Summary: Novel biodegradable copolymers derived from succinate, butan‐1,4‐diol, and butan‐1,4‐diamine were synthesized by two‐step polycondensation reactions. The obtained copolymers had a periodical‐sequence structure consisting of ester and amide units, and the melting temperatures of the periodic copolymers increased with an increase in amide content. The crystalline structure of the periodic copolymers differs from that of butylene succinate homopolymer (PBS), and these results suggest that the periodically introduced amide units are included in the crystalline phase forming a novel crystalline structure.
Periodic copolyester‐amides derived from succinate, butane‐1,4‐diol, and butan‐1,4‐diamine 相似文献
The development of a millimeter and submillimeter wave catheter for irradiation on living bodies using a gyrotron as the radiation power source is described. The GYROTRON FU-IV, optimized for such applications was used in the development. It was operated in both CW and pulsed regime at TE03 and TE32 modes with frequencies 302 GHz and 238 GHz respectively. Irradiation tests were made on thermal papers, beefs and liver of living rats. 相似文献
OCTA (Open Computational Tool for Advanced material technology) is an integrated simulation system for polymeric materials developed by a joint project of industry and academia supported by Japanese government. It aims at exploring the utility of mesoscale modelings developed in polymer science. OCTA consists of four simulation engines (molecular dynamics engine, rheology engine, interface engine, multi-phase engine) and a simulation platform. The system is designed to be open and extendable: all programs and source codes can be downloaded at http://octa.jp. 相似文献
The Li3MX6 compounds (M=Sc, Y, In; X=Cl, Br) are known as promising ionic conductors due to their compatibility with typical metal oxide cathode materials. In this study, we have successfully synthesized γ-Li3ScCl6 using high pressure for the first time in this family. Structural analysis revealed that the high-pressure polymorph crystallizes in the polar and chiral space group P63mc with hexagonal close-packing (hcp) of anions, unlike the ambient-pressure α-Li3ScCl6 and its spinel analog with cubic closed packing (ccp) of anions. Investigation of the known Li3MX6 family further revealed that the cation/anion radius ratio, rM/rX, is the factor that determines which anion sublattice is formed and that in γ-Li3ScCl6, the difference in compressibility between Sc and Cl exceeds the ccp rM/rX threshold under pressure, enabling the ccp-to-hcp conversion. Electrochemical tests of γ-Li3ScCl6 demonstrate improved electrochemical reduction stability. These findings open up new avenues and design principles for lithium solid electrolytes, enabling routes for materials exploration and tuning electrochemical stability without compositional changes or the use of coatings. 相似文献
We numerically investigated the dependence of the decryption characteristics in a message modulation type chaos secure communication system using optical fiber ring resonators (OFRRs) on the coherence condition of carrier light. Since the output dynamics of OFRRs were formed on the basis of interference phenomenon among the circulated components in OFRRs, the coherence condition of input light affected inherently the OFRR output dynamics, resulting in the decryption characteristics. It was found that the decryption characteristics degraded as coherence length increased, i.e., as the spectral width of the input light decreased. The decryption characteristics also grew worse as the parameter differences between the transmitter and the receiver became larger. 相似文献
The stereoselective one-pot three-component coupling reaction was accomplished by 1,4-addition of the protected cyanohydrin ether 9f to cyclohexenone 10g and subsequent addition of the resulting enolate to formaldehyde in high yield for the formation of the AC ring system of taxanes. We found that the bulky substituents at the 10-position in the A ring prevent the desired 1,4-addition. Similarly, the bulky trialkylsiloxy groups at the 4-position in the C ring prevent the 1,4-addition and electron-donating alkoxy groups at the same position induce the undesired retro-Michael reaction. 相似文献
The major products formed upon photolysis of ethyl 3-azido-4,6-difluorobenzoate in 2,2,2-trifluoroethanol-d3 has been elucidated by 1H NMR analysis of the product mixture. Among the products formed and structurally elucidated was a hitherto unreported product formed during photolysis of aryl azides, namely azoxybenzene 19. The structural assignments of the major components of the reaction mixture were aided by comparison with 1H NMR data from synthetic reference materials and compound isolation. MS, MS/MS, and HPLC analysis as well as UV spectroscopy was also employed in order to confirm and aid the structural analysis. 相似文献
The spectrofluorometric behavior of a membrane potential-sensitive dye, 1-(3-sulfonatopropyl)-4-[β-{2-(di-N-butylamino)-6-naphthyl}vinyl]pyridinium betaine (di-4-ANEPPS), at the polarized 1,2-dichloroethane/water interface was studied
by means of potential-modulated fluorescence (PMF) spectroscopy. The results, combined with those from cyclic and alternating
current voltammetry, clearly suggested that the dye adsorbed at the interface underwent a reorientation with increasing the
interfacial potential, giving a well-developed PMF response as well as a voltammetric response. In addition to the PMF response,
another PMF response was observed by addition of dilauroyl phosphatidylcholine (DLPC). This additional response was well explained
in terms of a reorientation of di-4-ANEPPS at the interface, which would be induced by the potential-dependent desorption
of DLPC from the interface. Thus, the present study supported the reorientation/solvatochromic mechanism for the membrane
potential-sensitive dye rather than the electrochromic mechanism. 相似文献
This study investigated the relationship of growth conditions, host strains and molecular weights of poly[(R)-3-hydroxybutyrate] [P(3HB)] synthesized by genetically engineered Escherichia coli. Various PHA synthases belonging to types I-IV enzymes were expressed in E. coli JM109 under the same experimental conditions, and the molecular weights of the polymers were characterized by gel permeation chromatography. The results demonstrate that P(3HB) polymers have varied molecular weights and polydispersities dependent on the characteristics of the individual PHA synthase employed. P(3HB) with high number-average molecular weights (Mn) [(1.5-4.0) × 106] and narrow polydispersities (1.6-1.8) were synthesized by PHA synthases from Ralstonia eutropha (type I), Delftia acidovorans (type I) and Allochromatium vinosum (type III). Contrary to these, P(3HB) with relatively low Mn [(0.17-0.79) × 106] and broad polydispersities (2.2-9.0) were synthesized by PHA synthases from Aeromonas caviae (type I), Pseudomonas sp. 61-3 (type II) and Bacillus sp. INT005 (type IV). Furthermore, the molecular weights of P(3HB) synthesized under various culture conditions, in various hosts of E. coli and by mutants of PHA synthase were characterized. It was found that, in addition to culture pH [Kusaka et al. Appl Microbiol Biotechnol 1997;47:140], other variances such as culture temperature, host strain and use of mutants are effective in changing polymer molecular weight. 相似文献