Carbon polymer dots (CPDs) were prepared by a one-pot aqueous synthetic route from ascorbic acid and diethylenetriamine at room-temperature. The CPDs under 350-nm excitation exhibit blue fluorescence peaking at 430 nm with a quantum yield of 47%. Other features include an average diameter of 5 nm, a fluorescence that is independent of the excitation wavelength, good water dispersibility and photostability, and excellent biocompatibility. The CPDs are shown to be viable fluorescent probes for ferric ion which acts as a strong quencher. The response to Fe(III) is linear in the 0.2 to 10 μM concentration range, and the detection limit is 0.1 μM. The probe was applied to the determination of Fe(III) in environmental waters and to intracellular imaging of ferric ions in HeLa cells.
Graphical abstract Carbon polymer dots (CPDs) are prepared from ascorbic acid and diethylenetriamine (DETA) at room-temperature (RT). The RT-CPDs exhibit excellent optical performance, biocompatibility and selectivity of quenching by ferric ions. This can be applied for determination and intracellular imaging of ferric ion.
We propose the use of a varied-line-spacing (VLS) holographic polymer-dispersed liquid crystal (H-PDLC) Bragg grating as a switchable image splitter to generate a compatible three-dimensional (3D) stereogram and to increase the viewing angle of the observer. To fabricate the VLS grating, a cylindrical lens is adopted to form a cylindrical wave, which interferes with a plane wave, generating an H-PDLC grating with a continuously varying period. The proposed holographic optical element (HOE)-based image splitter comprises two VLS H-PDLC gratings. It can be attached on a designed pattern, with two rectangles taking the place of conventional liquid crystal display panel pixels, and can separate them into right and left viewing fields with a wider range. Experimental results show that the movement of the eyes of the observer can reach 37.6 mm. A theoretical simulation indicates that a shorter focal length of the cylindrical lens can yield a larger movement range. Switching between two-dimensional and 3D modes can be performed by applying an external alternating-current voltage at ~80 V. The contrast ratio of the diffracted images induced by crosstalk is greater than 60%, which indicates the feasibility of the proposed HOE for 3D image splitting. 相似文献
In recent years, some investigators discussed the applicability of the HRR theory for engineering materials based on the results
of numerical analyses and experimental studies. In the present paper, the finite element method is employed to analyze the
crack tip fields of the engineering elastic-plastic material with a variety of geometry configurations of cracked specimens
from elastic state to intensely general yielded state in the plane strain case. The results indicate that the HRR theory loses
its validity of application for engineering elastic-plastic materials in the plane strain case. The reasons for this are analyzed.
A dual-parameter fracture criterion is suggested for this case. 相似文献
<正>In this article,a new 5-(p-maleicaminophenyl)-10,15,20-triphenylporphyrin(H_2P) and relative zinc compound(ZnP) were synthesized and characterized by means of elemental analyses,UV-vis,IR,MS and ~1H NMR spectroscopies.Furthermore,we have investigated the fluorescence spectroscopy of these compounds.The oxidation and reduction properties of the compounds were studied by the cyclic voltarnmetry,the oxidation-reduction potentials were obtained. 相似文献
The reaction of the Na2MoO4 or Na2WO4 salt with organic amine and PCl5, SiCl4 or TiCl4 in hydrochloric acid medium under hydrothermal conditions yields organic–polyoxometallate hybrid compounds, with the following reaction formula: Na2MO4 + Lewis-base + XCln + HCl → (Lewis-baseH)m(XM12O40) + NaCl + H2O (M = Mo or W; X = P, Si, Ti,; n = 3–5). By using this method, four new complexes, [(CH3)2NH]3[H3PW12O40] (1), (C2H5OH)3(H3PMo12O40) (2), [DMDA]2[H4SiW12O40]·H2O (3) (DMDA = 1 N,3 N-dimethyl-1,3-diazolidine) and [(DAN)6][H4TiW12O40]·4H2O (DAN = 4,4′-dianiline) (4), were obtained, and their crystal structures are reported. Thermal analysis of 1, 2 and 4 has been carried out. The thermal analysis indicates that the Keggin anion skeleton begins to decompose at about 300 °C. The possibility of constructing hydrogen-bond interactions by association between the polyoxometallate and the organic compound is explored. The roles of solvents and organic groups in the formation of specific crystalline architectures are discussed. The crystal structure of [H4TiW12O40], a hetero-transition-metal Keggin polyoxometallate with a square-plane TiO4, has been reported. Four architectures developed by hydrogen-bond associations of different Keggin polyoxometallates and organic bearing N–H or O–H donor functions are described. The selected organic modules (4,4′-dianiline, 1,3-dimethylimidazolidine, dimethylamine and ethanol) possess hydrogen-donor functions to allow them to act as bridges between polyoxometallate groups. Depending on the nature of the donor group, the number of hydrogens available for bonding, the geometric features and the sizes of the organic modules, diverse assembling patterns have been observed ranging from one-dimensional to three-dimensional networks. For all the networks, H3O+ and H+ act as actual linkers between the molecular units. 相似文献