The spectrochemical properties of bis-(α-methioninephosphonato)copper(ii) in aqueous solution

Spectroscopy Letters

Volumn 29, Issue 7, 1996, Pages 1307-1316

  Kurzak, K ^a   Kurzak, B ^a   Matczak Jon, E ^b   Hoffmann, M ^c  

^a SIEDLCE UNIVERSITY OF NATURAL SCIENCES AND HUMANITIES   (Poland)

^b WROCLAW UNIVERSITY OF TECHNOLOGY   (Poland)

^c GDANSK UNIVERSITY OF TECHNOLOGY   (Poland)

Author keywords

Angular overlap model; Copper(ii) complexes; Electronic spectra; Low symmetry; Phosphomethionine; Species in solution

Indexed keywords

EID: 0001131527     PISSN: 00387010     EISSN: None     Source Type: Journal    
DOI: 10.1080/00387019608007124     Document Type: Article

References (10)

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4. -) complexes in aqueous solution, ibid., 1994; 68. 1519-1528.
5. h and lower symmetries., 3-rd Conference Computers in Chemistry '94, Wroclaw-Poland, June 23-26, 1994;53.
6. Kurzak K., Kurzak B. The Spectrochemical properties of bis(amino hydroxamato)copper(II) complexes Spectrochim.Acta 1990, A46: 1561-1568.
7. Gans P., Sabatini A., Vacca A. SUPERQUAD: An improved general program for computation of formation constants from potentiometric data. J-Chem.Soc.,Dalton Trans. 1985; 1196.
8. Kiss T., Balla J., Nagy G , Kozlowski H., Kowalik Complexes of aminophosphonates. I. Transition metal complexes of aminophosphonic acid analogues of α-alanine, β-alanine, phenylalanine and tyrosine J.lnorg.Chim.Acta 1987; 138:25-30.
9. 2. Inorg.Chem. 1978; 17: 34-40.
10. Abreviations; α-Ala - α-alanine, Alaha - L-α-alaninehydroxamic acid, α-AlaP - α-alanine-phosphonic acid, Glyha - glycinehydroxamic acid, Hisha - L-histidinehydroxamic acid, Leuha - L-α-leucinehydroxamic acid, L-Met - methionine, α-MetP - methioninephosphonic acid, Sarha sarcosinehydroxamic acid.