Far-red fluorescence and chiroptical properties of pyrrolopyrrole aza-BODIPYs induced by the B , O -chelation

A titanium-mediated aza-BODIPY synthesis using diketopyrrolopyrrole bearing -anisyl substituents provided , -chelated pyrrolopyrrole aza-BODIPYs in a one-pot manner ether bond cleavage and chelation of the resulting nucleophilic oxygen to the boron atom. The , -chelation not only induces the redshif...

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Veröffentlicht in:Chemical communications (Cambridge, England) England), 2024-06, Vol.60 (48), p.6170-6173
Hauptverfasser: Fukami, Shuhei, Mori, Shigeki, Harada, Takunori, Shimizu, Soji
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Sprache:eng
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Zusammenfassung:A titanium-mediated aza-BODIPY synthesis using diketopyrrolopyrrole bearing -anisyl substituents provided , -chelated pyrrolopyrrole aza-BODIPYs in a one-pot manner ether bond cleavage and chelation of the resulting nucleophilic oxygen to the boron atom. The , -chelation not only induces the redshifts of absorption and fluorescence but also endows chiroptical properties.
ISSN:1359-7345
1364-548X
DOI:10.1039/d4cc01586j