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Träfflista för sökning "WFRF:(Jiang Jieying) "

Search: WFRF:(Jiang Jieying)

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1.
  • Hao, Fuying, et al. (author)
  • Design, crystal structures and enhanced frequency-upconverted lasing efficiencies of a new series of dyes from hybrid of inorganic polymers and organic chromophores
  • 2009
  • In: Journal of Materials Chemistry. - : RSC Publishing. - 0959-9428 .- 1364-5501. ; 19:48, s. 9163-9169
  • Journal article (peer-reviewed)abstract
    • A new series of hybrid dyes, trans-4-(4′-N,N-dialkylaminostyryl)-N-methyl pyridinium [Cd(SCN)3−]n [alkyl = Me(1), Et(2), Pr(3) and n–Bu(4)] have been successfully synthesized from hybrids of inorganic polymers and organic chromophores. The structures of four new hybrid dyes were characterized by single-crystal X-ray diffraction first. The particular features of the hybrid dyes are (1) the inorganic anions form isolated polymeric one-dimensional zig-zag chains of [Cd(SCN)3−]n with an extended π-conjugation system within the polymeric –[M–S–C≡N]–M… chain and high polarizabilities; and (2) the organic cationic chromophores determine their optical properties. Experimental results revealed that the TPA cross-section values and overall energy conversion efficiencies of hybrid dyes with different alkyl pendant groups have obviously increased from 1 to 4, and in particular, have been substantially enhanced compared to their corresponding iodide analogues 1′–4′. Therefore, we speculate that such increases are attributable to arrangements of infinite anionic [Cd(SCN)3−]n chains and synergic effects with chromophore cations.
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2.
  • Jiang, Jieying, et al. (author)
  • Association of genetic variations in aromatase gene with serum estrogen and estrogen/testosterone ratio in Chinese elderly men.
  • 2010
  • In: Clinica chimica acta. - : Elsevier BV. - 1873-3492 .- 0009-8981. ; 411:1-2, s. 53-8
  • Journal article (peer-reviewed)abstract
    • BACKGROUND: Single nucleotide polymorphism (SNP) rs2470152 of the gene CYP19A1 is associated with serum estradiol (E2) levels in Caucasian men. However, it remains to be verified if rs2470152 is the sole determinant accounting for the association. We determined whether 2 CYP19A1 SNPs tagging different haploblocks (rs2470152 and rs2899470) are associated with sex steroid levels in Chinese men. METHOD: Serum sex steroid level including E2, estrone (E1) and testosterone (T), of 1402 Chinese men aged > or = 65 years were analyzed. Genotyping of the two CYP19A1 SNPs was performed using Tm-shift allele-specific PCR. RESULTS: SNP rs2899470 was significantly associated with serum E2, E1 levels and E2/T ratio (p<0.001). However, SNP rs2470152 was only modestly associated with E2/T ratio (p=0.023). Analysis of haplotype showed a significant association between C-G, T-T haplotype with serum E2/T ratio (p=0.019 and p=1 x 10(-5), respectively). Similarly, E2 levels was also associated the T-T and T-G haplotypes (p=1 x 10(-5)). CONCLUSION: The genetic variation of CYP19A1 was associated with circulating estrogen levels in Chinese elderly men. In addition, it revealed that haplotype of rs2899470 and rs2470152, rather than rs2899470 alone, was a better indicator for the serum E2/T ratio and E2 levels.
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3.
  • Jiang, Jieying, et al. (author)
  • Association of SRD5A2 variants and serum androstane-3alpha,17beta-diol glucuronide concentration in Chinese elderly men.
  • 2010
  • In: Clinical chemistry. - : Oxford University Press (OUP). - 1530-8561 .- 0009-9147. ; 56:11, s. 1742-9
  • Journal article (peer-reviewed)abstract
    • Results of recent studies have demonstrated that genetic variants of the enzyme steroid 5α reductase type II (SRD5A2) are associated with serum concentrations of major androgen metabolites such as conjugates of androstane-3α,17β-diol-glucuronide (3α-diol-G). However, this association was not consistently found among different ethnic groups. Thus, we aimed to determine whether the association with SRD5A2 genetic variations exists in a cohort of healthy Chinese elderly men, by examining 2 metabolite conjugates: androstane-3α,l7β-diol-3-glucuronide (3α-diol-3G) and androstane-3α,17β-diol-17-glucuronide (3α-diol-17G).
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4.
  • Li, Shengli, et al. (author)
  • Formation of a Novel Polymeric Cadmium(II) Complex Bridged by Sulfur and Thiocyanato Ions
  • 2003
  • In: Chemistry Letters. - : Chemical Society of Japan. - 0366-7022 .- 1348-0715. ; 32:8, s. 748-749
  • Journal article (peer-reviewed)abstract
    • The title complex, {[N(CH3)4]2[Cd(SCN)2S]}n, was prepared by self-assembling from the reaction of a methanol/water (volume ratio, 1/1) solution containing cadmium(II) thiocyanate with equivalent amount of tetramethylammonium thiocyanate. The result of single X-ray determination for the complex reveals that a novel polymeric cadmium(II) complex bridged by sulfur and thiocyanato ions was obtained, which formed a two-dimensional (2D) structure.
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5.
  • Tian, Yupeng, et al. (author)
  • Structural diversity and properties of a series of dinuclear and mononuclear copper(II) and copper(I) carboxylato complexes
  • 2002
  • In: New Journal of Chemistry. - : RSC Publishing. - 1144-0546 .- 1369-9261. ; 26:10, s. 1468-1473
  • Journal article (peer-reviewed)abstract
    • The syntheses, crystal structures, magnetic and photoluminescence properties of a series of dinuclear and mononuclear copper(II) and copper(I)N-carbazolylacetate [N-carbazolylacetic acid=Hcabo] with different carboxylato coordination modes are reported. Although the carboxylato group has different coordination modes, the same carboxylate ligand binding to copper ion via four coordinating modes is rare. The crystal structure of complex [Cu2(Cabo)4(dmf)2]·2dmf (1) consists of a symmetrical dimeric Cu(II) carboxylato paddle-wheel core and oxygen atoms from dmf at the apical positions. The dinuclear complex [Cu2(Cabo)3(phen)2]ClO4·H2O·C2H5OH (2) (phen=1,10-phenanthroline) consists of an unusual dimeric core with two copper atoms bridged by three carboxylates one of which is in the η∶η∶μ2 bridging mode and the other two are in the rarer monoatomic bridging mode. To our knowledge, the present bridging mode has not been reported hitherto. Magnetic susceptibilities were measured in the temperature range 2–300 K. It is found that paddle-wheel copper(II) ions in 1 are strongly coupled antiferromagnetically with 2J=−356.4(6) cm−1, whereas complex 2 shows weak antiferromagnetic interaction with a 2J value of −12.8(4) cm−1. Copper(I)N-carbazolylacetate with strong fluorescence in the solid state as well as high thermal stability was obtained by reduction of the copper(II)N-carbazolylacetate using PPh3(triphenylphosphine) in dmf solution.
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6.
  • Tian, Yupeng, et al. (author)
  • Two novel two-photon polymerization initiators with extensive application prospects
  • 2004
  • In: Chemical Physics Letters. - : Elsevier. - 0009-2614 .- 1873-4448. ; 388:4-6, s. 325-329
  • Journal article (peer-reviewed)abstract
    • Two novel two-photon polymerization initiators, 10-ethyl-3-E-(4-(N,N′-di-n-butylamino)styryl)phenothiazine 5 and 10-ethyl-3,7-E,E-bis(4-(N,N′-di-n-butyl amino)styryl)phenothiazine 6, have been efficiently synthesized with room temperature solid phase Wittig reaction. Two initiators were found to exhibit good single-photon fluorescence emission and their quantum yields, lifetimes and solvent effects have been studied in detail. Two-photon fluorescence spectra were investigated under 800 nm fs laser pulse and two-photon absorption (TPA) cross-sections of the initiators have been evaluated by theoretical calculation.Two-photon initiating polymerization microfabrication experiments have been carried out and artificial defects were made and polymerization mechanism was also discussed.
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7.
  • Xue, Zhaoming, et al. (author)
  • Synthesis, Crystal Structure and Nonlinear Optical Properties of Nickel(Ⅱ) Complex with Schiff-base Ligand
  • 2003
  • In: Chinese journal of structural chemistry. - 0254-5861. ; 22:3, s. 265-269
  • Journal article (peer-reviewed)abstract
    • The nickel(Ⅱ) complex with the new ligand of S-benzyl-β-N-[10-ethylphenothiazine-3-methylene]dithiocarbazate(HL) crystallizes in the triclinic system, space group P1-with a = 7.516(1), b = 11.322(1), c = 13.366(1) (A),α= 84.818(1),β= 81.688(1), y= 76.037(1)°, V= 1090.26(3) (A)3, Z = 1, Dc=1.413 g/cm3, F(000) = 482,μ(MoKα)= 0.774 mm-1 (λ= 0.7103(A)),R = 0.0573 and wR =0.1375 for 3357 observed reflections withⅠ≥ 2σ(Ⅰ). The HL has lost a proton from its tautomeric thiol form and acts as a single negatively charged bidentate ligand coordinating to the nickel ion via the mercapto sulfur and β-nitrogen atoms. The geometry around Ni(Ⅱ) is almost square-planar with two equivalent Ni-N and Ni-S bonds. The nonlinear absorption of HL and NiL2 solutions (in DMF) was measured by open-aperture Z-scan technique at the wavelength of 532 nm.
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8.
  • Zhang, Mingliang, et al. (author)
  • Synthesis, crystal structure and two-photon property studies on a series of complexes derived from a novel Schiff base ligand
  • 2004
  • In: Transition metal chemistry (Weinheim). - : Kluwer Academic Publishers. - 0340-4285 .- 1572-901X. ; 29:6, s. 596-602
  • Journal article (peer-reviewed)abstract
    • A new Schiff base ligand derived from S-benzyldithiocarbazate and 4-[N-hydroxy ethyl-N-(methyl)amino]benzaldehyde (HL, where H is a dissociable proton) and its NiII, CuII, ZnII and PdII complexes were prepared and fully characterized. The structures of HL and Ni(L)2 were determined by X-ray diffraction analysis, which revealed that the geometry of the NiII ion is square-planar with two equivalent Ni=N and Ni=S bonds, and that the two neighboring molecules in two layers have weak contact. The electronic spectra and solution fluorescence of the ligand and the complexes were studied, and the quantum yields of single-photon fluorescence for the compounds were determined. The compounds possess two-photon absorption (t.p.a.) character and the t.p.a. coefficient β and t.p.a. cross-section σ were determined by the Z-scan technique. Especially, the Zn(L)2complex and the HL ligand exhibit intensive two-photon fluorescence (t.p.f.) at 800 nm laser pulses in the femtosecond regime.
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9.
  • Zhang, Xuanjun, et al. (author)
  • Self-assembly of Organic Chromophore with Cd-S Nanoclusters: Supramolecular Structures and Enhanced Emissions
  • 2005
  • In: Crystal Growth & Design. - : American Chemical Society (ACS). - 1528-7483 .- 1528-7505. ; 5:2, s. 565-570
  • Journal article (peer-reviewed)abstract
    • By combination of the large organic cation [trans-4-(4-dimethylanilino-styryl)-N-methyl-pyridinium with nanocluster anions ([Cd4(SC6H5)10]2- for compound 1 and [Cd4(SC6H5)6I4]2- for compound 2), two new hybrids were obtained and the structure of the [Cd4(SC6H5)6I4]2- cluster was first characterized by single-crystal X-ray diffraction. A novel supramolecular dimer {[Cd4(SC6H5)10]2-}2, connected via strong π−π interactions, was observed in 1, whereas every two [Cd4(SC6H5)6I4]2- clusters in 2 were linked by multiple C−H···I hydrogen bonds forming dimers, which, as building blocks, were further connected to each other via C−H···I hydrogen bonds and weak I···I interactions to form novel 1D helical chains. The UV−visible−near-IR spectra, one-photon excited photoluminescence, and two-photon pumped lasing were measured. The organic chromophore exhibits enhanced PL and two-photon pumped lasing in the two hybrids
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10.
  • Zhang, Xuanjun, et al. (author)
  • Two strong emitting coordination polymers with chain and ladder structures
  • 2003
  • In: Transition metal chemistry (Weinheim). - Netherlands : Kluwer Academic Publishers. - 0340-4285 .- 1572-901X. ; 28:6, s. 707-711
  • Journal article (peer-reviewed)abstract
    • Two coordination polymers [Zn(Cabo)2(EtOH)2(4,4′-Bipy)]n(1), and [Zn2(Cabo)2(NO3)2(4,4′-Bipy)2]n(2) (Cabo = carbazolylacetate, 4,4′-Bipy = 4,4′-bipyridine) with chain and ladder structures, respectively, were prepared and characterized by X-ray single-crystal structural analysis. The results showed that the different anions of metal salts have a large effect on the construction of coordination frameworks. Both complexes show strong emissions in the solid state as well as high thermal stability.
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