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991.
992.
Yan Yin Otoo Yamada Yoshiki Suto Takashi Mishima Kazuhiro Tanaka Hidetoshi Kita Ken‐ichi Okamoto 《Journal of polymer science. Part A, Polymer chemistry》2005,43(8):1545-1553
A series of sulfonated copolyimides (co‐SPIs) bearing pendant sulfonic acid groups were synthesized from 1,4,5,8‐naphthalenetetracarboxylic dianhydride (NTDA), bis(3‐sulfopropoxy) benzidines (BSPBs), and common nonsulfonated diamines via statistical or sequenced polycondensation reactions. Membranes were prepared by casting their m‐cresol solutions. The co‐SPI membrane had a microphase‐separated structure composed of hydrophilic and hydrophobic domains, but the connecting behavior of hydrophilic domains was different from that of the homo‐SPIs. The co‐SPI membranes displayed clear anisotropic membrane swelling in water with negligibly small dimensional changes in the plane direction of the membrane. With water uptake values of 39–94 wt %, they showed dimensional changes in membrane thickness of about 0.11–0.58, which were much lower than those of homo‐SPIs. The proton conductivity σ values of co‐SPI membranes with ion exchange capacity values ranging from 1.95–2.32 meq/g increased sigmoidally with increasing relative humidity. They displayed σ values of 0.05–0.16 S/cm at 50 °C in liquid water. Increasing temperature up to 120 °C resulted in further increase in proton conductivity. The co‐SPI membranes showed relatively good conductivity stability during the aging treatment in water at 100 °C for 300 h. © 2005 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 43: 1545–1553, 2005 相似文献
993.
Peng‐Fei Gou Wei‐Pu Zhu Ning Zhu Zhi‐Quan Shen 《Journal of polymer science. Part A, Polymer chemistry》2009,47(11):2905-2916
Novel amphiphilic eight‐arm star triblock copolymers, star poly(ε‐caprolactone)‐block‐poly(acrylic acid)‐block‐poly(ε‐caprolactone)s (SPCL‐PAA‐PCL) with resorcinarene as core moiety were prepared by combination of ROP, ATRP, and “click” reaction strategy. First, the hydroxyl end groups of the predefined eight‐arm SPCLs synthesized by ROP were converted to 2‐bromoesters which permitted ATRP of tert‐butyl acrylate (tBA) to form star diblock copolymers: SPCL‐PtBA. Next, the bromide end groups of SPCL‐PtBA were quantitatively converted to terminal azides by NaN3, which were combined with presynthesized alkyne‐terminated poly(ε‐caprolactone) (A‐PCL) in the presence of Cu(I)/N,N,N′,N″,N″‐pentamethyldiethylenetriamine in DMF to give the star triblock copolymers: SPCL‐PtBA‐PCL. 1H NMR, FTIR, and SEC analyses confirmed the expected star triblock architecture. The hydrolysis of tert‐butyl ester groups of the poly(tert‐butyl acrylate) blocks gave the amphiphilic star triblock copolymers: SPCL‐PAA‐PCL. These amphiphilic star triblock copolymers could self‐assemble into spherical micelles in aqueous solution with the particle size ranging from 20 to 60 nm. Their micellization behaviors were characterized by dynamic light scattering and transmission electron microscopy. © 2009 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 47: 2905–2916, 2009 相似文献
994.
A series of chiral Schiff bases ( L 1 – L 5 ) with different substituents in the salicylidenyl unit were prepared from condensation of 3‐aryl‐5‐ tert ‐butylsalicylaldehyde derivatives and optically active amino alcohols. Bromination of 3‐phenyl‐5‐ tert ‐butylsalicylaldehyde gave an unexpected product 3‐(4‐bromophenyl)‐5‐bromosalicylaldehyde, from which the corresponding Schiff base ligands L 6 and L 7 , derived from (S)‐valinol and (S)‐ tert ‐leucinol, respectively, were prepared. Ligands L 1 – L 7 were applied to the vanadium‐catalyzed asymmetric oxidation of aryl methyl sulfides. Under the optimal conditions, the oxidation of the thioanisole with H2O2 as oxidant in CH2Cl2 catalyzed by VO(acac)2‐ L 1 – L 7 gives good yields (74–83%) with moderate enantioselectivity (58–77% ee). Ligand L 7 , containing a 4‐bromophenyl group on the 3‐position and a Br atom on the 5‐position of the salicylidenyl moiety, displays an 80–90% ee for vanadium‐catalyzed oxidation of methyl 4‐bromophenyl sulfide and methyl 2‐naphthyl sulfide. Copyright © 2008 John Wiley & Sons, Ltd. 相似文献
995.
996.
A series of α-hydroxy esters were rapidly prepared (1.5 h) from α-keto esters via asymmetric transfer hydrogenation (ATH) in water by the use of surfactants for the first time. This green method, catalyzed by a water-soluble and recyclable Ru(II) complex, gave moderate to high enantioselectivities (up to 99.7% ee) with DTAB as an additive and HCOONa as the hydrogen source. 相似文献
997.
E. Polak R. S. Womersley H. X. Yin 《Journal of Optimization Theory and Applications》2008,138(2):311-328
We present a new active-set strategy which can be used in conjunction with exponential (entropic) smoothing for solving large-scale
minimax problems arising from the discretization of semi-infinite minimax problems. The main effect of the active-set strategy
is to dramatically reduce the number of gradient calculations needed in the optimization. Discretization of multidimensional
domains gives rise to minimax problems with thousands of component functions. We present an application to minimizing the
sum of squares of the Lagrange polynomials to find good points for polynomial interpolation on the unit sphere in ℝ3. Our numerical results show that the active-set strategy results in a modified Armijo gradient or Gauss-Newton like methods
requiring less than a quarter of the gradients, as compared to the use of these methods without our active-set strategy. Finally,
we show how this strategy can be incorporated in an algorithm for solving semi-infinite minimax problems. 相似文献
998.
Gang‐Yin Shi Xue‐Zhi Tang Cai‐Yuan Pan 《Journal of polymer science. Part A, Polymer chemistry》2008,46(7):2390-2401
The tadpole‐shaped amphiphilic copolymers with cyclic polystyrene as the head and a linear poly(N‐isopropylacrylamide) as the tail have been successfully synthesized by combination of reversible addition‐fragmentation chain transfer (RAFT) polymerization and “click” reaction. The synthesis involves two main steps: (1) preparation of a linear acetylene‐terminated PNIPAAM‐b‐PS with a side azido group anchored at the junction between two blocks; (2) intramolecular cyclization reaction to produce the cyclic PS block using “click” chemistry under high dilution. The structures, molecular weights, and molecular weight distributions of the resulted intermediates and the target polymers were characterized by their 1H NMR, FTIR, and gel permeation chromatography. The difference of surface property between tadpole‐shaped polymer and its linear precursor was observed, and the water contact angles on the former surface are larger than that of the latter surface. © 2008 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 46: 2390–2401, 2008 相似文献
999.
In this paper, we derive non-exponential asymptotic forms for solutions of defective renewal equations. These include as special
cases asymptotics for compound geometric distribution and the convolution of a compound geometric distribution with a distribution
function. As applications of these results, we study the Gerber-Shiu discounted penalty function in the classical risk model
and the reliability of a two-unit cold standby system in reliability theory.
相似文献
1000.
The silver chromate self-assembly necklace structures were synthesized using high-active acrylicamide template. The whole
length of the necklace structure was between 1.2 and 1.5 μm. The product was composed of single crystalline nanorods with
diameters of about 40 nm and lengths of 300 nm. The synthetic mechanism and product’s optical properties were also studied. 相似文献