Publications by authors named "Shuping Zhuo"

Organic luminescent materials are indispensable in optoelectronic displays and solid-state luminescence applications. Compared with single-component, multi-component crystalline materials can improve optoelectronic characteristics. This work forms a series of full-spectrum tunable luminescent charge-transfer (CT) cocrystals ranging from 400 to 800 nm through intermolecular collaborative self-assembly.

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Organic hierarchical branch micro/nanostructures constituted by single crystals with inherent multichannel characteristics exhibit superior potential in regulating photon transmission for photonic circuits. However, organic branch micro/nanostructures with precise branch positions are extremely difficult to achieve due to the randomness of the nucleation process. Herein, by taking advantage of the dislocation stress field-impurity interaction that solute molecules deposit preferentially along the dislocation line, twinning deformation was introduced into microcrystals to induce oriented nucleation sites, and ultimately organic branch microstructures with controllable branch sites were fabricated.

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Lithium-sulfur batteries have attracted extensive attention owing to their environmental friendliness, abundant reserves, high specific discharge capacity, and energy density. The shuttling effect and sluggish redox reactions confine the practical application of Li-S batteries. Exploring the new catalyst activation principle plays a key role in restraining polysulfide shuttling and improving conversion kinetics.

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The field of supramolecular metal-organic cage catalysis has grown rapidly in recent years. However, theoretical studies regarding the reaction mechanism and reactivity and selectivity controlling factors for supramolecular catalysis are still underdeveloped. Herein, we demonstrate a detailed density functional theory study on the mechanism, catalytic efficiency, and regioselectivity of the Diels-Alder reaction in bulk solution and within two [PdL] supramolecular cages.

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The oxidation of hypophosphorous acid (HPO) by a ruthenium(VI) nitrido complex, [(L)Ru(N)(OH)] (; L = ,'-bis(salicylidene)--cyclohexyldiamine dianion), has been studied in aqueous acidic solutions at pH 0-2.50. The reaction has the following stoichiometry: 2[(L)Ru(N)(OH)] + 3HPO + HO → 2[(L)Ru(NHP(OH))(OH)] + HPO.

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Peroxynitrite (ONOO ) as a major reactive oxygen species plays important roles in cellular signal transduction and homeostatic regulation. Precise detection of ONOO in biological systems is vital for exploring its physiological and pathological function. Among numerous detection methods, fluorescence imaging technology using fluorescent probes offers some advantages, including simple operation, high sensitivity and selectivity, as well as real-time and nondestructive detection.

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Herein, 3,6-di(thiophen-2-yl)-2,5-dihydropyrrolo[3,4-]pyrrole-1,4-dione (TDPP) and di--butyl 2,2'-(1,4-dioxo-3,6-di(thiophen-2-yl)pyrrolo[3,4-]pyrrole-2,5(1,4)-diyl)diacetate (TDPPA) were synthesized, which were then loaded in graphene aerogels. The as-prepared thiophene-diketopyrrolopyrrole-based molecules/reduced graphene oxide composites for lithium-ion battery (LIB) anode composites consist of DPPs nanorods on a graphene network. In relation to the DPPs part, embedding DPPs nanorods into graphene aerogels can effectively reduce the dissolution of DPPs in the electrolyte.

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Given their excellent reusability and environmental friendliness, solid acid catalysts have drawn considerable attention in acid-catalyzed reactions. However, the rational design and synthesis of solid acid catalysts with abundant Brønsted acid sites remains a challenge. In this paper, KIT-6, Zr-KIT-6, Mo-KIT-6, and ZrMo-KIT-6 solid acid catalysts are designed and synthesized.

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The anti-Markovnikov hydroamination reaction is considered to be a particular challenge, and one of the reactants, parent hydrazine, is also regarded as a troubling reagent. In this study, we first studied the hydrohydrazination of parent hydrazine an effective and green catalyst-external electric field (EEF). The calculation results demonstrated that the anti-Markovnikov and Markovnikov pathways are competitive when there was no catalyst.

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Endoplasmic reticulum (ER) is an indispensable organelle in eukaryotic cells involved in protein synthesis and processing, as well as calcium storage and release. Therefore, maintaining the quality of ER is of great importance for cellular homeostasis. Aberrant fluctuations of bioactive species in the ER will result in homeostasis disequilibrium and further cause ER stress, which has evolved to contribute to the pathogenesis of various diseases.

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Based on the idea of environmental friendliness, we first studied the hydrothiolation reactions of thiophenol with allylamine using a green catalyst-an external electric field (EEF). The hydrothiolation reactions could occur through Markovnikov addition (path M) and anti-Markovnikov addition (path AM) pathways. The calculation results demonstrated that when the EEF was oriented along , , and directions, path M was accelerated.

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Graphitic carbon nitride, regarded as a charming conjugated polymer, has been a visible light photocatalyst. Bulk carbon nitride endures the limited light absorption ability, few surface active sites and slow separation of photoinduced charge carriers, leading to the poor catalytic activity. Herein, a new carbon (C) and phosphorus (P) co-doped carbon nitride hollow tube with adjustable optical property (CPCN) was developed by applying melamine and polyacrylic amide as the precursors and phosphoric acid as the P source via a hydrothermal-thermal copolymerization way.

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Phosphorus-doped hierarchically porous carbon (HPC) is prepared with the assistance of freeze-drying using colloid silica and phytic acid dipotassium salt as a hard template and phosphorus source, respectively. Intensive material characterizations show that the freeze-drying process can effectively promote the porosity of HPC. The specific surface area and P content for HPC can reach up to 892 m g and 2.

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In this study, four thiophene-diketopyrrolopyrrole-based (TDPP-based) polymer derivatives modified by different groups and alkyl chains were synthesized. The effects of various functional groups on the electrochemical properties of the polymers for application in lithium-ion batteries were compared, where the carbazole (C) and tert-butyl acetate (TA) groups improved the capacity performance of the polymer electrodes, while hexane (H) and fluorene (F) groups enhanced the cycle stability of the polymer electrodes. The P(C-TDPP-TA) polymer electrode, i.

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Recent years have witnessed a rapid development of carbon dots (CDs), due to their outstanding luminescence properties and excellent biocompatibility. However, the internal structure and photoluminescent (PL) mechanism of CDs are still the subject of considerable debate, which is due to the fact that reaction products usually contain mixtures of several CD fractions as well as molecular intermediate and side products. Therefore, careful purification of the CDs is significant for analysis of structure and luminescence mechanism.

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The biomass-based carbons anode materials have drawn significant attention because of admirable electrochemical performance on account of their nontoxicity and abundance resources. Herein, a novel type of nickel-embedded carbon material (nickel@carbon) is prepared by carbonizing the dough which is synthesized by mixing wheat flour and nickel nitrate as anode material in lithium-ion batteries. In the course of the carbonization process, the wheat flour is employed as a carbon precursor, while the nickel nitrate is introduced as both a graphitization catalyst and a pore-forming agent.

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A new excited-state intramolecular proton transfer (ESIPT) based and polarity-sensitive fluorescent probe M-HA was easily developed by conjugated connection of indole and 2'-hydroxyacetophenone through (E)-2-chloro-3-(hydroxymethylene)cyclohex-1-enecarbaldehyde. M-HA shows near-infrared fluorescence, high molar absorption coefficient and a large Stokes shift in various common solvents. In particular, M-HA exhibits red-shifted maximum emission wavelength, and extraordinarily high fluorescence intensity and quantum yield in high-polarity solvents.

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Anti-Markovnikov selective oxidative amination reaction with simple alkenes is particularly promising but challenging because of the inherent electronic effect of the alkene substrate which is in favor of the Markovnikov product. In a recently reported Pd-catalyzed anti-Markovnikov oxidative amination reaction, the addition of quaternary ammonium salts is shown to be critical. We performed a comprehensive DFT study to elucidate the reaction mechanism and the origin of the regioselectivity, as well as the roles of the ammonium salts.

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Conductive polymers, such as polyaniline (PANI), polypyrrole (PPy), polythiophene (PTh) and poly 3,4-ethylenedioxythiophene (PEDOT), play an important role in the application of pseudocapacitors. It is necessary to explore the effects of different conductive polymers in electrode composites. Herein, we prepare zinc sulfide/reduced graphene oxide (ZnS/RGO) by the hydrothermal method, and conductive polymers (PANI, PPy, PTh and PEDOT) doped with the same mass ratio (polymer to 70 wt%) polymerization on the surface of ZnS/RGO composite.

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We herein develop a novel two-photon fluorescent probe termed L-pH for visualization of lysosomal pH within live cells. L-pH is composed of three moieties, including naphthalimide fluorophore as a fluorescence off-on response moiety, piperazine and morpholine groups as lysosomal targeting and pH responsive sites, as well as a reactive benzyl chloride segment for further lysosomal anchoring. The experimental results demonstrate that L-pH can instantaneously respond to various pH values with high sensitivity and selectivity, and has low cytotoxicity and excellent photostability.

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Carbon nitride, as an outstanding photocatalyst for hydrogen production, displays a limited photocatalytic performance on account of the insufficient light absorption and low surface area. Herein, three-dimensional mesoporous carbon nitride with large surface area was prepared by using freeze-dried cyanuric acid-melamine supramolecular aggregates and ionic liquid as precursor and template, respectively. The results find that as-prepared carbon nitride materials possess the 3D interconnected open-framework with porous channels owing to the decomposition of ionic liquid and precursor under high temperature calcination, which in favor of the contact between active sites and reactants as well as the improvement of charge carrier transport rate.

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Article Synopsis
  • The oxidative contraction of α-formal ketones, catalyzed by H₂O₂, is a key method for creating chiral cyclic ketones in natural product synthesis, with cyclic ketones being the primary products and ring-opening products being secondary.
  • DFT calculations reveal that both H₂O and H₂O₂ are effective in promoting the rate-determining step of the reaction, highlighting the significant role of solvent effects in the reaction mechanism.
  • The study found that steric hindrance and electronic effects of substituents on the ketone influence selectivity, with larger steric groups favoring cyclic products and electron-donating groups enhancing cyclic product formation.
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The excited-state properties of the "free" and "locked" pyrazine derivatives are investigated in solution. DCFP with "free" phenyls is theoretically calculated to be non-emissive due to the non-radiative energy dissipation through strong Duschinsky rotation effect, in agreement with the available experimental result. Surprisingly, DCBP with "bi-locked" phenyls is also calculated to be nonluminous.

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Mitochondria as essential organelles play critical roles in cellular metabolism. Mitochondrial pH is a vital parameter that directly affects the unique function of mitochondria. Herein, we present a new ratiometric fluorescent probe M-pH for monitoring the pH within the mitochondria.

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