Transition Metal Phthalocyanines as Nitrogen Oxydes Sensors

Author(s):  
Anna Maria Paoletti ◽  
Giovanna Pennesi ◽  
Gentilina Rossi ◽  
Amanda Generosi ◽  
Barbara Paci ◽  
...  
1993 ◽  
Vol 22 (8) ◽  
pp. 1299-1302 ◽  
Author(s):  
Naoki Toshima ◽  
Shin-ichi Kawamura ◽  
Tsuyoshi Tominaga

2019 ◽  
Vol 123 (14) ◽  
pp. 3214-3222
Author(s):  
Iulia Emilia Brumboiu ◽  
Soumyajyoti Haldar ◽  
Johann Lüder ◽  
Olle Eriksson ◽  
Heike C. Herper ◽  
...  

2012 ◽  
Vol 16 (07n08) ◽  
pp. 885-894 ◽  
Author(s):  
Abimbola O. Ogunsipe ◽  
Mopelola A. Idowu ◽  
Taofeek B. Ogunbayo ◽  
Isaac A. Akinbulu

The photophysics and photochemistry of phthalocyanine complexes of magnesium (MgPc), aluminum chloride (ClAlPc) and zinc (ZnPc) are studied in N,N′-dimethylformamide (DMF). The values obtained for the photophysical and photochemical parameters are normal for simple metallophthalocyanine (MPc) complexes. Protonation of the azomethine bridges reduced the photoactivities of the complexes considerably; however the excited triplet states of the protonated species are more stable towards ground state oxygen. The interaction of the non-protonated MPcs with ground state oxygen is shown to be diffusion-assisted, with bimolecular rate constant values of the order of 1010 M-1.s-1. MgPc could not be protonated; it was easily demetalated by the protonating acid. The kinetics of the demetalation yielded the rate equation: Rate = 0.1[MgPc][H+]2/3


2016 ◽  
Vol 52 (18) ◽  
pp. 3623-3626 ◽  
Author(s):  
K. Bader ◽  
M. Winkler ◽  
J. van Slageren

Transition metal phthalocyanines possess very long coherence times if the unpaired electron is in the plane of the ligand.


1982 ◽  
Vol 64 ◽  
pp. L23-L24 ◽  
Author(s):  
Kathy Schmatz ◽  
Subramaniam Muralidharan ◽  
Keith Madden ◽  
Richard Fessenden ◽  
Guillermo Ferraudi

1985 ◽  
Vol 89 (18) ◽  
pp. 3890-3894 ◽  
Author(s):  
D. K. Geiger ◽  
G. Ferraudi ◽  
K. Madden ◽  
J. Granifo ◽  
D. P. Rillema

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