A highly efficient cobalt(II)‐catalyzed alkynylation/annulation of terminal alkynes assisted by an N,O‐bidentate directing group is described. This protocol is characterized by wide substrate scope utilizing cheap cobalt catalysts, and offers a new approach to 3‐methyleneisoindolin‐1‐one, which can be converted into an oxadiazine salt in one step. Moreover, the directing group could be removed in three steps. 相似文献
Detonation nanodiamonds (DNDs) are emerging as bioimaging platforms due to their biocompability, small primary particle size, reactive surface, and stable fluorescence after modification. In this paper, a heteroatom engineering method is provided to fabricate the fluorescent DNDs through pyrolysis of dibenzyl disulfide. The quantum yield of these sulfur (S)-functionalized DNDs (SDNDs) increases with sulfur percentage. The solubility and stability of SDNDs in aqueous solution are also significantly increased due to the formation of hydrophilic sulfur groups on DND. Furthermore, these SDNDs are used to conjugate the stimuli-responsive poly(N-isopropylacrylamide) (PNIPAM) through the ‘graft from’ method. The conjugation demonstrated both pH- and thermo-responsive fluorescence behaviors, which shows promise to be used in ratiometric fluorescence sensing for the detection of intracellular pH and temperature values. 相似文献
A facile, efficient and environment friendly method is established to prepare poly(vinyl alcohol)(PVA) based graphene oxide-montmorillonite(GO-MMT) nanocomposites in aqueous media. GO-MMT nanohybrid is obtained by the combination of GO and MMT in water without any reducing or stabilizing agents. The formation of GO-MMT nanohybrid is due to the hydrogen bonding and crosslinking effects. The sodium ions within MMT sheets act as crosslinkers between GO sheets and MMT platelets. The resultant nanocomposites are characterized by means of X-ray diffraction(XRD), scanning electron microscopy(SEM), differential scanning calorimetry(DSC), thermogravimetric analysis(TGA) and mechanical testing. Compared to that of pure PVA, PVA nanocomposites show enhanced thermal stabilities and mechanical properties, which results from strong interfacial adhesion of the nanoadditives in PVA matrix. The further increase in the tensile strength and modulus results from strong interaction between PVA chains and layered GO-MMT as well as good mechanical properties of GO-MMT hybrid, compared to PVA/GO and PVA/MMT nanocompsoites. 相似文献
Nonlinear wave mixing in mesoscopic silicon structures is a fundamental nonlinear process with broad impact and applications. Silicon nanowire waveguides, in particular, have large third‐order Kerr nonlinearity, enabling salient and abundant four‐wave‐mixing dynamics and functionalities. Besides the Kerr effect, in silicon waveguides two‐photon absorption generates high free‐carrier densities, with corresponding fifth‐order nonlinearity in the forms of free‐carrier dispersion and free‐carrier absorption. However, whether these fifth‐order free‐carrier nonlinear effects can lead to six‐wave‐mixing dynamics still remains an open question until now. Here we report the demonstration of free‐carrier‐induced six‐wave mixing in silicon nanowires. Unique features, including inverse detuning dependence of six‐wave‐mixing efficiency and its higher sensitivity to pump power, are originally observed and verified by analytical prediction and numerical modeling. Additionally, asymmetric sideband generation is observed for different laser detunings, resulting from the phase‐sensitive interactions between free‐carrier six‐wave‐mixing and Kerr four‐wave‐mixing dynamics. These discoveries provide a new path for nonlinear multi‐wave interactions in nanoscale platforms.
Highly conductive poly(3,4‐ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS) films as transparent electrodes for organic light‐emitting diodes (OLEDs) are doped with a new solvent 1,3‐dimethyl‐2‐imidazolidinone (DMI) and are optimized using solvent post‐treatment. The DMI doped PEDOT:PSS films show significantly enhanced conductivities up to 812.1 S cm−1. The sheet resistance of the PEDOT:PSS films doped with DMI is further reduced by various solvent post‐treatment. The effect of solvent post‐treatment on DMI doped PEDOT:PSS films is investigated and is shown to reduce insulating PSS in the conductive films. The solvent posttreated PEDOT:PSS films are successfully employed as transparent electrodes in white OLEDs. It is shown that the efficiency of OLEDs with the optimized DMI doped PEDOT:PSS films is higher than that of reference OLEDs doped with a conventional solvent (ethylene glycol). The results present that the optimized PEDOT:PSS films with the new solvent of DMI can be a promising transparent electrode for low‐cost, efficient ITO‐free white OLEDs.
Here, a novel method is demonstrated for the preparation of three‐arm branched microporous organic nanotube networks (TAB‐MONNs) based on molecular templating of three‐arm branched core–shell bottlebrush copolymers and Friedel–Crafts alkylation reaction. The unique three‐arm branched bottlebrush copolymers are synthesized by a combination of atom transfer radical polymerization, reversible addition‐fragmentation chain transfer polymerization, and ring‐opening polymerization techniques. In this approach, the length and diameter of branched tube units can be well‐controlled by rational molecular design. Moreover, the as‐prepared TAB‐MONNs possess a high surface area and exhibit a superior adsorption capacity for Rhodamine 6G (R6G) and p‐cresol.
The polymerization of the photocleavable monomer, o‐nitrobenzyl methacrylate (NBMA), is investigated using photoinduced electron/energy transfer reversible addition‐fragmentation chain transfer polymerization. The polymerizations under visible red (λmax = 635 nm, 0.7 mW cm−2) and yellow (λmax = 560 nm, 9.7 mW cm−2) light are performed and demonstrate rational evidence of a controlled/living radical polymerization process. Well‐defined poly(o‐nitrobenzyl methacrylate) (PNBMA) homopolymers with good control over the molecular weight and polymer dispersity are successfully synthesized by varying the irradiation time and/or targeted degree of polymerization. Chain extension of a poly(oligo(ethylene glycol) methyl ether methacrylate) macro‐chain transfer agent with NBMA is carried out to fabricate photocleavable amphiphilic block copolymers (BCP). Finally, these self‐assembled BCP rapidly dissemble under UV light suggesting the photoresponsive character of NBMA is not altered during the polymerization under yellow or red light. Such photoresponsive polymers can be potentially used for the remote‐controlled delivery of therapeutic compounds.
In this study, the dye-doped polymer dispersed liquid crystals (PDLC) gratings techniques performed by the various research groups or being developed are briefly reviewed. Especially, the electrically switched diffraction and holographic gratings, have attained much attention by various research groups working in the PDLC-related display studies. The fabrication methodologies used for such grating texture, include like the conventional dye-doped PDLC grating, Azo-dye doped PDLC gratings, and lasing techniques etc., adopted for dye-doped PDLC gratings. The useful features and characteristics of their fabrication process of such gratings are discussed. Finally, some of the future perspectives on this particular research field are presented. 相似文献