Christoph ElschenbroichMatthias WolfJ. PeblerKlaus Harms
The paramagnetic boronic acid (η7-C7H7)V[η5-C5H4B(OH)2] (3•) has been prepared and characterized structurally, emphasis being placed on hydrogen bonding motives present in the crystal. EPR spectroscopy reveals that association of 3• is absent in fluid solution. Tri([5]trovacenyl)boroxine, 4•••, the cyclic anhydride of 3•, engages in antiferromagnetic exchange; magnetic susceptometry provides the value J(4•••) = −1.04 cm-1. Accordingly, the EPR spectrum of 4••• in fluid solution points to 22 51V hyperfine components separated by one-third of the coupling constant of mononuclear trovacene derivatives. Redox splittings δE1/2 between consecutive oxidation steps of 4••• are not resolved, i.e., δE1/2 ≤ 60 mV.
Christoph ElschenbroichFeng LuKlaus Harms
Malcolm L. H. GreenDileni K. SiriwardeneDermot O’HareLuet‐Lok Wong
D.R. MuhandiramG.Y. KielGerdy H. M. AartsIsabel M. SáezJohannes G. A. ReuversD. Michael HeinekeyW. A. G. GRAHAMJosef TakatsR. E. D. McClung
David A. BrownJohn C. BurnsCordula Mock‐KnoblauchW.K. Glass