56 research outputs found

    2-Isopropoxyphenyl N-methyl­carbamate

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    In the title compound, C11H15NO3, the mean planes of the carboxamide and isopropyl groups are inclined at 109.9 (1) and 128.7 (2)°, respectively, to the mean plane of the phen­oxy group. In the crystal structure, mol­ecules are stacked along the b axis, without any π–π inter­actions. The stacked columns are linked together by inter­molecular N—H⋯O hydrogen bonds, with an N⋯O distance of 2.842 (2) Å

    Photo-production of lowest Σ1/2\Sigma^*_{1/2^-} state within the Regge-effective Lagrangian approach

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    Since the lowest Σ\Sigma^{*} state, with quantum numbers spin-parity JP=1/2J^{P} =1/2^{-}, is far from established experimentally and theoretically, we have performed a theoretical study on the Σ1/2\Sigma^*_{1/2^-} photo-production within the Regge-effective Lagrangian approach. Taking into account that the Σ1/2\Sigma^*_{1/2^-} couples to the KˉN\bar{K}N channel, we have considered the contributions from the tt-channel KK exchange diagram. Moreover, these contributions from tt-channel KK^* exchange, ss-channel nucleon pole, uu-channel Σ\Sigma exchange, and the contact term, are considered. The differential and total cross sections of the process γnK+Σ1/2\gamma n \to K^{+}\Sigma^{*-}_{1/2^-} are predicted with our model parameters. The results should be helpful to search for the Σ1/2\Sigma^*_{1/2^-} state experimentally in future.Comment: 7 pages, 4 figure

    4-(4-Ethoxy­benz­yl)-1,3-oxazolidin-2-one

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    In the title compound, C12H15NO3, the ethoxy­benzyl ring plane forms a dihedral angle of 60.3 (4)° with the mean plane of the oxazolidine ring. The mol­ecules are linked through N—H⋯O hydrogen bonds into a chain running in the b direction

    Dimethyl 2-nitro­terephthalate

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    In the mol­ecule of the title compound, C10H9NO6, the two ester groups and the nitro group are inclined at 9.2 (2), 123.3 (6) and 135.2 (5)°, respectively to the mean plane of the benzene ring. In the crystal structure, mol­ecules are stacked along the a axis, without any π–π inter­actions. The stacked columns are linked together by non-classical intermolecular interactions of the type C—H⋯O

    Ethyl 3-carb­oxy-5-nitro­benzoate

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    In the title compound, C10H9NO6, the carb­oxy, ethoxy­carbonyl and nitro groups form dihedral angles of 3.8 (1), 4.5 (1) and 164.8 (1)°, respectively, with the mean plane of the benzene ring. In the crystal structure, mol­ecules lying about inversion centers are linked through O—H⋯O hydrogen bonds. C—H⋯O inter­actions are also present

    Isobutyl 3,5-dinitro­benzoate

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    In the structure of the title compound, C11H12N2O6, the mol­ecules are stacked along the b axis without any π–π inter­actions. The stacked columns are linked together by non-classical inter­molecular C—H⋯O inter­actions,. In the molecule, the nitro groups make dihedral angles of 9.4 (5) and 10.3 (5)° with the benzene ring

    Comparative analysis of SOFC-MGT top-level and new bottom-level system performance

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    In order to make the SOFC-MGT system more widely used, the mathematical simulation models of the SOFC-MGT top-level circulatory system and the new bottom circulatory system were first established, and then the performance of the two systems was analyzed and compared using Matlab/Simulink simulation software. The research results show that the output performance of the SOFC-MGT top-level circulation system is due to the new bottom-level circulation system, and the stack output performance of the two systems is not much different

    Genetic Analysis of Floral Symmetry Transition in African Violet Suggests the Involvement of Trans-acting Factor for CYCLOIDEA Expression Shifts

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    With the growing demand for its ornamental uses, the African violet (Saintpaulia ionantha) has been popular owing to its variations in color, shape and its rapid responses to artificial selection. Wild type African violet (WT) is characterized by flowers with bilateral symmetry yet reversals showing radially symmetrical flowers such as dorsalized actinomorphic (DA) and ventralized actinomorphic (VA) peloria are common. Genetic crosses among WT, DA, and VA revealed that these floral symmetry transitions are likely to be controlled by three alleles at a single locus in which the levels of dominance are in a hierarchical fashion. To investigate whether the floral symmetry gene was responsible for these reversals, orthologs of CYCLOIDEA (CYC) were isolated and their expressions correlated to floral symmetry transitions. Quantitative RT-PCR and in situ results indicated that dorsal-specific SiCYC1s expression in WT S. ionantha (SCYC1A and SiCYC1B) shifted in DA with a heterotopically extended expression to all petals, but in VA, SiCYC1s' dorsally specific expressions were greatly reduced. Selection signature analysis revealed that the major high-expressed copy of SCYC1A had been constrained under purifying selection, whereas the low-expressed helper SiCYC1B appeared to be relaxed under purifying selection after the duplication into SCYC1A and SiCYC1B. Heterologous expression of SCYC1A in Arabdiopsis showed petal growth retardation which was attributed to limited cell proliferation. While expression shifts of SCYC1A and SiCYC1B correlate perfectly to the resulting symmetry phenotype transitions in F1s of WT and DA, there is no certain allelic combination of inherited SiCYC1s associated with specific symmetry phenotypes. This floral transition indicates that although the expression shifts of SCYC1A/1B are responsible for the two contrasting actinomorphic reversals in African violet, they are likely to be controlled by upstream trans-acting factors or epigenetic regulations

    Identifying the pollution characteristics of atmospheric polycyclic aromatic hydrocarbons associated with functional districts in Ningbo, China

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    Duplicate polyurethane foam based passive air samplers (PUF-PAS) were deployed at seven sites in Ningbo from November 1, 2014 to October 31, 2015 and were used to analyze 15 priority polycyclic aromatic hydrocarbons (PAHs). Higher benzo[a]pyrene toxic equivalent concentrations were observed in the industrial areas during wintertime. Correspondence analysis (CA) was used to characterize the PAH congener profiles associated with each functional district and their temporal variations. It showed that different PAH composition profiles and seasonal variations were observed in mountain, rural area and residential areas; and different industrial layouts also led to different properties of PAH congener emissions. Higher levels of PAHs were observed around oil refinery in summer and at mountainous areas in winter, which might be attributed to the evaporation of petroleum and the impact of local biomass burning. This study also demonstrated that the factors influencing the representativeness of a site could be more clearly understood using PUF-PAS and CA analysis. © 2019, Springer Science+Business Media, LLC, part of Springer Nature
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