Publication | Closed Access
Application of <sup>13</sup>C and <sup>15</sup>N NMR spectroscopy to structural studies on nitramines
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Citations
34
References
1981
Year
Chemical EngineeringEngineeringBiochemistryElectronegativity EffectsSpectroscopyNatural SciencesStructure ElucidationSpectra-structure CorrelationOrganic ChemistryConformational FactorsMain Group ChemistryChemistrySolution Nmr SpectroscopyStructural StudiesMolecular ChemistryNuclear Magnetic Resonance SpectroscopyC Chemical ShiftsInorganic Compound
Abstract 15 N and 13 C chemical shifts and the 1 J ( 15 N 15 N), 1 J ( 15 N 13 C) and 1 J ( 13 CH) coupling constants have been determined for a number of 15 N‐enriched cyclic and acyclic secondary nitramines. The results are interpreted in terms of both electronegativity effects and conformational factors.
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