Crystal structure and NMR spectroscopic characterization of 1,5-bis(2-hydroxy-3-methoxybenzylidene)carbonohydrazide
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TALMACI, Natalia, DRAGANCEA, Diana, GORINCIOI, Elena, BOUROSH, Pavlina, KRAVTSOV, Victor. Crystal structure and NMR spectroscopic characterization of 1,5-bis(2-hydroxy-3-methoxybenzylidene)carbonohydrazide. In: Chemistry Journal of Moldova, 2023, nr. 2(18), pp. 53-60. ISSN 1857-1727. DOI: https://doi.org/10.19261/cjm.2023.1074
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Chemistry Journal of Moldova
Numărul 2(18) / 2023 / ISSN 1857-1727 /ISSNe 2345-1688

Crystal structure and NMR spectroscopic characterization of 1,5-bis(2-hydroxy-3-methoxybenzylidene)carbonohydrazide

DOI:https://doi.org/10.19261/cjm.2023.1074
CZU: 547.497

Pag. 53-60

Talmaci Natalia1, Dragancea Diana12, Gorincioi Elena1, Bourosh Pavlina3, Kravtsov Victor3
 
1 Institute of Chemistry, MSU,
2 Institute of Organic and Supramolecular Chemistry. "Costin D. Nenițescu" of the Romanian Academy,
3 Institute of Applied Physics, MSU
 
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Disponibil în IBN: 26 decembrie 2023


Rezumat

The solid-state structure of a symmetrical carbohydrazone, namely 1,5-bis(2-hydroxy-3-methoxybenzylidene)carbonohydrazide was determined by X-ray single crystal diffraction method. Compound 1 crystallizes in the monoclinic space group P21/n with unit cell parameters a= 10.1198(6), b= 22.7847(11), c= 15.1738(10) Å, β= 100.458(6)°, Z= 4, V= 3440.6(3) Å3, R1= 0.0540. Crystal structure of 1 is defined by two crystallographic independent molecules, which are bonded via N–H···O hydrogen bond. The organic molecules are as keto tautomers with respect to the carbamide fragment, and adopt the anti conformation. 1D and 2D NMR experiments have argued on the presence of the title compound in DMSO-d6 solution mostly as keto tautomer in syn conformation, and enol-imino form when considering o-vanillin residue.

Cuvinte-cheie
carbohydrazide, o-vanillin, syn-anti isomer, X-ray diffraction, NMR spectroscopy