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71.
T. Watanabe P. Bydžovský K. Dobashi S. Endo Y. Fujii O. Hashimoto T. Ishikawa K. Itoh H. Kanda M. Katoh T. Kinoshita O. Konno K. Maeda A. Matsumura F. Miyahara H. Miyase T. Miyoshi K. Mizunuma Y. Miura S.N. Nakamura H. Nomura Y. Okayasu T. Osaka M. Oyamada A. Sasaki T. Satoh H. Shimizu M. Sotona T. Takahashi T. Tamae H. Tamura T. Terasawa H. Tsubota K. Tsukada M. Ukai M. Wakamatsu H. Yamauchi H. Yamazaki 《Physics letters. [Part B]》2007
72.
Bartelt J Csorna SE Egyed Z Jain V Gibaut D Kinoshita K Pomianowski P Barish B Chadha M Chan S Cowen DF Eigen G Miller JS O'Grady C Urheim J Weinstein AJ Würthwein F Asner DM Athanas M Bliss DW Brower WS Masek G Paar HP Gronberg J Korte CM Kutschke R Menary S Morrison RJ Nakanishi S Nelson HN Nelson TK Qiao C Richman JD Roberts D Ryd A Tajima H Witherell MS Balest R Cho K Ford WT Lohner M Park H Rankin P Smith JG Alexander JP Bebek C Berger BE Berkelman K Bloom K Browder TE Cassel DG Cho HA 《Physical review D: Particles and fields》1995,52(9):4860-4867
73.
Kuwamura N Kitano K Hirotsu M Nishioka T Teki Y Santo R Ichimura A Hashimoto H Wright LJ Kinoshita I 《Chemistry (Weinheim an der Bergstrasse, Germany)》2011,17(38):10708-10715
Interchange between the nickel +2 and +3 oxidation states precisely controls the reversible rearrangement of the tris(2-pyridylthio)methanide (tptm) ligand in the organometallic nickel(II) complex [{Ni(μ-Br)-(tptm)}(2)] (2). Oxidation of 2 first gives the corresponding Ni(III) complex [{Ni(μ-Br)(tptm)}(2)][PF(6)](2) (4). However, in solution the tptm ligand in 4 slowly undergoes a rearrangement, in which the N and S atoms of one of the pyridylthiolate arms exchange Ni and C bonding partners, thereby resulting in an "N,S-confused" isomer of tptm in the product, [NiBr(bpttpm)]PF(6) (5; bpttpm= bis(2-pyridylthio)(2-thiopyridinium)-methyl). Reduction of 5 reverses this ligand rearrangement and 2 is reformed quantitatively. The individual steps involved in these unusual ligand rearrangements were investigated by a number of methods, including voltammetric analysis, and a mechanism for this process is proposed. X-ray crystal structure determinations of the key compounds 2, 4 and 5 have been obtained. 相似文献
74.
Takayuki Muro Yukako Kato Toyohiko Kinoshita Yoshio Watanabe 《Journal of synchrotron radiation》2009,16(4):595-596
A video camera system for observing a sample from the direction of an incident soft X‐ray beam has been developed. The sample is seen via two reflecting mirrors. The first mirror, which has a hole to allow the soft X‐ray beam to pass through, is set on the beam axis in a vacuum. The second mirror is used to cancel out the mirror inversion of the image. This camera system is used for efficient positioning of samples in a soft X‐ray beam. 相似文献
75.
76.
Masahiro Kinoshita Yuko Okamoto Fumio Hirata 《Journal of computational chemistry》1997,18(10):1320-1326
We have developed an algorithm for solving the reference interaction site model (RISM) equations for water near a solute molecule with many atomic sites (interaction sites). It is a hybrid of the Newton–Raphson and Picard methods and is judiciously constructed. Various considerations are given so that the computer time can be saved as much as possible. The robustness and high efficiency of the algorithm has been demonstrated for calculating hydration free energies of Met-enkephalin (a peptide with 75 sites) with different conformations. The Jacobian matrix is treated as part of the input data, and it has been found that the same matrix can be used for a considerably large set of different conformations of the solute molecule. © 1997 John Wiley & Sons, Inc. J Comput Chem 18: 1320–1326, 1997 相似文献
77.
Dominick J Lambrecht M Sanghera S Shelkov V Skwarnicki T Stroynowski R Volobouev I Wei G Zadorozhny P Artuso M Goldberg M He D Horwitz N Kennett R Mountain R Moneti GC Muheim F Mukhin Y Playfer S Rozen Y Stone S Thulasidas M Vasseur G Zhu G Bartelt J Csorna SE Egyed Z Jain V Kinoshita K Edwards KW Ogg M Britton DI Hyatt ER MacFarlane DB Patel PM Akerib DS Barish B Chadha M Chan S Cowen DF Eigen G Miller JS O'Grady C Urheim J Weinstein AJ Acosta D Athanas M Masek G Paar HP Sivertz M Gronberg J 《Physical review D: Particles and fields》1994,50(5):3027-3037
78.
Dina L. Kinoshita Luiz G. Ferreira Manoel L. De Siqueira 《International journal of quantum chemistry》1985,28(1):85-101
This is the third paper on the cellular method for polyatomic systems. We show how to deal with nonspherical Coulomb potentials. We also show how to modify the variational expression for the energy eigenvalues so as to obtain a faster convergence in the angular momentum series for the wavefunctions. We apply both techniques to the self-consistent calculation of SF6. Contrary to what we obtained in CH4 and SiH4, the cellular method cannot yield the correct equilibrium interatomic distance in the present case. The calculated ionization potentials are in the correct order but are all shifted by 2–3 eV. This shift is attributed to the wrong expression for exchange correlation. 相似文献
79.
80.
傅元勇 周书华T. Koike S. Kinoshita Y. Ma Y. Miura K. Miwa Y. Miyagi K. Shirotori T. Suzuki H. Tamura K. Tsukada M. Ukai K. Futatsukawa K. Hosomi M. Kawai M. Mimori N. Terada N. Maruyama K. Aoki H Fujioka Y Kakiguchi T. Nagae D. Nakajima H Noumi T Takahashi T.N. Takahashi A. Toyota M. Dairaku T. Fukuda S. Minami W. Imoto S. Aiimura K. Tanida 《中国物理快报》2007,24(8):2216-2218
From the ^12 C(π^+,K^+)^12 AC reaction the γ -rays of 261.6±0.24 ke V(7/2^+ →5/2^+)and 1481.7±0.7 ke V(1/2^+ →5/2^+) of ^11 A B,and 2667.3±2.8 keV(1^- 2 → 2^- 1)of ^12 A C hypernuclei have been identified using a large germanium detector array Hyperball2 at K6 beam line of KEK. The observed energies of the transitions 1481.7keV and 261.6 keV are significantly different from the values predicted by the shell model using the △ and SN parameters determined from the ^7 △ Li data. 相似文献