Conformation of the 1, 4, 7, 10-tetraoxocyclododeca-2, 3-dion was analysed by NMR and found out that the “gouch” from of a-diester carbonyls arrange the methylene groups as the “go«ch, gouch, anti” (g+ , gi, a) unitsin equilibrium of pseudorotermers so that o^ygens are in non corner positions of “sguare” conformation.
Birincil Dil | İngilizce |
---|---|
Konular | Kimya Mühendisliği |
Bölüm | Research Article |
Yazarlar | |
Yayımlanma Tarihi | 1 Ocak 1980 |
Yayımlandığı Sayı | Yıl 1980 Cilt: 26 |
Communications Faculty of Sciences University of Ankara Series B Chemistry and Chemical Engineering
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