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71.
Adriana Ionescu 《Journal of organometallic chemistry》2006,691(18):3806-3815
The ω-hydroxyolefins 3-buten-1-ol, 3-buten-1-methyl-1-ol and 4-penten-1-ol were subjected to hydroxycarbonylation conditions in water in the presence of PdCl2(PhCN)2 and 4-8 equiv. of water soluble tris(3-sodiumsulfonatophenyl)phosphine (TPPTS), or N-bis(N′,N′-diethyl-2-aminoethyl)-4-aminomethylphenyl-diphenylphosphine (N3P). Under conditions of high conversion, the olefins primarily undergo isomerisation through a chain walking mechanism with selectivities for aldehyde ranging from 65% to 98%, with the lower values for longer chain alcohols. The lactones formed as the minor product are almost exclusively branched, indicating that in the first step 2,1-insertion is strongly favoured over 1,2-insertion. In the N3P system also linear lactone is produced at lower conversion. Running the reaction in D2O produces multiple deuterium incorporation in all positions of the carbon chain. A mechanism is discussed. 相似文献
72.
73.
Reacting [PtCl(PTA)3]Cl(PTA = 1,3,5-triaza-7-phosphatricyclo[3.3.1.13,7]decane) with KSeCN in aqueous or MeOH medium results in the abstraction of the PTA ligands to yield SePTA. The reaction also proceeds quantitatively by direct reaction of PTA and KSeCN in water or methanol. The methylated PTA ligand, [PTA-Me]I (1-methyl-1-azonia-3,5-diaza-7-phosphatricyclo[3.3.1.13,7]decane iodide), reacts accordingly with KSeCN, albeit significantly slower. The crystal structure of SePTA, 1, and [SePTA-Me]I · CH3OH, 2, revealed PSe bond distances of 2.0991(19) and 2.100(2) Å, respectively. The first order phosphorous selenium coupling constants, 1JP-Se (D2O), of 722 and 788 Hz for SePTA and [SePTA-Me]I, respectively, indicates the latter is significantly less electron rich. 相似文献
74.
N-Terminal amino acid residues of Fractions IX, X, and XII were reinvestigated by DNP and DNS methods with two-dimensional polyamide thin-layer chromatography. It was found that our previous work1 had been erroneously concluded. By the present work, it was obvious that all three fractions had Leu as their N-terminal amino acid residues. 相似文献
75.
Xin-ping Duan Tianyi Chen Tianxiang Chen Lele Huang Li Ye Benedict T. W. Lo Youzhu Yuan Shik Chi Edman Tsang 《Chemical science》2021,12(25):8791
Coinage metal nanoparticles with high dispersion can serve as highly efficient heterogeneous catalysts. However, owing to their low melting point, poor thermal stability remains a major obstacle towards their application under reaction conditions. It is a common practice to use porous inorganic templates such as mesoporous silica SBA-15 to disperse Ag nanoparticles (NPs) against aggregation but their stability is far from satisfactory. Here, we show that the catalytic activity for hydrogenation of dimethyl oxalate (DMO) to methyl glycolate (MG) over Ag NPs dispersed on SBA-15 silica can be further promoted by incorporation of alkali metal ions at small loading, which follows the inverse order of their cationic size: Li+ > Na+ > K+ > Rb+. Among these, 5Ag1–Li0.05/SBA-15 can double the MG yield compared to pristine 5Ag/SBA-15 under identical conditions with superior thermal stability. Akin to the effect of an ionic surfactant on stabilization of a micro-emulsion, the cationic charge of an alkali metal ion can maintain dispersion and modulate the surface valence of Ag NPs. Interstitial Li in the octahedral holes of the face center packed Ag lattice is for the first time confirmed by X-ray pair distribution function and electron ptychography. It is believed that this interstitial-stabilization of coinage metal nanoparticles could be broadly applicable to multi-metallic nanomaterials for a broad range of C–O bond activating catalytic reactions of esters.Coinage metal nanoparticles with high dispersion can serve as highly efficient heterogeneous catalysts. 相似文献
76.
Marzano C Bettio F Chilin A Caffieri S Reddi E Bordin F 《Photochemistry and photobiology》2005,81(6):1371-1379
The molecular structure of 1,4,6,8-tetramethylfuro[2,3-h]quinolin-2(1H)-one (FQ), a recent furocoumarin-like photosensitizer, has been modified with the aim of reducing its strong genotoxicity, by replacing the methyl group at 4 position with a hydroxymethyl one, and so obtaining 4-hydroxymethyl-1,6,8-trimethylfuro[2,3-h]quinolin-2(1H)-one (HOFQ). This modification gave rise to a strong reduction of lipophilicity and dark interaction with DNA. The formation of monoadducts (MA) was deeply affected, whereas the induction of bifunctional adducts between DNA and proteins (DPC(L>0)) was replaced by an efficient production of DNA-protein cross-links at zero length (DPC(L=0)), probably via guanine damage. Because of its angular molecular structure, HOFQ does not form interstrand cross-links (ISC): therefore, DPC(L=0) and MA represent the main lesions induced by HOFQ in DNA. In comparison with FQ (which induces MA and DPC(L>0)) and 8-methoxypsoralen (8-MOP) (MA, ISC, DPC(L>0)), HOFQ seems to be a more selective agent. In fact, contrary to FQ and 8-MOP, HOFQ, together with a noticeable antiproliferative activity, shows low levels of point mutations in bacteria and of clastogenic effects in mammalian cells. HOFQ is also an efficient apoptosis inducer, especially in comparison with 8-MOP, when tested at equitoxic experimental conditions; this property might be correlated with the complete HOFQ inability of inducing skin erythemas, a well-known side effect of classic furocoumarin photosensitization. 相似文献
77.
A general formulation has been developed for the evaluation of the total electron spin-spin contact interaction in many-electron atoms, including both the intra- and inter-shell contributions. Calculations have been carried out, using existing analytical Hartree-Fock functions, for the positive ions, neutral systems, and negative ions for all the atoms from He to Kr.
This work has been supported in part by the National Research Council of Canada. 相似文献
Zusammenfassung Es wird ein allgemeiner Formalismus zur Berechnung der gesamten Elektronen-Spin-Spin-Kontakt-Wechselwirkung in Vielelektronen-Atomen angegeben, der sowohl die Anteile der Wechselwirkung innerhalb einer Schale als auch zwischen einzelnen Schalen berücksichtigt. Berechnungen wurden unter Benutzung vorhandener analytischer Hartree-Fock-Funktionen für die positiven Ionen, die neutralen Systeme und die negativen Ionen aller Atome von He bis Kr durchgeführt.
This work has been supported in part by the National Research Council of Canada. 相似文献
78.
A closed‐form expression has been derived to obtain the N‐dimensional rectangular atomic wave functions. The wave functions can be obtained straightforwardly with the knowledge of the angular momentum quantum numbers and the dimension and there is no need to employ recursive methods as in previous works. © 2002 Wiley Periodicals, Inc. Int J Quantum Chem 88: 263–274, 2002 相似文献
79.
80.
Simultaneous determination of berberine in rat blood,liver and bile using microdialysis coupled to high-performance liquid chromatography 总被引:5,自引:0,他引:5
High-performance liquid chromatography coupled to microdialysis was used for the simultaneous determination of unbound berberine in rat blood, liver and bile for a pharmacokinetic study. Microdialysis probes were simultaneously inserted into the jugular vein toward the right atrium, the median lobe of the liver, and the bile duct of male Sprague-Dawley rats for biological fluid sampling after administration of berberine (10 mg/kg) through the femoral vein. Berberine and dialysates were separated using a Zorbax SB-phenyl column and a mobile phase comprised of acetonitrile-methanol-20 mM monosodium phosphate (pH 3.0) (35:20:45, v/v) together with 0.1 mM 1-octanesulfonic acid. The detection limit for berberine was 10 ng/ml. The concentration-response relationship was linear (r2 > 0.995) over the concentration range 0.05-50 microg/ml; intra-assay and inter-assay precision and accuracy for berberine fell within predefined limits. The disposition of berberine in the blood, liver and bile fluid suggests that berberine might be metabolized in the liver and undergo hepatobiliary excretion. 相似文献