## Abstract The preferred conformations of the four isomers of 1,2,3,4,4a,6,7,8,9,13b‐decahydro‐9a__H__‐pyrido[1,2‐__f__] phenanthridine have been determined by 270 MHz ^1^H n.m.r. and i.r. spectroscopy. N.m.r. assignments are based on the specific chemical shifts of the protons adjacent to the nit
✦ LIBER ✦
The configuration of the tin-centered radical R3Sn (R = 2,4,6-tri-i-propyphenyl) as studied by ESR
✍ Scribed by M. Lehnig; Th. Apoussidid; W.P. Neumann
- Publisher
- Elsevier Science
- Year
- 1983
- Tongue
- English
- Weight
- 307 KB
- Volume
- 100
- Category
- Article
- ISSN
- 0009-2614
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✦ Synopsis
ESR data of the stannyl radical (i-PrsPh)&-at temperatures betxveen -140 and +200°C are presented. In solution, the isotropic l19Sn hyperfme coupling decreases with increasing temperature (20°C < T < 200°C) indicating that the radical is non-planar and configurationally stable. At -140°C in a toluene matrix, anisotropic features have been observed (A,, (--q 't9Sn) = 211 mT,Al( 'r9Sn) = 139 mT;gU = 1.995,gl= _ 7.016) leading to an out-of-plane angle of 12.7".
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🌐
English
⚖ 369 KB