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61.
Aubert B Barate R Boutigny D Gaillard JM Hicheur A Karyotakis Y Lees JP Robbe P Tisserand V Zghiche A Palano A Pompili A Chen JC Qi ND Rong G Wang P Zhu YS Eigen G Ofte I Stugu B Abrams GS Borgland AW Breon AB Brown DN Button-Shafer J Cahn RN Charles E Day CT Gill MS Gritsan AV Groysman Y Jacobsen RG Kadel RW Kadyk J Kerth LT Kolomensky YG Kral JF Kukartsev G LeClerc C Levi ME Lynch G Mir LM Oddone PJ Orimoto TJ Pripstein M Roe NA Romosan A Ronan MT Shelkov VG Telnov AV Wenzel WA Harrison TJ 《Physical review letters》2003,91(16):161801
We present measurements of the branching fractions of the decays B+-->eta'K+ and B0-->eta'K0. For B0-->eta(')K(0)(S) we also measure the time-dependent CP-violation parameters S eta'(K(0)(S)) and C eta'(K(0)(S)), and for B+-->eta'K+ the time-integrated charge asymmetry A(ch). The data sample corresponds to 88.9 x 10(6) BB pairs produced by e(+)e(-) annihilation at the Upsilon(4S). The results are B(B+-->eta'K+)=(76.9+/-3.5+/-4.4) x 10(-6), B(B0-->eta'K0)=(60.6+/-5.6+/-4.6) x 10(-6), S eta'(K(0)(S))=0.02+/-0.34+/-0.03, C eta'(K(0)(S))=0.10+/-0.22+/-0.04, and A(ch)=0.037+/-0.045+/-0.011. 相似文献
62.
Aubert B Barate R Boutigny D Gaillard JM Hicheur A Karyotakis Y Lees JP Robbe P Tisserand V Zghiche A Palano A Pompili A Chen JC Qi ND Rong G Wang P Zhu YS Eigen G Ofte I Stugu B Abrams GS Borgland AW Breon AB Brown DN Button-Shafer J Cahn RN Charles E Day CT Gill MS Gritsan AV Groysman Y Jacobsen RG Kadel RW Kadyk J Kerth LT Kolomensky YG Kral JF Kukartsev G LeClerc C Levi ME Lynch G Mir LM Oddone PJ Orimoto TJ Pripstein M Roe NA Romosan A Ronan MT Shelkov VG Telnov AV Wenzel WA Harrison TJ 《Physical review letters》2003,91(17):171801
We present results of a search for D0-D(-)0 mixing and a measurement of R(D), the ratio of doubly Cabibbo-suppressed decays to Cabibbo-favored decays, using D0-->K+pi- decays from 57.1 fb(-1) of data collected near sqrt[s]=10.6 GeV with the BABAR detector at the PEP-II collider. At the 95% confidence level, allowing for CP violation, we find the mixing parameters x('2)<0.0022 and -0.056相似文献
63.
A Danielewski surface is defined by a polynomial of the form P=x
nz
–p(y). Define also the polynomial P
=x
nz
–r(x)p(y) where r(x) is a non-constant polynomial of degree n–1 and r(0)=1. We show that, when n2 and deg p(y)2, the general fibers of P and P
are not isomorphic as algebraic surfaces, but that the zero fibers are isomorphic. Consequently, for every non-special Danielewski surface S, there exist non-equivalent algebraic embeddings of S in 3. Using different methods, we also give non-equivalent embeddings of the surfaces xz=(y
d
n
>–1) for an infinite sequence of integers d
n
.
We then consider a certain algebraic action of the orthogonal group
on 4 which was first considered by Schwarz and then studied by Masuda and Petrie, who proved that this action could not be linearized. This was done by comparing the strata of this action to those of the induced tangent space action. Inequivalent embeddings of a certain singular Danielewski surface S in 3 are found. We generalize their result and show how this leads to an example of two smooth algebraic hypersurfaces in 3 which are algebraically non-isomorphic but holomorphically isomorphic.
Partially supported by NSF Grant DMS 0101836. 相似文献
64.
Daniel Daigle Gene Freudenburg 《Proceedings of the American Mathematical Society》2001,129(3):657-662
For a field of characteristic zero, and for each integer , we construct a triangular derivation of whose ring of constants, though finitely generated over , cannot be generated by fewer than elements.
65.
Boto AN Kok P Abrams DS Braunstein SL Williams CP Dowling JP 《Physical review letters》2000,85(13):2733-2736
Classical optical lithography is diffraction limited to writing features of a size lambda/2 or greater, where lambda is the optical wavelength. Using nonclassical photon-number states, entangled N at a time, we show that it is possible to write features of minimum size lambda/(2N) in an N-photon absorbing substrate. This result allows one to write a factor of N2 more elements on a semiconductor chip. A factor of N = 2 can be achieved easily with entangled photon pairs generated from optical parametric down-conversion. It is shown how to write arbitrary 2D patterns by using this method. 相似文献
66.
In this study, an improved process for the synthesis of etorphine and dihydroetorphine from codeine with an overall yield of 2.7% and 1.5% respectively is described. The structure of 19‐propylthevinol 7 was verfied by X‐ray structure analysis. This result is promising for synthesizing various morphine‐based drugs. 相似文献
67.
Hugh Chaffey‐Millar Gene Hart‐Smith Christopher Barner‐Kowollik 《Journal of polymer science. Part A, Polymer chemistry》2008,46(5):1873-1892
A mass spectrometry analysis has been performed on complex architecture polymeric material produced during reversible addition fragmentation chain transfer (RAFT) polymerizations yielding star polymers. Para‐acetoxystyrene (AcOSty) has been polymerized at 60 °C, using azobisisobutyronitrile (AIBN) as the thermally decomposing initiator, in the presence of the R‐group approach tetrafunctional RAFT agent (1,2,4,5‐tetrakis‐(2‐phenyl‐thioacetyl‐sulfanylmethyl)‐benzene). In addition to ideal star material, a variety of products unique to this mode of polymerization have been identified. These include star–star couples, stars terminated with initiator fragments, star–star couples terminated with initiator fragments and linear polymers, supporting the notion that these species are responsible for the structured molecular‐weight distributions measured for these systems when analyzed via gel permeation chromatography. The analysis begins with a study of AcOSty polymerizing (i) in the absence of any mediating agent and (ii) in the presence of a monofunctional RAFT agent, revealing the mode of termination of propagating poly(AcOSty) radicals as combination and that some ionization biases exist among variants of poly (AcOSty). The interpretation of the mass spectrometry data has been aided by a novel kinetic model of star polymerizations, allowing the rationalization of experimental observations with theoretical expectations. © 2008 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 46: 1873–1892, 2008 相似文献
68.
69.
B. K. Mukhopadhyay K. K. Ahlquist V. Gruenman A. Lutz I. I. Kovalevski B. Schulze E. Rieger A. Noll W. Nagel J. Grant A. Abrams P. W. Codwise W. Staedel und J. D. Piper 《Fresenius' Journal of Analytical Chemistry》1936,105(5-6):212-222
Ohne Zusammenfassung 相似文献
70.
Yu‐Pin Wang Hsien‐Li Leu Tso‐Shen Lin Yu Wang Gene‐Hsiang Lee 《Acta Crystallographica. Section C, Structural Chemistry》2009,65(3):m131-m134
In the structures of each of the title compounds, [CrBr(C6H5O2)(NO)2], (I), and [CrBr(C12H9O)(NO)2], (II), one of the nitrosyl groups is located at a site away from the exocyclic carbonyl C atom of the cyclopentadienyl (Cp) ring, with twist angles of 174.5 (3) and 172.5 (1)°. The observed orientation is surprising, since the NO group is expected to be situated trans to an electron‐rich C atom in the ring. The organic carbonyl plane is turned away from the Cp ring plane by 5.6 (8) and 15.2 (3)°in (I) and (II), respectively. The exocyclic C—C bond in (I) is bent out of the Cp ring plane towards the Cr atom by 2.8 (3)°, but is coplanar with the Cp ring in (II); the angle is 0.1 (1)°. 相似文献