Synthesis of Ag(II) 2,3,7,8,12,13,17,18-octabromo-5,10,15,20-tetraphenylporphyrin and its facile demetalation to 2,3,7,8,12,13,17,18-octabromo-5,10,15,20-tetraphenylporphyrin

被引:1
|
作者
Ravindran, Sasitha Vidyarini [1 ]
Pennathur, Anuj Krishnasundar [2 ]
Devi, G. Nandhini [1 ]
Pennathur, Gautam [1 ]
机构
[1] Anna Univ, Ctr Biotechnol, Chennai 6000025, Tamil Nadu, India
[2] Indian Inst Sci Educ & Res, Dept Chem, Mohali, India
关键词
demetalation; halogenated porphyrin; metalloporphyrin; sodium sulphide; bromination; beta-pyrrole; in situ; IRON(III) PORPHYRINS; OXIDATION; METALLOPORPHYRINS; EPOXIDATION; ALKANES;
D O I
10.1142/S1088424616500462
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A novel one-step strategy for the synthesis of 2,3,7,8,12,13,17,18-octabromo-5,10,15,20-tetraphenylporphyrin using (AgOBP)-O-II is described. AgIIOBP was synthesized and was. Bromination of (AgTPP)-T-II was carried out in a one-step reaction by varying the subsequently demetalated using H2S time interval and stoichiometric addition of Br-2. The molecular weight of the halogenated porphyrin was confirmed by MALDI-TOF mass spectrometry. The synthesis of Ag(II) 2,3,7,8,12,13,17,18-octabromo-5,10,15,20-tetraphenylporphyrin was followed by demetalation of Ag(II) ion from the halogenated porphyrin. The demetalation of was carried out under mild conditions using sodium sulphide in trifluoroacetic acid. The time taken for the demetalation was considerably lesser than previously reported and which facilitated a simple way for the isolation of the final product in good yield. The yield of the free base was 98%. The formation of the product and purity was confirmed by H-1 NMR, Mass spectrometry. UV-visible spectrophotometer clearly showed the appearance of a characteristic Q-band of the octa-brominated porphyrin.
引用
收藏
页码:656 / 661
页数:6
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