Chemistry of dithiocarbamate derivatives of amino acids. Part III. X-ray photoelectron spectroscopy of Ba(S2CNHCH2CO2)�3H2O. I.r. and e.s.r. studies of ?-amino acid-dithiocarbamate complexes of copper(II)

1987 ◽  
Vol 12 (3) ◽  
pp. 225-229 ◽  
Author(s):  
Manuel Castillo ◽  
Ana Criado ◽  
Rosario Guzm�n ◽  
J. Julio Criado ◽  
Benigno Macias
Keyword(s):  
Amino Acids ◽  
Amino Acid ◽  
Photoelectron Spectroscopy ◽  
X Ray ◽  
Derivatives Of ◽  
Dithiocarbamate Derivatives

scholarly journals The Surface Composition of Amino Acid - KCl Solutions is pH-Dependent

2020 ◽  
Author(s):  
Geethanjali Gopakumar ◽  
Isaak Unger ◽  
Clara-Magdalena Saak ◽  
Gunnar Öhrwall ◽  
Arnaldo Naves de Brito ◽  
...  
Keyword(s):  
Amino Acids ◽  
Amino Acid ◽  
Aqueous Solutions ◽  
Photoelectron Spectroscopy ◽  
Surface Composition ◽  
Inorganic Ions ◽  
X Ray ◽  
Ph Dependent

The manuscript based on X-ray photoelectron spectroscopy on aqueous solutions containing KCl and different amino acids. Our analysis suggests that the presence of the inorganic ions at the surface of the liquid is strongly dependent on the pH of the solution and the type of amino acid.

scholarly journals The Surface Composition of Amino Acid - KCl Solutions is pH-Dependent

2020 ◽  
Author(s):  
Geethanjali Gopakumar ◽  
Isaak Unger ◽  
Clara-Magdalena Saak ◽  
Gunnar Öhrwall ◽  
Arnaldo Naves de Brito ◽  
...  
Keyword(s):  
Amino Acids ◽  
Amino Acid ◽  
Aqueous Solutions ◽  
Photoelectron Spectroscopy ◽  
Surface Composition ◽  
Inorganic Ions ◽  
X Ray ◽  
Ph Dependent

The manuscript based on X-ray photoelectron spectroscopy on aqueous solutions containing KCl and different amino acids. Our analysis suggests that the presence of the inorganic ions at the surface of the liquid is strongly dependent on the pH of the solution and the type of amino acid.

X-Ray Photoelectron Spectroscopy of Amino Acids, Polypeptides and Simple Carbohydrates

1995 ◽  
pp. 251-260 ◽  
Author(s):  
Kenneth E. Dombrowski ◽  
Stephen E. Wright ◽  
Jannine C. Birkbeck ◽  
William E. Moddeman
Keyword(s):  
Amino Acids ◽  
Photoelectron Spectroscopy ◽  
X Ray ◽  
Simple Carbohydrates

Sorption of α-amino-acids by copper montmorillonite

Clay Minerals ◽  
1967 ◽  
Vol 7 (2) ◽  
pp. 167-176 ◽  
Author(s):  
W. Bodenheimer ◽  
L. Heller
Keyword(s):  
Amino Acids ◽  
Amino Acid ◽  
Complex Formation ◽  
Glutamic Acid ◽  
Acid Complex ◽  
X Ray ◽  
Ray Methods

AbstractSorption of an acidic, amphoteric, sulphur containing and basic α-amino-acid (glutamic acid, glycine, methionine and lysine) by copper montmorillonite was studied by chemical and X-ray methods. With glutamic acid complex formation occurs only in solution but increasing basicity of the aminoacid favours complex formation in the clay interlayers.

X-ray studies on crystalline complexes involving amino acids and peptides. XL. Conformational variability, recurring and new features of aggregation, and effect of chirality in the malonic acid complexes of DL- and L-arginine

2002 ◽  
Vol 58 (6) ◽  
pp. 1051-1056 ◽  
Author(s):  
N. T. Saraswathi ◽  
M. Vijayan
Keyword(s):  
Amino Acids ◽  
Hydrogen Bonding ◽  
Amino Acid ◽  
Crystal Structures ◽  
Malonic Acid ◽  
Conformational Flexibility ◽  
X Ray ◽  
Conformational Variability ◽  
Aggregation Pattern ◽  
Positively Charged

The crystal structures of the complexes of malonic acid with DL- and L-arginine, which contain positively charged argininium ions and negatively charged semimalonate ions, further demonstrate the conformational flexibility of amino acids. A larger proportion of folded conformations than would be expected on the basis of steric consideration appears to occur in arginine, presumably because of the requirements of hydrogen bonding. The aggregation pattern in the DL-arginine complex bears varying degrees of resemblance to patterns observed in other similar structures. An antiparallel hydrogen-bonded dimeric arrangement of arginine, and to a lesser extent lysine, is a recurring motif. Similarities also exist among the structures in the interactions with this motif and its assembly into larger features of aggregation. However, the aggregation pattern observed in the L-arginine complex differs from any observed so far, which demonstrates that all the general patterns of amino-acid aggregation have not yet been elucidated. The two complexes represent cases where the reversal of the chirality of half the amino-acid molecules leads to a fundamentally different aggregation pattern.

N-DICHLOROACETYL DERIVATIVES OF SERINE AND THREONINE AND OF THEIR ESTERS AND SODIUM SALTS

1960 ◽  
Vol 38 (7) ◽  
pp. 1135-1140 ◽  
Author(s):  
I. Levi ◽  
A. E. Koller ◽  
G. Laflamme ◽  
J. W. R. Weed
Keyword(s):  
Amino Acids ◽  
Amino Acid ◽  
Antitumor Activity ◽  
Amino Acid Ester ◽  
Amino Group ◽  
Sodium Salts ◽  
Sarcoma 37 ◽  
Walker Carcinoma ◽  
Derivatives Of ◽  
Dichloroacetyl Chloride

The N-dichloroacetyl derivatives of DL-serine and DL-threonine were prepared by the Schotten–Baumann reaction from the amino acids and dichloroacetyl chloride. Negative ninhydrin tests coupled with elementary analyses indicated that only the amino group was acylated. The ester derivatives of these compounds were prepared either by esterification of the N-dichloroacetyl-DL-amino acid with diazomethane or by the reaction of the amino acid ester with dichloroacetyl chloride in the presence of triethylamine. The sodium salts and the esters were tested for antitumor activity against sarcoma 37 in mice and Walker carcinoma 256 in rats. In both cases regression of the tumors was obtained.

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