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Träfflista för sökning "WFRF:(Shi X.) srt2:(2000-2004)"

Sökning: WFRF:(Shi X.) > (2000-2004)

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1.
  • Zhang, Shi-Li, et al. (författare)
  • Abnormal anti-Stokes Raman scattering of carbon nanotubes
  • 2002
  • Ingår i: Physical Review B. Condensed Matter and Materials Physics. - 1098-0121 .- 1550-235X. ; 66:3
  • Tidskriftsartikel (refereegranskat)abstract
    • Abnormal anti-Stokes Raman scattering (AASR) was unambiguously observed in carbon nanotubes (CNT's). In contrast to traditional Raman scattering theory, the absolute value of the Raman frequency of the anti-Stokes peak is not the same as that of the corresponding Stokes peak. It was demonstrated that AASR scattering originates from the unique nanoscale cylindrical structure of CNT's that can be considered naturally as a graphite structure with an intrinsic defect from its rolling. The double-resonance Raman scattering theory was applied to interpret the scattering mechanism of the AASR phenomenon successfully and quantitatively.
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2.
  • Li, H. Y., et al. (författare)
  • Properties of a dinuclear Mn(III,III) complex with a tri-phenolate ligand N4O3 (3-) and a new complex containing a ligand covalently linked to ruthenium tris-bipyridine
  • 2004
  • Ingår i: Huaxue xuebao. - 0567-7351. ; 62:9, s. 916-922
  • Tidskriftsartikel (refereegranskat)abstract
    • A new high valent complex [Mn-2(III, III)L(mu-OAc)(2)].PF6 (2a) was prepared, where L was the trianion of 2, 6-bis {[(2-hydroxy-5-tert-butylbenzyl) (pyridyl-2-methyl)-amino]-methyl}-4-methylphenol, which contains two additional phenolate groups and two tert-butyl groups compared to its parent [Mn-2(II, II)(bpmp)(mu-OAc)(2)].ClO4 (1). These improvements narrowed the disparity between the new model and (Mn)(4) cluster (OEC in nature). Moreover, L was modified to be covalently linked with Ru(II) tris-bipyridine through an amide bond to construct a complex 2b for the study of photoinduced electron transfer (PET). UV-vis, IR, emission spectra and electrochemistry were used to investigate their photochemistry properties. The results showed that 2b has good photochemistry properties and the E-1/2 of Ru3+/Ru2+ was higher than those of phenol(+)/phenol and Mn(III, IV)/Mn(III, III). After coordination of manganese ions, the electron transfer process in the model complex conforms to the basic principles of electron donor side of photosystem II (PS II) in nature.
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4.
  • Shi, F., et al. (författare)
  • Synthesis and properties of a new donor model compound for PSII
  • 2004
  • Ingår i: Gaodeng xuéxiào huàxué xuébào. - 0251-0790. ; 25:9, s. 1666-1672
  • Tidskriftsartikel (refereegranskat)abstract
    • As a model compound for redox components on the donor side of photosystem II (PS II) in green plants, a supramolecular complex 2 was synthesized and characterized. In this complex, two {[(2-hydroxy-3-(morpholin-4-ylmethyl)-5-tert-butyl-benzyl)(pyridyl-2-methyl)amino]methyl} arms are linked to the ortho-positions of a phenol which is expected covalently to be linked to Ru(II) tris-bipyridine through an amide bond. The arms on the substituted-phenol can coordinate two Mn(III) ions. The structure of complex 2 was confirmed by electrospray ionization mass spectrometry (ESI-MS) and 2D-NMR (gCOSY, HSQC and HMBC). Its photochemical and electrochemical properties were studied. The results showed that the MLCT band of the compound was red-shifted compared to that of [Ru(byp)(3)](2+) and the luminescence quantum yield was enhanced. In addition, the oxidation potential of ruthenium was higher than the phenol(+)/phenol and Mn(III, IV)/Mn(III) which was consisted with the electron transfer sequence of the donor side of PS II in nature. All these showed that this compound was a good model to mimic the donor side of PS II.
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5.
  • Shi, F., et al. (författare)
  • Synthesis and spectral properties of a new ruthenium(II) tris-bipyridine with four ester groups and substituted phenol
  • 2004
  • Ingår i: Huaxue xuebao. - 0567-7351. ; 62:7, s. 713-719
  • Tidskriftsartikel (refereegranskat)abstract
    • A new ruthenium(II) complex (1) with four ester groups have been designed and synthesized, in which a phenol substituted by {[(2-hydroxy-3-(morpholin-4-ylmethyl)-5-tent-butylbenzyl) (pyridyl-2-methyl) amino]methyl} groups was covalently linked to ruthenium (II) tris-bipyridine. The structure of complex 1 was characterized by electrospray ionization mass spectrometer (ESI-MS) and 1D-NMR, 2D-NMR (gCOSY, HSQC and HMBC) spectra. The electrochemical and spectral properties were also studied. Introduction of the four carboxyl acid groups and the donor ligand tuned the spectra and the redox properties of compound 1. The MLCT transition was turned from 451 to 474 nm and the complex had long lifetime of the (MLCT)-M-3 state emission. Moreover, the oxidation potential of Ru3+/Ru2 + of compound 1 was similar to 360 mV higher than that of [Ru(bpy)(3)](2+) which would enhance the driving-force of electron transfer. These results showed that the compound 1 had proper redox potentials and was suitable for being used as photosensitizer of solar cell.
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6.
  • Zhang, L., et al. (författare)
  • Effects of intense laser irradiation on Raman intensity features of carbon nanotubes
  • 2002
  • Ingår i: Physical Review B. Condensed Matter and Materials Physics. - 1098-0121 .- 1550-235X. ; 65:7
  • Tidskriftsartikel (refereegranskat)abstract
    • The effect of intense laser irradiation on the features of Raman intensity of carbon nanotubes (CNT's) has been examined. The intensity of the D band decreases and the relative intensity between the G peaks changes with increasing laser power density (LPD) and remain unchanged with subsequent decrease in LPD. This behavior is different from the reversible variation of the G band frequency in the same process of power increase and subsequent decrease. It has been demonstrated that such irreversible change in intensity features originates from sample purification. This result suggests a simple and fast CNT purification method using intense laser irradiation.
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7.
  • Cooper, K., et al. (författare)
  • New Grid Scheduling and Rescheduling Methods in the GrADS Project
  • 2004
  • Konferensbidrag (refereegranskat)abstract
    • Summary form only given. The goal of the Grid Application Development Software (GrADS) project is to provide programming tools and an execution environment to ease program development for the grid. We present recent extensions to the GrADS software framework: 1. A new approach to scheduling workflow computations, applied to a 3D image reconstruction application; 2. A simple stop/migrate/restart approach to rescheduling grid applications, applied to a QR 3. A process-swapping approach to rescheduling, applied to an N-body simulation. Experiments validating these methods were carried out on both the GrADS MacroGrid (a small but functional grid) and the MicroGrid (a controlled emulation of the grid) and the results were demonstrated at the SC2003 conference.
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8.
  • Ma, P. X., et al. (författare)
  • An analytical model for space-charge region capacitance based on practical doping profiles under any bias conditions
  • 2001
  • Ingår i: Solid-State Electronics. - 0038-1101 .- 1879-2405. ; 45:1, s. 159-167
  • Tidskriftsartikel (refereegranskat)abstract
    • An analytical model is presented For quasi-static capacitance of the space-charge region in a p-n junction. The model is valid for realistic junction doping profiles under any bias conditions. It consists of local models in three bias regions. For the high-reverse bias region, a novel analytical model is derived. For the moderate-bias region, an empirical model commonly used in SPICE is adopted. Finally, for the high-forward bias region, the junction profiles are approximated by linearly-graded junctions. Existing analytical models are then modified appropriately to characterize both high-injection and heavy-doping effects for advanced bipolar transistors. Compared to previously developed analytical models or existing empirical models, as well as numerical simulation results, the analytical model presented here shows an improved accuracy and therefore provides a better tool For both device and circuit simulations.
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9.
  • Shi, L X, et al. (författare)
  • The low molecular mass PsbW protein is involved in the stabilization of the dimeric photosystem II complex in Arabidopsis thaliana
  • 2000
  • Ingår i: Journal of Biological Chemistry. - 0021-9258 .- 1083-351X. ; 275:48, s. 37945-37950
  • Tidskriftsartikel (refereegranskat)abstract
    • Arabidopsis thaliana plants have been transformed with an antisense gene to the psbW of photosystem II (PSII). Eight transgenic lines containing low levels of psbW mRNA have been obtained. Transgenic seedlings with low contents of PsbW protein (more than 96% reduced) were selected by Western blotting and used for photosynthetic functional studies. There were no distinct differences in phenotype between the antisense and wild type plants during vegetative period under normal growth light intensities. However, a sucrose gradient separation of briefly solubilized thylakoid membranes revealed that no dimeric PSII supracomplex could be detected in the transgenic plants lacking the PsbW protein. Furthermore, analysis of isolated thylakoids demonstrated that the oxygen-evolving rate in antisense plants decreased by 50% compared with the wild type, This was found to be due to up to 40% of D1 and D2 reaction center proteins of PSII disappearing in the transgenic plants. The absence of the PsbW protein also altered the contents of other PSII proteins to differing extents. These results show that in the absence of the PsbW protein, the stability of the dimeric PSII is diminished and consequently the total number of PSII complexes is greatly reduced. Thus the nuclear encoded PsbW protein may play a crucial role in the biogenesis and regulation of the photosynthetic apparatus.
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