Title of article :
Synthesis of meso-fluorotetrabenzoporphyrins
Author/Authors :
Ito، نويسنده , , Satoshi and Terada، نويسنده , , Noriaki and Seino، نويسنده , , Komei and Makihata، نويسنده , , Daishi and Sasaki، نويسنده , , Akira and Oba، نويسنده , , Toru، نويسنده ,
Issue Information :
هفته نامه با شماره پیاپی سال 2013
Pages :
4
From page :
5916
To page :
5919
Abstract :
Fluorination of quadruply bicyclo[2.2.2]octadiene-fused porphyrin (CP) with 1-chloromethyl-4-fluoro-1,4-diazoniabicyclo[2.2.2]octane bis(tetrafluoroborate) (Selectfluor) occurred at the meso positions to give a mixture of various meso-fluorinated CPs, which were separated and then quantitatively transformed to the corresponding meso-fluorinated tetrafluorobenzoporphyrins (BPs) at 240 °C for 30 min. X-ray analysis of the mono-fluoro BPs revealed that the BP skeleton remained flat, which is crucial for retaining aggregation behavior similar to that of the parent BP, thus producing highly crystalline BP derivatives.
Keywords :
Porphyrin , fluorination , retro Diels–Alder reaction
Journal title :
Tetrahedron Letters
Serial Year :
2013
Journal title :
Tetrahedron Letters
Record number :
1886420
Link To Document :
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