| 1. |
- Ablikim, M., et al.
(författare)
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Measurements of (XcJ)-> K+K-K+K- decays
- 2006
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Ingår i: Physics Letters B. - : Elsevier BV. - 0370-2693 .- 1873-2445. ; 642:3, s. 197-202
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Tidskriftsartikel (refereegranskat)abstract
- Using 14M psi(2S) events taken with the BESII detector, chi(cJ) -> 2(K+K-) decays are studied. For the four-kaon final state, the branching fractions are B(chi(c0,1,2) ->.2(K+K-)) = (3.48 +/- 0.23 +/- 0.47) x 10(-3), (0.70 +/- 0.13 +/- 0.10) x 10(-3), and (2.17 +/- 0.20 +/- 0.31) x 10(-3). For the phi K+K- final state, the branching fractions, which are measured for the first time, are B(chi(c0,1,2) -> phi K+K-) = (1.03 +/- 0.22 +/- 0.15) x 10(-3), (0.46 +/- 0.16 +/- 0.06) x 10(-3), and (1.67 +/- 0.26 +/- 0.24) x 10(-4). For the phi phi final state, B(chi(c0,2) -> phi phi) = (0.94 +/- 0.21 +/- 0.13) x 10(-3) and (1.70 +/- 0.30 +/- 0.25) x 10(-3).
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| 2. |
- Yu, G., et al.
(författare)
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Structures, electronic states, photoluminescence, and carrier transport properties of 1,1-disubstituted 2,3,4,5-tetraphenylsiloles
- 2005
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Ingår i: Journal of the American Chemical Society. - : American Chemical Society (ACS). - 0002-7863 .- 1520-5126. ; 127:17, s. 6335-6346
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Forskningsöversikt (refereegranskat)abstract
- The excellent electroluminescent (EL) properties of 1,1-disubstituted 2,3,4,5-tetraphenylsiloles, 1-methyl-1,2,3,4,5-pentaphenylsilole (MPPS), and 1,1,2,3,4,5-hexaphenylsilole (HPS) have been found. Despite some studies devoted to these materials, very little is known about the real origin of their unique EL properties. Therefore, we investigated the structures, photoluminescence (PL), and charge carrier transport properties of 1,1-disubstituted 2,3,4,5-tetraphenylsiloles as well as the effect of substituents on these characteristics. The single crystals of the three siloles involving 1,1-dimethyl-2,3,4,5-tetraphenylsilole (DMTPS), MPPS, and HIPS were grown and their crystal structures were determined by X-ray diffraction. Three siloles have nonplanar molecular structures. The substituents at 1,1-positions enhance the steric hindrance and have predominant influence on the twisted degree of phenyl groups at ring carbons. This nonplanar structure reduces the intermolecular interaction and the likelihood of excimer formation, and increases PL efficiency in the solid state. The silole films show high fluorescence quantum yields (75-85%), whereas their dilute solutions exhibit a faint emission. The electronic structures of the three siloles were investigated using quantum chemical calculations. The highest occupied molecular orbitals (HOMOs) and the lowest unoccupied molecular orbitals (LUMOs) are mainly localized on the silole ring and two phenyl groups at 2,5-positions in all cases, while the LUMOs have a significant orbital density at two exocyclic Si-C bonds. The extremely theoretical studies of luminescent properties were carried out. We calculated the nonradiative decay rate of the first excited state as well as the radiative one. It is found that the faint emission of DMTPS in solutions mainly results from the huge nonradiative decay rate. In solid states, molecular packing can remarkably restrict the intramolecular rotation of the peripheral side phenyl ring, which has a large contribution to the nonradiative transition process. This explains why the 1,1-disubstituted 2,3,4,5-tetraphenylsiloles in the thin films exhibit high fluorescence quantum yields. The charge carrier mobilities of the MPPS and HPS films were measured using a transient EL technique. We obtained a mobility of 2.1 x 10(-6) cm(2)/V(.)s in the MPPS film at an electric field of 1.2 x 10(6) V/cm. This mobility is comparable to that of Alq(3), which is one of the most extensively used electron transport materials in organic light-emitting diodes (LEDs), at the same electric field. The electron mobility of the HPS film is about similar to 1.5 times higher than that of the MPPS film. To the best of our knowledge, this kind of material is one of the most excellent emissive materials that possess both high charge carrier mobility and high PL efficiency in the solid states simultaneously. The excellent EL performances of MPPS and HPS are presumably ascribed to these characteristics.
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| 3. |
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| 4. |
- Liu, X., et al.
(författare)
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Synthesis, characterization and some properties of amide-linked porphyrin-ruthenium(II) tris(bipyridine) complexes
- 2005
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Ingår i: Tetrahedron. - : Elsevier BV. - 0040-4020 .- 1464-5416. ; 61:23, s. 5655-5662
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Tidskriftsartikel (refereegranskat)abstract
- A new molecular dyad, comprised of a zinc-porphyrin and a ruthenium(II) tris(bipyridine) complex linked through an amide bond has been synthesized and characterized by H-1, C-13 NMR, UV-vis, mass-spectrometry and elemental analysis. The electrochemistry as well as the steady-state emission properties were investigated. The redox behavior of the dyad exhibits a favorable reversible characteristic. Substantial quenching of porphyrin emission was found when the Q hand of 5 and 5-Zn was selectively photoexcited. This observation suggests a quenching mechanism with possible intramolecular electron transfer or energy transfer between the Ru(bpy)(3) moiety and the porphyrin free-base or Zn porphyrin moieties.
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| 5. |
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| 6. |
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| 7. |
- Shi, F., et al.
(författare)
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Synthesis and characterization of two novel high valent dinuclear complexes with a triphenolate ligand bearing functional groups
- 2005
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Ingår i: Chinese Chemical Letters. - 1001-8417 .- 1878-5964. ; 16:1, s. 89-92
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Tidskriftsartikel (refereegranskat)abstract
- Two novel high valent complexes [M-2(III, III)L(mu-OAc)(2)](PF6)-P-. (M=Mn, Fe; 9) were prepared, where L was the tri-anion of 2,6-bis{[(2-hydroxy-3-(morpholin-4-yl methyl)-5-tertbutyl benzyl)(pyridyl-2-methyl)amino]methyl}-4-methyl phenol which contained additional phenolic, tert-butyl and morpholin-4-yl methyl groups compared to its parent [Mn-2(II, II)(bpmp) (mu-OAc)(2)](CIO4)-C-. (10). These improvements decreased the difference between the new model and (Mn)(4) cluster (OEC in nature).
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| 8. |
- Sun, S. G., et al.
(författare)
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Studies of a series of novel rhenium(I) bipyridyl dyes for solar cells
- 2005
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Ingår i: Chinese Chemical Letters. - 1001-8417 .- 1878-5964. ; 16:5, s. 677-680
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Tidskriftsartikel (refereegranskat)abstract
- A series of novel rhenium(I) 2,2'-bipyridyl complexes [fac-Re(4,4'-di-COOEt-bpy)-(CO)(3)(Xpy)PF6], where bpy is 2,2'-bipyridine, py is pyridine and X is 3-methyl, 3-hydroxy, or 3-amino, were synthesized, their photophysical and electrochemical properties were studied. The Re(II/I) oxidation potentials decreased as the X group becomes more electron donating from H to 3-methyl, 3-hydroxy, or 3-amino, which might be a very convenient ways for adjusting the electron transfer driving force.
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| 9. |
- Wang, Y.-D., et al.
(författare)
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Grain-to-grain stress interactions in an electrodeposited iron coating
- 2005
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Ingår i: Advanced Materials. - : Wiley. - 0935-9648 .- 1521-4095. ; 17:10, s. 1221-1226
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Tidskriftsartikel (refereegranskat)abstract
- The distribution of residual stresses, in an iron electrolytic coating with the thickness of 1 mm, was discussed. It was found that the coating minimizes the influence of crystallographic texture and stress gradients. Scanning electron microscopy observations indicate that some cracks are produced in the direct current deposited layer. The results show that the grain size in the electrolytic coating observed by transmission electron microscopy is around 20 nm with an aspect ratio of 5:1
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| 10. |
- Yin, S., et al.
(författare)
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Aggregation-enhanced luminescence and vibronic coupling of silole molecules from first principles
- 2006
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Ingår i: Physical Review B Condensed Matter. - 0163-1829 .- 1095-3795. ; 73:20, s. 205409-
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Tidskriftsartikel (refereegranskat)abstract
- Aggregate formation in molecular solids usually quenches the luminescence, a piece of bad news for molecular electronic devices. However, siloles present extremely high luminescent efficiency in solid state as well as in aggregation, but have almost no luminescence in solution. By employing a first-principles calculation to study excited states and vibronic couplings, we find that it is the low-frequency twisting motions of side rings which enhance the nonradiative decay. These motions can be suppressed either by solid-state packing, by aggregation formation in polar solvents, or by increasing the solvent viscosity; thereby, the radiative decay becomes dominant, resulting in peculiar aggregate-induced emission phenomena in siloles.
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