Protonation constants of 1,4-benzodiazepin-2-one derivatives in inductive parameter models

1984 ◽  
Vol 24 (4) ◽  
pp. 648-650
Author(s):  
S. P. Smul'skii ◽  
I. V. Yudanova ◽  
Yu. A. Kruglyak
Keyword(s):  
Protonation Constants ◽  
Inductive Parameter

Studies on the Coordination Reaction of VO2+ and Tannic Acid in the Tannin Extract Desulfurization

2012 ◽  
Vol 239-240 ◽  
pp. 1573-1576
Author(s):  
Zhu Qing Gao ◽  
Xiao Dong Cai ◽  
Kai Cheng Ling
Keyword(s):  
Stability Constants ◽  
Tannic Acid ◽  
Ph Value ◽  
Protonation Constants ◽  
Conditional Stability ◽  
Tannin Extract ◽  
Acid Effect ◽  
Different Temperatures ◽  
The Stability ◽  
Apparent Stability

At different temperatures, the protonation constants of tannic acid and the complex apparent stability constants between tannic acid and VO2+ were determined by using pH potentimetric method. The results showed that the protonation constants and the complex apparent stability constants slightly decreased with the raising temperature. In accordance with the pH value in the tannin extract technology, the conditional stability constants of the complex were calculated on the basis of the acid effect of tannic acid and the hydrolysis effect of VO2+. It was found that pH greatly affected the stability constants of the complex , so pH must be strictly controlled in the tannin extract technology.

Formation Constants of Copper(II) and Zinc(II) with N-salicylideneanthranilic Acid in 50–50 Water–dioxane

1972 ◽  
Vol 50 (10) ◽  
pp. 1609-1611
Author(s):  
R. K. Mehta ◽  
R K Gupta
Keyword(s):  
Sodium Perchlorate ◽  
Formation Constants ◽  
Protonation Constants ◽  
Fair Agreement ◽  
Complex Species ◽  
Color Changes

Protonation constants of N-salicylideneanthranilic acid and formation constants of its Cu(II) and Zn(II)complexes have been studied potentiometrically in 50% dioxane (vol/vol) solutions (μ = 0.1 sodium perchlorate) at 30 ± 0.2 °C. The color changes observed during titrations have been related to the formation of different complex species in solution. The formation constants are in fair agreement with the Irving and Williams rule.

Ionic Strength Dependence of Protonation Constants ofN-Alkyl Substituted Open Chain Diamines in NaClaq

2004 ◽  
Vol 49 (1) ◽  
pp. 109-115 ◽  
Author(s):  
Francesco Crea ◽  
Concetta De Stefano ◽  
Ottavia Giuffrè ◽  
Silvio Sammartano
Keyword(s):  
Ionic Strength ◽  
Protonation Constants ◽  
Ionic Strength Dependence ◽  
Open Chain ◽  
Strength Dependence

Ethylenediamine-N,N′-diacetic acid complexes with divalent manganese, zinc, cadmium, and lead: a thermodynamic study

1979 ◽  
Vol 57 (1) ◽  
pp. 113-118 ◽  
Author(s):  
R. J. Gualtieri ◽  
W. A. E. McBryde ◽  
H. K. J. Powell
Keyword(s):  
Protonation Constants ◽  
Thermodynamic Study ◽  
Diacetic Acid ◽  
Calorimetric Data ◽  
Nmr Studies ◽  
Aqueous Acid ◽  
Manganese Zinc ◽  
Proton Dissociation ◽  
Zinc Cadmium ◽  
Cadmium And Lead

The four protonation constants are reported for the dianion of ethylenediamine-N,N′-diacetic acid(H2L),25°C, I = 0.10 M(KNO3), (log ki = 9.60, 6.51, 2.12, 1.3). log K(potentiometric) and ΔH(calorimetric) data are reported for the formation of the complexes [ML], M = Mn2+, Zn2+, Cd2+, and Pb2+ (log K = 6.87, 10.99, 9.16, and 10.66; ΔH = −2.9, −24.4, −16.7, and −28.0 kJ mol−1 respectively). The complexes [ZnL] and [PbL] undergo (aqua) proton dissociation reactions, [Formula: see text] log KD = −10.56 and −11.02, ΔHD = +60.7 and +38.5 kJ mol−1, respectively. Potentiometric and nmr studies indicate that the ligand undergoes a slow (metal catalysed) hydrolysis or rearrangement in aqueous acid.

IONIZATION OF ORGANIC COMPOUNDS: III. BASICITIES OF PROPIONIC ACID AND PROPIONAMIDE

1962 ◽  
Vol 40 (5) ◽  
pp. 966-975 ◽  
Author(s):  
J. T. Edward ◽  
I. C. Wang
Keyword(s):  
Sulphuric Acid ◽  
Propionic Acid ◽  
Organic Compounds ◽  
Acid Concentration ◽  
Ultraviolet Absorption ◽  
Protonation Constants ◽  
Acidity Function ◽  
Hammett Acidity Function ◽  
Ionization Ratio

Protonation constants (pKBH+) of −6.8 and −0.9 have been determined for propionic acid and propionamide, respectively, from measurements of their ultraviolet absorption in various concentrations of sulphuric acid. The ionization ratio of propionamide and of other amides increases more slowly than the Hammett acidity function, h0, with increase in acid concentration. This may be explained by assuming that in a given concentration of sulphuric acid the protonated amide is more heavily hydrated than the protonated Hammett indicator used to establish the h0 scale for this region of acid concentrations.

scholarly journals Synthesis and Complexation Properties of 2-Hydroxy-5-methoxyphenylphosphonic Acid (H3L1). Crystal Structure of the [Cu(H2L1)2(Н2О)2] Complex

2021 ◽  
Vol 91 (11) ◽  
pp. 2176-2186
Author(s):  
G. S. Tsebrikova ◽  
Yu. I. Rogacheva ◽  
I. S. Ivanova ◽  
A. B. Ilyukhin ◽  
V. P. Soloviev ◽  
...  
Keyword(s):  
Crystal Structure ◽  
Hydrogen Bond ◽  
Methoxy Group ◽  
Protonation Constants ◽  
Water Molecules ◽  
X Ray Diffraction ◽  
X Ray ◽  
The Stability ◽  
Intramolecular Hydrogen ◽  
Oxygen Atoms

Abstract 2-Hydroxy-5-methoxyphenylphosphonic acid (H3L1) and the complex [Cu(H2L1)2(H2O)2] were synthesized and characterized by IR spectroscopy, thermogravimetry, and X-ray diffraction analysis. The polyhedron of the copper atom is an axially elongated square bipyramid with oxygen atoms of phenolic and of monodeprotonated phosphonic groups at the base and oxygen atoms of water molecules at the vertices. The protonation constants of the H3L1 acid and the stability constants of its Cu2+ complexes in water were determined by potentiometric titration. The protonation constants of the acid in water are significantly influenced by the intramolecular hydrogen bond and the methoxy group. The H3L1 acid forms complexes CuL‒ and CuL24‒ with Cu2+ in water.

Sign in / Sign up

Export Citation Format

Share Document