scholarly journals Preparation, Analytical, IR Spectral, and Thermal Studies of Some New Hydrazinium Carboxylates

2012 ◽  
Vol 2012 ◽  
pp. 1-5 ◽  
Author(s):  
R. Manimekalai ◽  
C. R. Sinduja ◽  
K. Kalpanadevi

Hydrazinium salts of 2,4-dichlorophenylacetic acid, phenoxyacetic acid, 2,4-dichlorophenoxyacetic acid, diphenylacetic acid, cinnamic acid, and picolinic and nicotinic acids have been prepared by accomplishing neutralization of aqueous hydrazine hydrate with the respective acids. Formation of these hydrazinium salts has been confirmed by analytical, IR spectral, and thermal studies. IR spectra of the salts register N–N stretching frequencies of ion in the region 963–951 cm−1 and the frequencies of ion in the region 1047–1026 cm−1. Thermal decomposition studies show that the hydrazinium salts undergo melting followed by endothermic decomposition into carbon residue as the endproduct.

2018 ◽  
Vol 52 (1) ◽  
pp. 53-57 ◽  
Author(s):  
M. D. Vedenyapina ◽  
L. R. Sharifullina ◽  
S. A. Kulaishin ◽  
E. D. Strel’tsova ◽  
A. A. Vedenyapin ◽  
...  

2002 ◽  
Vol 106 (29) ◽  
pp. 6743-6749 ◽  
Author(s):  
Robert Zona ◽  
Sonja Solar ◽  
Knud Sehested ◽  
Jerzy Holcman ◽  
Stephen P. Mezyk

1957 ◽  
Vol 3 (6) ◽  
pp. 821-840 ◽  
Author(s):  
G. R. Bell

A new Achromobacter species which decomposed 2,4-dichlorophenoxyacetic acid (2,4-D), apparently to small molecules, was isolated from a soil treated with successive closes of the herbicide. The organism grew poorly or not at all on common laboratory media in the presence or absence of 2,4-D. Investigation of its carbon, nitrogen, mineral, and vitamin requirements in agar containing 2,4-D showed that the best growth stimulants were the dicarboxylic acids of the tricarboxylic acid cycle, bicarbonate, formate, urea, and L-histidine. Calcium or magnesium and probably iron were required for maximum growth. Some aryloxy acids, phenolic compounds, and an ester were tested for their ability to replace 2,4-D as growth substrate or to inhibit growth in the presence of 2, 4-D, and it was found that the ethyl ester of 2,4-D and chlorophenolic substances were most toxic. Only 2-methyl-4-chlorophenoxyacetic acid (MCPA) and less readily, 4-chlorophenoxyacetic acid, phenoxyacetic acid, and resorcinol could substitute for 2,4-D. Good cell multiplication and herbicide decomposition were obtained in an aerated mineral salts medium containing 2,4-D, yeast extract, and 0.005 ML-malic acid. Maximum growth (ca. 109cells/ml.) occurred in 4 to 5 days and 2,4-D decomposition was essentially complete in 6 to 7 days. Resting cells were able to oxidize 2,4-D, MCPA, 2,4,5-trichlorophenoxyacetic acid (2,4,5-T), and 2,4-dichlorophenol (2,4-DCP) and to release 94% of the 2,4-D chlorine as chloride. High concentrations of yeast extract caused growing cells to accumulate 2,4-DCP.


1969 ◽  
Vol 24 (8) ◽  
pp. 1046-1052 ◽  
Author(s):  
Josef Weigl

A strong physical association of indoleacetic acid. 2.4-dichloro-phenoxyacetic acid, indolepropionic acid and indolebutyric acid with lecithin was found which might have physiological significance (regulation, polar mobility). The association is assumed to be mainly due to bonding between the complementary charged groups of the phospholipid and auxin molecules and to specific interaction of the more hydrophobic parts of the molecules.The following interactions were established:Lecithin dissolved in CCl4 moves indoleacetic acid and 2.4-dichloro-phenoxyacetic acid out of an aqueous phase. Cholesterol, long chain fatty acids and amines did not give this interaction with indoleacetic acid and 2.4-dichlorophenoxyacetic acid 4, 5.1 mole lecithin was found to bind up to 0.8 mole indoleacetic acid. Cephalin and phosphatidylserin exhibit a weaker interaction. Indolepropionic acid and indolebutyric acid were found to compete with indoleacetic acid. There was no effective competition of benzoic acid, phenoxyacetic acid, phenylacetic acid, cholesterol and several fatty aids with indoleacetic acid for the binding sites on the lecithin molecule. 2,4-dichlorophenoxyacetic acid appears to be bound stronger than indoleacetic acid and phenoxyacetic acid. Indoleacetic acid and 2.4-dichlorophenoxyaetic acid were incorporated into swollen lecithin lamellae.Similar interactions are to be expected for other hormones and phospholipids. The lipoprotein structures of cell membranes may be visualized to interact even more specificly with growth hormones than our model system. It is suggested that interaction of hormones with membranes should be considered in theories on regulation. Experiments on ion permeability indicate an influence of indoleacetic acid on cell membranes.


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