Maria Micha-Screttas, George A. Heropoulos and Barry R. Steele
The paramagnetic nuclear magnetic resonance shifts for 6(7)Li in tetrahydrofuran solutions of lithium biphenyl, naphthalene, phenanthrene, anthracene and trans-stilbene radical anions have been measured as a function of the radical anion concentration. The shift vs. concentration relationships are linear except in the case of naphthalene. Both the observed molar shifts, δobs[6(7)Li], and the corresponding contact shifts, δc, are equal for the two isotopes. The paramagnetic shifts observed for THF solutions of 6(7)Li naphthalene radical anion increase with increasing dilution resulting in a non-linear shift vs. concentration relationship. This relationship becomes linear in the presence of 6(7)LiCl. A qualitative interpretation is proposed based on dynamic processes involving lithium cation exchange. The relevance of these results to SRN1 reactions is noted.