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101.
The reaction of [ReOCl3(PPh3)2] with 5,6-diphenyl-3-(2-pyridyl)-1,2,4-trazine (dppt) has been examined and [ReCl3(OPPh3)(dppt)] has been obtained. The triphenylphosphine oxide can be easily replaced by PPh3 in the reaction of [ReCl3(OPPh3)(dppt)] with an excess of triphenylphosphine. The [ReCl3(OPPh3)(dppt)] and [ReCl3(PPh3)(dppt)] complexes have been structurally and spectroscopically characterized. Their molecular orbital diagrams have been calculated with the density functional theory (DFT) method, and their electronic spectra have been discussed on the basis of time-dependent DFT calculations. The compound [ReCl3(OPPh3)(dppt)] has been studied additionally by magnetic measurement. The magnetic behavior is characteristic of mononuclear complexes with d4 low-spin octahedral Re(III) complexes (3T1g ground state) and arise because of the large spin–orbit coupling (ζ = 2500 cm−1), which gives diamagnetic ground state. 相似文献
102.
Yan Ping Wang Wen Fa Xie Bin Li Wen Lian Li 《中国化学快报》2007,18(12):1501-1504
A new 1,3,4-oxadiazole-contanining rhenium(I) complex,with the formula [Re(CO)_3(Bphen)(PTOP)],(Bphen=bathophe- nardine,PTOP=4-(5-p-tolyl-1,3,4-oxadiazd-2-yl)pyridine),is synthesized and characterized by elemental analysis,IR,~1H NMR, UV-vis and luminescence spectroscopy.The double-layer electroluminescence devices based on the Re(I) complex have been fabricated by spin-coating technique.The turn-on voltage,maximum efficiency,and brightness for green emission obtained from the devices are 9V,2.1cd/A and 165cd/m~2,respectively. 相似文献
103.
A coalesced high-intensity dc discharge is maintained between three cathodes and a single anode, stabilized by using resistors on each cathode leg. Jets of plasma gas are produced from either the cathode area or the anode area of the device. Cathode jets are generated by the self-induced pumping at the cathode tips and augmented by central gas injection. Arc voltage-current characteristics show classical convection-stabilized arc behavior. Anode heat transfer rates may be substantially increased by central gas injection toward the anode. Temperature fields in the coalesced, axially symmetric portion of the arc are determined spectrometrically and compared to those of a classical single-cathode free-burning arc. 相似文献
104.
105.
New mixed-ligand copper(I) complexes, [Cu(Phca2en)(PPh3)X], [Phca2en = N,N′-bis(β-phenylci-nnamaldehyde)-1,2-diiminoethane and X=Cl (1), Br (2), I (3), NCS (4), N3 (5)] have been synthesized and characterized by various techniques. 1H and 13C-NMR and IR spectral data of these copper(I) complexes are compared with the free ligand to elucidate some structural features. The structures of [Cu(Phca2en)(PPh3)Br] (2) and [Cu(Phca2en)(PPh3)I] (3) have been determined from single-crystal data showing that the coordination geometry around copper atom is a distorted tetrahedron. Furthermore, these Cu(I) complexes exhibit supramolecular motifs of the type multiple phenyl embraces resulting from attractive interactions between phenyl rings of PPh3 moieties. The presence of the C–H…Cu weak intramolecular hydrogen bonds, due to the trapping of C–H bonds in the vicinity of the metal atoms, is also reported. 相似文献
106.
107.
M. SenŌ H. Noritomi Y. Kuroyanagi K. Iwamoto G. Ebert 《Colloid and polymer science》1984,262(9):727-733
The conformation of various basic poly (-amino acid)s was investigated by CD measurements in aqueous solutions containing bis (2-ethylhexyl)sodium sulfosuccinate (AOT) as well as in the AOT reversed micelles. The addition of AOT into an aqueous solution of poly(L-lysine) induces the conformational transition from coil to ordered structure, followed by aggregation. On the other hand, poly(L-lysine) assumes-structure in the reversed micelles at low wovalue (wo=[H2O]/[AOT]). Similarly to poly(L-lysine), poly(L-ornithine) takes an ordered structure in the aqueous solution containing AOT and-structure in the reversed micelles. In this case, however, these ordered structures are not so stable, compared with that of poly(L-lysine). Poly(L-arginine) undergoes the conformational transition from coil to helix by addition of AOT into the aqueous solution. Further addition of AOT allows transformation into-structure. Copoly(L-lysyl-L-leucine) with 63% leucine residue was shown to take a stable helical conformation even in pure water. In the reversed micelles, however, this ordered structure is significantly changed probably because the hydrophobic interaction among the leucyl residues is lowered in the reversed micelles. 相似文献
108.
After the next revision of the ISO-standards for hardness testing (ISO 6506–6508) an estimation of the uncertainty (ISO/IEC 17025, ISO 5725) is mandatory. The two proposed approaches of part one (ISO 6506–6508) of the ISO Standards for hardness are exemplified. The calculation approach implemented in an Excel-based file, which is available via , is announced.Presented at the Metro Trade Workshop on Traceability and Measurement Uncertainty in Testing, 30–31 January 2003, Berlin, Germany 相似文献
109.
Kai-Ming Chi Hung-Chang Houa Kuo-Hsien Chen Shin-Guang Shyu Yuh-Sheng Wen 《中国化学会会志》1995,42(3):547-554
Copper(I) complexes of general formula (β-diketonate)Cu(7-AcO-NBD), where 7-AcO-NBD = 7-norbornadienyl acetate and β-diketonate = 1,1,1,5,5,5-hexafluoro-2,4-pentanedionate (1), 1,1,1-trifluoro-2,4-pentanedionate (2), 2,4-pentanedionate (3), 4,4,4-trifluoro-1-(2-thienyl)-1,3-butanedionate (4), 4,4,4-trifluoro-1-phenyl-1,3-butanedionate (5), were prepared from reactions of CuCl with Na(β-diketonate) in the presence of 7-AcO-NBD. AH compounds were characterized by elemental analyses, 1H, 13C, 19F NMR and IR spectra. Single-crystal strucutre of compound 1 was determined by X-ray diffraction analysis that showed a mononuclear copper species with coordination of a chelating β-diketonate ligand through two oxygen atoms and the 7-AcO-NBD through its C? C double bond and an oxygen atom in the solid state. For compound 1, the crystal data are: triclinic, space group $ {\rm P}\bar 1 $, a= 5.4519(14) Å, b= 11.852(3) Å, c= 13.304(3) Å, α = 74.721(20)° β = 80.220(20)°, γ= 76.848(19)°, Z = 2, RF = 0.060 and Rw = 0.064. Hot-wall chemical vapor deposition experiments revealed that compound 1 is suitable as a precursor for deposition of copper films in the temperature range 170–260 °C. 相似文献
110.
Alkyl substituted chromium Fischer carbene complexes react with 1,1-diphenylallene in the presence of rhodium(I) catalysts (10 mol%) to yield highly substituted dienyl indenone derivatives. In this process a catalytic chromium(0)-rhodium(I) exchange occurs, four new C-C bonds are created, and four-components (two allenes, the carbene ligand and one CO ligand) are joined in a chemo- and regioselective manner. 相似文献