Structural characterisation of flavonoids and flavonoid-O-glycosides extracted from Genista tenera by fast-atom bombardment tandem mass spectrometry

Genista tenera is a plant native to the Madeira Island (Portugal). From the ethanol extract of its powdered aerial parts, two flavones, three isoflavones and one 7-O-glucosyl isoflavone were isolated. A mass spectrometric study of these compounds was performed using liquid secondary ion mass spectrometry (LSIMS) in combination with high-energy collision-induced dissociation (CID) and tandem mass spectrometry (MS/MS). Characteristic fragmentation patterns were observed in all the investigated compounds; the loss of small neutral species from the protonated molecules was useful for identifying the presence of specific functional groups in the A- and B-rings. In order to help to establish the proposed structures, NMR and UV studies were also performed.     

Bethe ansatz results for Hubbard chains with toroidal boundary conditions

We solve exactly the problem of a one-dimensional repulsive-U Hubbard chain with toroidal boundary conditions (HTB) using the Bethe ansatz approach. We calculate analytically the finite-size corrections to the ground-state energy in the half-filled case and use this expression to derive charge and spin stiffnesses with no assumptions. We then use a particle-hole transformation to calculate the finite-size corrections for the half-filledattractive- U case, and again derive the resulting expressions for the charge and spin stiffnesses. Lastly, we discuss how the repulsive-U corrections relate to those of a Heisenberg model with toroidal boundary conditions.On leave from Departamento de Fisica, Universidade Federal de S. Carlos, S. Carlos, 13560, Brazil.