The author of 《Improved synthesis of β-ketoenamine-linked covalent organic frameworks via monomer exchange reactions》 were Daugherty, Michael C.; Vitaku, Edon; Li, Rebecca L.; Evans, Austin M.; Chavez, Anton D.; Dichtel, William R.. And the article was published in Chemical Communications (Cambridge, United Kingdom) in 2019. Recommanded Product: 2,4,6-Trihydroxybenzene-1,3,5-tricarbaldehyde The author mentioned the following in the article:
β-Ketoenamine-linked covalent organic frameworks (COFs) offer excellent structural versatility and outstanding aqueous stability, but their stability complicates obtaining samples with high crystallinity and surface areas. In contrast, imine-linked COFs are often isolated with superior materials quality. Here we synthesize several β-ketoenamine-linked COFs, including two unreported structures, with unmatched crystallinity and high surface areas by preparing the corresponding imine-linked COF and exchanging its triformylbenzene monomers with triformylphloroglucinol. After reading the article, we found that the author used 2,4,6-Trihydroxybenzene-1,3,5-tricarbaldehyde(cas: 34374-88-4Recommanded Product: 2,4,6-Trihydroxybenzene-1,3,5-tricarbaldehyde)
2,4,6-Trihydroxybenzene-1,3,5-tricarbaldehyde(cas: 34374-88-4) is a member of phloroglucinol derivatives. Regarding monomeric phloroglucinols, this group encompasses acryl phloroglucinols, phloroglucinol-terpene adducts, phloroglucinol glycosides, halogenated phloroglucinols, prenylated phloroglucinols, and cyclicroup polyketides.Recommanded Product: 2,4,6-Trihydroxybenzene-1,3,5-tricarbaldehyde
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