Deutero-malonsaeure-dinitril | 2658-86-8

• 分子结构分类: 有机化合物 - 有机氮化合物
• 英文名称: Deutero-malonsaeure-dinitril
• 英文别名: Monodeutero-malononitril；Deuterio-malonsaeure-dinitril；Deutero-malodinitril；Monodeutero-malonsaeure-dinitril；deuterio-malononitrile；Malononitril-D(1)；Malonnitril-1-d
• CAS: 2658-86-8
• 化学式: C₃H₂N₂
• 分子量: 67.0543
• InChiKey: CUONGYYJJVDODC-MICDWDOJSA-N

反应信息

• 作为产物：
  描述：

  丙二腈 在 重水 作用下， 生成 Deutero-malonsaeure-dinitril 、 alkaline earth salt of/the/ methylsulfuric acid
  参考文献：
  名称：

  Angular Dependence of Electron‐Coupled Proton Interactions in CH₂ Groups

  摘要：

  Experimental and theoretical studies have been made of the dependence upon HCH angle of the electron-coupled proton-proton interactions in CH2 groups. A valence-bond approximation is used in the theoretical treatment which predicts that the coupling constant AgemHH decreases from 32 cps to 0 cps for HCH angles of 100° to 125°. For angles greater than 125°, AgemHH is predicted to be negative. Experimental values of AgemHH have been obtained from analyses of the proton magnetic-resonance spectra of a number of compounds, including several partially deuterated species. Insofar as the HCH angles are known in these compounds, there is good agreement between the theoretical and experimental coupling constants, especially for angles smaller than 120°, for which AgemHH changes more rapidly with angle. Moreover, a negative value is found experimentally for AgemHH in vinyl bromide at an HCH angle which is approximately that at which the theory predicts the coupling to become negative. The substituted ethylenes constitute the largest group of compounds studied experimentally. In them, AgemHH has been found to vary from 3.2 cps to —1.8 cps, while the Ac isHH values range from 6.9 cps to 12 cps and the AtransHH from 14.3 cps to 18.4 cps. The various results presented indicate that the value of the coupling constant can serve as a measure of the HCH angle. However, further work is needed to confirm the reliability of the method and investigate the effects of substituent perturbations.

  DOI：

  10.1063/1.1730585