Publications by authors named "Zhenzhen Xue"

Breeding resistant cultivars is the most effective strategy to control stripe rust in cereal crops. The hexaploid triticale line Xinyi is highly resistant to stripe rust at the seedling and adult plant stages. A segregating F population derived from a cross between Xinyi and the susceptible hexaploid triticale cultivar Zhongsi1048 was assessed to understand the genetic architecture of stripe rust resistance.

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In this study, we utilized the pyridine derivative tri(pyridin-3-yl)amine (TPA) and terephthalic acid (HPTA) as coordination ligands to synthesize two Cd-organic frameworks, namely [Cd(PTA)(TPA)] () and [Cd(PTA)(TPA)(DMA)]•2DMA () (DMA = ,-dimethylacetamide). It was demonstrated that both compounds possess room-temperature phosphorescence (RTP). Specifically, compound exhibited an interesting excitation-responsive RTP emission, with the phosphorescence covering half of the visible spectrum, while compound was found to display a distinct blue-green phosphorescence.

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A strategy combining a tailored database and high-throughput activity screening that discover bioactive metabolites derived from Magnoliae Officinalis Cortex (MOC) was developed and implemented to rapidly profile and discover bioactive metabolites derived from traditional Chinese medicine (TCM). The strategy possessed four characteristics: 1) The tailored database consisted of metabolites derived from big data-originated reference compound, metabolites predicted , and MOC chemical profile-based pseudomolecular ions. 2) When profiling MOC-derived metabolites , attentions were paid not only to prototypes of MOC compounds and metabolites directly derived from MOC compounds, as reported by most papers, but also to isomerized metabolites and the degradation products of MOC compounds as well as their derived metabolites.

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In virtue of the cationic tri(pyridin-4-yl)amine (TPA) derivatives acting as the templates, two iodometallates, [MeHTPA][CuI][CuI] () and [MeTPA][AgI] (), were constructed with different architectures. Compound features a discrete [CuI] cluster, which is further combined with [CuI] and two [MeHTPA] moieties through electrostatic interactions to result in a 3D supramolecular framework. Two types of infinite Ag-I chains with different orientations are formed in iodoargentate , and adjacent chains, together with in situ -methylated cations, are further aggregated into a final 3D supramolecule.

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Article Synopsis
  • Zero-dimensional hybrid organic-inorganic bismuth halides, specifically two mixed-cation-phase bismuth chlorides, are being explored as lead-free materials due to their unique properties.
  • These compounds exhibit interesting photoluminescence effects, with one showing dual emissions (blue fluorescence and yellow-green phosphorescence) and the other displaying a wide-band yellow-green emission.
  • Additionally, their structures allow for significant electron transfer and temperature-dependent proton conduction, which can be enhanced by light, indicating potential applications in smart materials.
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Introduction: Magnoliae officinalis cortex (MOC) is an important traditional Chinese medicine (TCM), and both raw and stir-fried MOC were commonly used in clinic.

Objectives: This study aimed to discriminate MOC and MOC stir-fried with ginger juice (MOCG) using an integrated approach combining liquid chromatography/mass spectrometry (LC/MS), gas chromatography/mass spectrometry (GC/MS), intelligent sensors, and chemometrics.

Methods: The sensory characters of the samples were digitalized using intelligent sensors, i.

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Assembling a heterostructure is an effective strategy for enhancing the electrocatalytic activity of hybrid materials. Herein, CoFe-layered double hydroxide and Co-metal-organic framework (CoFe-LDH/Co-MOF) hollow heterostructure nanorod arrays are synthesized. First, [Co(DIPL)(HBTC)(HO)] [named as Co-MOF, DIPL = 2,6-di(pyrid-4-yl)-4-phenylpyridine, HBTC = 1,3,5-benzenetricarboxylic acid] crystalline materials with a uniform hollow structure were prepared on the nickel foam.

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Aroma or fragrance in rice is a genetically controlled trait; Its high appreciation by consumers increases the rice market price. Previous studies have revealed that the rice aroma is controlled by a specific gene called BETAINE ALDEHYDE DEHYDROGENASE (OsBADH2), and mutation of this gene leads to the accumulation of an aromatic substance 2-acetyl-1-pyrroline (2-AP). The use of genetic engineering to produce aroma in commercial and cultivated hybrids is a contemporary need for molecular breeding.

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Chlorophyll degradation is an important physiological process and is essential for plant growth and development. However, how chlorophyll degradation is controlled at the cellular and molecular level remains largely elusive. Pectin is a main component of the primary cell wall, and polygalacturonases (PGs) is a group of pectin-hydrolases that cleaves the pectin backbone and release oligogalacturonide.

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Color-tunable room-temperature phosphorescence (RTP) with potential in many fields is of great importance but extremely challenging. It is necessary to comprehend the correlation between the molecular structure and property to design and synthesize such materials. Metal-organic coordination polymers (CPs) with good predesignability and precise structure have become a platform to construct RTP materials.

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This study aimed to investigate the impact of ginger juice on chemical profile of Magnoliae Officinalis Cortex(MOC) when they were processed together. Ultra-high-performance liquid chromatography coupled to quadrupole-orbitrap high-resolution mass spectrometry(UHPLC-Q-Orbitrap HRMS) was used for qualitative analysis of the chemical component of MOC samples before and after being processed with ginger juice. UPLC was performed to observe the content variation of eight main components in processed MOC.

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Photocatalytic degradation of organic pollutants via semiconductors with high visible light response and effective carrier separation is an economical and green route to greatly achieve environmental remediation. Herein, an efficient BiOI/BiMoO p-n heterojunction was in situ fabricated through hydrothermal method by substituting MoO species for I ions. The characteristic p-n heterojunction exhibited a strongly enhanced visible light responsive absorption from 500 to 700 nm owing to the narrow band gap of BiOI and a greatly effective separation of photoexcited carriers because of the built-in electric field on the interface between BiOI and BiMoO.

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Delicate design and bottom-up synthesis of hollow nanostructures for oxygen evolution electrocatalysts is a promising way to accelerate the reaction kinetics of overall water splitting. Herein, an efficient and versatile strategy for the controllable preparation of Pd-Cu alloy nanoparticles encapsulated in carbon nanopillar arrays (PD-Cu@HPCN) is developed. Core-shell structured MOF@imidazolium-based ionic polymers (ImIPs) have been prepared and adopted as a template, along with the decomposition of the inner Cu-MOFs when an anion exchange occurs between sodium tetrachloropalladate in solution and bromides in the external ImIP shell.

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Background: The expression changes of some proteins are associated with cancer progression, and can be used as biomarkers in cancer diagnosis. Automated systems have been frequently applied in the large-scale detection of protein biomarkers and have provided a valuable complement for wet-laboratory experiments. For example, our previous work used an immunohistochemical image-based machine learning classifier of protein subcellular locations to screen biomarker proteins that change locations in colon cancer tissues.

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The rational design of 2D polyoxometalate-based metal-organic framework (POMOF) nanosheets on a conductive substrate as a self-supporting electrode is highly attractive but a great challenge. Herein is the first demonstration of POMOF nanopillar arrays consisting of 2D nanosheets as a self-supported electrode for the hydrogen evolution reaction (HER) in acidic conditions. Single-crystal X-ray analysis reveal that our as-prepared 2D [Co(TIB)(PMoO)]·Cl·4HO [named CoMo-POMOF; TIB = 1,3,5-tris(1-imidazoly)benzene] crystalline materials are connected by Co-α-Keggin polymolybdate units act as secondary building blocks and TIB as the organic ligands.

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When the N- and O-donor ligands are combined as coligands, two noncentrosymmetric (NCS) complexes of [Ni(p-bdc)(tipa)(HO)]·HO () and Ni(npdc)(tipa)HO () [tipa = tris[4-(1-imidazol-1-yl)phenyl]amine, p-Hbdc = 1,4-benzenedicarboxylic acid, and Hnpdc = 2,6-naphthalenedicarboxylic acid] were achieved under solvothermal conditions. For both structures, N-donor ligands are responsible for the generation of a layered structure, while the O-donor ligands are hung on the layers and are responsible for enhancing the polarity, giving rise to the NCS structures. Because of the different connection modes between the metal centers and different carboxylate ligands (p-bdc in and npdc in ), and show some structural differences.

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Rational design of metal-organic frameworks (MOFs) into ultrathin two-dimensional (2D) nanosheets with controllable thickness is significantly attractive but is also a significant challenge. Herein, the authors report, for the first time, the synthesis of ultrathin 2D nickel-based MOF nanosheets with a thickness of only about 2 nm via a ligand-assisted controllable growth strategy, which cannot be acquired from the exfoliation of their bulky counterparts or the conventional hydrothermal method. The correlation between 2D nanosheets and crystal growth preference was demonstrated through a judicious choice of a specific [Ni(BIP)(-BDC)(HO)] framework (BIP = (3,5-bis(1-imidazoly)pyridine), -HBDC = terephthalic acid) to underlie the geometry of the resultant morphology.

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The assembly of a tetradentate pyridine-derived ligand with CuX has afforded two isostructural Cu(I)-organic frameworks [CuX(TBD)·DMF] (X = Cl for and Br for ) in this work. Structural analysis indicates that the compounds feature hybrid layered architectures, and the three-dimensional supramolecular frameworks are finally fabricated through the alternative stacking of adjacent layers wherein large open channels are simultaneously constructed. The chemical stability has been studied showing the excellent skeleton maintenance of the prepared solids in various solvents and even in water.

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Room-temperature phosphorescence (RTP) materials with recognizable afterglow property have gained widespread attraction. Multicolor RTP has added benefits in multiplexed biological labeling, a zero background ratiometric sensor, a multicolor display, and other fields. However, it is a great challenge to prepare multicolor RTP from a single-component compound according to Kasha's rule.

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Electron transfer photochromic materials with photo-triggered radicals have received huge interest from chemists due to their potentialities in anticounterfeiting, displays, energy conversion, and information storage. However, utilizing the sole carboxylic acid to synthesize novel electron transfer photochromic species is still confronted with huge challenges. Herein, an acentric three-dimensional network Cd(ADC)(DMF)(HO) (; ADC = anthracene-9,10-dicarboxylate; DMF = ,-dimethylformamide) and a two-dimensional layer Zn(ADC)(HO)·DMA·HO (; DMA = ,-dimethylacetamide) were synthesized and characterized via a photoactive HADC ligand.

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Catalases (CATs) are important self-originating enzymes and are involved in many of the biological functions of plants. Multiple forms of CATs suggest their versatile role in lesion mimic mutants (LMMs), H2O2 homeostasis and abiotic and biotic stress tolerance. In the current study, we identified a large lesion mimic mutant9428 (llm9428) from Ethyl-methane-sulfonate (EMS) mutagenized population.

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Hybrid photochromic materials (HPMs) have potential applications in numerous fields, such as display, protection, and information storage. The generation of HPMs with tunable photochromic performance is meaningful for the availability of smart photoresponsive materials. As a good platform, crystalline HPMs (CHPMs) provide possibilities to generate desirable products because of their synthetic tunability.

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Background: The quality of traditional Chinese medicines (TCMs) has been closely related to their growth regions. The geo-herbalism of TCMs is just like the protected destination of origin on foodstuffs and wines, telling us the specific geographic regions could yield TCMs with superior quality. However, the impact of habitat on TCMs could hardly been indicated in current quality evaluation, defects were as follows: (1) few studies involved the effect of environmental factors, (2) more attentions were paid to several abundant compounds, while global components especially water-soluble compounds were prone to be ignored.

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Oxygenated fuel has the function of self-supplying oxygen during the combustion process, which can greatly improve emission performance and reduce diesel fuel soot production. In this paper, a novel oxygenated fuel poly(oxymethylene) dibutyl ether (PODBE ) is designed and synthesized through experiments in combination with density functional theory (DFT) calculation. The experimental results show that PODBE has the advantages of high cetane number (73.

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The subcellular locations of proteins are closely related to their functions. In the past few decades, the application of machine learning algorithms to predict protein subcellular locations has been an important topic in proteomics. However, most studies in this field used only amino acid sequences as the data source.

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