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Re-investigation of the conformational interconversion of the 1,2,3,6,7,8-hexahydropyrene cation radical by EPR, ENDOR and TRIPLE spectroscopy

✍ Scribed by Reijo Mäkelä; Mikko Vuolle


Publisher
John Wiley and Sons
Year
1985
Tongue
English
Weight
374 KB
Volume
23
Category
Article
ISSN
0749-1581

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✦ Synopsis


The conformational interconversion of the 1,2,3,6,7,8-hexahydropyrene cation radical has been re-examined by EPR, ENDOR and TRIPLE spectroscopy, and the Arrhenius plot is presented for a wider temperature range than that used earlier. The EPR spectra were measured from 143 to 369 K and the ENDOR spectra from 143 to 263 K. The thermodynamic constants of the conformational interconversion of the cation radical were determined on the basis of the temperature-dependent spectra. The high-resolution spectra clearly show that there are two overlapping spectra at low temperature, and this is confirmed by simulation.


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## 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