Synthesis and characterisation of the unsubstituted dipyrrin and 4,4-dichloro-4-bora-3a,4a-diaza-s-indacene: improved synthesis and functionalisation of the simplest BODIPY framework.

نویسندگان

  • Brandon R Groves
  • Sarah M Crawford
  • Travis Lundrigan
  • Chérif F Matta
  • Shahin Sowlati-Hashjin
  • Alison Thompson
چکیده

An improved and scalable synthesis of the unsubstituted 4,4-difluoro-4-bora-3a,4a-diaza-s-indacene framework facilitates access to the previously unreported parent dipyrrin HCl salt, as well as 4,4-dichloro-4-bora-3a,4a-diaza-s-indacene.

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منابع مشابه

Modulation of the spectroscopic property of Bodipy derivates through tuning the molecular configuration.

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Axially chiral BODIPYs.

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A colorimetric probe for the selective naked-eye detection of Pb(II) ions in aqueous media.

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Determination of progesterone and 17-hydroxyprogesterone by high performance liquid chromatography after pre-column derivatization with 4,4-difluoro-5,7-dimethyl-4-bora-3a,4a-diaza-s-indacene-3-propionohydra zide.

Progesterone, 17-hydroxyprogesterone and four other 3-keto steroids were determined by high performance liquid chromatography with fluorescence detection. Each steroid was derivatized with 4,4-difluoro-5,7-dimethyl-4-bora-3a,4a-diaza-s-indacene++ +-3- propionohydrazide (BODIPY FL hydrazide) and separated on a Wakosil 5C4 column with acetonitrile-water (7 + 3) as mobile phase. The limits of dete...

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عنوان ژورنال:
  • Chemical communications

دوره 49 8  شماره 

صفحات  -

تاریخ انتشار 2013