Oxidation States of Manganese Methyl Phæophorbide a in Aqueous Solution

Nature ◽  
1964 ◽  
Vol 202 (4930) ◽  
pp. 343-345 ◽  
Author(s):  
PAUL A. LOACH ◽  
MELVIN CALVIN
Biochemistry ◽  
1963 ◽  
Vol 2 (2) ◽  
pp. 361-371 ◽  
Author(s):  
Paul A. Loach ◽  
Melvin Calvin

1963 ◽  
Vol 41 (1) ◽  
pp. 108-111 ◽  
Author(s):  
Ruth M. Bennett ◽  
Owen G. Holmes

When dissolved in fused alkali nitrate, manganese (II) is oxidized to MnO2. In the same solvent MnO4− decomposes to MnO2. Peroxide ion arrests the decomposition at MnO42−, while the presence of hydroxide ion results in the formation of MnO43−. The spectra of MnO42− and MnO43− in molten nitrate show great similarity to their spectra in alkaline aqueous solution.


1953 ◽  
Vol 75 (22) ◽  
pp. 5652-5654 ◽  
Author(s):  
Loren G. Hepler ◽  
Z Z. Hugus ◽  
Wendell M. Latimer

1988 ◽  
Vol 41 (9) ◽  
pp. 1433 ◽  
Author(s):  
TA Odonnell

Recently observed spectra of solvated d- and f-transition element cations in superacidic media, together with spectra of aqua cations in acidic aqueous solution, are used to propose that cationic speciation is much more general in acidic solvents and melts than is usually accepted. It will be shown that cations in unusually low oxidation states are stabilized in highly acidic media, and that these cations disproportionate as the acidity of the medium is decreased and that in general these latter phenomena are independent of the chemical nature or the temperature domain of the medium.


ChemInform ◽  
1988 ◽  
Vol 19 (33) ◽  
Author(s):  
U. W. SCHERER ◽  
J. V. KRATZ ◽  
M. SCHAEDEL ◽  
W. BRUECHLE ◽  
K. E. GREGORICH ◽  
...  

1949 ◽  
Vol 71 (2) ◽  
pp. 687-693 ◽  
Author(s):  
J. C. Hindman ◽  
L. B. Magnusson ◽  
T. J. LaChapelle

1988 ◽  
Vol 146 (2) ◽  
pp. 249-254 ◽  
Author(s):  
U.W. Scherer ◽  
J.V. Kratz ◽  
M. Schädel ◽  
W. Brüchle ◽  
K.E. Gregorich ◽  
...  

2019 ◽  
Vol 54 (1) ◽  
Author(s):  
Fabiola Monroy-Guzman ◽  
Didier Trubert ◽  
Lucette Brillard ◽  
Michel Hussonnois ◽  
Olimpus Constantinescu ◽  
...  

Studies of the chemical property of transactinide elements are very difficult due to their short half-lives and extremely small production yields. However it is still possible to obtain considerable information about their chemical properties, such as the most stable oxidation states in aqueous solution, complexing ability, etc., comparing their behaviour with their lighter homologous in the periodic table. In order to obtain a better knowledge of the behavior of rutherfordium, Rf (element 104), dubnium, Db (element 105) in HF medium, the sorption properties of Zr, Hf, Nb, Ta and Pa, homologues of Rf and Db, were studied in NH4F/HClO4 medium in this work. Stability constants of the fluoride complexes of these elements were experimentally obtained from Kd obtained at different F- and H+ concentrations. The anionic complexes: [Zr(Hf)F5]-, [Zr(Hf)F6]2-, [Zr(Hf)F7]3-, [Ta(Pa)F6]-, [Ta(Pa)F7]2-, [Ta(Pa)F8]3-, [NbOF4]- and [NbOF5]2- are present as predominant species in the HF range over investigation.    


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