Titlebook: Specific Intermolecular Interactions of Nitrogenated and Bioorganic Compounds; Alexei K. Baev Book 2014 Springer-Verlag Berlin Heidelberg

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myalgia

Specific Intermolecular Interactions and Energies of Compounds with Peptidic Structure,f these acids, simple peptides, dipeptides, and polypeptides, allow us to conduct a correct thermodynamic analysis of each series of compounds, using the enthalpy characteristics of the processes of vaporization and sublimation to obtain the energies of the hydrogen bonds and the specific interactio

TERRA

Specific Intermolecular Interactions of Urea, Uracile, and Their Derivatives,[1]. “Pure” crystalline urea is a mixture of mono crystals with a tetragonal system, the lattice constants of which belong to the structural class P42.m, Z = 2(mm.), and have the values a = 0.5645, b = 0.5645, and c = 0.4704 nm [2]. The crystalline structures of urea have the shapes of needles and s

PARA

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CESS

Specific Intermolecular Interactions of Methoxyamines, Methoxynitriles, and Amides,n their condensed condition. Shifting of the electron density at the carbon atoms of the methyl groups leads to an insignificant negative charge [1–3], reducing the positive value as a result of the intermolecular reverse dative bond [4–8]

Gyrate

Specific Intermolecular Interactions and Energies of Compounds with Peptidic Structure,the enthalpy characteristics of the processes of vaporization and sublimation to obtain the energies of the hydrogen bonds and the specific interactions, formed in its liquid and crystalline conditions.

MEET

Book 2014ed methodology their energies are determined. The new concept of the extra stabilizing effect of isomeric methyl groups on the structure and stability of nitrogenated organic molecules and bioorganic compounds is introduced and the destabilization action on specific interactions is outlined.

Amplify

Hydrogen Bonds and Specific Intermolecular Interactions of Nitrogenated and Bio-organic Compounds aomic distances of atoms in the molecule (in the X–H bond distance), and this is observed in the fundamental X–H stretching vibration frequencies [2]. A practically similar definition of the hydrogen bond is given in Pauling’s monograph titled “The Nature of the Chemical Bond” [3].

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