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Träfflista för sökning "WFRF:(Jiang Minhua) "

Sökning: WFRF:(Jiang Minhua)

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1.
  • Hao, Fuying, et al. (författare)
  • Design, crystal structures and enhanced frequency-upconverted lasing efficiencies of a new series of dyes from hybrid of inorganic polymers and organic chromophores
  • 2009
  • Ingår i: Journal of Materials Chemistry. - : RSC Publishing. - 0959-9428 .- 1364-5501. ; 19:48, s. 9163-9169
  • Tidskriftsartikel (refereegranskat)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.
  • Li, Shengli, et al. (författare)
  • Formation of a Novel Polymeric Cadmium(II) Complex Bridged by Sulfur and Thiocyanato Ions
  • 2003
  • Ingår i: Chemistry Letters. - : Chemical Society of Japan. - 0366-7022 .- 1348-0715. ; 32:8, s. 748-749
  • Tidskriftsartikel (refereegranskat)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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3.
  • Tian, Yu-peng, et al. (författare)
  • Synthesis, crystal structure and NLO properties of a novel ruthenium(II) complex with unusual coordination mode
  • 2005
  • Ingår i: Transition metal chemistry (Weinheim). - : Kluwer Academic Publishers. - 0340-4285 .- 1572-901X. ; 30:7, s. 778-785
  • Tidskriftsartikel (refereegranskat)abstract
    • A new Schiff base 4-[N-hydroxyethyl-N-(methyl)amino]benzaldehyde S-methyl dithiocarbazate (HL, where H is a dissociable proton) and the ruthenium complex [Ru(bpy)2L]PF6 (bpy = 2,2′-bipyridine) have been synthesized. The structural determinations of the ligand and its ruthenium complex, by X-ray crystallography, show that the ligand is coordinated as a monoanionic bidentate N, S-donor, forming a four-member chelate ring with a bite angle of 65.91°. The complex shows intense MLCT transitions in the visible region. Fluorescent and electrochemical properties have been also studied. The complex in DMF solution exhibited a strong two-photon absorption (t.p.a.) at 532 nm nanosecond laser pulses. The t.p.a. coefficient β, t.p.a. cross-section σ and the third-order optical nonlinearity χ(3) of the complex and the ligand have been determined by the Z-scan technique.
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4.
  • Tian, Yupeng, et al. (författare)
  • Structural diversity and properties of a series of dinuclear and mononuclear copper(II) and copper(I) carboxylato complexes
  • 2002
  • Ingår i: New Journal of Chemistry. - : RSC Publishing. - 1144-0546 .- 1369-9261. ; 26:10, s. 1468-1473
  • Tidskriftsartikel (refereegranskat)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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5.
  • Tian, Yupeng, et al. (författare)
  • Two novel two-photon polymerization initiators with extensive application prospects
  • 2004
  • Ingår i: Chemical Physics Letters. - : Elsevier. - 0009-2614 .- 1873-4448. ; 388:4-6, s. 325-329
  • Tidskriftsartikel (refereegranskat)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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6.
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7.
  • Xue, Zhaoming, et al. (författare)
  • Synthesis, Crystal Structure and Nonlinear Optical Properties of Nickel(Ⅱ) Complex with Schiff-base Ligand
  • 2003
  • Ingår i: Chinese journal of structural chemistry. - 0254-5861. ; 22:3, s. 265-269
  • Tidskriftsartikel (refereegranskat)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. (författare)
  • Synthesis, crystal structure and two-photon property studies on a series of complexes derived from a novel Schiff base ligand
  • 2004
  • Ingår i: Transition metal chemistry (Weinheim). - : Kluwer Academic Publishers. - 0340-4285 .- 1572-901X. ; 29:6, s. 596-602
  • Tidskriftsartikel (refereegranskat)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. (författare)
  • Formation of A Novel 1D Supramolecule [HgCl2(ptz)]2·HgCl2 (ptz = Phenothiazine) : A New Precursor to Submicrometer Hg2Cl2 Rods
  • 2003
  • Ingår i: Inorganic Chemistry. - : American Chemical Society (ACS). - 0020-1669 .- 1520-510X. ; 42:12, s. 3734-3737
  • Tidskriftsartikel (refereegranskat)abstract
    • A novel supramolecule [HgCl2(ptz)]2·HgCl2 (ptz = phenothiazine) with uncoordinated inorganic salt HgCl2 presented in a 1D chain was first prepared and then successfully applied as a new precursor in the preparation of submicrometer Hg2Cl2 rods. Single crystal X-ray analysis showed that the 1D chain structure is stabilized by hydrogen bonds between adjacent chains and the coordination mode of the ligand phenothiazine is unusual with large steric inhibition other than the chain directions. The results revealed that the particular chain structure plays a significant role in the formation of the Hg2Cl2 rods.
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10.
  • Zhang, Xuanjun, et al. (författare)
  • Self-assembly of Organic Chromophore with Cd-S Nanoclusters: Supramolecular Structures and Enhanced Emissions
  • 2005
  • Ingår i: Crystal Growth & Design. - : American Chemical Society (ACS). - 1528-7483 .- 1528-7505. ; 5:2, s. 565-570
  • Tidskriftsartikel (refereegranskat)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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