Through the challenging synthesis of tetraphenylporphyrin derivatives bearing nitroxide moieties

2019 ◽  
Vol 23 (04n05) ◽  
pp. 584-588
Author(s):  
Emel Önal ◽  
Ismail Fidan ◽  
Dominique Luneau ◽  
Catherine Hirel

Tetraphenylporphyrin derivatives a synthetic heterocycles with convenient preparation and a richness of properties which make them attractive in broad fields such as energy, life and materials sciences. Thus, in the quest for new radical architectures, tetraphenylporphyrins are prime candidates. To this end, we designed free-base tetraphenylporphyrins bearing nitronyl and imino nitroxide moieties covalently bonded to the para-position of the meso-phenyl substituent. Their detailed synthesis and characterization are reported here.

2008 ◽  
Vol 16 (13) ◽  
pp. 6544-6551 ◽  
Author(s):  
Angela Mammana ◽  
Tomohiro Asakawa ◽  
Klaus Bitsch-Jensen ◽  
Amanda Wolfe ◽  
Saireudee Chaturantabut ◽  
...  

1997 ◽  
Vol 50 (9) ◽  
pp. 939 ◽  
Author(s):  
Fang Chen ◽  
Parveen Akhtar ◽  
Leon A. P. Kane-Maguire ◽  
Gordon G. Wallace

A range of optically active pyrrole monomers have been synthesized in which a chiral sub- stituent is covalently bonded either to the pyrrole N or C3 ring position, namely (–)-(1R)-4-methyl-N-(1-phenylethyl)pyrrole-3-carboxamide, (+)-(1S)-4-methyl-N-(1-phenylethyl)pyrrole-3-carboxamide, (–)-(1R)-4-methyl-N-(1-naphthylethyl)pyrrole-3-carboxamide, (+)-(1S)-4-methyl-N-(1-naphthylethyl)pyrrole-3-carboxamide, (+)-(2S)-2-(1H-pyrrol-1-yl)propionic acid, (+)-(1S)-N-(1-phenyl-ethyl)pyrrole, and (–)-(1R)-N-(1-phenylethyl)pyrrole. Their chiroptical properties have been established by circular dichroism spectroscopy. Electropolymerization of the three N-substituted pyrrole monomers provided films of chiral conducting polymers, whose electrical and spectroscopic properties are described. Although oxidation of the C3 substituted pyrrole monomers was also facile, electrodeposition was poor and films of the associated polymers could not be obtained.


2005 ◽  
Vol 8 (3-4) ◽  
pp. 655-661 ◽  
Author(s):  
Barbara Onida ◽  
Luisa Borello ◽  
Sonia Fiorilli ◽  
Barbara Bonelli ◽  
Claudia Barolo ◽  
...  

2012 ◽  
Vol 2012 (36) ◽  
pp. 5915-5920 ◽  
Author(s):  
Di Gao ◽  
Gabriel Canard ◽  
Michel Giorgi ◽  
Teodor Silviu Balaban

2001 ◽  
Vol 40 (19) ◽  
pp. 4845-4855 ◽  
Author(s):  
Roger Guilard ◽  
Claude P. Gros ◽  
Frédéric Bolze ◽  
François Jérôme ◽  
Zhongping Ou ◽  
...  

2008 ◽  
Vol 63 (2) ◽  
pp. 183-186 ◽  
Author(s):  
Ming-Xue Li ◽  
Hong-Yu Niu ◽  
Wei Wang ◽  
Jing-Ping Wang

A Keggin-type arsenotungstate anion-supported iron-bipyridine complex, [Fe(2,2'-bipy)3]1.5- [AsWVI10WV2O40Fe(2,2'-bipy)2(H2O)] · 0.25H2O, has been hydrothermally synthesized and characterized by IR and ESR spectra, TG-DTA analysis, and single crystal X-ray diffraction. Each structural unit of the title compound consists of one [AsWVI10WV2O40Fe(2,2'-bipy)2(H2O)]3− heteropolyanion, one and a half [Fe(2,2'-bipy)3]2+ cations, and a quarter of an H2O molecule. In the heteropolyanion the [Fe(2,2'-bipy)2(H2O)]2+ unit is covalently bonded to the reduced Keggin polyoxoanion [AsWVI10WV2O40]5−. The complex ismonoclinic, space group C2/c with a = 46.8079(13), b = 14.3990(4), c = 26.1085(8) Å , β = 90.00(5)°, Z = 8, Dc = 3.10 g/cm3


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