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(12) United States Patent (10) Patent N0.: US 8,304,580 B2 Nanmyo Et A]
US008304580B2 (12) United States Patent (10) Patent N0.: US 8,304,580 B2 Nanmyo et a]. (45) Date of Patent: Nov. 6, 2012 (54) METHOD FOR PRODUCING TRIS(PER FOREIGN PATENT DOCUMENTS FLUORO-ALKANESULFONYL)METHIDE EP 0813521 B1 * 9/2000 ACID SALT JP 2000-226392 A 8/2000 JP 2000-256348 A 9/2000 (75) Inventors: Tsutomu Nanmyo, Ube (JP); Shintaro JP 2000-256348 A * 9/2000 Sasaki, Ube (JP); Takashi Kume, OTHER PUBLICATIONS KaWagoe (JP) English translation of JP-2000-256348-A; “machine translation” (73) Assignee: Central Glass Company, Limited, from JPO link at: http://WWW4.ipd1.inpit.go.jp/Tokujitu/ Ube-shi (JP) tj sogodbenkipdl accessed Oct. 25, 201 1; relevant part of document.* European Search Report dated Jun. 8, 2011 (four (4) pages). ( * ) Notice: Subject to any disclaimer, the term of this Waller et al., “Tris (tri?uoromethanesulfonyl) methide (“Tri?ide”) patent is extended or adjusted under 35 Anion: Convenient Preparation, X-ray Crystal Structures, and U.S.C. 154(b) by 528 days. Exceptional Catalytic Activity as a Counterion With Ytterbium (III) and Scandium (111)”, Journal of Organic Chemistry, vol. 64, 1999, pp. (21) Appl. N0.: 12/520,17s 2910-2913, XP-002636992. Turowsky et al., “Tris ((tri?uoromethyl) sulfonyl) methane, HC (22) PCT Filed: Dec. 18, 2007 (SO2CF3)3”, Journal of Inorganic Chemistry, vol. 27, 1988, pp. 2135-2137, XP-002636993. (86) PCT No.: PCT/JP2007/074296 International Search Report and PCT/ISN237 W/translation dated Feb. 12, 2008 (Seven (7) pages). § 371 (0X1)’ LutZ Turowsky et al., “Tris((tri?uoromethyl)sulfonyl)methane, (2), (4) Date: Jun. -
Lecture Notes
Solid State Physics PHYS 40352 by Mike Godfrey Spring 2012 Last changed on May 22, 2017 ii Contents Preface v 1 Crystal structure 1 1.1 Lattice and basis . .1 1.1.1 Unit cells . .2 1.1.2 Crystal symmetry . .3 1.1.3 Two-dimensional lattices . .4 1.1.4 Three-dimensional lattices . .7 1.1.5 Some cubic crystal structures ................................ 10 1.2 X-ray crystallography . 11 1.2.1 Diffraction by a crystal . 11 1.2.2 The reciprocal lattice . 12 1.2.3 Reciprocal lattice vectors and lattice planes . 13 1.2.4 The Bragg construction . 14 1.2.5 Structure factor . 15 1.2.6 Further geometry of diffraction . 17 2 Electrons in crystals 19 2.1 Summary of free-electron theory, etc. 19 2.2 Electrons in a periodic potential . 19 2.2.1 Bloch’s theorem . 19 2.2.2 Brillouin zones . 21 2.2.3 Schrodinger’s¨ equation in k-space . 22 2.2.4 Weak periodic potential: Nearly-free electrons . 23 2.2.5 Metals and insulators . 25 2.2.6 Band overlap in a nearly-free-electron divalent metal . 26 2.2.7 Tight-binding method . 29 2.3 Semiclassical dynamics of Bloch electrons . 32 2.3.1 Electron velocities . 33 2.3.2 Motion in an applied field . 33 2.3.3 Effective mass of an electron . 34 2.4 Free-electron bands and crystal structure . 35 2.4.1 Construction of the reciprocal lattice for FCC . 35 2.4.2 Group IV elements: Jones theory . 36 2.4.3 Binding energy of metals . -
A STUDY of the BINARY SYSTEM Na-Cs
C oo|p ef A STUDY OF THE BINARY SYSTEM Na-Cs BY L. M. COOPER THESIS FOR THE DEGREE OF BACHELOR OF SCIENCE IN CHEMICAL ENGINEERING COLLEGE OF LIBERAL ARTS AND SCIENCES UNIVERSITY OF ILLINOIS 1917 1*3 »T UNIVERSITY OF ILLINOIS .Maz..25. i^ilr. THIS IS TO CERTIFY THAT THE THESIS PREPARED UNDER MY SUPERVISION BY LiiOU...M...,..C.O,Qm T3E.. BINARY.. ENTITLED A... SI.UM.. .PI.. S^^^^^ THE IS APPROVED BY ME AS FULFILLING THIS PART OF THE REQUIREMENTS FOR DEGREE OF., BA.GHELOR...Qii...S.C.IM.C.E. Instructor in Charge Approved : HEAD OF DEPARTMENT OF. 3 UHJC -13- IX TABLE OF CONTENTS Page I Introduction 1 II Source and purification of materials 2 III Method 6 IV Table 7 V Temperature-concentration diagram of the binary system Na-Gs 8 VI Discussion of diagram 9 VII Conclusions 11 VIII Bibliography 12 IX Table of Contents 13 X Acknowledgement 14 Digitized by the Internet Archive in 2013 http://archive.org/details/studyofbinarysysOOcoop . I INTRODUCTION Systems of two alkali metals have been little studied. Lithium in its alloy forming properties resembles magnesium rather than sodium, and its behavior is in some respects anom- alous. Molten lithium is hardly miscible with sodium or potas- (1) sium. Sodium forms a single compound NaoK, with potassium, (3) but this compound dissociates below its melting point. It is probable that both lithium and sodium would prove, on investi- gation, to form compounds with rubidium and caesium, but that the metals of the potassium sub-group would not combine with one another In the second sub-group, copper, silver, and gold alloy together, forming solid solutions either completely or to a limited extent. -
Safety Data Sheet According to 1907/2006/EC, Article 31 Printing Date 21.07.2021 Revision: 21.07.2021
Page 1/6 Safety data sheet according to 1907/2006/EC, Article 31 Printing date 21.07.2021 Revision: 21.07.2021 SECTION 1: Identification of the substance/mixture and of the company/undertaking · 1.1 Product identifier · Trade name: Cesium chloride (99.999%-Cs) PURATREM · Item number: 93-5542 · CAS Number: 7647-17-8 · EC number: 231-600-2 · 1.2 Relevant identified uses of the substance or mixture and uses advised against No further relevant information available. · 1.3 Details of the supplier of the safety data sheet · Manufacturer/Supplier: Strem Chemicals, Inc. 7 Mulliken Way NEWBURYPORT, MA 01950 USA [email protected] · Further information obtainable from: Technical Department · 1.4 Emergency telephone number: EMERGENCY: CHEMTREC: + 1 (800) 424-9300 During normal opening times: +1 (978) 499-1600 SECTION 2: Hazards identification · 2.1 Classification of the substance or mixture · Classification according to Regulation (EC) No 1272/2008 The substance is not classified according to the CLP regulation. · 2.2 Label elements · Labelling according to Regulation (EC) No 1272/2008 Void · Hazard pictograms Void · Signal word Void · Hazard statements Void · Precautionary statements P231 Handle under inert gas. P262 Do not get in eyes, on skin, or on clothing. P305+P351+P338 IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing. P403+P233 Store in a well-ventilated place. Keep container tightly closed. P422 Store contents under inert gas. P501 Dispose of contents/container in accordance with local/regional/national/international regulations. · 2.3 Other hazards · Results of PBT and vPvB assessment · PBT: Not applicable. -
WO 2016/074683 Al 19 May 2016 (19.05.2016) W P O P C T
(12) INTERNATIONAL APPLICATION PUBLISHED UNDER THE PATENT COOPERATION TREATY (PCT) (19) World Intellectual Property Organization International Bureau (10) International Publication Number (43) International Publication Date WO 2016/074683 Al 19 May 2016 (19.05.2016) W P O P C T (51) International Patent Classification: (81) Designated States (unless otherwise indicated, for every C12N 15/10 (2006.01) kind of national protection available): AE, AG, AL, AM, AO, AT, AU, AZ, BA, BB, BG, BH, BN, BR, BW, BY, (21) International Application Number: BZ, CA, CH, CL, CN, CO, CR, CU, CZ, DE, DK, DM, PCT/DK20 15/050343 DO, DZ, EC, EE, EG, ES, FI, GB, GD, GE, GH, GM, GT, (22) International Filing Date: HN, HR, HU, ID, IL, IN, IR, IS, JP, KE, KG, KN, KP, KR, 11 November 2015 ( 11. 1 1.2015) KZ, LA, LC, LK, LR, LS, LU, LY, MA, MD, ME, MG, MK, MN, MW, MX, MY, MZ, NA, NG, NI, NO, NZ, OM, (25) Filing Language: English PA, PE, PG, PH, PL, PT, QA, RO, RS, RU, RW, SA, SC, (26) Publication Language: English SD, SE, SG, SK, SL, SM, ST, SV, SY, TH, TJ, TM, TN, TR, TT, TZ, UA, UG, US, UZ, VC, VN, ZA, ZM, ZW. (30) Priority Data: PA 2014 00655 11 November 2014 ( 11. 1 1.2014) DK (84) Designated States (unless otherwise indicated, for every 62/077,933 11 November 2014 ( 11. 11.2014) US kind of regional protection available): ARIPO (BW, GH, 62/202,3 18 7 August 2015 (07.08.2015) US GM, KE, LR, LS, MW, MZ, NA, RW, SD, SL, ST, SZ, TZ, UG, ZM, ZW), Eurasian (AM, AZ, BY, KG, KZ, RU, (71) Applicant: LUNDORF PEDERSEN MATERIALS APS TJ, TM), European (AL, AT, BE, BG, CH, CY, CZ, DE, [DK/DK]; Nordvej 16 B, Himmelev, DK-4000 Roskilde DK, EE, ES, FI, FR, GB, GR, HR, HU, IE, IS, IT, LT, LU, (DK). -
Standardless, Automated Determination of Chlorine-35 by 35Cl Nuclear Magnetic Resonance
Standardless, Automated Determination of Chlorine-35 by 35Cl Nuclear Magnetic Resonance Watson, Simon A1; Edwards, Andy J1; Parkinson, John A2 1GlaxoSmithKline Medicines Research Centre, Stevenage, Hertfordshire, UK 2 WestCHEM Department of Pure and Applied Chemistry, University of Strathclyde, Glasgow, UK Corresponding author: Watson, Simon A; GlaxoSmithKline, Gunnelswood Road, Stevenage, Hertfordshire, UK, SG1 2NY; 01438 766685; [email protected] We present an example of a robust, fully automated, walk-up method to quantify chloride concentration in sample solutions using 35Cl nuclear magnetic resonance (NMR). Minimal user input is required, no standards are acquired at the time of analysis and the submission, acquisition, processing and production of results are seamlessly integrated within existing NMR automation software. The method demonstrated good linearity with R2 = 0.999 over three orders of magnitude of analyte concentration, results that are highly independent of analyte functionality, and the stability of instrument response was such that analyses of additional standards were not required for a period of several months. At a nominal sample concentration of 10 mg/ml in D2O at 400 MHz, a detection limit and a quantitation limit of 0.1 and 0.5% w/w, respectively, was achieved in a 1 hour run time. Robust methodology was achieved by applying a rigorous approach to method development and validation to determine and evaluate fully the time- and sample-dependent factors that affect quantitation in this experiment. 1 Keywords: NMR, 35Cl, chloride, quantitation, walk-up, automation, pharmaceutical analysis Introduction The maxim that “nuclear magnetic resonance (NMR) is inherently quantitative” has become a central dogma of NMR spectroscopy in literature and presentations. -
Simple Cubic Lattice
Chem 253, UC, Berkeley What we will see in XRD of simple cubic, BCC, FCC? Position Intensity Chem 253, UC, Berkeley Structure Factor: adds up all scattered X-ray from each lattice points in crystal n iKd j Sk e j1 K ha kb lc d j x a y b z c 2 I(hkl) Sk 1 Chem 253, UC, Berkeley X-ray scattered from each primitive cell interfere constructively when: eiKR 1 2d sin n For n-atom basis: sum up the X-ray scattered from the whole basis Chem 253, UC, Berkeley ' k d k d di R j ' K k k Phase difference: K (di d j ) The amplitude of the two rays differ: eiK(di d j ) 2 Chem 253, UC, Berkeley The amplitude of the rays scattered at d1, d2, d3…. are in the ratios : eiKd j The net ray scattered by the entire cell: n iKd j Sk e j1 2 I(hkl) Sk Chem 253, UC, Berkeley For simple cubic: (0,0,0) iK0 Sk e 1 3 Chem 253, UC, Berkeley For BCC: (0,0,0), (1/2, ½, ½)…. Two point basis 1 2 iK ( x y z ) iKd j iK0 2 Sk e e e j1 1 ei (hk l) 1 (1)hkl S=2, when h+k+l even S=0, when h+k+l odd, systematical absence Chem 253, UC, Berkeley For BCC: (0,0,0), (1/2, ½, ½)…. Two point basis S=2, when h+k+l even S=0, when h+k+l odd, systematical absence (100): destructive (200): constructive 4 Chem 253, UC, Berkeley Observable diffraction peaks h2 k 2 l 2 Ratio SC: 1,2,3,4,5,6,8,9,10,11,12. -
Crystal Structure Transformations in Binary Halides
1 A UNITED STATES DEPARTMENT OF A111D3 074^50 IMMERCE JBLICAT10N NSRDS—NBS 41 HT°r /V\t Co^ NSRDS r #C£ DM* ' Crystal Structure Transformations in Binary Halides u.s. ARTMENT OF COMMERCE National Bureau of -QC*-| 100 US73 ho . 4 1^ 72. NATIONAL BUREAU OF STANDARDS 1 The National Bureau of Standards was established by an act of Congress March 3, 1901. The Bureau's overall goal is to strengthen and advance the Nation’s science and technology and facilitate their effective application for public benefit. To this end, the Bureau conducts research and provides: (1) a basis for the Nation’s physical measure- ment system, (2) scientific and technological services for industry and government, (3) a technical basis for equity in trade, and (4) technical services to promote public safety. The Bureau consists of the Institute for Basic Standards, the Institute for Materials Research, the Institute for Applied Technology, the Center for Computer Sciences and Technology, and the Office for Information Programs. THE INSTITUTE FOR BASIC STANDARDS provides the central basis within the United States of a complete and consistent system of physical measurement; coordinates that system with measurement systems of other nations; and furnishes essential services leading to accurate and uniform physical measurements throughout the Nation’s scien- tific community, industry, and commerce. The Institute consists of a Center for Radia- tion Research, an Office of Measurement Services and the following divisions: Applied Mathematics—Electricity—Heat—Mechanics—Optical Physics—Linac Radiation 2—Nuclear Radiation 2—Applied Radiation 2—Quantum Electronics 3— Electromagnetics 3—Time and Frequency 3—Laboratory Astrophysics 3—Cryo- 3 genics . -
Cesium Chloride and Dmso Protocol
Cesium Chloride And Dmso Protocol Undistilled Xavier suffumigates her alamedas so impalpably that Hartley locomote very unflaggingly. Heliconian Rabi still blathers: expectable and unconverted Bernie alternating quite adjectivally but staving her listeria proximo. Sometimes true Zackariah strewings her inns ceaselessly, but costive Stephanus eternised conservatively or perpetrated twelvefold. The best alternative cancer treatments actually consist of several protocols which fulfil different things. Nieper has passed away. Lammers T, Peschke P, Kuhnlein R, et al. DNAse mix: made up her end of binding incubations. Likewise, blockade of these channels produces early afterdepolarizations, which can produce to arrhythmias, including torsade de pointes. The greed is to caught the lowest values reported as causing the way adverse effects, and stout the broadest possible safety margins for adolescent substance. Here because the degree of dying cancer and cesium dmso protocol. Values are generally displayed in milligram per kilo food. The solubilities of these hydroxylic bases are also shown in Table IX for comparative purposes. However, there is no evidence the support these claims, while serious adverse reactions have been reported. This bench an immensely powerful cancer treatment, but the rules are fresh, and they ought be respected. This reversible characteristic provides a strategy for both solvent removal from the products of reaction as longer as solvent recovery and reuse. Already, the truck below can start time help visualize aspects of motion comparison. Cesium Chloride Protocol actually follow and complete protocol. On scene and reading initial presentation she was treated with standard advanced cardiac life support. Electromedicine devices cannot cut cancer cells directly because fault cannot differentiate between a cancer cell first a normal cell. -
Chemical Names and CAS Numbers Final
Chemical Abstract Chemical Formula Chemical Name Service (CAS) Number C3H8O 1‐propanol C4H7BrO2 2‐bromobutyric acid 80‐58‐0 GeH3COOH 2‐germaacetic acid C4H10 2‐methylpropane 75‐28‐5 C3H8O 2‐propanol 67‐63‐0 C6H10O3 4‐acetylbutyric acid 448671 C4H7BrO2 4‐bromobutyric acid 2623‐87‐2 CH3CHO acetaldehyde CH3CONH2 acetamide C8H9NO2 acetaminophen 103‐90‐2 − C2H3O2 acetate ion − CH3COO acetate ion C2H4O2 acetic acid 64‐19‐7 CH3COOH acetic acid (CH3)2CO acetone CH3COCl acetyl chloride C2H2 acetylene 74‐86‐2 HCCH acetylene C9H8O4 acetylsalicylic acid 50‐78‐2 H2C(CH)CN acrylonitrile C3H7NO2 Ala C3H7NO2 alanine 56‐41‐7 NaAlSi3O3 albite AlSb aluminium antimonide 25152‐52‐7 AlAs aluminium arsenide 22831‐42‐1 AlBO2 aluminium borate 61279‐70‐7 AlBO aluminium boron oxide 12041‐48‐4 AlBr3 aluminium bromide 7727‐15‐3 AlBr3•6H2O aluminium bromide hexahydrate 2149397 AlCl4Cs aluminium caesium tetrachloride 17992‐03‐9 AlCl3 aluminium chloride (anhydrous) 7446‐70‐0 AlCl3•6H2O aluminium chloride hexahydrate 7784‐13‐6 AlClO aluminium chloride oxide 13596‐11‐7 AlB2 aluminium diboride 12041‐50‐8 AlF2 aluminium difluoride 13569‐23‐8 AlF2O aluminium difluoride oxide 38344‐66‐0 AlB12 aluminium dodecaboride 12041‐54‐2 Al2F6 aluminium fluoride 17949‐86‐9 AlF3 aluminium fluoride 7784‐18‐1 Al(CHO2)3 aluminium formate 7360‐53‐4 1 of 75 Chemical Abstract Chemical Formula Chemical Name Service (CAS) Number Al(OH)3 aluminium hydroxide 21645‐51‐2 Al2I6 aluminium iodide 18898‐35‐6 AlI3 aluminium iodide 7784‐23‐8 AlBr aluminium monobromide 22359‐97‐3 AlCl aluminium monochloride -
Short Communications
SHORT COMMUNICATIONS CARBONYL HALIDES OF THE GROUP VIII TRANSITION METALS By R. COLTON?and R. H. FARTHING? [Manuscript received April 24, 19691 Introduction In the preparation of dichlorodicarbonylruthenium(~~)by the interaction of a mixture of formic acid and hydrochloric acid on ruthenium trichloride, it was observed1 that the solution turned from its initial red colour to bright green before finally becoming yellow or orange. The dicarbonyl complex was isolated from the orange solution1 and we now report the isolation of the intermediate compound, dichloroaquocarbonylruthenium(~~),from the green solution. In the course of an elegant kinetic study of this system, Halpern and Kemp2 isolated the anion [RuCO(H20)C14]2-,which is derived from our new aquocarbonyl halide, simply by addition of ammonium chloride to the green solution; and they suggested that dichloroaquocarbonylruthenium(~~)was an intermediate in the formation of the dicarbonyl compound. Results and Discussion Ruthenium trichloride is readily reduced by formic acid in the presence of hydrochloric acid to give, initially, a green solution.1 Slow evaporation of this solution in a vacuum desiccator gave pure dichloroaquocarbonylruthenium(~~)as a black powder. The complex is involatile and remarkably stable thermally since it can be heated to 200"in vacuum without loss of the coordinated water molecule. However, unlike the corresponding dicarbonyl complex it is susceptible to oxidation in solution. It is soluble in water, hydrochloric acid solution, acetone, methanol, and other coordinating solvents, but insoluble in chloroform, dichloromethane, and carbon tetrachloride. In hydrochloric acid solution it undoubtedly exists as the tetrachloro- aquocarbonylruthenate(~~)anion, since addition of the chlorides of suitable large cations such as caesium is sufficient to precipitate the appropriate salt of this anion. -
289. Problem 22.35P (HRW) in the Basic Cscl (Caesium Chloride) Crystal Structure, Cs Ions Form the Corners of a Cube and A
289. Problem 22.35P (HRW) In the basic CsCl (caesium chloride) crystal structure, Cs+ ions form the corners of a cube and a Cl− ion is at the cube’s centre. The edge length of the cube is 0.40 nm. The ions are each deficient by one electron (and thus each has a charge of +e), and the Cl− ion has one excess electron (and thus has a charge of −e). (a) We have to find the magnitude of the net electrostatic force on the ion by the eight ions at the corners of the cube. (b) If one of the ions is missing the crystal is said to have a defect. We have to find the magnitude of the net electrostatic force exerted on the ion by the remaining ions. Solution: (a) We not that relative to the ion at the centre of the cubic crystal there are a pair of ions which exert equal and Csopposite+ electrostatic forces on the ion. Therefore, the magnitude of the net electrostatic force on the ion due to the eight ions located at the vertices of the cubic lattice will be zero. Cl− (b) When one of the ions is missing there will be an imbalance of force on the ion. The magnitude of the force on the ion due to the remaining seven ions will therefore be equal to the force that the missing ion would have exerted on the ion. It is given that the edge length of the cube is 0.40 nm. Therefore, the distance of the centre of the cube from any of the vertices of the cube will be 33 da= = 0.40 10−−9 m = 3.46 10 10 m.