Conformational ;f;ects in 1,3-dioxans and 1,3-dithianes have been recently largely elucidated. -That is why we started a systematic study of alkyl-substituted 1,3-oxathianes to compare their conformational features with those of their above-mentioned symmetric analogs. GELAN and ANTEURIS investigat
✦ LIBER ✦
Ionisation and appearance potentials in the evaluation of nonbonded interactions—IV: Conformational effects in methyl-substituted 1,3-oxathianes
✍ Scribed by Jorma Jalonen; Paavo Pasanen; Kalevi Pihlaja
- Publisher
- John Wiley and Sons
- Year
- 1973
- Tongue
- English
- Weight
- 370 KB
- Volume
- 7
- Category
- Article
- ISSN
- 1076-5174
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## Abstract Three empirical equation which have been used to calculate ionisation potentials of para and __meta__ disubstituted benzenes are evalyated according to their ability to predict the IP's of __para__ and __meta__ YC~6~H~4~COX, (where x OH, NH~2~, CL).
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