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Organic materials with both high electron mobility and strong solid‐state emission are rare although for their importance to advanced organic optoelectronics. In this paper, triphenylethylenes with varying number of perylenediimide (PDI) unit (TriPE‐nPDIs, n = 1?3) are synthesized and their optical and charge‐transporting properties are systematically investigated. All the molecules exhibit strong solid‐stated near infrared (NIR) emission and some of them exhibit aggregation‐enhanced emission characteristics. Organic field‐effect transistors (OFETs) using TriPE‐nPDIs are fabricated. TriPE‐3PDI shows the best performance with maximum quantum yield of ≈30% and optimized electron mobility of over 0.01 cm2 V?1 s?1, which are the highest values among aggregation‐induced emission luminogens with NIR emissions reported so far. Photophysical property investigation and theoretical calculation indicate that the molecular conformation plays an important role on the optical properties of TriPE‐nPDI, while the result from film microstructure study reveals that the film crystallinity influences greatly their OFET device performance.  相似文献   
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Control yourself! A two-color molecular beacon with non-nucleosidic chromophores in a triplex stem is presented. Pyrene and PDI fluorophores act as mutual quenchers by formation of a donor-acceptor complex in the closed form. Hybridization with the target results in two independent fluorescence signals. The two-color read-out provides a "self-control" feature, which helps to eliminate false positive signals in imaging and screening applications.  相似文献   
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The synthesis and photophysical properties of water‐soluble, fluorescent polyglycerol‐dendronized perylenediimides 1–4 are reported. The polyglycerol dendrons, which are known to be highly biocompatible, are found to confer high water‐solubility on the perylenediimide in aqueous media while retaining its excellent fluorescent properties. Furthermore, intramolecular crosslinking of the polyglycerol dendrons using the ring‐closing metathesis reaction not only enhances the photostability but also reduces the size of perylenediimide‐cored dendrimers. The permeability of the various dendritic shells is probed using heavy metal ion quenchers and compared to non‐dendritic but water‐soluble perylenediimide 5 .  相似文献   
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In this study, electropolymerization of pre-synthesized N,N′-di-[3-[2-(3-thienyl)ethyl] phenyl] perylene-3,4,9,10-bis(dicarboximide) (ThPDITh) was performed on Au button electrode and the properties of the resultant polymer P(ThPDITh) were investigated by electrochemical techniques. Effect of the polymerization charge on the redox behaviors of the polymer film was investigated by cyclic voltammetry (CV) and the polymer film was further characterized by electrochemical impedance spectroscopy (EIS) measurements. Corresponding electrical equivalent circuit was applied to the experimental data to explain the electrochemical phenomenon on the interface of the Au/P(ThPDITh). In order to obtain information on the energy storage properties of P(ThPDITh) as a pseudo-capacitive electrode material, important cell characteristics, such as redox process in anodic and cathodic potential ranges, stability of galvanostatic charge–discharge (GCD) curves, coulombic efficiency, capacitance, energy and power density values were determined. Capacitance values, obtained through different measurements (CV, EIS and GCD) are all in good agreement with each other. All the results suggested that P(ThPDITh) is capable of undergoing multiple reversible redox processes, and a good candidate for improving the capacitance and energy density of electrode material while still offering high power capability.  相似文献   
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