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41.
Multiple-zero multiple-pole optical filter transfer functions may be implemented more efficiently in an integrated optics architecture if higher order N × M optical couplers are utilized. For example, a coherent ring resonator made from two 3×3 couplers offers some advantages over the three mirror Fabry-Perot etalon, which is its analog. To this end we develop the formalism for obtaining the transfer functions and scattering matrices of ring resonators made from two N × M couplers. We then present a methodology for analyzing serial and parallel systems of N × M optical coupler ring resonators. 相似文献
42.
C. Scheidenberger K. Beckert P. Beller F. Bosch C. Brandau D. Boutin L. Chen B. Franzke H. Geissel R. Knöbel C. Kozhuharov J. Kurcewicz S. A. Litvinov Yu. A. Litvinov M. Mazzocco G. Münzenberg F. Nolden W. R. Plaß M. Steck B. Sun H. Weick M. Winkler 《Hyperfine Interactions》2006,173(1-3):61-66
One important goal of the ILIMA project at FAIR is the study of masses and decay properties of relativistic isomeric beams
stored and cooled in the planned storage-ring complex. A new scheme is described, where a storage-cooler ring is used for
high-resolution mass separation. Experimental results on the separation of the isobaric pair 140Pr-140Ce are presented.
P. Beller, deceased. 相似文献
43.
Carleson测度与Bloch的刻画 总被引:1,自引:0,他引:1
在文中,对于C^n中有界强拟凸域。我们得到Carleson测度,消没Carleson测度的刻画。利用Carleson测度,我们还得到Bloch,小Bloch的刻画。 相似文献
44.
Let R be a ring. R is called right AP-injective if, for any a ∈ R, there exists a left ideal of R such that lr(a) = Ra (?) Xa. We extend this notion to modules. A right .R-module M with 5 = End(MR) is called quasi AP-injective if, for any s ∈ S, there exists a left ideal Xs of S such that ls(Ker(s)) = Ss (?) Xs. In this paper, we give some characterizations and properties of quasi AP-injective modules which generalize results of Page and Zhou. 相似文献
45.
46.
T. V. Ramakrishnan H. R. Krishnamurthy S. R. Hassan G. Venketeswara Pai 《Journal of Chemical Sciences》2003,115(5-6):767-774
Manganites of the LA1−x
Ca
x
MnO3 family show a variety of new and poorly understood electronic, magnetic and structural effects. Here we outline a new approach
recently proposed by us, where we argue that due to strong Jahn-Teller (JT) coupling with phonons the twofold degeneratee
g
states at the Mn sites dynamically reorganize themselves into localised, JT polaronsl with exponentially small inter-site hopping, and band-like, nonpolaronic statesb, leading to anew 2-band model for manganites which includes strong Coulomb and Hund’s couplings. We also discuss some results from a dynamical mean-field theory treatment
of the model which explains quantitatively a wide variety of experimental results, including insulator-metal transitions and
CMR, in terms of the influence of physical conditions on the relative energies and occupation of thel andb states. We argue that this microscopic coexistence of the two types of electronic states, and their relative occupation and
spatial correlation is the key to manganite physics.
Dedicated to Professor C N R Rao on his 70th birthday 相似文献
47.
Anette Munch Elmr Patric Jannasch 《Journal of polymer science. Part A, Polymer chemistry》2006,44(7):2195-2205
Methacrylate‐functionalized poly(ethylene oxide‐co‐ethylene carbonate) macromonomers were prepared in two steps by the anionic ring‐opening polymerization of ethylene carbonate at 180 °C, with potassium methoxide as the initiator, followed by the reaction of the terminal hydroxyl groups of the polymers with methacryloyl chloride. The molecular weight of the polymer went through a maximum after approximately 45 min of polymerization, and the content of ethylene carbonate units in the polymer decreased with the reaction time. A polymer having a number‐average molecular weight of 2650 g mol?1 and an ethylene carbonate content of 28 mol % was selected and used to prepare a macromonomer, which was subsequently polymerized by UV irradiation in the presence of different concentrations of lithium bis(trifluoromethanesulfonyl)imide salt. The resulting self‐supportive crosslinked polymer electrolyte membranes reached ionic conductivities of 6.3 × 10?6 S cm?1 at 20 °C. The coordination of the lithium ions by both the ether and carbonate oxygens in the polymer structure was indicated by Fourier transform infrared spectroscopy. © 2006 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 44: 2195–2205, 2006 相似文献
48.
Makoto Kume Atsunori Hirano Bungo Ochiai Takeshi Endo 《Journal of polymer science. Part A, Polymer chemistry》2006,44(11):3666-3673
A spiro orthoester with an exomethylene group (exoSOE) was radically copolymerized with acrylonitrile or vinyl acetate at several feed ratios to obtain the corresponding copolymers having spiro orthoester moieties in the side chain. The obtained copolymers could be crosslinked via the double ring‐opening polymerization of the spiro orthoester moieties in their side chain by a treatment with BF3OEt2. The volume changes upon the crosslinking of the copolymers were evaluated by density measurements with a micromeritics gas pycnometer. The copolymers experienced less than 1% volume expansion instead of volume shrinkage during typical cationic crosslinking, regardless of the copolymer compositions. Negligible shrinkage was observed during the thermal cationic crosslinking of a film cast from a nitrobenzene solution of the copolymers containing a benzylthiophenium salt as a thermally latent cationic initiator. The constantly low volume changes during the crosslinking of the copolymers from exoSOE probably depended on the almost zero volume change during the cationic polymerizations of spiro orthoester derivatives. This indicates that exoSOE is an effective monomer for crosslinkable polymers without volume changes. © 2006 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 44: 3666–3673, 2006 相似文献
49.
Hisatoyo Morinaga Bungo Ochiai Hideharu Mori Takeshi Endo 《Journal of polymer science. Part A, Polymer chemistry》2006,44(12):3778-3786
Natural human hair was modified by the graft polymerization of propylene sulfide in an aqueous medium. The amount of the polymer grafted onto the reduced hair was 0.15–0.19 g on 1.0 g of hair. The grafted polymer was isolated by the hydrolysis of the hair in the polymer‐grafted hair under basic conditions and was confirmed to be poly(propylene sulfide) by 1H NMR, 13C NMR, and Fourier transform infrared spectra. The number‐average molecular weights of the isolated polymers from the grafted products were 10,000–12,000. © 2006 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 44: 3778–3786, 2006 相似文献
50.
Ye Lin Feng Zeng‐Guo Zhao Yu‐Mei Wu Feng Chen Shi Wang Guo‐Qing 《Journal of polymer science. Part A, Polymer chemistry》2006,44(11):3650-3665
A novel cyclic ether monomer 3‐{2‐[2‐(2‐hydroxyethoxy)ethoxy]ethoxy‐methyl}‐3′‐methyloxetane (HEMO) was prepared from the reaction of 3‐hydroxymethyl‐3′‐methyloxetane tosylate with triethylene glycol. The corresponding hyperbranched polyether (PHEMO) was synthesized using BF3·Et2O as initiator through cationic ring‐opening polymerization. The evidence from 1H and 13C NMR analyses revealed that the hyperbranched structure is constructed by the competition between two chain propagation mechanisms, i.e. active chain end and activated monomer mechanism. The terminal structure of PHEMO with a cyclic fragment was definitely detected by MALDI‐TOF measurement. A DSC test implied that the resulting polyether has excellent segment motion performance potentially beneficial for the ion transport of polymer electrolytes. Moreover, a TGA assay showed that this hyperbranched polymer possesses high thermostability as compared to its liquid counterpart. The ion conductivity was measured to reach 5.6 × 10?5 S/cm at room temperature and 6.3 × 10?4 S/cm at 80 °C after doped with LiTFSI at a ratio of Li:O = 0.05, presenting the promise to meet the practical requirement of lithium ion batteries for polymer electrolytes. © 2006 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 44: 3650–3665, 2006 相似文献