Investigation of the molecular structure of the radical anions of some pyrimidine-type bases in aqueous solution by comparison of calculated hyperfine coupling constants with EPR resultsElectronic supplementary information (ESI) available: calculated hfc constants depending on the level of geometry optimisation and structure of the hydrogen bonded complex of a uracil radical anion with 5 water molecules. See http://www.rsc.org/suppdata/cp/b2/b207732a/

2002 ◽  
Vol 5 (1) ◽  
pp. 64-72 ◽  
Author(s):  
S. Naumov ◽  
J. Reinhold ◽  
D. Beckert
2000 ◽  
Vol 2000 (7) ◽  
pp. 342-343 ◽  
Author(s):  
Martyn C.R. Symons

Although ·PF2 radicals have been extensively studied there does not seem to be any spectroscopic evidence for ·PF3-radical anions. Here it is proposed that an EPR spectrum previously assigned to ·PF2 radicals is almost certainly due to ·PF3-centres. The 31P and 19F hyperfine coupling constants for these radicals are expected to be very similar. However, the ·PF3-radicals should show an extra coupling to the third 19F nucleus. This is clearly present.


1971 ◽  
Vol 49 (21) ◽  
pp. 3529-3535 ◽  
Author(s):  
F. C. Adam ◽  
C. R. Kepford

The radical anions of biphenyl and some of its bridged derivatives have been studied by e.s.r. It is found that the proton hyperfine coupling constants change monotonically through the series of radical anions derived from biphenyl, 9,10-dihydrophenanthrene, fluorene, dibenzothiophene, and dibenzofuran. Deuterations have been carried out for the latter two compounds and the hyperfine coupling constants are assigned to specific positions in these anions. The data are displayed in the form of a correlation diagram from which assignments for other bridged biphenyl anions can be made.


1972 ◽  
Vol 25 (11) ◽  
pp. 2353 ◽  
Author(s):  
RFC Claridge ◽  
BM Peake

The hyperfine coupling constants for the radical anions of 2,3-dihydro- phenalene (perinaphthane) and 7,8,9,l0-tetrahydrocyclohepta[de]naphthalene have been determined from analysis of the electron spin resonance spectra in solution. The results are compared with data from other mono- and di-peri- substituted naphthalenes. A simple H�ckel molecular orbital treatment is used to describe the inductive effect of the aliphatic substituent.


2018 ◽  
Vol 123 (2) ◽  
pp. 505-516
Author(s):  
Victoria A. Sannikova ◽  
Maria P. Davydova ◽  
Peter S. Sherin ◽  
Simon V. Babenko ◽  
Valeri V. Korolev ◽  
...  

2007 ◽  
Vol 111 (38) ◽  
pp. 11221-11227 ◽  
Author(s):  
Alexey S. Kiryutin ◽  
Olga B. Morozova ◽  
Lars T. Kuhn ◽  
Alexandra V. Yurkovskaya ◽  
P. J. Hore

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