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Synthesis and Luminescence of Soluble meso-Unsubstituted Tetrabenzo- and Tetranaphtho23porphyrins

机译:可溶性内消旋未取代的四苯并和四萘并23卟啉的合成和发光

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摘要

Syntheses of soluble tetrabenzoporphyrins (TBP) and tetranaphtho[2,3]porphyrins (TNP), with multiple substituents in the conjugated aromatic rings but bearing no substituents in the meso-positions, is reported. Both types of porphyrins were obtained by direct aromatization of precursor porphyrins, annealed with either cyclohexene or dihydronaphthalene fragments. TBPs and TNPs possess powerful absorption bands in the near-infrared (λ 610-710 nm, ϵ = 100,000-300,000 M-1 cm-1) and exhibit strong luminescence. Free bases and Zn complexes fluoresce with quantum yields of up to 50%, whereas Pd and Pt complexes phosphoresce in solutions at ambient temperatures. Remarkably, the phosphorescence quantum yields of Pd and Pt TBPs reach as high as 20-50%, which places them among the brightest near-infrared phosphors known to date.
机译:据报道,可溶性四苯并卟啉(TBP)和四萘并[2,3]卟啉(TNP)的合成是在共轭芳环上具有多个取代基,但在中间位没有取代基。两种类型的卟啉均通过对前体卟啉进行直接芳构化,并与环己烯或二氢萘片段进行退火而获得。 TBPs和TNPs在近红外波段(λ610-710 nm,ϵ = 100,000-300,000 M -1 cm -1 )具有很强的吸收谱带,并具有较强的发光特性。游离碱和Zn络合物发荧光,量子产率高达50%,而Pd和Pt络合物在室温下在溶液中发磷。值得注意的是,Pd和Pt TBP的磷光量子产率高达20-50%,这使它们成为迄今为止已知的最亮的近红外磷光体之一。

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