The nonisothermal decomposition kinetics of copper(II) complexes with phthalanilic acids and amino acids
β Scribed by Li-Ping Ren; Wei-Lin Dai; Yong Cao; He-Xing Li; Xiao-Hui Zheng; Kangnian Fan
- Publisher
- John Wiley and Sons
- Year
- 2003
- Tongue
- English
- Weight
- 93 KB
- Volume
- 35
- Category
- Article
- ISSN
- 0538-8066
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β¦ Synopsis
Fifteen new kinds of mixed ligand complexes Cu(x-P)A [P = 2-(COO)C 6 H 4 CONH-C 6 H 4 ; x = H, 2-Cl, 2-CH 3 , 2-OCH 3 , 4-OCH 2 CH 3 ; A = dehydronium Met, Leu, Phen] were synthesized. The thermal decomposition behavior of each complex is studied by TG. Coats-Redfern, MacCallum-Tammer, and Zsako methods are adopted to estimate the values of the apparent activation energy E a , the activation entropy S = , the reaction order n, and the frequency factor A. The results showed that the reaction order is 2/3 for each of the complex. Studies on the mechanism of the thermal decomposition reactions suggested that these reactions all fit the kinetic equation 1 -(1Ξ±) 1/3 = kt.
π SIMILAR VOLUMES
In this study, the overall stability constants of copper(II) complexes with some β£-amino acids (glycine, DL-alanine, DL-valine, L-leucine, L-asparagine, L-glutamine) were determined by potentiometric titration in water, 25% dioxan-75% water, 35% dioxan-65% water, 50% dioxan-50% water, and 60% dioxan
## Abstract The acidity of malondialdehyde as well as the stability of its 1 :1βcomplexes with Ni^II^ and Cu^II^ have been determined (Table). In comparison with the enolates of aliphatic Ξ²βdikeβtones the anion C~3~H~3~O~2~β has not only a strikingly reduced basicity, but is also a grossly inferior