The reduction of the central manganese ion in MnCl tetraphenylporphyrinate upon hydrogen diffusion through a palladium membrane

Author(s):  
N. S. Enikolopov ◽  
V. M. Gryaznov ◽  
A. B. Solov'eva ◽  
I. G. Rish ◽  
S. I. Zavodchenko ◽  
...  

2015 ◽  
Vol 71 (11) ◽  
pp. 1307-1310 ◽  
Author(s):  
Elena A. Buvaylo ◽  
Olga Yu. Vassilyeva ◽  
Brian W. Skelton

The title compound, [Mn(C12H15NO5)2]·0.39H2O, is a 0.39 hydrate of the isostructural complex bis(2-{[1,1-bis(hydroxymethyl)-2-oxidoethyl]iminomethyl}-6-methoxyphenolato)manganese(IV) that has previously been reported by Back, Oliveira, Canabarro & Iglesias [Z. Anorg. Allg. Chem.(2015),641, 941–947], based on room-temperature data. The current structure that was determined at 100 K reveals a lengthening of theccell parameter compared with the published one due to the incorporation of the partial occupancy water molecule. The title compound crystallizes in the tetragonal chiral space groupP41212; the neutral [MnIV(C12H15NO5)2] molecule is situated on a crystallographicC2axis. The overall geometry about the central manganese ion is octahedral with an N2O4core; each ligand acts as a meridional ONO donor. The coordination environment of MnIVat 100 K displays a difference in one of the two Mn–O bond lengths, compared with the room-temperature structure. In the crystal, the neutral molecules are stacked in a helical fashion along thec-axis direction.



1993 ◽  
Vol 3 (7) ◽  
pp. 1643-1648
Author(s):  
N. Adnani ◽  
J. M. Titman


1979 ◽  
Vol 40 (C2) ◽  
pp. C2-635-C2-638
Author(s):  
F. Pröbst ◽  
F. E. Wagner ◽  
M. Karger ◽  
G. Wortmann


2003 ◽  
Vol 173 (10) ◽  
pp. 1107 ◽  
Author(s):  
Aleksei V. Gapontsev ◽  
Vladimir V. Kondrat'ev


1992 ◽  
Vol 1 (1) ◽  
pp. 685-692
Author(s):  
D. Lupu ◽  
R. Grecu ◽  
S. I. Fărcaș


1992 ◽  
Vol 1 (1) ◽  
pp. 631-635
Author(s):  
U. Stuhr ◽  
D. Steinbinder ◽  
H. Wipf ◽  
B. Frick


1992 ◽  
Vol 1 (1) ◽  
pp. 792-792
Author(s):  
J. Tóth ◽  
K. Tompa ◽  
I. Bakonyi
Keyword(s):  


Author(s):  
E. I. Maslikova ◽  
V. D. Andreeva ◽  
E. L. Alekseeva ◽  
Yu. A. Yakovlev

Research of hydrogen diffusion in VT6 alloy is carried out considering different types of heat treating and hydrogen charging. The influence of microalloying on the susceptibility to hydride formation and embrittlement of titanium alloys is analyzed, and also effects of an oxide film on hydrogen charging during heat treatment without protective atmosphere, are studied.



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