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John GH May I Sharrad CA Sutton AD Collison D Helliwell M Sarsfield MJ 《Inorganic chemistry》2005,44(21):7606-7615
We report the synthesis, structural, and spectroscopic characterization of a series of uranium(IV)-perrhenato complexes. Three isostructural complexes with general formula [U(ReO4)4(L)4] (where L = tri-n-butylphosphine oxide/TBPO (2), triethyl phosphate/TEP (3), or tri-iso-butyl phosphate/TiBP (4)), have been synthesized, both through the photoreduction of ethanolic {UO2}2+ solutions and also via a novel U(IV) starting material, U(ReO4)4.5H2O (1). Compound 1 has also been used in the preparation of [U(ReO4)4(TPPO)3(CH3CN)].2CH3CN (5) and [U(ReO4)(DPPMO2)3(OH)][ReO4]2.2CH3CN (6), where TPPO represents triphenylphosphine oxide and DPPMO2 represents bis(diphenylphosphino)methane dioxide. All six complexes have been spectroscopically characterized using NMR, UV-vis-NIR, and IR techniques, with 2, 3, 5, and 6 also fully structurally characterized. The U atoms in compounds 2-6 all exhibit eight-coordinate geometry with up to four perrhenate groups in addition to three (DPPMO2 and TPPO) or four (TEP, TiBP, TBPO) coordinated organic ligands. In the case of compounds 5 and 6, the coordination of eight ligands to the U(IV) center is completed by the binding of a solvent molecule (CH3CN) and OH-, respectively. Solid-state physical analysis (elemental and thermogravimetric) and infrared spectroscopy are in agreement with the structural studies. The crystallographic data suggest that the strength of the U(IV)-O-donor ligand bonds decreases across the series R3PO > [ReO4]- > (RO)3PO. Solution-state IR and 31P NMR spectroscopy appear to be in agreement with these solid-state results. 相似文献
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The enantiomeric separation of three selenoamino acids, D,L-selenomethionine, D,L-selenoethionine and D,L-selenocystine is described. Both sulfated beta-cyclodextrin and vancomycin have been successfully used to separate all enantiomers of the compounds with UV detection. Reproducible separations, in terms of peak area and migration time were obtained using sulfated beta-cyclodextrin with reversed polarity and UV detection. With vancomycin as a chiral selector, reversed polarity was found to be more reproducible than positive polarity in terms of peak migration times. 相似文献
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Gold nanoparticle/polymer nanocomposites: dispersion of nanoparticles as a function of capping agent molecular weight and grafting density 总被引:2,自引:0,他引:2
Corbierre MK Cameron NS Sutton M Laaziri K Lennox RB 《Langmuir : the ACS journal of surfaces and colloids》2005,21(13):6063-6072
The dispersion of polymer-covered gold nanoparticles in high molecular weight (MW) polymer matrixes is reported. Complete particle dispersion was achieved for PS125-Au in the polystyrene (PS) matrixes studied (up to and including Mn = 80 000 g/mol). PS19-Au, on the other hand, exhibits complete dispersion in a low MW PS matrix (Mn = 2000 g/mol) but only partial dispersion in higher MW matrixes (up to 80 000 g/mol). Similarly, PEO45-Au is fully dispersed in a low MW poly(ethylene oxide) (PEO) matrix (Mn = 1000 g/mol) but only partially in a higher MW PEO matrix (Mn = 15 000 g/mol). Wetting of the polymer-Au brushes by the polymer matrix is associated with dispersibility. Theory predicts that, for dense polymer brushes, wetting is achieved when the MW of the polymer brush equals (and is greater than) that of the polymer matrix. The observed partial dispersion of the PS19-Au and PEO45-Au nanoparticles in matrixes whose MW is greater than the brush MW is attributable to the existence of a high volume fraction of voids within the brush. These voids arise from the unique geometry of the nanoparticle surface arising from the juxtaposed facets of the gold nanoparticle. PS125-Au brushes are wetted by PS matrixes whose degree of polymerization is larger than 125, probably because of their lower grafting density on the gold core or the high fraction of void volumes caused by the facets on the gold cores. Dispersion thus occurs when the matrix MW is greater than that of the brush. 相似文献
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Thermal desorption gas chromatograph mass spectrometry (TD GC/MS) was used to study weight loss in thermogravimetric analysis (TGA). The technique of thermal desorption utilizes the same temperature heating rate as the TGA to thermally desorb volatiles from solid sample matrices. Volatiles were cryo-trapped at −60 °C. After thermal desorption is complete, the trapped volatiles are separated by a GC capillary column and identified by mass spectrometry. In this study, the TD GC/MS was applied in pharmaceutical development to understand the chemical reactions attributed to the weight loss in the thermal decomposition of two dicarboxylic acid salts of a drug substance. These two salts exhibited different thermal stabilities. The thermally induced chemical reactions obtained from these two salts included dehydration and decarboxylation. Thermal degradation compounds were identified and reaction pathways for decomposition were proposed. The stability of the salts is dependent on the identity of the dicarboxylic acids from which they were generated. The information obtained from TD GC/MS helps better understand the weight loss process in thermogravimetric analysis. 相似文献
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Dassié D Eschbach R Hubert F Hubert P Isaac MC Izac C Leccia F Mennrath P Vareille A Longuemare C Mauger F Danevich F Kouts V Tretyak VI Vassilyev Y Zdesenko Y Barabash AS Kornoukov VN Lepikhin YB Umatov VI Vanushin IA Augier C Blum D Campagne JE Jullian S Lalanne D Laplanche F Natchez F Pichenot G Szklarz G Arnold R Guyonnet JL Lamhamdi T Linck I Piquemal F Scheibling F Brudanin V Egorov V Kochetov O Nozdrin A Vylov T Zaparov S Nicholson HW Sutton CS 《Physical review D: Particles and fields》1995,51(5):2090-2100