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Novel wide band-gap polymer of PBTFT containing dibenzosexithiophene-alt-bithiophene backbone was designed and synthesized via the Stille cross-coupling reaction.
In this work, an amphiphilic copolymer, PCL-SS-P PEGMA-co-MAEBA), which contained a disulfide joint in backbone was designed and synthesized.
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The channel allocation method in the backbone is designed, and MIMO is used to cancel inter-hop interference.
Two host materials, SFCA and SFCC, consist of a diphenylamine or carbazole unit linking to spiro-fused phenyl carbazole (SFC) backbone, were designed and synthesized.
A series of water-soluble cationic polyfluorene copolymer containing 2,2′-bipyridine moieties (PFP-P1 3) PFP-P1 3ackbone were desinned and synthesized as the fluorescent probackboneCu2+ ions.
A series of butynediol-ethoxylate based polysiloxanes (PSi-EOs) with same composition but different lengths of siloxane backbone were designed and synthesized via hydrosilylation reaction.
Two copolymers based on 2,1,3-benzoxadiazole (BO) as the acceptor unit and quaterthiophene as the donor unit, which possess different steric hindrance in the backbone, were designed and synthesized.
A novel Jeffamine based Quaternary Ammonium Iodide (JQAI) melt which contains ether group in backbone were designed and synthesized as non-volatile iodide resource for fabrication of dye sensitized solar cells.
Two scaffolds based on 5,6-fused heterocyclic backbones were designed and synthesized as Raf kinase inhibitors.
Two pyrene derivatives, substituted with 2-methylnaphthalene units on 1,3-position and 1,6-position of pyrene backbones, were designed and synthesized.
A series of new planar and central chiral ligands based on [2.2]paracyclophane backbones were designed and prepared from enantiomerically pure 4-amino-13-bromo[2.2]paracyclophane and commercially available chiral amino alcohols.
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