Tautomerism and 1H, 13C and 15N MMR spectral assignments of some nitro derivatives of malonic acid diamide

Magnetic Resonance in Chemistry

Volumn 43, Issue 7, 2005, Pages 563-566

  Sebban, Muriel ^a   Guillard, Jérome ^a   Palmas, Pascal ^a   Poullain, Didier ^a  

^a DIF   (France)

Author keywords

13C NMR; 15N NMR; 1H NMR; Energetic compounds; Furoxan; Imine; Malonic acid diamide; Nitration; NMR; Oxadiazole

Indexed keywords

CARBOXYLIC ACIDS; DECOMPOSITION; DETONATION; MASS SPECTROMETRY; X RAY ANALYSIS;

13C NMR; 15N NMR; 1H NMR; ENERGETIC COMPOUNDS; FUROXAN; IMINE; MALONIC ACID; MALONIC ACID DIAMIDE; OXADIAZOLES; SPECTRAL ASSIGNMENTS;

NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY;

ALCOHOL DERIVATIVE; DIAMINE; IMINE; MALONIC ACID DERIVATIVE; NITRO DERIVATIVE; OXADIAZOLE DERIVATIVE; CARBON; DIAMIDE; MALONIC ACID; NITROGEN DERIVATIVE; PROTON;

ARTICLE; CALCULATION; CARBON NUCLEAR MAGNETIC RESONANCE; CHEMICAL STRUCTURE; DECOMPOSITION; ENERGY TRANSFER; INFRARED SPECTROSCOPY; MASS SPECTROMETRY; NITRATION; NITROGEN NUCLEAR MAGNETIC RESONANCE; OXIDATION; PROTON NUCLEAR MAGNETIC RESONANCE; X RAY ANALYSIS; CHEMISTRY; COMPARATIVE STUDY; EVALUATION; ISOMERISM; METHODOLOGY; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY;

CARBON ISOTOPES; DIAMIDE; ISOMERISM; MAGNETIC RESONANCE SPECTROSCOPY; MALONATES; NITROGEN COMPOUNDS; PROTONS;

EID: 20544446942     PISSN: 07491581     EISSN: None     Source Type: Journal    
DOI: 10.1002/mrc.1592     Document Type: Article

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