Epicoccum sorghinum Causing Leaf Spot on Polygonatum cyrtonema in China.

Polygonatum cyrtonema Hua (family Asparagaceae) is a traditional Chinese medicinal plant that is widely cultivated in various parts of China, including Hunan Province. In summer 2022, a leaf spot disease was observed in 10% of the P. cyrtonema plants (Huang jing) in 18 hectares of this crop in the Hongjiang District (27°18'4″N, 110°11'1″E) of Hunan Province. The initial symptoms of the disease were brown spots on young leaves, and adjacent tissues gradually changed from green to yellow. The entire leaf then became yellow, withered, and eventually exhibited a thn and black appearance. In total, 12 diseased plants from four sampling sites (three plants per site) were collected for laboratory analysis to address the concerns of P. cyrtonema growers. Symptomatic leaf samples were selected, and the leaf fragments containing infected parts of the plants were disinfected with 75% ethanol for 1 min, then immersed in 2.5% hypochlorite for 45 s. After disinfection, symptomatic leaf samples were rinsed three times with sterile water, placed on potato saccharose agar containing 50 µg/ml kanamycin and incubated at 25°C for 2 days. Subsequently, 12 fungal isolates were isolated from various leaf samples through hyphal tip transferring. Ten of the 12 fungal isolates had similar morphological features, and one of them (isolate hjh) was used as the representative isolate for the study. With a growth rate of 6.3 mm per day, its white colonies transformed into red concentric rings in five days; they gradually became black after 10 days of growth. The chlamydospores were round (4.0-9.9 × 3.1-9.3 µm, n = 30), whereas the conidia were ovate (8.0-12.1 × 3.2-6.5 µm, n = 30). The morphological features of the isolate hjh were similar to the features of Epicoccum spp. (Aveskamp et al. 2010). The internal transcribed spacer (ITS) region (including the partial ITS1 sequence and the 5.8S and ITS2 complete sequences), ß-tubulin (tub) gene, and large subunit (LSU) rRNA gene, were amplified from the isolate hjh using the primer pairs ITS5/ITS4, Bt2a/Bt2b, and LROR/LR5, respectively (Taguiam et al. 2021). BLASTn analysis showed that the ITS (OR253745), tub (OR253764), and LSU (OR253746) sequences generated from the isolate hjh were 98-99% similar to the sequences of E. sorghinum strains CBS 179.80 and CBS 627.68. Subsequently, the ITS, tub, and LSU sequences were combined using Sequence Matrix software; phylogenetic analysis via Bayesian and maximum likelihood methods (Vaidya et al. 2011; Li et al. 2021) classified the isolate hjh into the E. sorghinum clade. To fulfill Koch's postulates, pathogenicity tests were conducted on healthy (lesion-free and disease-free) 2-year-old P. cyrtonema plants. Three healthy plants were inoculated by spraying whole plant until run-off with a spore suspension of the isolate hjh (1 × 106 conidia/ml); Three other healthy plants were sprayed with sterile water as controls. The inoculated plants were incubated in a growth chamber at 25 ± 2°C with 85% humidity for 28 days(Chen et al. 2021). Leaves from the inoculated plants gradually became brown within 15 days. Finally, the plants died 28 days after inoculation. The control plants showed no symptoms throughout the experimental period. Isolates (isolate hjh1, hjh2 and hjh3) that were reisolated from the inoculated plants exhibited morphologically similar characteristics and molecularly identical to the original isolate hjh. To our knowledge, this is the first report of E. sorghinum causing leaf spot disease on P. cyrtonema. The results of this study may facilitate the production of P. cyrtonema in China.

Study on the molecular mechanism of dihydromyricetin in alleviating liver cirrhosis based on network pharmacology.

Dihydromyricetin (DHM) is a bioactive flavonoid extracted from Hovenia dulcis, which has various activities. In the present study, the molecular mechanism of dihydromyricetin (DHM) in relieving liver cirrhosis was investigated through network pharmacology and experimental verification. The cell model was induced by TGF-ß1 activating the human hepatic stellate cell line (HSC; LX-2). The protein levels of α-SMA, collagen I, and collagen III and pathway-related proteins within LX-2 cells were detected using Western blot. EdU staining was conducted to detect cell proliferation. Immunofluorescence staining was performed to detect the expression levels of α-SMA and collagen I. Next, the drug targets of DHM were screened from the PubChem database. The differentially expressed genes in the liver cirrhosis dataset GSE14323 were identified. The expression of the identified drug targets in LX-2 cells was verified using qRT-PCR. The results showed that TGF-ß1 treatment notably increased LX-2 cell viability, promoted cell proliferation, and elevated α-SMA, collagen I, and collagen III protein contents. DHM treatment could partially eliminate TGF-ß1 effects, as evidenced by the inhibited cell viability and proliferation and reduced α-SMA, collagen I, and collagen III contents. After network pharmacology analysis, nine differentially expressed target genes (MMP2, PDGFRB, PARP1, BCL2L2, ABCB1, TYR, CYP2E1, SQSTM1, and IL6) in liver cirrhosis were identified. According to qRT-PCR verification, DHM could inhibit the expression of MMP2, PDGFRB, PARP1, CYP2E1, SQSTM1, and IL6, and enhance ABCB1 expression levels within LX-2 cells. Moreover, DHM inhibited mTOR and MAPK signaling pathways in TGF-ß1-induced HSCs. In conclusion, DHM could inhibit HSC activation, which may be achieved via acting on MMP2, PDGFRB, PARP1, CYP2E1, SQSTM1, IL6, and ABCB1 genes and their downstream signaling pathways, including mTOR and MAPK signaling pathway.

Lattice Boltzmann Simulation of the Kinetics Process of Methane Diffusion with the Adsorption-Desorption Hysteresis Effect in Coal.

The occurrence of coalbed methane adsorption-desorption hysteresis has been widely observed, but a unified understanding of its mechanism is lacking, and the factors affecting its degree are unclear. This study introduces a microscale LB model for gas diffusion-adsorption-desorption in porous media that also accounts for the adsorption-desorption hysteresis effect. The accuracy of the model has been validated using previous experimental data, and the primary controlling factors of adsorption-desorption hysteresis were analyzed. The findings are as follows: (1) In the process of methane diffusion-adsorption-desorption, Knudsen diffusion dominates in micro- and mesopores, while viscous flow prevails in macropores; our model can adaptively adjust gas transport regimes across a broad range of pore sizes and pressures. (2) The desorption amount and rate are close relative to the correction factors α and ß. A higher α value corresponds to greater initial adsorption as well as longer desorption time, whereas a lower ß value implies weaker desorption capacity and a slower desorption rate. (3) Pore size can affect gas diffusion-adsorption-desorption kinetics, where larger pore size corresponds to efficient gas diffusivity; when r < 10 nm, the desorption process is mainly controlled by the desorption rate. Overall, this study has offered new insights into the mechanism behind methane adsorption-desorption hysteresis at the microscale, identified primary controlling factors of methane diffusion-adsorption-desorption process, and provided a foundation for numerical simulations and experiments related to the adsorption-desorption hysteresis.

Apparent Permeability Model of Coalbed Methane in Moist Coal: Coupling Gas Adsorption and Moisture Adsorption.

Under specific conditions, moisture in natural coal seams can be adsorbed in the pores of the coal matrix, reducing the amount of methane adsorption sites and the effective area of the transport channels. This makes the prediction and evaluation of permeability in CBM exploitation more challenging. In this paper, we developed an apparent permeability model of coalbed methane coupling viscous flow, Knudsen diffusion, and surface diffusion which considers the effects of adsorbed gas and moisture in the pores of the coal matrix on the permeability evolution. The predicted data of the present model are compared with those of other models, and the results show good agreement, verifying the accuracy of the model. The model was employed to study the apparent permeability evolution characteristics of coalbed methane under different pressure and pore size distribution conditions. The main findings are as follows: (1) moisture content increases with saturation, with a slower increase for smaller porosities and an accelerated non-linear increase for porosities greater than 0.1. (2) Gas adsorption in pores decreases permeability, further weakened by moisture adsorption under high pressure but negligible at pressures below 1 MPa. (3) Higher water saturation weakens gas transport capacity, especially with pore sizes smaller than 10 nm. (4) The non-Darcy effect weakens with higher initial porosity, and neglecting moisture adsorption may significantly deviate from actual values in modeling methane transport in coal seams. The present permeability model can capture the transport characteristics of CBM in moist coal seams more realistically and is more applicable for predicting and evaluating the gas transport performance under dynamic variations of pressure, pore size, and moisture. The results in this paper can explain the transport behavior of gas in moist, tight, porous media and also provide a foundation for coalbed methane permeability evaluation.

Study of Viscoelastic Properties of Graphene Foams Using Dynamic Mechanical Analysis and Coarse-Grained Molecular Dynamics Simulations.

As a promising nano-porous material for energy dissipation, the viscoelastic properties of three-dimensional (3D) graphene foams (GrFs) are investigated by combining a dynamic mechanical analysis (DMA) and coarse-grained molecular dynamic (CGMD) simulations. The effects of the different factors, such as the density of the GrFs, temperature, loading frequency, oscillatory amplitude, the pre-strain on the storage and loss modulus of the GrFs as well as the micro-mechanical mechanisms are mainly focused upon. Not only the storage modulus but also the loss modulus are found to be independent of the temperature and the frequency. The storage modulus can be weakened slightly by bond-breaking with an increasing loading amplitude. Furthermore, the tensile/compressive pre-strain and density of the GrFs can be used to effectively tune the viscoelastic properties of the GrFs. These results should be helpful not only for understanding the mechanical mechanism of GrFs but also for optimal designs of advanced damping materials.

Nucleation and growth mechanism in the early stages of nickel coating in jet electrodeposition: a coarse-grained molecular simulation and experimental study.

In jet electrodeposition, microscopic nucleation and growth in the early stages of nickel coating are curcial and directly related to the consistency and reliability of the coating structure. We set up a three-electrode device with flow-injection function based on the vertical distribution and further studied the early stages of nanocluster formation corresponding to parallel and vertical distribution states. According to the nucleation diffusion and growth analysis, a coarse-grained molecular dynamics model is established for the first time to reveal the influences of different growth environments on the microscopic nucleation growth of the coating structure. Thus, the ion dynamic diffusion and nucleation kinetic mechanism could be further achieved, these vary under different electrodeposition conditions. In addition, the physical structure of the surface coating can be obtained by element analysis and density functional theory (DFT) calculations. These findings provide a theoretical and experimental basis for the efficient preparation of nickel coatings.

Mechanical Properties and Deformation Mechanisms of Graphene Foams with Bi-Modal Sheet Thickness by Coarse-Grained Molecular Dynamics Simulations.

Graphene foams (GrFs) have been widely used as structural and/or functional materials in many practical applications. They are always assembled by thin and thick graphene sheets with multiple thicknesses; however, the effect of this basic structural feature has been poorly understood by existing theoretical models. Here, we propose a coarse-grained bi-modal GrF model composed of a mixture of 1-layer flexible and 8-layer stiff sheets to study the mechanical properties and deformation mechanisms based on the mesoscopic model of graphene sheets (Model. Simul. Mater. Sci. Eng. 2011, 19, 54003). It is found that the modulus increases almost linearly with an increased proportion of 8-layer sheets, which is well explained by the mixture rule; the strength decreases first and reaches the minimum value at a critical proportion of stiff sheets ~30%, which is well explained by the analysis of structural connectivity and deformation energy of bi-modal GrFs. Furthermore, high-stress regions are mainly dispersed in thick sheets, while large-strain areas mainly locate in thin ones. Both of them have a highly uneven distribution in GrFs due to the intrinsic heterogeneity in both structures and the mechanical properties of sheets. Moreover, the elastic recovery ability of GrFs can be enhanced by adding more thick sheets. These results should be helpful for us to understand and further guide the design of advanced GrF-based materials.

Multiscale Lattice Boltzmann Simulation of the Kinetics Process of Methane Desorption-Diffusion in Coal.

The methane desorption and diffusion characteristics in coal are key factors affecting coalbed methane productivity. In this paper, we developed a lattice Boltzmann model for methane migration in the multiscale porous media of coal. In the simulation, the diffusion of methane in macropores/fractures is assumed to follow Fick's law, and that in the coal matrix is treated as Knudsen diffusion. In addition, the Langmuir adsorption kinetics equation is employed to describe the dynamic process of methane adsorption and desorption. The results indicated the following: (1) The specific surface area and fracture proportion of the coal will increase with the employment of hydraulic fracturing, which may prompt the gas desorption-diffusion efficiency. (2) The flow and diffusion of methane are closely related to each other. When the gas diffusivity is poor, the desorption-diffusion can be effectively accelerated by increasing the drainage intensity, but when the gas diffusivity is fine, the flow velocity has little influence on the methane desorption. In practice, if the estimated methane diffusion coefficient is below the order of 10-5 m2/s, more attention should be paid to its accuracy; otherwise, the obtained results may have a large deviation from the real value. (3) In the typical range of average pore sizes of coal, gas desorption rate growth with the increase of pore size makes the low-rank coal more advantageous in exploitation due to its larger average pore size. With the decline of reservoir pressure, the low- and high-rank coals more easily desorb methane than medium-rank coal. (4) In the kinetic study of the coalbed methane desorption-diffusion process, the accuracy of the obtained results may depend on the adsorption and desorption rate constants if the desorption rate constant is less than 106 1/s.

Anions effect construction of 1D naphthalene diimide supramolecular chains by π interactions and fluorescence detect iodide anion.

Five diverse 1D supramolecular chains, {[4-pmntd]}n(1), {H2[4-pmntd]•2Br-}n(2), {H2[4-pmntd]•2NO3-}n(3), {H2[4-pmntd]•2ClO4-}n(4), {H2[4-pmntd]•2BF4-}n(5), (where 4-pmntd was N,N'-bis (4-pyridylmethyl)naphthalene diimide) were synthesized and characterized by X-ray single-crystal structure analysis, IR spectroscopy, elemental analyses, thermogravimetric analyses, fluorescence detection. The anions effect construction of their 1D chain structural diversity through different π interactions. Compound 1 through the adjacent pyridine rings parallel π∙∙∙π interactions formed 1D linear chain structure. Compound 2 through Br- anion∙∙∙π interactions and halogenbond interactions formed 1D zigzag chain structure. Compound 3 through lone pair∙∙∙π interactions of naphthalene diimide and the adjacent carboxyl group formed 1D stairway chain structure. Compound 4 through ClO4- anion∙∙∙π interactions formed 1D ribbon chain structure. Compound 5 through parallel π∙∙∙π interactions of the adjacent naphthalene diimide planes and pyridine rings formed 1D ladder chain structure. The five compounds' fluorescence properties and thermal stabilities were investigated. The compound 2 solution could fluorescence detection for iodide anion via fluorescence quenching.

Diverse 1D chains supramolecular structures of N,N'-bis(3-pyridylmethyl)pyromellitic diimide and fluorescence iodide sensing.

Three diverse supramolecular compounds, {[3-pmpmd]}n(1), {H2[3-pmpmd]·2NO3-}n(2), {H2[3-pmpmd]·2tbb}n(3), (where 3-pmpmd was N,N'-bis(3-pyridylmethyl)pyromellitic diimide; tbb was tertiary butyl benzoic acid) were synthesized and characterized by elemental analyses, IR spectroscopy, thermogravimetric analyses, and X-ray single-crystal structure analysis. The co-crystal anions affect their structural diversity. Compound 1 is a 1D stairway chain structure by perpendicular π⋯π interactions of pyromellitic diimide and the neighboring pyridine rings. Compound 2 is a typical 1D ladder chain structure by hydrogen bond of nitrate arranged in a parallel array. Compound 3 is a 1D zigzag chain structure of one 3-pmpmd and two tbb by parallel π⋯π interactions and hydrogen bond interactions. Thermal stabilities and fluorescence properties of all compounds were investigated. The solution of compound 2 in DMF can fluorescence sense for iodide ions by remarkably quenching fluorescence intensity.

Selective Adsorption of Water, Methanol, and Ethanol by Naphthalene Diimide-Based Coordination Polymers with Constructed Open Cu2+ Metal Sites and Separation of Ethanol/Acetonitrile.

The selective separation of ethanol/acetonitrile by porous materials has rarely been observed owing to their similar physicochemical properties. In this work, we report a new coordination network, [Cu2(4-pmntd)2(opd)2](4-pmntd = N,N'-bis(4-pyridymethy)naphthalene diimide, opd = disodium 1,2-benzenedicarboxylate), which exhibits selective separation of ethanol over acetonitrile. The weak coordination bonds formed by unsaturated Cu2+ sites and hydroxyl groups are the key to such performance.

Synthesis, crystal structure, fluorescence properties of 1D chain Manganese (II) and Cadmium (II) complexes.

Two complexes, {[Mn(3-pmpmd)2(Cl)2]·2H2O}n(1), {[Cd(3-pmpmd) (I)2]·CHCl3·H2O}n(2), (3-pmpmd, N,N'-bis(3-pyridylmethyl)pyromellitic diimide) were synthesized and characterized by elemental analyses, IR spectroscopy, thermogravimetric analyses, and X-ray single-crystal structure analysis. The conformations of 3-pmpmd ligand affect their structural diversity. Complex 1 is a 1D double chain structure in edge-to-edge arrangement by π⋯π interactions. Complex 2 is a typical 1D zigzag chain structure arranged in a parallel array containing 1D channel to accommodate the chloroform and water guest molecules. Thermal stabilities and fluorescence properties of both complexes were investigated. The solution of complex 2 in DMF can sense for I- anion by quenching fluorescence intensity, whereas other anions increasing fluorescence intensity.

Synthesis, structure, photoluminescence and antitumour activity of zinc complex based on 2-(2-(1H-benzo-[d]imidazol-2-yl)benzyl)-1H-benzo-[d]imidazole.

A new complex [Zn(bbb)Cl2]·DMF, where bbb is 2-(2-(1H-benzo[d]imidazol-2-yl)benzyl)-1H-benzo[d]imidazole, was synthesized and characterized by element analysis, (1)H NMR and X-ray single crystal structure analyses. For complex: crystal system, triclinic, space group, P-1, a=9.4661(13), b=10.3534(14), c=13.0025(18)Å, α=73.477(2), ß=80.743(2), γ=88.658(2)°, V=1205.5(3)Å(3), Z=2. In this complex, the Zn(2+) distorted tetrahedron geometry is coordinated by two nitrogen atoms from 2-(2-(1H-benzo[d]imidazol-2-yl)benzyl)-1H-benzo[d]imidazole and two Cl(-). The complex emits yellow green luminescence with the maximal emission peak at 550 nm in DMF solution. The complex exhibits inhibition on the growth of Eca109 cancer cell with IC50 value of 8.9±1.1 µM, which was lower than that of cisplatin (14.3±1.4 µM). This complex has potential application in treatment of esophageal cancer.

Dinuclear zinc(II) complexes containing (benzimidazol-2-yl)benzene that overcome drug resistance in hepatocellular carcinoma cells through induction of mitochondria fragmentation.

Herein we demonstrated that dinuclear zinc complexes could overcome drug resistance in R-HepG2 drug resistance hepatocellular carcinoma cells through induction of mitochondria-mediated apoptosis or by triggering mitochondria fragmentation, depletion of the membrane potential and intracellular ATP levels.

Transcriptome analysis of Houttuynia cordata Thunb. by Illumina paired-end RNA sequencing and SSR marker discovery.

BACKGROUND: Houttuynia cordata Thunb. is an important traditional medical herb in China and other Asian countries, with high medicinal and economic value. However, a lack of available genomic information has become a limitation for research on this species. Thus, we carried out high-throughput transcriptomic sequencing of H. cordata to generate an enormous transcriptome sequence dataset for gene discovery and molecular marker development. PRINCIPAL FINDINGS: Illumina paired-end sequencing technology produced over 56 million sequencing reads from H. cordata mRNA. Subsequent de novo assembly yielded 63,954 unigenes, 39,982 (62.52%) and 26,122 (40.84%) of which had significant similarity to proteins in the NCBI nonredundant protein and Swiss-Prot databases (E-value <10(-5)), respectively. Of these annotated unigenes, 30,131 and 15,363 unigenes were assigned to gene ontology categories and clusters of orthologous groups, respectively. In addition, 24,434 (38.21%) unigenes were mapped onto 128 pathways using the KEGG pathway database and 17,964 (44.93%) unigenes showed homology to Vitis vinifera (Vitaceae) genes in BLASTx analysis. Furthermore, 4,800 cDNA SSRs were identified as potential molecular markers. Fifty primer pairs were randomly selected to detect polymorphism among 30 samples of H. cordata; 43 (86%) produced fragments of expected size, suggesting that the unigenes were suitable for specific primer design and of high quality, and the SSR marker could be widely used in marker-assisted selection and molecular breeding of H. cordata in the future. CONCLUSIONS: This is the first application of Illumina paired-end sequencing technology to investigate the whole transcriptome of H. cordata and to assemble RNA-seq reads without a reference genome. These data should help researchers investigating the evolution and biological processes of this species. The SSR markers developed can be used for construction of high-resolution genetic linkage maps and for gene-based association analyses in H. cordata. This work will enable future functional genomic research and research into the distinctive active constituents of this genus.

Zinc(II) complexes containing bis-benzimidazole derivatives as a new class of apoptosis inducers that trigger DNA damage-mediated p53 phosphorylation in cancer cells.

In the present study, two zinc(II) complexes containing bis-benzimidazole derivatives, Zn(bpbp)Cl2 (1) and [Zn(bpbp)2](ClO4)2·CH3CH2OH·H2O (2) (bpbp = 2,6-bis(1-phenyl-1H-benzo[d]imidazol-2-yl)pyridine), have been designed, synthesized and evaluated for their in vitro anticancer activities. The underlying molecular mechanisms through which they caused the cancer cell death were also elucidated. The complexes were identified as potent antiproliferative agents against a panel of five human cancer cell lines by comparing with cisplatin. Complex 2 demonstrated dose-dependent growth inhibition on MCF-7 human breast carcinoma cells with IC50 at 2.9 µM. Despite this potency, the complexes possessed great selectivity between human cancer cells and normal cells. Induction of apoptosis in MCF-7 cells by complex 2 was evidenced by accumulation of sub-G1 cell population, DNA fragmentation and nuclear condensation. Further investigation on intracellular mechanisms revealed that complex 2 was able to induce p53-dependent apoptosis in cancer cells by triggering DNA damage. On the basis of this evidence, we suggest that Zn(II) complexes containing bis-benzimidazole derivatives may be candidates for further evaluation as chemotherapeutic agents for human cancers.

The synthesis and luminescence of europium (III) complex based on deprotonated 1-(4-ethyl-4H-thieno[3,2-b]indol-6-yl)-4,4,4-trifluorobutane-1,3-dionate and 1,10-phenanthroline.

A new ß-diketone ligand, 1-(4-ethyl-4H-thieno[3,2-b]indol-6-yl)-4,4,4-trifluoro-butane-1,3-dione(HL) was synthesized by four steps reaction (Suzuki-Miyaura cross-coupling, Cadogan cyclization, N-ethylation and Claisen condensation reaction) from 1-(4-bromo-3-nitrophenyl)ethanone and thiophen-2-ylboronic acid. Deprotonated ligand (L(-1)) and 1,10-phenanthroline (phen) coordinated to Eu(3+) to obtain a new europium (III) complex, EuL(3)(phen). The complex was characterized by elementary analysis, IR, (1)H NMR, UV-Visible absorption spectroscopy, thermogravimetric analysis (TGA) and photoluminescence (PL) measurements in detail. TGA shows that the decomposition temperature of the complex is up to 320 °C. PL measurement results indicate that the Eu(III) complex exhibit intense red-emission with the characteristic of europium ion. Red LED device was successfully fabricated by employing the complex onto 380 nm-emitting InGaN chip, which shows that the complex can act as red phosphor in combination with 380 nm-emitting chips.

Syntheses, crystal structure and luminescent properties of cadmium complexes based on 2,6-bis(1-phenylbenzimidazol-2-yl)pyridine.

Two cadmium complexes, Cd(bpbp)Cl(2) (complex 1) and [Cd(bpbp)(2)](ClO(4))(2) (complex 2), based on 2,6-bis(1-phenylbenzimidazol-2-yl)pyridine (bpbp), were synthesized and characterized by X-ray single crystal structure analyses. For complex 1: crystal system, monoclinic, space group, C2/c, a=27.427(3)Å, b=13.4495(15)Å, c=14.8381(17)Å, ß=106.635(2)°, V=5244.4(10)Å(3), Z=8. It is a neutral complex. The Cd(II) ion distorted trigonal bipyramidal geometry is five-coordinated by three nitrogen atoms from ligand (bpbp) and two chlorine ions. For complex 2: crystal system, triclinic, space group, P-1, a=13.4791(15)Å, b=13.8506(16)Å, c=16.5839(19)Å, α=94.202(2)°, ß=106.948(2)°, γ=94.872(2)°, V=2935.3(6)Å(3), Z=2. It is an ionic complex. The Cd(II) ion octahedral geometry is six-coordinated by six nitrogen atoms from two ligand (bpbp). Both complexes emit blue luminescence with emission peaks at 420 and 430 nm in solid state and with emission peaks at 415 and 425 nm in DMF solution. In complex 1 absorption spectra, there is not only the free ligand absorption peak at 310 nm, but also shows strong Cd-Cl charge transfer peak at 350 nm in DMF solution.

[Synthesis and luminiescence of Eu(III) complex based on 4,4,4-trifluoro-1-(4'-m-terphenyl)-1, 3-butanedione and 1,10-phenanthroline].

A new europium (III) complex, EuL3 phen, [HL = 4,4,4-trifluoro-1-(4'-m-terphenyl)-1,3-butanedione, phen = 1, 10-phenanthroline] was synthesized. Its structure was characterized by elemental analysis, IR and FAB-MS. The complex exhibits strongly red emission due to the 5D0-7F(J) (J = 0-4) transitions of Eu3+ ions under irradiation of UV or 395 nm emission light of InGaN chip. The strongest emission peak is located at 613 nm. The luminescence quantum yield is 13%. The lifetime of the complex is 470 micros. The decay curve can be fit with a single exponential. The thermogravimetric analyses curve for the complex shows that the complex is stable up to 220 degrees C, which meets the requirement of fabrication of LED device. A red luminescent LED was successfully fabricated by coating complex EuL3 phen onto 395 nm emitting InGaN chip. The mass ratio of complex to the silicone is related to the chromaticity coordinates and efficiency of fabricated LED. When the mass ratio of complex to the silicone is 1 : 25, the chromaticity coordinates of the fabricated LED with the europium complex are x = 0.64 and y = 0.35 and the efficiency achieves 0.89 lm x W(-1). The results indicate that the complex may act as a potential red component in the fabrication of white LEDs.

Effect of different alkyl groups at the N-position on the luminescence of carbazole-based beta-diketonate europium(III) complexes.

A series of carbazole-based beta-diketone derivatives and their europium(III) ternary complexes Eu(N-Cx)(3)phen were designed and synthesized, where N-Cx denotes carbazole-based beta-diketonates with different alkyl substituents at N-position of the carbazole ring and phen is 1,10-phenethroline. Thermogravimetric analysis (TGA) shows that the decomposition temperature of the complexes is over 360 degrees C. UV-visible absorption spectroscopy, photoluminescence (PL), and the luminescence quantum yield of the Eu(III) complexes were measured and compared with each other, and the effect of different substituted-alkyls at N-position in the carbazole ring on the photoluminescence was discussed in details, indicating there exists a competition between the absorption capacity and the energy transfer efficiency for the complexes when the structure of the substituted-alkyls changes. The triplet state energy levels of the beta-diketonate ligands in the complexes are higher than that of the lowest excited level of Eu(3+) ion, (5)D(0), so the photoluminescence mechanism of the Eu(III) complexes was proposed as a ligand-sensitized luminescence process. Red LEDs were fabricated by precoating the complexes onto 395 nm emitting InGaN chips. All the results show that this series of Eu(III) complexes is a promising candidate as a red component in fabrication of NUV-based white LEDs.