Interhalogen Compounds
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Transport of Dangerous Goods
ST/SG/AC.10/1/Rev.16 (Vol.I) Recommendations on the TRANSPORT OF DANGEROUS GOODS Model Regulations Volume I Sixteenth revised edition UNITED NATIONS New York and Geneva, 2009 NOTE The designations employed and the presentation of the material in this publication do not imply the expression of any opinion whatsoever on the part of the Secretariat of the United Nations concerning the legal status of any country, territory, city or area, or of its authorities, or concerning the delimitation of its frontiers or boundaries. ST/SG/AC.10/1/Rev.16 (Vol.I) Copyright © United Nations, 2009 All rights reserved. No part of this publication may, for sales purposes, be reproduced, stored in a retrieval system or transmitted in any form or by any means, electronic, electrostatic, magnetic tape, mechanical, photocopying or otherwise, without prior permission in writing from the United Nations. UNITED NATIONS Sales No. E.09.VIII.2 ISBN 978-92-1-139136-7 (complete set of two volumes) ISSN 1014-5753 Volumes I and II not to be sold separately FOREWORD The Recommendations on the Transport of Dangerous Goods are addressed to governments and to the international organizations concerned with safety in the transport of dangerous goods. The first version, prepared by the United Nations Economic and Social Council's Committee of Experts on the Transport of Dangerous Goods, was published in 1956 (ST/ECA/43-E/CN.2/170). In response to developments in technology and the changing needs of users, they have been regularly amended and updated at succeeding sessions of the Committee of Experts pursuant to Resolution 645 G (XXIII) of 26 April 1957 of the Economic and Social Council and subsequent resolutions. -
Periodic Trends in the Main Group Elements
Chemistry of The Main Group Elements 1. Hydrogen Hydrogen is the most abundant element in the universe, but it accounts for less than 1% (by mass) in the Earth’s crust. It is the third most abundant element in the living system. There are three naturally occurring isotopes of hydrogen: hydrogen (1H) - the most abundant isotope, deuterium (2H), and tritium 3 ( H) which is radioactive. Most of hydrogen occurs as H2O, hydrocarbon, and biological compounds. Hydrogen is a colorless gas with m.p. = -259oC (14 K) and b.p. = -253oC (20 K). Hydrogen is placed in Group 1A (1), together with alkali metals, because of its single electron in the valence shell and its common oxidation state of +1. However, it is physically and chemically different from any of the alkali metals. Hydrogen reacts with reactive metals (such as those of Group 1A and 2A) to for metal hydrides, where hydrogen is the anion with a “-1” charge. Because of this hydrogen may also be placed in Group 7A (17) together with the halogens. Like other nonmetals, hydrogen has a relatively high ionization energy (I.E. = 1311 kJ/mol), and its electronegativity is 2.1 (twice as high as those of alkali metals). Reactions of Hydrogen with Reactive Metals to form Salt like Hydrides Hydrogen reacts with reactive metals to form ionic (salt like) hydrides: 2Li(s) + H2(g) 2LiH(s); Ca(s) + H2(g) CaH2(s); The hydrides are very reactive and act as a strong base. It reacts violently with water to produce hydrogen gas: NaH(s) + H2O(l) NaOH(aq) + H2(g); It is also a strong reducing agent and is used to reduce TiCl4 to titanium metal: TiCl4(l) + 4LiH(s) Ti(s) + 4LiCl(s) + 2H2(g) Reactions of Hydrogen with Nonmetals Hydrogen reacts with nonmetals to form covalent compounds such as HF, HCl, HBr, HI, H2O, H2S, NH3, CH4, and other organic and biological compounds. -
IODINE Its Properties and Technical Applications
IODINE Its Properties and Technical Applications CHILEAN IODINE EDUCATIONAL BUREAU, INC. 120 Broadway, New York 5, New York IODINE Its Properties and Technical Applications ¡¡iiHiüíiüüiütitittüHiiUitítHiiiittiíU CHILEAN IODINE EDUCATIONAL BUREAU, INC. 120 Broadway, New York 5, New York 1951 Copyright, 1951, by Chilean Iodine Educational Bureau, Inc. Printed in U.S.A. Contents Page Foreword v I—Chemistry of Iodine and Its Compounds 1 A Short History of Iodine 1 The Occurrence and Production of Iodine ....... 3 The Properties of Iodine 4 Solid Iodine 4 Liquid Iodine 5 Iodine Vapor and Gas 6 Chemical Properties 6 Inorganic Compounds of Iodine 8 Compounds of Electropositive Iodine 8 Compounds with Other Halogens 8 The Polyhalides 9 Hydrogen Iodide 1,0 Inorganic Iodides 10 Physical Properties 10 Chemical Properties 12 Complex Iodides .13 The Oxides of Iodine . 14 Iodic Acid and the Iodates 15 Periodic Acid and the Periodates 15 Reactions of Iodine and Its Inorganic Compounds With Organic Compounds 17 Iodine . 17 Iodine Halides 18 Hydrogen Iodide 19 Inorganic Iodides 19 Periodic and Iodic Acids 21 The Organic Iodo Compounds 22 Organic Compounds of Polyvalent Iodine 25 The lodoso Compounds 25 The Iodoxy Compounds 26 The Iodyl Compounds 26 The Iodonium Salts 27 Heterocyclic Iodine Compounds 30 Bibliography 31 II—Applications of Iodine and Its Compounds 35 Iodine in Organic Chemistry 35 Iodine and Its Compounds at Catalysts 35 Exchange Catalysis 35 Halogenation 38 Isomerization 38 Dehydration 39 III Page Acylation 41 Carbón Monoxide (and Nitric Oxide) Additions ... 42 Reactions with Oxygen 42 Homogeneous Pyrolysis 43 Iodine as an Inhibitor 44 Other Applications 44 Iodine and Its Compounds as Process Reagents ... -
Chemistry of the Noble Gases*
CHEMISTRY OF THE NOBLE GASES* By Professor K. K. GREE~woon , :.\I.Sc., sc.D .. r".lU.C. University of N ewca.stle 1tpon Tyne The inert gases, or noble gases as they are elements were unsuccessful, and for over now more appropriately called, are a remark 60 years they epitomized chemical inertness. able group of elements. The lightest, helium, Indeed, their electron configuration, s2p6, was recognized in the gases of the sun before became known as 'the stable octet,' and this it was isolated on ea.rth as its name (i]A.tos) fotmed the basis of the fit·st electronic theory implies. The first inert gas was isolated in of valency in 1916. Despite this, many 1895 by Ramsay and Rayleigh; it was named people felt that it should be possible to induce argon (apy6s, inert) and occurs to the extent the inert gases to form compounds, and many of 0·93% in the earth's atmosphere. The of the early experiments directed to this end other gases were all isolated before the turn have recently been reviewed.l of the century and were named neon (v€ov, There were several reasons why chemists new), krypton (KpVn'TOV, hidden), xenon believed that the inert gases might form ~€vov, stmnger) and radon (radioactive chemical compounds under the correct con emanation). Though they occur much less ditions. For example, the ionization poten abundantly than argon they cannot strictly tial of xenon is actually lower than those of be called rare gases; this can be illustrated hydrogen, nitrogen, oxygen, fl uorine and by calculating the volumes occupied a.t s.t.p. -
Halogen Fluorides Chlorine Trifluoride ( Clf3 )
Journal content Halogen fluorides Chlorine trifluoride ( ClF3), Bromine trifluoride (BrF3) Trifluorides of bromine and chlorine are strong fluorinating reagents and chlorine trifluoride is among the most reactive and aggressive compounds and does not yield to fluorine in chemical activity. Main constants of these compounds are as follows: ClF3 BrF3 Molecular mass 92.46 136.91 Boiling temperature,oC 11.75 125.75 Melting temperature, oC -76.3 8.77 Density at 25oC,g/cm3 1.8094 2.8 ClF3 was obtained and identified by O.Ruff and H.Krug in 1930 [2], BrF3 was produced by P.Leberau [3] and E.B.R.Prideaux [4] in 1905. Both halogen fluorides are produced in industry by direct fluorination of Cl2(Br2) in a nickel equipment followed by further purification from admixtures by fractional distillation [5]. Methods to produce ClF3 and BrF3, their chemical and physical properties, molecular structure etc. have been reviewed in detail in a number of papers including [1,6,7,8], while there are few data about their application except application in nuclear [1,8] and space [8] engineering. Since the reviews contain information up to the late 60-s ( 1966-1967), it seems expedient to examine improvements in a technology of production and purification of ClF3 and BrF3 and also data about their application published since 1967. 1. Technology of production and purification of ClF3 and BrF3 There are practically no records for the period under review (1967-1999). Three reports [9,10,11] relate to investigation of kinetics of reactions to produce ClF3 under specific conditions. -
Inorganic Seminar Abstracts
C 1 « « « • .... * . i - : \ ! -M. • ~ . • ' •» »» IB .< L I B RA FLY OF THE. UN IVERSITY Of 1LLI NOIS 546 1^52-53 Return this book on or before the Latest Date stamped below. University of Illinois Library «r L161— H41 Digitized by the Internet Archive in 2012 with funding from University of Illinois Urbana-Champaign http://archive.org/details/inorganicsemi195253univ INORGANIC SEMINARS 1952 - 1953 TABLE OF CONTENTS 1952 - 1953 Page COMPOUNDS CONTAINING THE SILICON-SULFUR LINKAGE 1 Stanley Kirschner ANALYTICAL PROCEDURES USING ACETIC ACID AS A SOLVENT 5 Donald H . Wilkins THE SOLVENT PHOSPHORYL CHLORIDE, POCl 3 12 S.J. Gill METHODS FOR PREPARATION OF PURE SILICON 17 Alex Beresniewicz IMIDODISULFINAMIDE 21 G.R. Johnston FORCE CONSTANTS IN POLYATOMIC MOLECILES 28 Donn D. Darsow METATHESIS IN LIQUID ARSENIC TRICHLORIDE 32 Harold H. Matsuguma THE RHENI DE OXIDATION STATE 40 Robert L. Rebertus HALOGEN CATIONS 45 L.H. Diamond REACTIONS OF THE NITROSYL ION 50 M.K. Snyder THE OCCURRENCE OF MAXIMUM OXIDATION STATES AMONG THE FLUOROCOMPLEXES OF THE FIRST TRANSITION SERIES 56 D.H. Busch POLY- and METAPHOSPHATES 62 V.D. Aftandilian PRODUCTION OF SILICON CHLORIDES BY ELECTRICAL DISCHARGE AND HIGH TEMPERATURE TECHNIQUES 67 VI. £, Cooley FLUORINE CONTAINING OXYHALIDES OF SULFUR 72 E.H. Grahn PREPARATION AND PROPERTIES OF URANYL CARBONATES 76 Richard *• Rowe THE NATURE OF IODINE SOLUTIONS 80 Ervin c olton SOME REACTIONS OF OZONE 84 Barbara H. Weil ' HYDRAZINE BY ELECTROLYSIS IN LIQUID AMMONIA 89 Robert N. Hammer NAPHTHAZARIN COMPLEXES OF THORIUM AND RARE EARTH METAL IONS 93 Melvin Tecotzky THESIS REPORT 97 Perry Kippur ION-PAIR FORMATION IN ACETIC ACID 101 M.M. -
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 -
Mean Amplitudes of Vibration of Iodine Trifluoride
Note 333 Mean Amplitudes of Vibration of Iodine Table 1. Calculated mean amplitudes of vibration (in A) of IF3. Trifluoride HK) MI-F(ax) «I-F(eq) u F(ax)...F(ax) MF(ax)...F(eq) E. J. Baran 0 0.0448 0.0401 0.057 0.057 Centro de Qufmica Inorgänica (CEQUINOR/CONICET, 100 0.0448 0.0401 0.057 0.058 UNLP), Facultad de Ciencias Exactas, 200 0.0460 0.0405 0.058 0.062 Universidad Nacional de La Plata, C. Correo 962, 298.16 0.0489 0.0420 0.061 0.068 1900-La Plata, Argentina 300 0.0489 0.0420 0.061 0.068 400 0.0528 0.0444 0.066 0.075 Reprint requests to Prof. E. J. B.; 500 0.0568 0.0474 0.071 0.082 E-mail: [email protected] 600 0.0609 0.0500 0.075 0.089 700 0.0648 0.0529 0.080 0.095 Z. Naturforsch. 56a, 333-334 (2001); 800 0.0686 0.0558 0.085 0.101 received January 12, 2001 900 0.0723 0.0586 0.089 0.107 1000 0.0759 0.0613 0.094 0.113 Mean amplitudes of vibration of IF3 have been calculated from vibrational spectroscopic data in the temperature range between 0 and 1000 K. Bond properties of the molecule are dis cussed on the basis of these results. Some comparison with relat Table 2. Comparison of the mean amplitudes of vibration (in A ed species are made. and at 298. 16 K) of the three isostructural XF3 species. -
1 Unit 4.4 Chemistry of Non-Transition Elements Few Facts of Halogens: A
Unit 4.4 Chemistry of Non-transition Elements Few facts of halogens: a) Ionisation energy of halogens is very high. This indicates that it has very little tendency to lose electrons. Due to gradual increase in size, it decreases down the group. b) The halogen molecules are held by weak Vander Waals forces, which increase down the group. This is responsible for the solid state of iodine. c) Chlorine has highest electron affinity in the group. Due to small size, fluorine has lower electron affinity than chlorine. d) All halogens are coloured as shown below: Halogens Fluorine Chlorine Bromine Iodine Colour Light Yellow Greenish Yellow Reddish Yellow Dark Violet The origin of colours of halogens is due to the absorption of visible light which excite the outermost electron to a higher energy level. Fluorine, being very small in size require very large excitation energy (obtained from the blue or violet part) of light, hence light yellow. Iodine being very large in size, the required lower excitation energy is obtained by absorption of yellow part of light. Interhalogen compounds: Halogen elements have different electro-negativity. Due to this they combine with each other to form covalent compounds (binary). “The binary compounds formed by halogens amongst themselves are known as Inter- halogen compounds”. These compounds have general formula; XYn, where n = 1, 3, 5 & 7. Ternary compounds of halogens are not known; as such a complex molecule might be unstable. Classification: Various types of inter-halogen compounds are tabulated below: Element Fluorine Chlorine Bromine Iodine Fluorine ------ ----- ----- ----- Chlorine ClF, ClF3, ClF5 --- --- --- Bromine BrF, BrF3, BrF5 BrCl --- --- Iodine IF, IF3, IF5, IF7 ICl, ICl3 IBr --- From the above table, the following points may be noted: • The inter-halogen compounds may be regarded as the halide of the more electronegative halogen. -
5.04 Principles of Inorganic Chemistry II Fall 2008
MIT OpenCourseWare http://ocw.mit.edu 5.04 Principles of Inorganic Chemistry II Fall 2008 For information about citing these materials or our Terms of Use, visit: http://ocw.mit.edu/terms. Chemistry 5.04 (F08) Practice Problem Set Practice vibrational and MO problems for the exam 1. Chatt prepared the dinitrogen complexes, trans-Mo(N2)2(PR3)4 in which the surprising result of two π-acid ligands coordinate trans to each other. Build the MO diagram for the complex. Draw the frontier d-orbital MOs and indicate the HOMO and LUMO orbitals. 2. Shown below are two electronically different metal carbides. Use MO arguments to address the following: a. Draw the HOMO for each complex. b. Explain the vacant site trans to the carbide atom in the square pyramidal, Ru complex. c. How many pi electrons are donated from the anilides into the metal in the moly complex (assume that for each sp2 hybirdized N-atom the tert-butly group point up, towards the apical carbide, and the aryl groups point down). Do the anilides and carbide compete for π symmetry orbitals on moly? d. Estimate the relative acidity of both carbide-carbon atoms. Which of these acids will protonate the carbide: MeC6H5, HCPh3, H3CCOOH, H(OEt2)B[3,5-C6H3(CF3)2] (answer yes or no for each acid/carbide combination)? 8 3. The synthesis of uranocene, [(η -C8H8)2U], is considered as the beginning of modern organoactinide chemistry. Organoactinides are distinguished by covalent interactions between the 5f orbitals of the 2– actinoids as well as the 6d orbitals. -
Bromine Trifluoride As a Solvent*
OpenStax-CNX module: m33061 1 Bromine Trifluoride as a Solvent* Andrew R. Barron This work is produced by OpenStax-CNX and licensed under the Creative Commons Attribution License 3.0 warning: Bromine triuoride is a toxic, colorless, and corrosive liquid with a pungent choking smell that is soluble in sulfuric acid but explodes on contact with water and organic compounds. Vapors severely irritate and may burn the eyes, skin, and respiratory system. The liquid burns all human tissue and causes severe damage. ◦ ◦ Bromine triuoride (BrF3) has a liquid range similar to water (Mp = 8.8 C and Bp = 127 C), and like water it auto ionizes, (1). (1) + - The products, like those of water's self-ionization, are an acid (BrF2 ) and a base (BrF4 ). However, unlike water, BrF3 reacts with uoride acids and bases not proton acids and bases. Thus, in BrF3 a base is a salt - that provides F , i.e., potassium uoride (KF) is a base in BrF3 solution in the same manner as potassium hydroxide (KOH) is a base in water. The product from the reaction of a uoride donor salt with BrF3 is the - formation of the conjugate base, BrF4 , (2). (2) Other examples of this type of reaction include: (3) (4) - By analogy, an acid in BrF3 solution is a compound that acts as a uoride (F ) acceptor, i.e., a Lewis acid, (5). (5) Exercise 1 (Solution on p. 3.) What are the products from the reaction of HF with BrF3? *Version 1.3: Jan 19, 2010 5:32 pm -0600 http://creativecommons.org/licenses/by/3.0/ http://cnx.org/content/m33061/1.3/ OpenStax-CNX module: m33061 2 1 Bromine triuoride as a uorinating agent Bromine triuoride is a strong uorinating agent that is able to convert a metal (e.g., vanadium) to its associated uoride compound, (i.e., VF5). -
Physical Properties and Association of the Liquid Halogen Fluorides
PHYSICAL PROPERTIES AND ASSOCIATION OF THE LIQUID HALOGEN FLUORIDES By Emerson E. Garver A THESIS Submitted to the School for Advanced Graduate Studies of Michigan State University of Agriculture and Applied Science in partial fulfillment of the requirements for the degree of DOCTOR OF PHILOSOPHY Department of Chemistry 1957 ProQuest Number: 10008509 All rights reserved INFORMATION TO ALL USERS The quality of this reproduction is dependent upon the quality of the copy submitted. In the unlikely event that the author did not send a complete manuscript and there are missing pages, these will be noted. Also, if material had to be removed, a note will indicate the deletion. uest ProQuest 10008509 Published by ProQuest LLC (2016). Copyright of the Dissertation is held by the Author. All rights reserved. This work is protected against unauthorized copying under Title 17, United States Code Microform Edition © ProQuest LLC. ProQuest LLC. 789 East Eisenhower Parkway P.O. Box 1346 Ann Arbor, Ml 48106- 1346 ACKNOWLEDGMENT The author wishes to express his sincere appreciation to Professor Max T. Rogers, without whom this manuscript could not have been written. Throughout the course of this investigation he has offered encouragement, helpfulness and much-needed advice. He also wishes to make known his debt to J. L, Speirs for aid in instrumentation, to H. B, Thompson for his cogent observations, and to E, Forest Hood for some excellent glass blowing. The Atomic Energy Commission has made this work possible through a research grant. VITA Emerson E, Garver was born May 1, 1929 at Akron, Ohio. After attending Western Reserve Academy located at Hudson, Ohio, he spent one year at Swarthmore College and received the Bachelor of Science degree from Kent State University in 1951* He attended graduate school at the Ohio State University for a year and the following year enrolled at Michigan State University.