Nomenclature of Inorganic Chemistry (IUPAC Recommendations 2005)
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Densifying Metal Hydrides with High Temperature and Pressure
3,784,682 United States Patent Office Patented Jan. 8, 1974 feet the true density. That is, by this method only theo- 3,784,682 retical or near theoretical densities can be obtained by DENSIFYING METAL HYDRIDES WITH HIGH making the material quite free from porosity (p. 354). TEMPERATURE AND PRESSURE The true density remains the same. Leonard M. NiebylsM, Birmingham, Mich., assignor to Ethyl Corporation, Richmond, Va. SUMMARY OF THE INVENTION No Drawing. Continuation-in-part of abandoned applica- tion Ser. No. 392,370, Aug. 24, 1964. This application The process of this invention provides a practical Apr. 9,1968, Ser. No. 721,135 method of increasing the true density of hydrides of Int. CI. COlb 6/00, 6/06 metals of Groups II-A, II-B, III-A and III-B of the U.S. CI. 423—645 8 Claims Periodic Table. More specifically, true densities of said 10 metal hydrides may be substantially increased by subject- ing a hydride to superatmospheric pressures at or above ABSTRACT OF THE DISCLOSURE fusion temperatures. When beryllium hydride is subjected A method of increasing the density of a hydride of a to this process, a material having a density of at least metal of Groups II-A, II-B, III-A and III-B of the 0.69 g./cc. is obtained. It may or may not be crystalline. Periodic Table which comprises subjecting a hydride to 15 a pressure of from about 50,000 p.s.i. to about 900,000 DESCRIPTION OF THE PREFERRED p.s.i. at or above the fusion temperature of the hydride; EMBODIMENT i.e., between about 65° C. -
The Synthesis of Molecules Containing Quaternary Stereogenic Centers Via the Intramolecular Asymmetric Heck Reaction
The Synthesis of Molecules Containing Quaternary Stereogenic Centers via the Intramolecular Asymmetric Heck Reaction Reported by Eric P. Gillis April 19, 2007 INTRODUCTION The enantioselective synthesis of compounds containing quaternary stereocenters continues to be a challenging endeavor and is a field of intense interest and development.1,,,,2 3 4 5 From the perspective of methods development, the asymmetric synthesis of compounds containing quaternary stereocenters poses a distinct challenge due to the sterically congested environment in which C-C bonds must be formed and stereochemical information must be transferred. Existing asymmetric methods have been applied successfully in desymmetrization processes that transform prochiral quaternary centers into stereodefined quaternary centers. However, for processes in which a quaternary stereocenter is created directly via a C-C bond forming reaction, only a few asymmetric reactions have been fruitful. The diversity in the array of methods that exist for the synthesis of compounds containing quaternary stereocenters is necessitated in part because of the number of distinct quaternary stereocenter architectures that are possible (Scheme 1). The construction of acyclic quaternary stereocenters is particularly challenging due to the number of degrees of freedom associated with these structures. However, promising results for the construction of these stereocenters via allylation,6 allylic alklyation,7 and Michael addition8 have been reported recently. For the synthesis of cyclic quaternary stereocenters a number of methods have been employed successfully including the intramolecular Heck reaction,9 alkylation,10 arylation,11 and Michael addition12. Fused bicyclic quaternary stereocenters are generally accessed via the desymmetrization of a prochiral quaternary center. In this regard, theoretically any SCHEME 1. -
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. -
Triazene (H2NNNH) Or Triimide (HNHNNH) Markofçrstel,[A, D] Yetsedaw A
DOI:10.1002/cphc.201600414 Articles On the Formation of N3H3 Isomers in Irradiated Ammonia Bearing Ices:Triazene (H2NNNH) or Triimide (HNHNNH) MarkoFçrstel,[a, d] Yetsedaw A. Tsegaw,[b] Pavlo Maksyutenko,[a, d] Alexander M. Mebel,[c] Wolfram Sander,[b] and Ralf I. Kaiser*[a, d] The remarkable versatility of triazenesinsynthesis, polymer theoretical studies with our novel detection scheme of photo- chemistry and pharmacology has led to numerousexperimen- ionization-driven reflectron time-of-flight mass spectroscopy tal and theoretical studies.Surprisingly,only very little is we can obtain information on the isomersoftriazene formed known aboutthe most fundamental triazene:the parentmole- in the films. Using isotopically labeled starting material, we can cule with the chemical formula N3H3.Here we observe molecu- additionally gain insightinthe formation pathways of the iso- lar,isolated N3H3 in the gas phase after it sublimes from ener- mers of N3H3 under investigation and identify the isomers getically processed ammonia and nitrogen films. Combining formedastriazene (H2NNNH) andpossibly triimide(HNHNNH). 1. Introduction During the last decades, triazenes—a class of organic mole- life time of at least 1mswas also inferred as an intermediate cules carrying the =N N=N moiety—have received substan- in the radiolysis of an aqueous solution of hydrazine based on À À tial attention both from the theoretical and organic chemistry asingle absorption feature at 230 nm.[6] The cyclic isomer of [1] communities. Derived from cis-and trans-triazene (HN=NNH2 ; triazene, cyclotriazane, was first reported crystallographically in Scheme1), the substituted counterparts have significant appli- zeolite A, where it was stabilized by asilver cation as [1a,c] [1d] + [7] + cations in synthetic chemistry, polymer science, and phar- Ag(N3H3) . -
A Germaaluminocene†
Chemical Science View Article Online EDGE ARTICLE View Journal | View Issue A germaaluminocene† Cite this: Chem. Sci., 2020, 11, 2982 Lena Albers, * Patrik Tholen, Marc Schmidtmann and Thomas Muller¨ * All publication charges for this article The reactions of dipotassium germacyclopentadienediide with two Group 13 dichlorides, Cp*BCl and have been paid for by the Royal Society 2 * ff of Chemistry Cp AlCl2, yield two structurally di erent products. In the case of boron a borole complex of germanium(II) is obtained. The aluminium halide gives an unprecedented neutral Received 21st January 2020 Accepted 7th February 2020 germaaluminocene. Both compounds were fully characterised by multinuclear NMR spectroscopy supported by DFT computations. The molecular structure of the germaaluminocene was DOI: 10.1039/d0sc00401d determined by XRD. rsc.li/chemical-science Introduction conversion and aer work-up complex 2c was isolated as a brown oil in 35% yield (Scheme 2). NMR spectroscopy evi- The aim of utilizing readily available and environmentally denced the presence of the expected borole ring with a h1- benign main group element compounds for activation of bound cyclopentadienyl substituent. Interestingly, the NMR Creative Commons Attribution-NonCommercial 3.0 Unported Licence. unreactive materials and strong bonds instead of transition data indicated frozen rotation around the B-Ca single bond, metal-based complexes became increasingly popular during the giving rise to ten 13C NMR signals for the cyclopentadienyl last decade.1 We attempted to follow this lead by establishing substituent (Table S3, ESI†). In addition, all four carbon atoms polarised heteroalkenes I as they mimic the electronic situation of the borole ring are magnetically non-equivalent. -
New Generation Cadmium‑Free Quantum Dots for Biophotonics and Nanomedicine
This document is downloaded from DR‑NTU (https://dr.ntu.edu.sg) Nanyang Technological University, Singapore. New Generation Cadmium‑Free Quantum Dots for Biophotonics and Nanomedicine Xu, Gaixia; Zeng, Shuwen; Zhang, Butian; Swihart, Mark T.; Yong, Ken‑Tye; Prasad, Paras N. 2016 Xu, G., Zeng, S., Zhang, B., Swihart, M. T., Yong, K.‑T., & Prasad, P. N. (2016). New Generation Cadmium‑Free Quantum Dots for Biophotonics and Nanomedicine. Chemical Reviews, 116(19), 12234‑12327. https://hdl.handle.net/10356/83973 https://doi.org/10.1021/acs.chemrev.6b00290 © 2016 American Chemical Society. This is the author created version of a work that has been peer reviewed and accepted for publication by Chemical Reviews, American Chemical Society. It incorporates referee’s comments but changes resulting from the publishing process, such as copyediting, structural formatting, may not be reflected in this document. The published version is available at: [http://dx.doi.org/10.1021/acs.chemrev.6b00290]. Downloaded on 06 Oct 2021 00:28:06 SGT Page 1 of 288 Submitted to Chemical Reviews 1 2 3 4 5 6 New Generation Cadmium-Free Quantum Dots for 7 8 Biophotonics and Nanomedicine 9 10 11 12 13 14 Gaixia Xu1,5†, Shuwen Zeng2,5†, Butian Zhang2, Mark T. Swihart3*, 15 2* 4* 16 Ken-Tye Yong and Paras N. Prasad 17 18 19 20 1 21 Key Laboratory of Optoelectronics Devices and Systems of Ministry of Education/Guangdong 22 Province, College of Optoelectronic Engineering, Shenzhen University, Shenzhen, P. R. 23 China 24 2 25 School of Electrical and Electronic Engineering, -
Parallels to Frustrated Lewis/Radical Pair Chemistry
klh00 | ACSJCA | JCA11.2.5208/W Library-x64 | manuscript.3f (R5.0.i3:5004 | 2.1) 2020/02/05 13:43:00 | PROD-WS-121 | rq_481292 | 7/01/2020 12:12:45 | 10 | JCA-DEFAULT pubs.acs.org/IC Article 1 Redox-Controlled Reactivity at Boron: Parallels to Frustrated Lewis/ 2 Radical Pair Chemistry ⊥ ⊥ 3 Anthony Wong, Jiaxiang Chu, Guang Wu, Joshua Telser, Roman Dobrovetsky, and Gabriel Menard́ * Cite This: https://dx.doi.org/10.1021/acs.inorgchem.0c01464 Read Online ACCESS Metrics & More Article Recommendations *sı Supporting Information 4 ABSTRACT: We report the synthesis of new Lewis-acidic boranes μ 5 tethered to redox-active vanadium centers, (Ph2N)3V( -N)B(C6F5)2 μ 6 (1a)and(N(CH2CH2N(C6F5))3)V( -N)B(C6F5)2 (1b). Redox IV/V 7 control of the V couple resulted in switchable borane versus 8 “hidden” boron radical reactivity, mimicking frustrated Lewis versus 9 frustrated radical pair (FLP/FRP) chemistry, respectively. Whereas V 10 heterolytic FLP-type addition reactions were observed with the V 11 complex (1b) in the presence of a bulky phosphine, homolytic peroxide, IV 12 or Sn−hydride, bond cleavage reactions were observed with the V * μ 13 complex, [CoCp2 ][(N(CH2CH2N(C6F5))3)V( -N)B(C6F5)2](3b), 14 indicative of boron radical anion character. The extent of radical 15 character was probed by spectroscopic and computational means. IV/V 16 Together, these results demonstrate that control of the V oxidation 17 states allows these compounds to access reactivity observed in both FLP 18 and FRP chemistry. -
Bismuth Chloride Solution SDS US
SAFETY DATA SHEET Issue Date 10-Nov-2015 Revision Date 11-Nov-2015 Version 1 1. IDENTIFICATION Product identifier Product Name Bismuth Trichloride Solution Other means of identification Product Code 0650 UN/ID no. UN1760 Synonyms Bismuth chloride; Trichlorobismuth, Trichlorobismuthine Recommended use of the chemical and restrictions on use Recommended Use Laboratory chemicals. Uses advised against No information available Details of the supplier of the safety data sheet Manufacturer Address Harrell Industries, Inc. 2495 Commerce Drive Rock Hill, SC 29730 www.harrellindustries.com Emergency telephone number Company Phone Number 803-327-6335 Fax Number 803-327-7808 24 Hour Emergency Phone Number (800) 633-8253 PERS Emergency Telephone (800) 633-8253 (PERS) 2. HAZARDS IDENTIFICATION Classification OSHA Regulatory Status This chemical is considered hazardous by the 2012 OSHA Hazard Communication Standard (29 CFR 1910.1200) Acute toxicity - Inhalation (Gases) Category 4 Acute toxicity - Inhalation (Dusts/Mists) Category 4 Skin corrosion/irritation Category 1 Sub-category A Serious eye damage/eye irritation Category 1 Specific target organ toxicity (single exposure) Category 3 Label elements Emergency Overview Warning Hazard statements Corrosive to metals. Causes severe skin burns and eye damage May cause respiratory irritation _____________________________________________________________________________________________ Page 1 / 8 0650 - Bismuth Trichloride Solution Revision Date 11-Nov-2015 _____________________________________________________________________________________________ Appearance Clear, colorless to yellow Physical state liquid Odor Faint hydrochloric acid odor. liquid Precautionary Statements - Prevention Wash skin thoroughly after handling Wear eye protection/ face protection Wear protective gloves Precautionary Statements - Response Immediately call a POISON CENTER or doctor IF ON SKIN: Wash with plenty of soap and water IF IN EYES: Rinse cautiously with water for several minutes. -
1 Structure, Properties, and Preparation of Boronic Acid Derivatives Overview of Their Reactions and Applications Dennis G
j1 1 Structure, Properties, and Preparation of Boronic Acid Derivatives Overview of Their Reactions and Applications Dennis G. Hall 1.1 Introduction and Historical Background Structurally, boronic acids are trivalent boron-containing organic compounds that possess one carbon-based substituent (i.e., a CÀB bond) and two hydroxyl groups to fill the remaining valences on the boron atom (Figure 1.1). With only six valence electrons and a consequent deficiency of two electrons, the sp2-hybridized boron atom possesses a vacant p-orbital. This low-energy orbital is orthogonal to the three substituents, which are oriented in a trigonal planar geometry. Unlike carbox- ylic acids, their carbon analogues, boronic acids, are not found in nature. These abiotic compounds are derived synthetically from primary sources of boron such as boric acid, which is made by the acidification of borax with carbon dioxide. Borate esters, one of the key precursors of boronic acid derivatives, are made by simple dehydration of boric acid with alcohols. The first preparation and isolation of a boronic acid was reported by Frankland in 1860 [1]. By treating diethylzinc with triethylborate, the highly air-sensitive triethylborane was obtained, and its slow oxidation in ambient air eventually provided ethylboronic acid. Boronic acids are the products of a twofold oxidation of boranes. Their stability to atmospheric oxidation is considerably superior to that of borinic acids, which result from the first oxidation of boranes. The product of a third oxidation of boranes, boric acid, is a very stable and relatively benign compound to humans (Section 1.2.2.3). Their unique properties and reactivity as mild organic Lewis acids, coupled with their stability and ease of handling, are what make boronic acids a particularly attractive class of synthetic intermediates. -
Safety Data Sheet
Safety data sheet Page: 1/13 BASF Safety data sheet according to UN GHS 4th rev. Date / Revised: 23.10.2017 Version: 2.0 Product: Pearl-Glo® SF PG1099 (ID no. 30322522/SDS_COS_00/EN) Date of print 24.10.2017 1. Identification Product identifier Pearl-Glo® SF PG1099 Chemical name: Pearl-Glo SF CAS Number: 7787-59-9 Relevant identified uses of the substance or mixture and uses advised against Relevant identified uses: cosmetic ingredient Details of the supplier of the safety data sheet Company: BASF SE 67056 Ludwigshafen GERMANY Telephone: +49 621 60-48799 E-mail address: [email protected] Emergency telephone number International emergency number: Telephone: +49 180 2273-112 2. Hazards Identification Classification of the substance or mixture According to UN GHS criteria No need for classification according to GHS criteria for this product. Page: 2/13 BASF Safety data sheet according to UN GHS 4th rev. Date / Revised: 23.10.2017 Version: 2.0 Product: Pearl-Glo® SF PG1099 (ID no. 30322522/SDS_COS_00/EN) Date of print 24.10.2017 Label elements Globally Harmonized System (GHS) The product does not require a hazard warning label in accordance with GHS criteria. Other hazards According to UN GHS criteria No specific dangers known, if the regulations/notes for storage and handling are considered. 3. Composition/Information on Ingredients Substances Chemical nature INCI Name: BISMUTH OXYCHLORIDE Contains: Bismuth chloride oxide CAS Number: 7787-59-9 EC-Number: 232-122-7 Hazardous ingredients (GHS) According to UN GHS criteria No particular hazards known. Mixtures Not applicable 4. First-Aid Measures Description of first aid measures Remove contaminated clothing. -
1 Abietic Acid R Abrasive Silica for Polishing DR Acenaphthene M (LC
1 abietic acid R abrasive silica for polishing DR acenaphthene M (LC) acenaphthene quinone R acenaphthylene R acetal (see 1,1-diethoxyethane) acetaldehyde M (FC) acetaldehyde-d (CH3CDO) R acetaldehyde dimethyl acetal CH acetaldoxime R acetamide M (LC) acetamidinium chloride R acetamidoacrylic acid 2- NB acetamidobenzaldehyde p- R acetamidobenzenesulfonyl chloride 4- R acetamidodeoxythioglucopyranose triacetate 2- -2- -1- -β-D- 3,4,6- AB acetamidomethylthiazole 2- -4- PB acetanilide M (LC) acetazolamide R acetdimethylamide see dimethylacetamide, N,N- acethydrazide R acetic acid M (solv) acetic anhydride M (FC) acetmethylamide see methylacetamide, N- acetoacetamide R acetoacetanilide R acetoacetic acid, lithium salt R acetobromoglucose -α-D- NB acetohydroxamic acid R acetoin R acetol (hydroxyacetone) R acetonaphthalide (α)R acetone M (solv) acetone ,A.R. M (solv) acetone-d6 RM acetone cyanohydrin R acetonedicarboxylic acid ,dimethyl ester R acetonedicarboxylic acid -1,3- R acetone dimethyl acetal see dimethoxypropane 2,2- acetonitrile M (solv) acetonitrile-d3 RM acetonylacetone see hexanedione 2,5- acetonylbenzylhydroxycoumarin (3-(α- -4- R acetophenone M (LC) acetophenone oxime R acetophenone trimethylsilyl enol ether see phenyltrimethylsilyl... acetoxyacetone (oxopropyl acetate 2-) R acetoxybenzoic acid 4- DS acetoxynaphthoic acid 6- -2- R 2 acetylacetaldehyde dimethylacetal R acetylacetone (pentanedione -2,4-) M (C) acetylbenzonitrile p- R acetylbiphenyl 4- see phenylacetophenone, p- acetyl bromide M (FC) acetylbromothiophene 2- -5- -
C7sc03595k1.Pdf
Electronic Supplementary Material (ESI) for Chemical Science. This journal is © The Royal Society of Chemistry 2018 Mechanistic insights into boron-catalysed direct amidation reactions Sergey Arkhipenko,a Marco T. Sabatini,b Andrei Batsanov,a Valerija Karaluka,b Tom D. Sheppard,b Henry S. Rzepac and Andrew Whitinga* aCentre for Sustainable Chemical Processes, Department of Chemistry, Durham University, Science Site, South Road, Durham, DH1 3LE, UK. Email: [email protected] bDepartment of Chemistry, University College London, 20 Gordon Street, London, WC1H 0AJ, UK. cDepartment of Chemistry, Imperial College London, South Kensington Campus, London, SW7 2AZ, UK. Contents Page 1. General experimental 2 2. Synthetic procedures and compound characterisation§ 2.A. Reaction of monomeric acyloxyboron species with amines 3 2.B. Synthesis of borinic acids and studies of their interactions 6 with amines and carboxylic acids 2.C. Interactions of boronic acids with amines and carboxylic acids 10 2.D. Interaction of B2O3 and B(OH)3 with amines and carboxylic acids 21 2.E. Kinetic studies 22 3. Tabulated summary of spectroscopic data 29 4. X-ray crystallographic information# 30 5. References 36 §Note that all NMR data and .cif crystallographic data is available for download from site: DOI: 10.14469/hpc/1620 and sub-collections therein. GENERAL EXPERIMENTAL All starting materials and solvents were obtained commercially from standard chemical suppliers and were used as received unless otherwise stated. Dry solvents were prepared using the Innovative Technology Inc. solvent purification system, or dried by known methods, including standing over 4 Å molecular sieves for 24 h in the case of toluene and CDCl3.