2-(2-Aminoethylamino)ethanol (L) reacts with cupric bromide in dimethylformamide to give a mononuclear complex of Cu(II) [L2Cu]Br2, with six-coordinate distorted octahedral geometry, in which two molecules of tridentate (N,N,O) ligand are involved. The structure was confirmed by spectroscopic methods, elemental and thermogravimetric analyses, and magnetic measurements. Optimization of possible configurations indicated the formation of the trans structure of the complex. Experimental results indicate that the investigated complex, bis[2-(2-aminoethylamino)ethanol] copper(II) bromide, behaves as a semiconductor in the studied temperature range of 298–388 K. Gas sensing properties of the film for the volatile organic compounds (VOCs): acetone, tetra-chloromethane, chloroform, ethanol, and methanol, were also investigated as a function of vapor concentration and temperature in dark. The film showed maximum sensitivity to tetrachloromethane and ethanol vapors at room temperature. Responses of the film to the tested gases are reversible. 相似文献
Hydrogels are attractive biomaterials for three-dimensional cell culture and tissue engineering applications. The preparation of hydrogels using alginate and gelatin provides cross-linked hydrophilic polymers that can swell but do not dissolve in water. In this work, we first reinforced pure alginate by using polyoxyethylene as a supporting material. In an alginate/PEO sample that contains 20 % polyoxyethylene, we obtained a stable hydrogel for cell culture experiments. We also prepared a stable alginate/gelatin hydrogel by cross-linking a periodate-oxidized alginate with another functional component such as gelatin. The hydrogels were found to have a high fluid uptake. In this work, preparation, characterization, swelling, and surface properties of these scaffold materials were described. Lyophilized scaffolds obtained from hydrogels were used for cell viability experiments, and the results were presented in detail. 相似文献
Structure of products formed in polyethylene oxidation by nitric acid was studied by NMR, IR, and electronic absorption spectroscopies
and derivatography. 相似文献
Hydrogen-transfer reduction processes are attracting increasing interest from synthetic chemists in view of their operational simplicity. The new chiral C2-symmetric ligands N,N′-bis-[(1S)-1-sec-butyl-2-O-(diphenylphosphinite)ethyl]ethanediamide, 1 and N,N′-bis-[(1S)-1-phenyl-2-O-(diphenylphosphinite)ethyl]ethanediamide, 2 and the corresponding ruthenium complexes 3 and 4 have been prepared and their structures have been elucidated by a combination of multi-nuclear NMR spectroscopy, IR spectroscopy, and elemental analysis. 1H–31P NMR, DEPT, 1H–13C HETCOR, or 1H–1H COSY correlation experiments were used to confirm the spectral assignments. The catalytic activity of complexes 3 and 4 in transfer hydrogenation of acetophenone derivatives by iso-PrOH has also been studied. Under optimized conditions, these chiral ruthenium complexes serve as catalyst precursors for the asymmetric transfer hydrogenation of acetophenone derivatives in iso-PrOH and act as excellent catalysts, giving the corresponding chiral alcohols in 99% yield and up to 75% ee. This transfer hydrogenation is characterized by low reversibility under these conditions. 相似文献
The polydendate bis(phosphino)amine, tris{2-(N,N-bis(diphenylphosphino)aminoethyl}amine 1 has been prepared in a single step from the reaction of tris(2-aminoethyl)amine with six equivalents of PPh2Cl in the presence of NEt3 in THF. Oxidation of 1 with aqueous H2O2, elemental sulfur or grey selenium gave the corresponding oxide, sulfide or selenide derivatives. [{(P(E)Ph2)2NCH2CH2}3N] (E: 2a O, 2b S, 2c Se), respectively. Reaction of [{(PPh2)2NCH2CH2}3N] with 3 equiv. of PdCl2(cod) or PtCl2(cod) gave the corresponding chelate complexes, [Pd3Cl61] or [Pt3Cl61]. The new compounds were fully characterized by NMR, IR spectroscopy and elemental analysis. The catalytic activity of the Pd(II) complex was tested in the Suzuki coupling and Heck reactions. The Pd(II) complex catalyzed the Suzuki coupling and Heck reaction affording biphenyls and stilbenes, respectively, in high yields. 相似文献
The transition of a solvated flexible macromolecular chain from random coil behavior in the θ‐state to a globular compact form in the collapsed state has been the subject of extensive theoretical and experimental studies. Most of the coil‐globule transition studies of macromolecules have concentrated on the prototypical polystyrene‐cyclohexane system. However, chain contractions reported in this system have been around 75% of those in the unperturbed θ‐state. This relatively small decrease in size does not satisfy the criterion for a densely packed, collapsed globule. Experimentally, the collapse from a coil to a true compact globular state has now been established for two flexible macromolecules: poly(N‐isopropylacrylamide) in water and poly(methyl methacrylate) in various solvents. In this contribution, we review recent theoretical studies covering phenomenological and Langevin models as well as computer simulations. In addition, we outline recent experimental studies of the coil‐globule transition of various flexible polymers, copolymers, and polyelectrolytes.
Expansion factor, αequation/tex2gif-stack-1.gif, versus temperature for NaPSS in 4.17 M aqueous NaCl solution. (•): NaPSS‐1, (○): NaPSS‐2. 相似文献