Intramolecular hydrogen bonding and molecular structure of 2-nitroresorcinol from gas-phase electron diffraction

1993 ◽  
Vol 97 (16) ◽  
pp. 4080-4084 ◽  
Author(s):  
Konstantin B. Borisenko ◽  
Istvan Hargittai
Keyword(s):  
Molecular Structure ◽  
Hydrogen Bonding ◽  
Electron Diffraction ◽  
Gas Phase ◽  
Intramolecular Hydrogen Bonding ◽  
Intramolecular Hydrogen ◽  
Gas Phase Electron Diffraction

scholarly journals MOLECULAR STRUCTURE OF TRYPTOPHAN: GAS PHASE ELECTRON DIFFRACTION AND QUANTUM-CHEMICAL STUDIES

2020 ◽  
Vol 63 (3) ◽  
pp. 37-45
Author(s):  
Valeriya V. Dunaeva ◽  
Georgiy V. Girichev ◽  
Nina I. Giricheva
Keyword(s):  
Molecular Structure ◽  
Amino Acids ◽  
Electron Diffraction ◽  
Gas Phase ◽  
Quantum Chemical ◽  
Structural Parameters ◽  
Electron Diffraction Data ◽  
Geometrical Parameters ◽  
Intramolecular Hydrogen ◽  
Gas Phase Electron Diffraction

The molecular structure and conformational properties of tryptophan have been investigated by gas-phase electron diffraction and theoretical methods. Quantum chemical calculations realized by program Gaussian 03 (B3LYP/cc-pVTZ) have been predicted the existence of six conformers at the temperature of experiment (T = 495 K). The ability of gas-phase electron diffraction method to distinguish the structure of conformers was estimated theoretically. Conformers have different orientations of carboxylic and amine group, backbone and indole fragment to each other. These conformers can be divided on two groups: distinguishable parameters (with different torsion angle C(OOH)-C(HNH2)-C(H2)-C(ind)) and weekly distinguishable ones (with different torsion angles H-N-C-C and H-O-C-C) by gas-phase electron diffraction. The molecular parameters of the conformers were determined. The conformers have intramolecular hydrogen bonding of the H2N···HO. The analysis of the gas-phase electron diffraction data have been carried out assuming the saturated vapor of tryptophan at T = 495 K consists of mixture at least of two conformers with lowest energy. It was shown that optimal ratio between conformers I : II was 50 : 50, respectively. The geometrical parameters of amino acids molecules (glycine, alanine, tryptophan) obtained by gas-phase electron diffraction were compared. The influence of the intramolecular hydrogen bond was established onto the structural parameters of the backbone of the above amino acids molecules.

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