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1.
Ren‐Shen Lee Jen‐Ming Yang Tz‐Feng Lin 《Journal of polymer science. Part A, Polymer chemistry》2004,42(10):2303-2312
Water‐soluble poly(ester‐carbonate) having pendent amino and carboxylic groups on the main‐chain carbon is reported for the first time. This article describes the melt ring‐opening/condensation reaction of trans‐4‐hydroxy‐N‐benzyloxycarbonyl‐L ‐proline (N‐CBz‐Hpr) with 5‐methyl‐5‐benzyloxycarbonyl‐1,3‐dioxan‐2‐one (MBC) at a wide range of molar fractions. The influence of reaction conditions such as catalyst concentration, polymerization time, and temperature on the number average molecular weight (Mn) and molecular weight distribution (Mw/Mn) of the copolymers was investigated. The polymerizations were carried out in bulk at 110 °C with 3 wt % stannous octoate as a catalyst for 16 h. The poly(ester‐carbonate)s obtained were characterized by Fourier transform infrared spectroscopy, 1H NMR, differential scanning calorimetry, and gel permeation chromatography. The copolymers synthesized exhibited moderate molecular weights (Mn = 6000–14,700 g mol?1) with reasonable molecular weight distributions (Mw/Mn = 1.11–2.23). The values of the glass‐transition temperature (Tg) of the copolymers depended on the molar fractions of cyclic carbonate. When the MBC content decreased from 76 to 12 mol %, the Tg increased from 16 to 48 °C. The relationship between the poly(N‐CBz‐Hpr‐co‐MBC) Tg and the compositions was in approximation with the Fox equation. In vitro degradation of these poly(N‐CBz‐Hpr‐co‐MBC)s was evaluated from weight‐loss measurements and the change of Mn and Mw/Mn. Debenzylation of 3 by catalytic hydrogenation led to the corresponding linear poly(ester‐carbonate), 4 , with pendent amino and carboxylic groups. © 2004 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 42: 2303–2312, 2004 相似文献
2.
Anna Jenčová 《International Journal of Theoretical Physics》2004,43(7-8):1635-1649
We use a class of generalized relative entropies on density matrices to obtain one-parameter families of torsion-free affine connections. 相似文献
3.
Pal Jen Wei 《Journal of Non》2008,354(33):3911-3918
Through the arrangement of the applied load, experimental nanoindentation results of polymethylmethacrylate (PMMA) and polyurethane (PU) employed to establish a mechanical model. The proposed model consists of irreversible delayed plastic (viscoplastic) deformation, irreversible viscous deformation, and reversible delayed elastic (viscoelastic) deformations. The phase lag exhibited between the responding depth and the oscillating load is found to be linear proportional to frequency in the range of 1-50 Hz. The residual cavity profile of the PMMA scanned by an atomic force microscope gives a validity of accommodation assumption applied in the present model. The effects of overshooting, which occurred in the dwelling process, are also discussed. 相似文献
4.
5.
Jenó Szigeti 《Order》1990,7(1):77-81
Given a linearly ordered set (A,
R
) and an R-monotone function f: AA, we give a necessary and sufficient condition on A, f,
R
, involving generating sets and forbidden subalgebras, for
R
to be a well-ordering.Partially supported by Hungarian National Foundation for Scientific Research Grant nr. 1813. 相似文献
6.
Three new hetero‐bischelated rhodium (III) complexes of cis‐[Rh(PA)(L)Cl2]Cl (where PA = phenylpyridin‐2‐ylmethylene‐amine; L = 2,2′‐bipyridine, 2,2′‐dipyridylamine and 1,10‐phenanthroline) have been successfully prepared and characterized. Each complex shows high intensity bands in the UV region, and these are assigned to spin‐allowed π‐π* transitions. The medium‐intensity absorption band profile in the lower energy region can be explained by convolution of spin‐allowed CT and d‐d* transitions. The emission spectra at low temperature (77 K) of these complexes in EtOH/MeOH (4:1 v/v) are virtually identical. They all exhibit a broad, symmetric, and structureless red emission with a microsecond lifetime and hence are assigned as the d‐d* phosphorescence. 相似文献
7.
The photochemistry of diazomethane in toluene and p-xylene solutions was investigated. The reactions of methylene with toluene gave eight products. In the diazomethane p-xylene solution, p-ethyltoluene, 1,2,4-trimethylbenzene, 1,4-dimethylcyclohepatriene-1,3,5 and three unidentified compounds were found as products of the reaction of methylene with p-xylene. The relative rates of addition and insertion reaction of methylene with toluene and p-xylene have been calculated. 相似文献
8.
9.
It is well known how the Kostant-Rowen Theorem extends the validity of the famous Amitsur-Levitzki identity to skew-symmetric matrices. Here we give a general method, based on a graph theoretic approach, for deriving extensions of known permanental-type identities to skew-symmetric and symmetric matrices over a commutative ring of prime characteristic. Our main result has a typical Kostant-Rowen flavour: IfM≥p[n+1/2] then $C_M (X,Y) = \sum\limits_{\alpha ,\beta \in Sym(M)} {x_{\alpha (1)} y_{\beta (1)} x_{\alpha (2)} y_{\beta (2)} } ...x_{\alpha (M)} y_{\beta (M)} = 0$ is an identity onM n ? (Ω), the set ofnxn skew-symmetric matrices over a commutative ring Ω withp1Ω=0 (provided that $P > \sqrt {[n + 1/2)} $ ). Otherwise, the stronger conditionM≥pn implies thatC M(X,Y)=0 is an identity on the full matrix ringM n(Ω). 相似文献
10.
K. W. Cheah L. C. Ho J. B. Xia J. Li W. H. Zheng W. R. Zhuang Q. M. Wang 《Applied Physics A: Materials Science & Processing》1995,60(6):601-606
Photoluminescence studies on porous silicon show that there are luminescence centers present in the surface states. By taking photoluminescence spectra of porous silicon with respect to temperature, a distinct peak can be observed in the temperature range 100–150 K. Both linear and nonlinear relationships were observed between excitation laser power and the photoluminescence intensity within this temperature range. In addition, there was a tendency for the photoluminescence peak to red shift at low temperature as well as at low excitation power. This is interpreted as indicating that the lower energy transition becomes dominant at low temperature and excitation power. The presence of these luminescence centers can be explained in terms of porous silicon as a mixture of silicon clusters and wires in which quantum confinement along with surface passivation would cause a mixing of andX band structure between the surface states and the bulk. This mixing would allow the formation of luminescence centers. 相似文献