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首页> 外文期刊>Journal of Molecular Structure >Stabilization of c-lactam and lactone ring-fused norcaradienes by protonation: DFT calculations of norcaradiene and the corresponding cycloheptatriene structures
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Stabilization of c-lactam and lactone ring-fused norcaradienes by protonation: DFT calculations of norcaradiene and the corresponding cycloheptatriene structures

机译:通过质子化稳定c-内酰胺和内酯环稠合的正二十碳烯:正二十碳烯和相应的环庚三烯结构的DFT计算

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摘要

Stabilization of norcaradiene structures of c-lactone and lactam ring-fused 7-vinylnorcaradienes 1a–1e in their norcaradiene – cycloheptatriene valence isomerization was achieved by protonation. Induced 13C NMR chemical shifts caused by protonation were monitored for the cyclopropane ring carbons (C1, C6 and C7) of the norcaradiene structures as indices of their stabilities. DFT calculations (B3LYP/6- 311+G(d) level) of norcaradienes, the corresponding cycloheptatrienes, and their protonated structures supported the experimental results.
机译:通过质子化作用,可以使c-内酯和内酰胺环稠合的7-乙烯基降冰片烯1a-1e降冰片烯结构稳定。监测由质子化引起的诱导的13 C NMR化学位移,以测定降冰片烯结构的环丙烷环碳(C1,C6和C7),作为其稳定性的指标。降冰片烯,相应的环庚烯及其质子化结构的DFT计算(B3LYP / 6- 311 + G(d)含量)支持了实验结果。

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