Conformation and Stability of 1,1-Diphenylmethyleneiminyl

被引：19

作者：

Hudson, Robert F. ^{[1
]}

Lawson, Alexander J. ^{[1
]}

Record, Keith A. F. ^{[1
]}

机构：

[1] Univ Chem Lab, Canterbury CT2 7NH, Kent, England

来源：

JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS | 1974年 / 12期

关键词：

D O I：

10.1039/c39740000488

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

The magnitudes of ring-proton coupling in the title radical are consistent with those calculated for the conformation (III) which is also estimated to be the most stable rotamer.

引用

页码：488 / 489

页数：2

共 8 条

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[2] NITROXIDE RADICALS .7. NUCLEAR AND ELECTRON RESONANCE SPECTRA OF SOME AROMATIC TERT-BUTYL NITROXIDES
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[3] HUDSON RF, 1971, CHEM COMMUN, P807
[4] DELOCALIZATION OF UNPAIRED ELECTRON DENSITY OF PI RADICALS INTO SUBSTITUENT PHENYL GROUPS
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[J]. JOURNAL OF CHEMICAL PHYSICS, 1968, 49 (10) : 4725 - +
[5] THEORY AND APPLICATION OF PHOTOELECTRON SPECTROSCOPY .18. SEMIQUANTITATIVE PROOF OF HYPERCONJUGATION
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SCHWEIG, A
[J]. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION IN ENGLISH, 1973, 12 (04): : 307 - 308
[6] ESR-SPECTRUM OF A PERPENDICULAR BENZYL RADICAL
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BERNDT, A
[J]. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 1974, 13 (02) : 144 - 145
[7] SEIFERT KG, 1974, TETRAHEDRON LETT, P829
[8] SYMONS MCR, 1973, TETRAHEDRON, V29, P615

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