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991.
992.
We classify all unitary modular tensor categories (UMTCs) of rank ≤ 4. There are a total of 35 UMTCs of rank ≤ 4 up to ribbon
tensor equivalence. Since the distinction between the modular S-matrix S and −S has both topological and physical significance, so in our convention there are a total of 70 UMTCs of rank ≤ 4. In particular,
there are two trivial UMTCs with S = (±1). Each such UMTC can be obtained from 10 non-trivial prime UMTCs by direct product, and some symmetry operations. Explicit
data of the 10 non-trivial prime UMTCs are given in Sect. 5. Relevance of UMTCs to topological quantum computation and various
conjectures are given in Sect. 6. 相似文献
993.
Haihui Cao Guoxing Lin Alan A. Jones 《Journal of Polymer Science.Polymer Physics》2005,43(18):2433-2444
Deuterium solid echo line shapes were measured on deuterated poly(ethylene oxide) (d4PEO) in a blend with protonated poly(methyl methacrylate) to characterize chain dynamics of this component in the blend. Line shapes were observed as a function of temperature from 183 to 243 K and echo delay times from 10 to 100 μs on a blend containing 20 wt % d4PEO. The line shapes and the associated relative intensities were quantitatively interpreted in terms of segmental motion and libration. The results of the interpretation are compared to an earlier study of deuterium spin‐lattice relaxation times over the temperature range of 313 to 413 K. A combined interpretation of both sets of data is developed based on bimodal distribution of correlation times that are separated by about 2 orders of magnitude in time. The faster mode is 30% of the correlation function with a stretched exponent near one while the slower mode is characterized by an exponent of 0.5. The source of the bimodal character is not revealed by the line shape and relaxation data but is consistent with the presence of two glass transition temperatures in this miscible blend and anomalous translational diffusion of diethyl ether through the blend. © 2005 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 43: 2433–2444, 2005 相似文献
994.
995.
996.
Eric Rivard Andrew R. McWilliams Alan J. Lough Ian Manners 《Phosphorus, sulfur, and silicon and the related elements》2013,188(4-5):845-847
An unusual, reversible skeletal substitution reaction involving boron- and aluminum-based heterophosphazenes is described. 相似文献
997.
Richard Bonnett Robert G. Guy David Lanigan 《Phosphorus, sulfur, and silicon and the related elements》2013,188(1-3):95-103
Abstract Thiocyanogen reacts slowly with alkenes, in the presence of a radical inhibitor in benzene or acetic acid in the dark at 25°, to yield α,β-dithiocyanates, α-isothiocyanates-β-thiocyanates and, in acetic acid, α-acetoxy-β-thiocyanates in varying proportions. The additions to alkyl alkenes are trans-stereospecific, and, in the case of the α-isothiocyanato-β-thiocyanates, non-regiospecific. The additions to aryl alkenes are trans-stereoselective and regiospecific, yielding the Markownikov-orientated α-isothiocyanato-β-thiocyanates. A heterolytic mechanism involving a two-step, kinetically controlled addition, with the formation of a cyano-sulfonium ion intermediate, e.g., 35, in the case of alkyl alkenes and an open carbonium ion, e.g., 36, in the case of aryl alkenes, is suggested. The diothiocyanate: isothiocyanato-thiocyanate ratios are discussed in terms of kinetic and steric control of reaction. 相似文献
998.
Jozsef Béres Wesley G. Bentrude Jeno Tomasz Alan E. Sopchik 《Phosphorus, sulfur, and silicon and the related elements》2013,188(3-4)
Abstract An investigation of the effects of changing the nature of X, nitrogen base (B), and amino substituent (R2N) on the equilibrium 1?2 was carried out. The influence of the above structural changes on the time-averaged coupling constants JAP and JBP, determined at 300 MHz, were used to follow changes in Keq. With constant R2N, small effects from variation of X and B were found. A large range in Keq arose from changes in the steric size of R2N. These results will be related to the question of the ease of chair to twist interconversion of the phosphate ring essential to the biological activities of the naturally occurring diesters, cAMP and cGMP. 相似文献
999.
Richard Cremlyn Naseem Akhtar 《Phosphorus, sulfur, and silicon and the related elements》2013,188(3):247-255
Abstract Pyrrolidine, morpholine, and β-hydroxyethylmorpholine have been phosphorylated with phosphorus oxychloride, phenylphosphorodichloridate, p-chlorophenylphosphorodichloridate and thiophosphoryl chloride. The resultant phosphorodichloridates have been condensed with a wied range of nucleophilic reagents, e.g. amines, hydrazines, phenols and isobutanol. Piperazine with phosphorus oxychloride (2 mols) gave the N(1) N(4)-diphosphorotetrachloridate, which was characterized as the tetracyclohexylamidate. β-Hydroxyethylpiperazine was similarly phosphorylated to the N,O-diphosphorotetrachloridate which was characterized as the tetraphenylhydrazidate. Condensation of pyrrolidine (2 mols) with phosphorus oxychloride (1 mol) afforded N,N′-dipyrrolidinophosphorochloridate which was reacted with phenylhydrazide and sodium azide. The phosphoroazide with triphenylphosphine afforded the corresponding triphenylphosphinimine. N-Phenyl N′-pyrrolidinophosphorochloridate with aqueous pyridine gave the corresponding pyrophosphoramide and the stability of the pyrophosphoramide towards hydrolysis was examined. 1,2-Cyclohexanediol was phosphorylated with phenylphosphorodichloridate and thiophosphorylchloride. Trans-4-t-Butylcyclohexyl N,N′-diphenylhydrazinophosphorothioate by reaction with formaldehyde gave a tetra-azaphosphorine P-sulfide. Trans-4-t-Butylcyclohexyl N-phenyl N′-phenylphosphorodiamidic hydrazide reacted with 1,4-dibromobut-2-ene to give a 1,2-diazahex-4-ene. 相似文献
1000.
R. Alan Aitken Nazira Karodia Tracy Massil Robert J. Young 《Phosphorus, sulfur, and silicon and the related elements》2013,188(1)
Abstract We recently reported the thermal elimination of Ph3PO from suitably protected aminoacyl ylides 1 as a route to acetylenic amino acid analogues 2. Pyrolysis of ylides such as 3 with a free amino group takes a different course. Ethanol is eliminated to give the c h i d cyclic ylides 4 which can be viewed as 3-triphenylphosphoranylidene tetramic acids. Specific examples prepared include 4 (R = Me, Pri), the parent compound 5 (from glycine) and the six-membered ring compound 6 (from p-alanine). Using a similar approach, bicyclic ylides such as 7 (from proline) can be prepared. In the case of the glutamate derived ylide 8, thermolysis initially gives a mixturc of 9 and 10 but these both cyclise to the bicyclic product 11 with time. The structure and reactivity of these interesting cyclic ylides are now being examined. 相似文献