The first utilization of acidic ionic liquid for preparation of tetraarylporphyrins

Chemical Communications

Volumn , Issue 17, 2004, Pages 1902-1903

  Kitaoka, Satoshi ^a   Nobuoka, Kaoru ^a   Ishikawa, Yuichi ^a  

^a OITA UNIVERSITY   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

BENZALDEHYDE; DICHLOROMETHANE; IONIC LIQUID; PORPHYRIN DERIVATIVE; PYRROLE; TETRAPHENYLPORPHYRIN DERIVATIVE;

ACIDITY; ARTICLE; CATALYSIS; CATALYST; CHEMICAL REACTION; CONCENTRATION RESPONSE; LIQUID; REACTION ANALYSIS; RECYCLING; REPRODUCIBILITY; ROOM TEMPERATURE; SYNTHESIS; TECHNIQUE;

EID: 5044234663     PISSN: 13597345     EISSN: None     Source Type: Journal    
DOI: 10.1039/b404241g     Document Type: Article

References (19)

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16. 4), 0.1% (Br).
17. 7 between the yields of NC-TTP and of TTP in the biphasic reaction is currently under progress.
18. Preparing 1.0 g TPP and 1.0g NC-TPP require 2 L and 5 L dichloromethane, respectively, under the optimal condition of the Lindsey method employing MSA at room temperature.
19. Pure dichloromethane was pre-equilibrated with the acidic IL by shaking vigorously or just placing on the interface as described in Table 1.