing a high molecular weight, 80 % cis ‐1,4 regularity and a T g=−94 °C without an obvious melting point owing to short polyethylene sequences even at its content up to 45 mol %, was isolated. This new rubber material exhibited excellent anti‐flowing performance and strong tensile strength.  相似文献   

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Homoleptic uranium(IV) amidate complexes have been synthesized and applied as single‐source molecular precursors for the chemical vapor deposition of UO2 thin films. These precursors decompose by alkene elimination to give highly crystalline phase‐pure UO2 films with an unusual branched heterostructure.  相似文献   

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All‐polymer solar cells (all‐PSCs) offer unique morphology stability for the application as flexible devices, but the lack of high‐performance polymer acceptors limits their power conversion efficiency (PCE) to a value lower than those of the PSCs based on fullerene derivative or organic small molecule acceptors. We herein demonstrate a strategy to synthesize a high‐performance polymer acceptor PZ1 by embedding an acceptor–donor–acceptor building block into the polymer main chain. PZ1 possesses broad absorption with a low band gap of 1.55 eV and high absorption coefficient (1.3×105 cm−1). The all‐PSCs with the wide‐band‐gap polymer PBDB‐T as donor and PZ1 as acceptor showed a record‐high PCE of 9.19 % for the all‐PSCs. The success of our polymerization strategy can provide a new way to develop efficient polymer acceptors for all‐PSCs.  相似文献   

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