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41.
Armstrong TA Bettoni D Bharadwaj V Biino C Borreani G Broemmelsiek D Buzzo A Calabrese R Ceccucci A Cester R Church M Dalpiaz P Dalpiaz PF Dimitroyannis D Fabbri M Fast J Gianoli A Ginsburg CM Gollwitzer K Govi G Hahn A Hasan M Hsueh S Lewis R Luppi E Macrí M Majewska AM Mandelkern M Marchetto F Marinelli M Marques J Marsh W Martini M Masuzawa M Menichetti E Migliori A Mussa R Palestini S Pallavicini M Passaggio S Pastrone N Patrignani C Peoples J Petrucci F Pia MG Pordes S Rapidis P Ray R 《Physical review D: Particles and fields》1996,54(11):7067-7070
42.
We report a study of the 4 A 2g →2 T 1g absorption band of Mn4+ in Cs2SiF6. The band shows several lines or groups of lines associated with transitions from the 4 A 2g ground state to the spin-orbit components (2 T 1g )Γ8 and (2 T 1g )Γ6 coupled to the three odd-parity vibrations v 6(t 2u ), v 4(t 1u ) and v 3(t 1u ). The absorptions associated with the (2 T 1g )Γ8 electronic state have structure whereas those associated with the (2 T 1g )Γ6 do not. It is shown that the structure is a consequence of splitting of the Γ8 × v vibronic multiplets by electron-vibration interaction. The intensity of the 4 A 2g →(2 T 1g )Γ i + vj vibronic transitions are expressed in terms of a small number of parameters; two parameters for v(t 1u ) modes and three for v(t 2u ) modes. Plausible but not good fits to the low temperature Zeeman data and vibronic splitting patterns are obtained. The excitation spectrum of the Cs2SiF6 : Mn4+ in the region of the 4 A 2g →2 Eg and 4 A 2g →2 T 1g is recorded using a c.w. dye laser. This reveals numerous weaker lines involving combinational modes and even-parity modes v5 (t 2g ), v 2(eg ) and v 1(a 1g ). Several interesting electron-vibrational effects are observed. These are illustrated and discussed qualitatively. 相似文献
43.
Qamrul Hasan Ansari Siegfried Schaible Jen-Chih Yao 《Journal of Global Optimization》2002,22(1-4):3-16
In this paper, we introduce the system of generalized vector equilibrium problems which includes as special cases the system of generalized implicit vector variational inequality problems, the system of generalized vector variational and variational-like inequality problems and the system of vector equilibrium problems. By using a maximal element theorem, we establish existence results for a solution of these systems. As an application, we derive existence results for a solution of a more general Nash equilibrium problem for vector-valued functions. 相似文献
44.
In this study, a more general version of F-expansion method is proposed. With this offered method, more than one Jacobi elliptic functions are located in the solution function. We seek analytical solutions of the space-time fractional cubic Schrodinger equation by use of the new type of F-expansion method. Consequently, multifarious exact analytical solutions consisting of single, double, and multiple combined Jacobi elliptic functions solutions are acquired. 相似文献
45.
46.
Zarife Sibel ahin Fatma Sevindi Hasan budak amil Ik 《Acta Crystallographica. Section C, Structural Chemistry》2010,66(10):m314-m318
The title compounds, trans‐bis(trans‐cyclohexane‐1,2‐diamine)bis(6‐methyl‐2,2,4‐trioxo‐3,4‐dihydro‐1,2,3‐oxathiazin‐3‐ido)copper(II), [Cu(C4H4NO4S)2(C6H14N2)2], (I), and trans‐diaquabis(cyclohexane‐1,2‐diamine)zinc(II) 6‐methyl‐2,2,4‐trioxo‐3,4‐dihydro‐1,2,3‐oxathiazin‐3‐ide dihydrate, [Zn(C6H14N2)2(H2O)2](C4H4NO4S)2·2H2O, (II), are two‐dimensional hydrogen‐bonded supramolecular complexes. In (I), the CuII ion resides on a centre of symmetry in a neutral complex, in a tetragonally distorted octahedral coordination environment comprising four amine N atoms from cyclohexane‐1,2‐diamine ligands and two N atoms of two acesulfamate ligands. Intermolecular N—H...O and C—H...O hydrogen bonds produce R22(12) motif rings which lead to two‐dimensional polymeric networks. In contrast, the ZnII ion in (II) resides on a centre of symmetry in a complex dication with a less distorted octahedral coordination environment comprising four amine N atoms from cyclohexane‐1,2‐diamine ligands and two O atoms from aqua ligands. In (II), an extensive two‐dimensional network of N—H...O, O—H...O and C—H...O hydrogen bonds includes R21(6) and R44(16) motif rings. 相似文献
47.
The title ion–molecule reaction has been proposed to play an important role in interstellar chemistry if it yields acrylonitrile ions CH2CH–CN+. This question was probed by examining the formation of HCCH+ and HCN from low-energy ions CH2CH–CN+ and related isomers, using tandem mass spectrometry based experiments (D and 13C labelling) in conjunction with model chemistry calculations (CBS-QB3/APNO). We conclude that the title reaction is a barrierless multistep rearrangement that may not effectively compete with the straightforward formation of stable distonic ions HCCH–NCH+ from HCCH+(ion)–HCN(dipole) encounter complexes. 相似文献
48.
Dual‐responsive micrometer‐sized core‐shell composite polymer particles were prepared by dispersion polymerization followed by seeded copolymerization. Polystyrene (PS) particles prepared by dispersion polymerization were used as core particles. N‐isopropyl acrylamide (NIPAM) and methacrylic acid (MAA) were used to induce dual‐responsive that is thermo‐ and pH‐responsive properties in the shell layer of composite polymer particles, prepared by seeded copolymerization with PS core particles. Temperature‐ and pH‐dependent adsorption behaviors of some macromolecules on composite polymer particles indicate that produced composite polymer particles exhibit dual‐responsive surface properties. Copyright © 2007 John Wiley & Sons, Ltd. 相似文献
49.
Hasan K Fowler C Kwong P Crane AK Collins JL Kozak CM 《Dalton transactions (Cambridge, England : 2003)》2008,(22):2991-2998
The structures and properties of six new iron(iii) diamine-bis(phenolate) complexes are reported. Reaction of anhydrous FeX(3) salts (where X = Cl or Br) with the diprotonated tripodal tetradentate ligands 2-pyridylamino-N,N-bis(2-methylene-4-methyl-6-tert-butylphenol), H(2)[L(1)], and N,N-dimethyl-N',N'-bis(2-methylene-4-methyl-6-tert-butylphenol)ethylenediamine, H(2)[L(2)], produces the trigonal bipyramidal iron(iii) complexes, [L(1)]FeCl , [L(1)]FeBr , [L(2)]FeCl and [L(2)]FeBr . Reaction of FeX(3) with the related linear tetradentate ligand N,N'-bis(4,6-tert-butyl-2-methylphenol)-N,N'-bismethyl-1,2-diaminoethane, H(2)[L(3)], generates square pyramidal iron(iii) complexes, [L(3)]FeCl and [L(3)]FeBr . Complexes have been characterized using electronic absorption spectroscopy and magnetometry. Single crystal X-ray molecular structures have been determined for complexes 1, 3, 5 and 6. 相似文献
50.
In recent years there has been an increase in use of botanicals with antioxidant properties as skin photoprotective agents. Pomegranate (Punica granatum L.) fruit possesses strong antioxidant and antiinflammatory properties. Recently, we have shown that pomegranate-derived products rich in anthocyanidins and ellagitannins inhibit UVB-mediated activation of nuclear factor kappa B and modulate UVA-mediated cell proliferation pathways in normal human epidermal keratinocytes. In this study, we evaluated the effect of polyphenol-rich pomegranate fruit extract (POMx) on UVB-induced oxidative stress and photoaging in human immortalized HaCaT keratinocytes. Our data show that pretreatment of HaCaT cells with POMx (10-40 microg mL(-1)) inhibited UVB (15-30 mJ cm(-2))-mediated (1) decrease in cell viability, (2) decrease in intracellular glutathione content and (3) increase in lipid peroxidation. Employing immunoblot analysis we found that pretreatment of HaCaT cells with POMx inhibited UVB-induced (1) upregulation of MMP-1, -2, -7 and -9, (2) decrease in TIMP-1, (3) phosphorylation of MAPKs and (iv) phosphorylation of c-jun, whereas no effect was observed on UVB-induced c-fos protein levels. These results suggest that POMx protects HaCaT cells against UVB-induced oxidative stress and markers of photoaging and could be a useful supplement in skin care products. 相似文献