Synthesis and characterization of new molecular complexation between free base meso-tetraarylporphyrins and nitrosonium ion as π-acceptor

2012 ◽  
Vol 384 ◽  
pp. 133-136 ◽  
Author(s):  
Halimeh Molaei ◽  
Hossein Dehghani
2008 ◽  
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pp. 6544-6551 ◽  
Author(s):  
Angela Mammana ◽  
Tomohiro Asakawa ◽  
Klaus Bitsch-Jensen ◽  
Amanda Wolfe ◽  
Saireudee Chaturantabut ◽  
...  

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 ◽  
...  

2010 ◽  
Vol 49 (12) ◽  
pp. 5766-5774 ◽  
Author(s):  
Giuseppe Pomarico ◽  
Xiao Xiao ◽  
Sara Nardis ◽  
Roberto Paolesse ◽  
Frank R. Fronczek ◽  
...  

2018 ◽  
Vol 22 (01n03) ◽  
pp. 173-180 ◽  
Author(s):  
Ümit İşci ◽  
Sevinc Zehra Topal ◽  
Emel Önal ◽  
İsmail Fidan ◽  
Savaş Berber ◽  
...  

A meso-tetra-6b,10b-dihydrobenzo[j]cyclobut[a]acenaphthylene free-base porphyrin was synthesised and its photophysical, photochemical and electrochemical properties were compared with those of free-base meso-tetraphenylporphyrin. The frontier orbitals and the HOMO–LUMO energy gaps of both compounds were also determined. It was demonstrated that the meso6b,10b-Dihydrobenzo[j]cyclobut[a]acenaphthylene porphyrin retained the same properties as the tetraphenylporphyrin.


2011 ◽  
Vol 15 (11n12) ◽  
pp. 1326-1334 ◽  
Author(s):  
Shun Sugawara ◽  
Megumi Kodama ◽  
Yusuke Hirata ◽  
Satoshi Kojima ◽  
Yohsuke Yamamoto

Previously unreported octaisopropyltetraphenylporphyrin (OiPTPP) was prepared from 3,4-diisopropylpyrrole, an unstable previously unisolated heterocyclic compound. Purification of the free-base 18π porphyrin required conversion to its 18π zinc(II) complex, chromatographic separation, and acid mediated demetalation. Oxidation of the 18π porphyrin with SbCl5 furnished metal-free 16π octaisopropyltetraphenylporphyrin (OiPTPP). X-ray structural determination revealed that the novel species is the most distorted 16π porphyrin to date. The time course of decomposition of the oxidized species monitored by UV-vis spectra implied that the introduction of high steric repulsion was effective for enhancing stability of the 16π porphyrin. The reaction of metal-free 16π OiPTPP with LiBF4 followed by Pd2(dba)3 gave the corresponding 18π OiPTPP palladium(II) complex via reduction of the OiPTPP lithium(I) complex as previously reported for 16π octaisobutyltetraphenylporphyrin (OiBTPP). The new 18π porphyrin system could be characterized by the X-ray analysis of the 18π OiPTPP palladium(II) complex. The X-ray structure of the 18π metal complex also indicated that the distortion of the porphyrin ring had become larger than that of previously known 18π porphyrins


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