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We present an efficient and convenient synthesis of 3,8-dibromophenanthridine derivatives and their conjugated polymers and demonstrate that phenanthridine-containing conjugated polymers can be used as luminescent chemosensor materials. High molecular weight poly(phenanthridine-co-fluorene)s (P1, P2) and poly(phenanthridine-co-p-phenylene) (P3) were synthesized by palladium-catalyzed Suzuki−Miyaura−Schlüter polycondensation (SMSPC). These phenanthridine-containing polymers are of high quantum yields in solution and show reversible optical response to protonation and deprotonation of the phenanthridine rings. [ABSTRACT FROM AUTHOR]

N,N'-Bicarbazole with almost spatially vertical structure was synthesized by a facile method and was demonstrated as a versatile building block for conjugated microporous polymers (CMPs) through transition metal catalyzed coupling polymerizations including Yamamoto, Suzuki, and Sonogashira polymerizations. The porosities and morphologies of four N,N'-bicarbazole-based CMPs were systematically studied and compared. With high surface area, good thermal stability and microporous structure, the CMP synthesized by Yamamoto polymerization exhibited excellent adsorption capacities of CO2 and organic dyes, and the maximum adsorption capacity of methylene blue (MB) in water reached up to 1016 mg g-1. The good adsorption properties of N,N'-bicarbazole CMPs could be a good candidate for potential applications in water purification and treatment. [ABSTRACT FROM AUTHOR]

A novel type of π-extended 1,10-phenanthroline, specifically with fused thiophene groups at the less exploited 3-, 4-, 7-, and 8-positions of the phenanthroline ring, and its conjugated polymers were designed and synthesized. The current developed route is based on the Bischler-Napieralski cyclization of the (1,2-phenylene)diamide precursor, which offers a facile and versatile strategy for preparing soluble and well-defined 1,10-phenanthroline derivatives and their analogues. High molecular weight poly(phenanthroline-co-fluorene)s with good solubility in common organic solvents or water were prepared by palladium-catalyzed Suzuki-Miyaura-Schlüter polycondensation. The optical responsive properties of these thiophene-fused 1,10-phenanthroline-containing polymers have demonstrated these polymers could be a good candidate for potential applications as luminescent chemosensor materials thanks to the specific repeating unit along the backbone. [ABSTRACT FROM AUTHOR]