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Curcuminoid-BF2 complexes: Synthesis, fluorescence and optimization of BF2 group cleavage.


ABSTRACT: Eight difluoroboron complexes of curcumin derivatives carrying alkyne groups containing substituents have been synthesized following an optimised reaction pathway. The complexes were received in yields up to 98% and high purities. Their properties as fluorescent dyes have been investigated. Furthermore, a strategy for the hydrolysis of the BF2 group has been established using aqueous methanol and sodium hydroxide or triethylamine.

SUBMITTER: Weiss H 

PROVIDER: S-EPMC5669223 | biostudies-literature | 2017

REPOSITORIES: biostudies-literature

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Curcuminoid-BF<sub>2</sub> complexes: Synthesis, fluorescence and optimization of BF<sub>2</sub> group cleavage.

Weiss Henning H   Reichel Jeannine J   Görls Helmar H   Schneider Kilian Rolf Anton KRA   Micheel Mathias M   Pröhl Michael M   Gottschaldt Michael M   Dietzek Benjamin B   Weigand Wolfgang W  

Beilstein journal of organic chemistry 20171026


Eight difluoroboron complexes of curcumin derivatives carrying alkyne groups containing substituents have been synthesized following an optimised reaction pathway. The complexes were received in yields up to 98% and high purities. Their properties as fluorescent dyes have been investigated. Furthermore, a strategy for the hydrolysis of the BF<sub>2</sub> group has been established using aqueous methanol and sodium hydroxide or triethylamine. ...[more]

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