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- W2784400101 endingPage "439" @default.
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- W2784400101 abstract "How to get two bonds for the price of one For more than a century, we have known how to couple aryl chlorides at the sites of their C-Cl bonds to form a single C-C bond. Koga et al. found that palladium catalysis can instead activate these C-Cl bonds to attack nearby aromatic C-H bonds in a terphenyl molecular framework. The reaction thereby produces a new ring, fused to the original rings on either side. Polycyclic compounds of this sort are of particular interest in optoelectronics research because of their expansive electron delocalization. Science , this issue p. 435" @default.
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- W2784400101 date "2018-01-26" @default.
- W2784400101 modified "2023-10-18" @default.
- W2784400101 title "Synthesis of partially and fully fused polyaromatics by annulative chlorophenylene dimerization" @default.
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- W2784400101 doi "https://doi.org/10.1126/science.aap9801" @default.
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