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951.
Maryam Sadat Majdolashrafi 《Phosphorus, sulfur, and silicon and the related elements》2018,193(7):415-422
The complex [Pt2(μ-mtrzt)4(mtrzt)2] (1) was synthesized from the reaction of a mixture of 4-methyl-4H-1,2,4-triazole-3-thiol (Hmtrzt) and ethylenediamine (en) with K2PtCl4 in CH3OH/H2O (2:1) as solvent. The complex [Pt2(μ-mtrzt)4] (2) was synthesized by the same procedure as described for preparation of complex 1 but in the absence of ethylenediamine. Both complexes were characterized by elemental analysis, IR,1H NMR,13C{1H}NMR, UV-Vis, as well as luminescence spectroscopy and their structures were analyzed by single-crystal X-ray diffraction method. The X-ray structure determinations show that complexes of 1 and 2 have binuclear structures in a paddle-wheel fashion with Pt-Pt distances of 2.6628(7) and 2.7977(16)Å, respectively. In complex 1, each platinum(III) atom has a distorted octahedral coordination geometry with the sulfur atom and the second platinum subunit in axial positions and two nitrogen and two sulfur atoms in equatorial positions. Also, in complex 2, each platinum(II) atom has a distorted square-pyramidal coordination geometry with the second platinum subunit in axial position and two nitrogen and two sulfur atoms in equatorial positions. In addition, intermolecular C?H···N and C?H···S hydrogen bonds in 1 and 2 as well as intermolecular anagostic C?H···Pt and C?H···π interactions in 2 are effective in the stabilization of the crystal packing of these complexes. 相似文献
952.
Hossein Aghabozorg Abolghasem Moghimi Faranak Manteghi Maryam Ranjbar 《无机化学与普通化学杂志》2005,631(5):909-913
Starting with a zirconium salt and LH2 , (pydaH2)2+(pydc)2?, (pyda=2, 6‐pyridinediamine; pydcH2=2,6‐pyridinedicarboxylic acid), as a 1:1 proton transfer self‐associated compound, two different compounds were resulted. One of them is a new complex of ZrIV with a flat pyridine containing ligand and structure of (pydaH)2[Zr(pydc)3] · 5H2O (1) and the other, (pydaH)+(NO3)? (2) is an ion pair with no zirconium ion. The zirconium(IV) complex (1) is crystallized in triclinic system with space group and Z = 2, the crystallographic parameters are: a = 10.612(5) Å, b = 10.617(5) Å, c = 16.815(8) Å, α = 103.654(9)°, β = 95.821(9)°, γ = 98.891(9)° and R‐value for 16767 collected reflections is 0.0592. The ion pair (2) has crystals of monoclinic system with P21 space group and Z = 2. Its crystallographic parameters are: a = 3.6227(11) Å, b = 10.034(4) Å, c = 10.296(4) Å, β = 93.422(9)° and R‐value for 4031 collected reflections is 0.0521. The two compounds were characterized with elemental analysis, ESI/MS, NMR and IR spectroscopy. 相似文献
953.
Akbar Heydari Samad Khaksar Maryam Esfandyari Mahmoud Tajbakhsh 《Tetrahedron letters》2007,48(7):1135-1138
A simple and convenient procedure for direct reductive amination of aldehydes and ketones with sodium borohydride is described. The reaction has been carried out in methanol in the presence of a catalytic amount of H3PW12O40 (0.5 mol %). α,β-Unsaturated aldehydes and ketones can be easily converted into the corresponding allyl alcohols by reaction with H3PW12O40 (0.5 mol %)/NaBH4. 相似文献
954.
Akbar Heydari Roohollah Kazem Shiroodi Hossein Hamadi Maryam Esfandyari Mehrdad Pourayoubi 《Tetrahedron letters》2007,48(33):5865-5868
The commercially available heteropoly acid H3PW12O40 (0.5 mol %) is a very efficient and environmentally benign catalyst for N-tert-butoxycarbonylation of amines (primary, secondary) with di-tert-butyl dicarbonate at room temperature in short reaction times (<10 min). No competitive side products such as isocyanates, ureas, N,N-di-tert-butoxycarbonyls, O-Boc and oxazolidinones were observed. Chiral α-amino alcohols and esters afforded the corresponding N-Boc derivatives chemoselectively in excellent yields. 相似文献
955.
Issa Yavari Zinatossadat Hossaini Maryam Sabbaghan Majid Ghazanfarpour-Darjani 《Tetrahedron》2007,63(38):9423-9428
The reaction of ethyl propiolate with triphenylphosphine (Ph3P) in the presence of N-alkylisatins led to ethyl 2,2,2-triphenyl-2,5-dihydro-1,2-λ5-oxaphosphole-4-carboxylate-spiro-1-alkyl-1,3-dihydro-2H-indol-2-ones in good yield. The reaction of dialkyl acetylenedicarboxylates with Ph3P in the presence of N-alkylisatins led to dialkyl 2,2,2-triphenyl-2,5-dihydro-1,2-λ5-oxaphosphole-3,4-dicarboxylate-spiro-1-alkyl-1,3-dihydro-2H-indol-2-ones and alkyl 4-(alkoxy)-5-oxo-2,5-dihydro-3-furancarboxylate-spiro-1-alkyl-1,3-dihydro-2H-indol-2-ones. 相似文献
956.
Two new ZnII(μ‐4,4′‐bipy) coordination polymers with acetate anions, [Zn(4,4′‐bipy)(AcO)2] ( 1 ) and [Zn2(4,4′‐bipy)(AcO)4] ( 2 ), have been synthesized. The compounds were characterized with elemental analysis, IR‐, 1H NMR‐, 13C NMR spectroscopy and studied by thermal analysis, fluorescence measurements and x‐ray crystallography. The structural studies of compound 1 suggest the structure is a coordination polymer of zinc(II) consisting of linear double chains formed by bridging 4,4′‐bipy ligand and connection of the acetate‐bridged centrosymmetric [Zn2(OAc)2]2+ nodes. 相似文献
957.
958.
Second-order standard addition for deconvolution and quantification of fatty acids of fish oil using GC-MS 总被引:1,自引:0,他引:1
In the present work two second-order calibration methods, generalized rank annihilation method (GRAM) and multivariate curve resolution-alternating least square (MCR-ALS) have been applied on standard addition data matrices obtained by gas chromatography-mass spectrometry (GC-MS) to characterize and quantify four unsaturated fatty acids cis-9-hexadecenoic acid (C16:1ω7c), cis-9-octadecenoic acid (C18:1ω9c), cis-11-eicosenoic acid (C20:1ω9) and cis-13-docosenoic acid (C22:1ω9) in fish oil considering matrix interferences. With these methods, the area does not need to be directly measured and predictions are more accurate. Because of non-trilinear conditions of GC-MS data matrices, at first MCR-ALS and GRAM have been used on uncorrected data matrices. In comparison to MCR-ALS, biased and imprecise concentrations (%R.S.D. = 27.3) were obtained using GRAM without correcting the retention time-shift. As trilinearity is the essential requirement for implementing GRAM, the data need to be corrected. Multivariate rank alignment objectively corrects the run-to-run retention time variations between sample GC-MS data matrix and a standard addition GC-MS data matrix. Then, two second-order algorithms have been compared with each other. The above algorithms provided similar mean predictions, pure concentrations and spectral profiles. The results validated using standard mass spectra of target compounds. In addition, some of the quantification results were compared with the concentration values obtained using the selected mass chromatograms. As in the case of strong peak-overlap and the matrix effect, the classical univariate method of determination of the area of the peaks of the analytes will fail, the “second-order advantage” has solved this problem successfully. 相似文献
959.
Shayessteh Dadfarnia Ali Mohammad Haji Shabani Fatema Tamadon Maryam Rezaei 《Mikrochimica acta》2007,158(1-2):159-163
A simple and rapid flow injection system is proposed for indirect determination of cyanide by flame atomic absorption spectrometry.
It consists of a microcolumn of immobilized salen (N,N′-bis(salicylidene)ethylenediamine) on sodium dodecyl sulfate (SDS)-coated
alumina saturated with silver ion and a carrier of dilute solution of sodium hydroxide (10−5 mol L−1). The micro-column was located between the injection valve and nebulizer of atomic absorption spectrometry. Injection of
250 μL of aqueous cyanide standard or sample solution at pH range of 9–11 cause elution of silver as silver cyanide complexes,
which was then measured by flame atomic absorption spectrometry. The absorbance was proportional to the concentration of cyanide
in the sample. The graph of absorbance (as peak height) vs. cyanide concentration was linear over the concentration range
of 0.1–10 mg L−1 of cyanide, and the detection limit was 0.06 mg L−1. The relative standard deviation at 1 and 3 mg L−1 of cyanide concentration were 4.1 and 4.7%, respectively. The method was successfully applied to determination of cyanide
in water and industrial waste waters, and the accuracy was examined through independent analysis by accepted method of pyridine-barbituric
acid. 相似文献
960.
Minoo Dabiri Mostafa Baghbanzadeh Maryam S. Nikcheh 《Monatshefte für Chemie / Chemical Monthly》2007,138(12):1249-1252
Summary. Oxalic acid is used as an efficient catalyst in the condensation of 2-aminoaryl ketones with carbonyl compounds leading to
the formation of quinolines in excellent yields under solvent-free conditions. This methodology offers significant improvements
for the synthesis of quinolines with regard to the yield of products, simplicity in operation, inexpensive reagents, and green
aspects by avoiding toxic catalysts and solvents. 相似文献