Chiral Symmetry of Baryons

We study chiral symmetry aspects of the positive and negative parity baryons by identifying them with linear representations of the chiral group $SU(N_{f}) \otimes SU(N_{f})$. It is shown that there are two distinctive schemes: naive and mirror assignments. We construct linear sigma models for baryons in the two assignments and examine their physical implications. Then we investigate properties of the naive and mirror nucleons microscopically by using QCD interpolating fields. Finally, we propose experiments to distinguish the two chiral assignments for the nucleon.Comment: 36 pages, To appear in Prog. Theor. Phy

Quark Confinement for Multi-Quark Systems -- Application to Fully-Charmed Tetraquarks

A new color basis system and confinement mechanism for multi-quark systems are proposed according to the string-type picture of QCD. The color string configurations in the strong coupling QCD are implemented in the set of color basis states. The extended color Hilbert space for $QQ\bar Q\bar Q$ systems includes a ''hidden color'' state, which mixes with two-meson states $Q\bar Q+Q\bar Q$, This mixing effect leads to an attractive potential sufficient to form a bound state. We apply a realistic Hamiltonian model with the new scheme to fully charmed tetraquark states, $cc\bar c\bar c$, and find a bound and two resonant states, which could potentially correspond to the $cc\bar c\bar c$ tetraquark candidates recently observed in experiments.Comment: 6 pages, 3 figure

Antioxidant Activity and Oxidation Products of 1,2,3,4- Tetrahydroquinoxalines in Peroxyl Radical Scavenging Reactions, Part I

This paper studies the antioxidant activity of 1,2,3,4-tetrahydroquinolines, 3,4-dihydro-2H-benzo[1,4]thiazines and 1,2,3,4-tetrahydroquinoxalines in the inhibition of the peroxidation of tetralin induced by an azo initiator. Neither 1,2,3,4- tetrahydroquinoline nor 3,4-dihydro-2H-benzo[1,4]thiazine alone acted as an antioxidant, but when they have an electron-donating group at the para position to the NH group, they act as potent antioxidants. On the other hand, 1,2,3,4- tetrahydroquinoxaline on its own showed good antioxidant activity. However, 1,2,3,4-tetrahydroquinoxalines with methyl and methoxy groups in the phenyl ring have reactivities similar to or less than that of unsubstituted 1,2,3,4-tetrahydroquinoxaline. The induction periods of 1,2,3,4-tetrahydroquinoxalines with an alkyl group or phenyl group at the 2-position were all longer than the value for the unsubstituted 1,2,3,4-tetrahydroquinoxaline, except for a compound with a t-butyl group. The oxidation of 1,2,3,4-tetrahydroquinoxalines by peroxyl radicals generated from an azo initiator in tetralin or benzene yields quinoxalines and a dimer product of quinoxalines, 6-(1,2,3,4-tetrahydroquinoxalin-1-yl)-quinoxaline