Possible singlet and triplet superconductivity on honeycomb lattice

We study the possible superconducting pairing symmetry mediated by spin and charge fluctuations on the honeycomb lattice using the extended Hubbard model and the random-phase-approximation method. From $2\%$ to $20\%$ doping levels, a spin-singlet $d_{x^{2}-y^{2}}+id_{xy}$-wave is shown to be the leading superconducting pairing symmetry when only the on-site Coulomb interaction $U$ is considered, with the gap function being a mixture of the nearest-neighbor and next-nearest-neighbor pairings. When the offset of the energy level between the two sublattices exceeds a critical value, the most favorable pairing is a spin-triplet $f$-wave which is mainly composed of the next-nearest-neighbor pairing. We show that the next-nearest-neighbor Coulomb interaction $V$ is also in favor of the spin-triplet $f$-wave pairing.Comment: 6 pages, 4 figure

Revisiting Bohr's principle of complementarity using a quantum device

Bohr's principle of complementarity lies at the central place of quantum mechanics, according to which the light is chosen to behave as a wave or particles, depending on some exclusive detecting devices. Later, intermediate cases are found, but the total information of the wave-like and particle-like behaviors are limited by some inequalities. One of them is Englert-Greenberger (EG) duality relation. This relation has been demonstrated by many experiments with the classical detecting devices. Here by introducing a quantum detecting device into the experiment, we find the limit of the duality relation is exceeded due to the interference between the photon's wave and particle properties. However, our further results show that this experiment still obey a generalized EG duality relation. The introducing of the quantum device causes the new phenomenon, provides an generalization of the complementarity principle, and opens new insights into our understanding of quantum mechanics.Comment: 5 pages, 4 figure

Functional Characterization of Dark Sleeper (Odontobutis obscura) TBK1 on IFN Regulation

In East Asia, the dark sleeper, Odontobutis obscura (O. obscura) is a crucial commercial species of freshwater fish; however, its molecular biology research is still undeveloped, including its innate immune system, which is pivotal to antiviral responses. In this study, we cloned and identified the characterization and kinase function of dark sleeper TANK-binding kinase 1 (TBK1), supplementing the evidence of the conservation of this classical factor in fish. First, the ORF of Odontobutis obscurus (O. obscura) TBK1 (OdTBK1) was cloned from liver tissue by RACE-PCR. Subsequent nucleic acid and amino acid sequence analysis suggested that OdTBK1 is homologous with other fish TBK1, and the N-terminal Serine/Threonine protein kinases catalytic domain (S_TKc) and C-terminal coiled coil domain (CCD) are conserved. Subsequently, the cellular distribution demonstrated that OdTBK1 was located in the cytoplasm region. With regard to the identification of functions, OdTBK1 activated several interferon (IFN) promoters' activity and induced downstream IFN-stimulated genes (ISGs) expression. In a canonical manner, wild-type OdTBK1 significantly phosphorylated interferon regulatory factor 3 (IRF3) but failed when the N-terminal region was truncated. Furthermore, overexpression of OdTBK1 decreased viral proliferation remarkably. Collectively, these data systematically analyzed the characterization and function of OdTBK1, initiating the study of the innate antiviral response of dark sleeper

6-Benzyl-6,7-dihydro-5H-pyrrolo­[3,4-b]pyridine-5,7-dione

In the title compound, C14H10N2O2, the dihedral angle between the heterocyclic ring system and the phenyl ring is 45.8 (5)°. Weak inter­molecular C—H⋯N hydrogen bonding is present in the crystal structure

Ethyl 8-chloro-1-cyclo­propyl-6,7-difluoro-4-oxo-1,4-dihydro­quinoline-3-carboxyl­ate

In the mol­ecule of the title compound, C15H12ClF2NO3, the quinoline ring system is not planar, the dihedral angle between the pyridine and benzene rings being 3.55 (8)°. In the crystal, inter­molecular C—H⋯O hydrogen bonds link the mol­ecules into layers parallel to (101)