Stallingslinde1601

Throughout the process, no droplet microfluidic expertise or equipment is required. learn more More importantly, the proposed system enables multiple samples to be processed simultaneously with a detection limit of 10 copies/μL. The test is simple and intuitive to operate in most laboratories for multi-sample detection, significantly enhancing the accessibility and detection throughput of the ddLAMP technique.Although Pb harbors a strong spin-orbit coupling effect, pristine plumbene (the last group-IV cousin of graphene) hosts topologically trivial states. Based on first-principles calculations, we demonstrate that epitaxial growth of plumbene on the BaTe(111) surface converts the trivial Pb lattice into a quantum spin Hall (QSH) phase with a large gap of ∼0.3 eV via a selective substrate-orbital-filtering effect. Tight-binding model analyses show the pz orbital in half of the Pb overlayer is selectively removed by the BaTe substrate, leaving behind a pz-px,y band inversion. Based on the same working principle, the gap can be further increased to ∼0.5-0.6 eV by surface adsorption of H or halogen atoms that filters out the other half of the Pb pz orbitals. The mechanism of selective substrate-orbital-filtering is general, opening an avenue to explore large-gap QSH insulators in heavy-metal-based materials. It is worth noting that plumbene has already been widely grown on various substrates experimentally.Cooperation between single-molecule magnets and electrical conductivity holds promise for preparing high-density magnetic devices; however, there are only a few reports so far. Here we report a 4f-π-based molecular hybrid, k-(ET)5Dy(NCS)7(KCl)0.5 (1) (ET = bis(ethylenedithio)tetrathiafulvalene, NCS- = thiocyanate), which undergoes slow relaxation of the magnetization and electrical conductivity. Unlike common ET-based conductive salts, K+ ions were intercalated into ET layers and coordinated with ET radicals. We found that the ET charges were sensitive to temperature, resulting in rich conductive phases at 75-300 K. In particular, the upturn in conductivity with a clear hysteresis loop was explained by the formation of partially oxidized states with charges close to 0.5+, which accounts for a metallic state. From the results of electronic structure calculations, the hole concentration increased to 125 K, which is consistent with a partially oxidized state upon cooling. The weak antiferromagnetic interactions accompanied by a dual magnetic relaxation process below 4 K are closely associated with the weak 4f-π interactions.Meridional tridentate N-heterocyclic carbene (NHC)-based pincer ligands contribute to a substantial growth in modern organometallic chemistry in both homogeneous catalysis and luminescence materials. Among all NHC-based pincer ligands, the dianionic LX2-type CCC-pincer ones constitute the smallest subcategory owing to their limited ligand frameworks suitable for complexation. This work reports a one-pot, high-yield synthesis of a homoleptic anionic all-carbon bis-pincer iridium(III) complex (4) directly from a bis(aryl)-substituted dipyrido-annulated (dpaAr2) imidazolium salt and [Ir(COD)Cl]2 via a cascade of deprotonation/C-H activation processes. Both experimental complexation chemistry and computational mechanistic investigation suggest that the large bite angle and π-rich character of the dpaAr2 NHC are responsible for its facile complexation as a dianionic LX2-type CCC-pincer ligand precursor. The all-carbon ligated iridium(III) complex (4) bearing a π-conjugated ligand scaffold showed remarkably low oxidation potentials, which allows future investigations in its redox chemistry and photophysical properties.Nitroxides are an important class of radical trapping antioxidants whose promising biological activities are connected to their ability to scavenge peroxyl (ROO•) radicals. We have measured the rate constants of the reaction with ROO• (kinh) for a series of 2,2,6,6-tetramethyl-1-piperidinyloxy (TEMPO) derivatives as 5.1 × 106, 1.1 × 106, 5.4 × 105, 3.7 × 105, 1.1 × 105, 1.9 × 105, and 5.6 × 104 M-1 s-1 for -H, -OH, -NH2, -COOH, -NHCOCH3, -CONH(CH2)3CH3, and ═O substituents in the 4 position, with a good Marcus relationship between log (kinh) and E° for the R2NO•/R2NO+ couple. Newly synthesized Pluronic-silica nanoparticles (PluS) having nitroxide moieties covalently bound to the silica surface (PluS-NO) through a TEMPO-CONH-R link and coumarin dyes embedded in the silica core, has kinh = 1.5 × 105 M-1 s-1. Each PluS-bound nitroxide displays an inhibition duration nearly double that of a structurally related "free" nitroxide. As each PluS-NO particle bears an average of 30 nitroxide units, this yields an overall ≈60-fold larger inhibition of the PluS-NO nanoantioxidant compared to the molecular analogue. The implications of these results for the development of novel nanoantioxidants based on nitroxide derivatives are discussed, such as the choice of the best linkage group and the importance of the regeneration cycle in determining the duration of inhibition.We used N,N'-dicyclohexylcarbodiimide (DCC) coupling chemistry to synthesize (1) heterostructures of CdSe and CdTe quantum dots (QDs) in colloidal dispersions and (2) heterostructures of CdSe and CdTe QDs, as well as CdS and CdSe QDs, immobilized on metal oxide thin films. The DCC-mediated formation of amide bonds between terminal carboxylic acid and amine groups of ligands on different QDs drove the formation of heterostructures. This cross-linking mechanism selectively yields heterostructures and prohibits the undesired formation of homostructures consisting of just one type of QD. Products of adsorption, ligand-exchange, and covalent-coupling reactions were characterized by transmission electron microscopy and ATR-FTIR, 1H NMR, electronic absorption, steady-state emission, and time-resolved emission spectroscopy. Ground-state absorption spectra of constituent QDs were unperturbed upon incorporation into heterostructures, enabling control over electronic properties. Heterostructures of CdSe and CdTe QDs exhibit type-II interfacial energetic offsets that promote charge separation following excitation of either QD. Indeed, photoexcited CdTe QDs transferred electrons to CdSe, and photoexcited CdSe QDs transferred holes to CdTe, on time scales of 10-100 ns, as evidenced by dynamic quenching of band-edge and trap-state emission. Mixed dispersions of noninteracting QDs did not undergo excited-state charge transfer. Constructing heterostructures on TiO2 thin films introduced an additional charge-transfer pathway, electron transfer from QDs to TiO2, which occurred on subnanosecond time scales and enabled extended spatial separation of photogenerated electrons and holes. Our results reveal that carbodiimide coupling chemistry can be used to tether colloidal QDs selectively and covalently to each other, yielding dispersed or immobilized heterostructures with programmable compositions and energetic offsets that can undergo efficient excited-state interfacial electron transfer.