Concentrations of Polycyclic Aromatic Hydrocarbons in New Jersey Soils
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Determination of Parent and Alkylated Polycyclic Aromatic Hydrocarbons (Pahs) in Biota and Sediment
ICES TECHNIQUES IN MARINE ENVIRONMENTAL SCIENCES NO. 45 NOVEMBER 2009 Determination of parent and alkylated polycyclic aromatic hydrocarbons (PAHs) in biota and sediment L. WEBSTER • J. TRONCZYNSKI P. KORYTAR • K. BOOIJ • R. LAW International Council for the Exploration of the Sea Conseil International pour l’Exploration de la Mer H. C. Andersens Boulevard 44 – 46 DK‐1553 Copenhagen V Denmark Telephone (+45) 33 38 67 00 Telefax (+45) 33 93 42 15 www.ices.dk [email protected] Our cover photo was taken by N. Penny Holliday aboard the RRS “Discovery” in rough seas in the Rockall Trough. Recommended format for purposes of citation: Webster, L., Tronczynski, J., Korytar, P., Booij, K., and Law, R. 2010. Determination of parent and alkylated polycyclic aromatic hydrocarbons (PAHs) in biota and sediment. ICES Techniques in Marine Environmental Sciences. No. 45. 26 pp. Series Editor: Paul D. Keizer For permission to reproduce material from this publication, please apply directly to the General Secretary. Correspondence concerning the details of any method or procedure should be directed to the author(s). This series presents detailed descriptions of methods and procedures relating to chemical and biological measurements in the marine environment. Most techniques described have been selected for documentation based on performance in ICES or other intercalibration or intercomparison exercises: they have been carefully evaluated and shown to yield good results when correctly applied. They have also been subject to review by relevant ICES working groups, but this is not to be construed as constituting official recommendation by the Council. ISBN 978-87-7482-074-1 978-87-7482-297-4 https://doi.org/10.17895/ices.pub.5070 ISSN 0903 – 2606 2707-6997 © 2010 International Council for the Exploration of the Sea ICES Techniques in Marine Environmental Sciences No. -
Mild Synthesis of Perylene Tetracarboxylic Monoanhydrides with Potential Applications in Organic Optoelectronics
City University of New York (CUNY) CUNY Academic Works All Dissertations, Theses, and Capstone Projects Dissertations, Theses, and Capstone Projects 5-2019 Mild Synthesis of Perylene Tetracarboxylic Monoanhydrides with Potential Applications in Organic Optoelectronics Xizhe Zhao The Graduate Center, City University of New York How does access to this work benefit ou?y Let us know! More information about this work at: https://academicworks.cuny.edu/gc_etds/3258 Discover additional works at: https://academicworks.cuny.edu This work is made publicly available by the City University of New York (CUNY). Contact: [email protected] Mild Synthesis of Perylene Tetracarboxylic Monoanhydrides with Potential Applications in Organic Optoelectronics By Xizhe Zhao A dissertation submitted to the Graduate Faculty in Chemistry in partial fulfillment of the requirements for the degree of Doctor of Philosophy The City University of New York. 2019 © 2019 Xizhe Zhao All Rights Reserved ii Mild Synthesis of Perylene Tetracarboxylic Monoanhydrides with Potential Applications in Organic Optoelectronics by Xizhe Zhao This manuscript has been read and accepted for the Graduate Faculty in Chemistry in satisfaction of the dissertation requirement for the degree of Doctor of Philosophy. 04/29/19 Prof. Shi Jin _________________________ __________________________________________________ Date Chair of Examining Committee 04/29/19 Prof. Brian R. Gibney _________________________ __________________________________________________ Date Executive Officer Supervisory Committee: Prof. Krishnaswami Raja Prof. Sanjai Kumar Pathak THE CITY UNIVERSITY OF NEW YORK iii ABSTRACT Mild Synthesis of Perylene Tetracarboxylic Monoanhydrides with Potential Applications in Organic Optoelectronics By Xizhe Zhao Advisor: Professor Shi Jin Perylene tetracarboxylic derivatives are considered good n-type semi-conductors. In past decades, there has been extensive study on their synthesis and electronic properties. -
Polycyclic Aromatic Hydrocarbon Structure Index
NIST Special Publication 922 Polycyclic Aromatic Hydrocarbon Structure Index Lane C. Sander and Stephen A. Wise Chemical Science and Technology Laboratory National Institute of Standards and Technology Gaithersburg, MD 20899-0001 December 1997 revised August 2020 U.S. Department of Commerce William M. Daley, Secretary Technology Administration Gary R. Bachula, Acting Under Secretary for Technology National Institute of Standards and Technology Raymond G. Kammer, Director Polycyclic Aromatic Hydrocarbon Structure Index Lane C. Sander and Stephen A. Wise Chemical Science and Technology Laboratory National Institute of Standards and Technology Gaithersburg, MD 20899 This tabulation is presented as an aid in the identification of the chemical structures of polycyclic aromatic hydrocarbons (PAHs). The Structure Index consists of two parts: (1) a cross index of named PAHs listed in alphabetical order, and (2) chemical structures including ring numbering, name(s), Chemical Abstract Service (CAS) Registry numbers, chemical formulas, molecular weights, and length-to-breadth ratios (L/B) and shape descriptors of PAHs listed in order of increasing molecular weight. Where possible, synonyms (including those employing alternate and/or obsolete naming conventions) have been included. Synonyms used in the Structure Index were compiled from a variety of sources including “Polynuclear Aromatic Hydrocarbons Nomenclature Guide,” by Loening, et al. [1], “Analytical Chemistry of Polycyclic Aromatic Compounds,” by Lee et al. [2], “Calculated Molecular Properties of Polycyclic Aromatic Hydrocarbons,” by Hites and Simonsick [3], “Handbook of Polycyclic Hydrocarbons,” by J. R. Dias [4], “The Ring Index,” by Patterson and Capell [5], “CAS 12th Collective Index,” [6] and “Aldrich Structure Index” [7]. In this publication the IUPAC preferred name is shown in large or bold type. -
Organic Chemistry Name Formula Isomers Methane CH 1 Ethane C H
Organic Chemistry Organic chemistry is the chemistry of carbon. The simplest carbon molecules are compounds of just carbon and hydrogen, hydrocarbons. We name the compounds based on the length of the longest carbon chain. We then add prefixes and suffixes to describe the types of bonds and any add-ons the molecule has. When the molecule has just single bonds we use the -ane suffix. Name Formula Isomers Methane CH4 1 Ethane C2H6 1 Propane C3H8 1 Butane C4H10 2 Pentane C5H12 3 Hexane C6H14 5 Heptane C7H16 9 Octane C8H18 18 Nonane C9H20 35 Decane C10H22 75 Isomers are compounds that have the same formula but different bonding. isobutane n-butane 1 Naming Alkanes Hydrocarbons are always named based on the longest carbon chain. When an alkane is a substituent group they are named using the -yl ending instead of the -ane ending. So, -CH3 would be a methyl group. The substituent groups are named by numbering the carbons on the longest chain so that the first branching gets the lowest number possible. The substituents are listed alphabetically with out regard to the number prefixes that might be used. 3-methylhexane 1 2 3 4 5 6 6 5 4 3 2 1 Alkenes and Alkynes When a hydrocarbon has a double bond we replace the -ane ending with -ene. When the hydrocarbon has more than three carbon the position of the double bond must be specified with a number. 1-butene 2-butene Hydrocarbons with triple bonds are named basically the same, we replace the -ane ending with -yne. -
Stoichiometric and Catalytic Reactions Involving Si-H Bond Activations by Rh and Ir Complexes Containing a Pyridylindolide Ligand Dmitry Karshtedt,†,‡ Alexis T
Organometallics 2006, 25, 4471-4482 4471 Stoichiometric and Catalytic Reactions Involving Si-H Bond Activations by Rh and Ir Complexes Containing a Pyridylindolide Ligand Dmitry Karshtedt,†,‡ Alexis T. Bell,*,§,‡ and T. Don Tilley*,†,‡ Departments of Chemistry and Chemical Engineering, UniVersity of California, Berkeley, Berkeley, California 94720, and Chemical Sciences DiVision, Lawrence Berkeley National Laboratory, 1 Cyclotron Road, Berkeley, California 94720 ReceiVed June 5, 2006 New rhodium and iridium complexes containing the bidentate, monoanionic 2-(2′-pyridyl)indolide (PyInd) ligand were prepared. The bis(ethylene) complex (PyInd)Rh(C2H4)2 (3) reacted with triethylsilane at 60 °C to produce the 16-electron Rh(V) bis(silyl)dihydride complex (PyInd)RhH2(SiEt3)2 (4). Both 3 and 4 catalyzed the chloride transfer reaction of chlorobenzene and Et3SiH to give Et3SiCl and benzene i in the absence of base. In the presence of LiN Pr2, catalytic C-Si coupling was observed, to produce Et3SiPh. Analogous Ir complexes of the type (PyInd)IrH2(SiR3)2, where R3 ) Et3 (6a), Me2Ph (6b), Ph2Me (6c), or Ph3 (6d), were not catalytically active in this chloride transfer chemistry. The molecular structure of 6c, determined by X-ray crystallography, may be described as having a highly unusual bicapped tetrahedral geometry. DFT calculations indicate that this distortion is associated with the d4 electron count and the presence of highly trans-influencing silyl ligands. The reaction of 6a with PMe3 (5 equiv) produced (PyInd)IrH(SiEt3)(PMe3)2 (7), while the reaction with PPh3 (1 equiv) generated a mixture of isomers that was converted to (PyInd)IrH(SiEt3)(PPh3)(8) upon heating in benzene at 80 °C. -
Addition of Hydrogen Bromide to Unsymmetrical Olefins
AN ABSTRACT OF TH TESIS OF Charles runior Rogers for the Ph.D. in Chemistry (Name) (Degree) (Lajor1 Date thesis is presented August 22, 1952 - Title ADDITION OF HYDROGEN BROMIDE Abstract approved Redacted for privacy (Ljr Pro'essor) (j In this investigation the addition o1 hydrogen bromide to 3-methylcyclohexene has been studied in order to see if the theory of hyperconjugation could be extended to include olefins of' this type. Since the olefin has an equal number of hydrogens on both carbons carrying the double bond, a mixture o± bromides was expected in the addition product. The bromides expected were cis-2- or trans-2-bromomethyl- cyclobexane or a mixture of the isomers and ois-3- or trans-3-broraomethylcyclohexane or a mixture or those isomers. An infrared method ol' analyzing the addition product was used. To use this method it was necessary to make up 1own mixtures of the compounds expected in the addition product. In order to prepare some of the isomeric bromides, trams-2- and trans-3-rnethylcyclohexanol were prepared. Then, because no good. methods could be found in the literature for the conversion of isomeric alcohols to isonieric bromides, the alcohols were not used. Instead, the Imown mixtures for the infrared work were prepared from 2-bromo- and 3-bromo- methylcyclohexanes, both containing unknown amounts of the cis-trans isomers. The 3-methylcyclohexene used in the hydrogen bromide addition was prepared from. 3-bromom.ethylcyclohexene and methylnìagnesium iodide. The addition of hydrogen bromide was conducted at 0°C and at room temperature using glacial acetic acid as a solvent. -
Highly Soluble Monoamino-Substituted Perylene Tetracarboxylic Dianhydrides: Synthesis, Optical and Electrochemical Properties
Int. J. Mol. Sci. 2014, 15, 22642-22660; doi:10.3390/ijms151222642 OPEN ACCESS International Journal of Molecular Sciences ISSN 1422-0067 www.mdpi.com/journal/ijms Article Highly Soluble Monoamino-Substituted Perylene Tetracarboxylic Dianhydrides: Synthesis, Optical and Electrochemical Properties Kew-Yu Chen * and Che-Wei Chang Department of Chemical Engineering, Feng Chia University, Taichung 40724, Taiwan; E-Mail: [email protected] * Author to whom correspondence should be addressed; E-Mail: [email protected]; Tel.: +886-4-2451-7250 (ext. 3683); Fax: +886-4-2451-0890. External Editor: Dennis N. Kevill Received: 8 November 2014; in revised form: 21 November 2014 / Accepted: 1 December 2014 / Published: 8 December 2014 Abstract: Three dialkylamino-substituted perylene tetracarboxylic dianhydrides with different n-alkyl chain lengths (n = 6, 12 or 18), 1a–1c, were synthesized under mild conditions in high yields and were characterized by 1H NMR, 13C NMR and high resolution mass spectroscopy. Their optical and electrochemical properties were measured using UV-Vis and emission spectroscopic techniques, as well as cyclic voltammetry (CV). This is the first time that the structures and the properties of monoamino-substituted perylene tetracarboxylic dianhydrides have been reported. These molecules show a deep green color in both solution and the solid state and are soluble in most organic solvents. They all show a unique charge transfer emission in the near-infrared region, and the associated peaks exhibit solvatochromism. The dipole moments of the compounds have been estimated using the Lippert-Mataga equation, and upon excitation, they show slightly larger dipole moment changes than those of corresponding perylene diimides, 2a–2c. -
Polycyclic Aromatic Hydrocarbon Structure Index
United States Department of Commerce Technology Administration National Institute of Standards and Technology NIST Special Publication 922 Polycyclic Aromatic Hydrocarbon Structure Index Lane C. Sander and Stephen A. Wise This publication is available free of charge from: https://doi.org/10.6028/NIST.SP.922e2020 NIST Special Publication 922 Polycyclic Aromatic Hydrocarbon Structure Index Lane C. Sander and Stephen A. Wise Chemical Science and Technology Laboratory National Institute of Standards and Technology Gaithersburg, MD 20899-0001 December 1997 revised August 2020 This publication is available free of charge from: https://doi.org/10.6028/NIST.SP.922e2020 U.S. Department of Commerce Wilbur L. Ross, Jr., Secretary National Institute of Standards and Technology Walter Copan, NIST Director and Under Secretary of Commerce for Standards and Technology Errata for SP 922 (printed document) Corrected entries are listed below 2 1 3 19 Acephenanthrylene CH 9 10 4 201-06-9 16 10 202 1.291 8 5 Cyclopenta[jk]phenanthrene 11.70 7 6 9.067 3.890 10 1 9 2 27208-37-3 226 1.200 33 8 3 Cyclopenta[cd]pyrene CH18 10 7 4 11.52 6 5 Acepyrene Acepyrylene 9.602 3.887 10 9 1 34 Benz[mno]aceanthrylene 203-13-4 CH 226 8 2 18 10 1.222 7 3 Naphtho[1,8,7,6-cdef]fluorene 11.83 6 5 4 9.679 3.884 2 HC2 1 3 41 11 4 1H-Cyclopenta[e]pyrene 109587-09-9 CH19 12 240 10 5 9 8 6 7 11 1 10 2 9 3 52 5H-Benzo[cd]pyrene 191-34-4 CH19 12 240 1.233 8 5 4 7 6 Pyrenindene 11.92 C 9.674 H2 4.207 14 1 13 2 12 3 160 4 Cyclopent[b]indeno[4,5-g]- 72088-81-4 CH24 14 302 10 11 9 phenanthrene 8 5 7 6 2 3 1 4 14 5 Cyclopent[b]indeno[5,6-g]- 72088-82-5 CH 302 161 6 24 14 12 13 phenanthrene 11 10 7 89 Polycyclic Aromatic Hydrocarbon Structure Index Lane C. -
Polycyclic Aromatic Hydrocarbons (Pahs)
Polycyclic Aromatic Hydrocarbons (PAHs) Factsheet 4th edition Donata Lerda JRC 66955 - 2011 The mission of the JRC-IRMM is to promote a common and reliable European measurement system in support of EU policies. European Commission Joint Research Centre Institute for Reference Materials and Measurements Contact information Address: Retiewseweg 111, 2440 Geel, Belgium E-mail: [email protected] Tel.: +32 (0)14 571 826 Fax: +32 (0)14 571 783 http://irmm.jrc.ec.europa.eu/ http://www.jrc.ec.europa.eu/ Legal Notice Neither the European Commission nor any person acting on behalf of the Commission is responsible for the use which might be made of this publication. Europe Direct is a service to help you find answers to your questions about the European Union Freephone number (*): 00 800 6 7 8 9 10 11 (*) Certain mobile telephone operators do not allow access to 00 800 numbers or these calls may be billed. A great deal of additional information on the European Union is available on the Internet. It can be accessed through the Europa server http://europa.eu/ JRC 66955 © European Union, 2011 Reproduction is authorised provided the source is acknowledged Printed in Belgium Table of contents Chemical structure of PAHs................................................................................................................................. 1 PAHs included in EU legislation.......................................................................................................................... 6 Toxicity of PAHs included in EPA and EU -
Methane Or Pentane Calibration
July 10, 2003 Applications Note: Use of "pentane equivalent" calibration gas mixtures Introduction The gas that is used to verify accuracy is every bit as important as the detector itself when it comes to worker safety. Choosing (and using) the right mixture is critical to the success of your atmospheric monitoring program. BW understands the importance of calibration, and we are always on the lookout for ways to improve the process. To that end, BW is pleased to announce the introduction of a new series of "pentane equivalent" calibration gas mixtures. These mixtures are designed to provide an even more dependable (and easy) means for the verification of accuracy of instruments that include a sensor for the detection of combustible gas. What are "pentane equivalent" mixtures and why are they better? Using BW’s new "equivalent" mixtures is exactly like using our older mixtures. In the case of the GasAlertMicro and GasAlertMax, all you have to do is press the "cal" button, attach the adaptor, and flow gas to the sensors. All the adjustments are made automatically. The difference comes from what's in the cylinder of gas. In the past, BW has usually recommended using mixtures that include 50% LEL methane as the combustible gas used for general purpose calibration. BW's new equivalent mixtures are still based on methane, but in concentrations that are designed to produce a level of sensitivity "equivalent" to that provided by a mixture that contains a 50% LEL concentration of pentane. The reasoning behind the development of these new formulations has to do with how combustible sensors detect gas, and what happens to sensitivity in the event that a combustible sensor ever becomes "poisoned". -
Health Risks of Structural Firefighters from Exposure to Polycyclic
International Journal of Environmental Research and Public Health Systematic Review Health Risks of Structural Firefighters from Exposure to Polycyclic Aromatic Hydrocarbons: A Systematic Review and Meta-Analysis Jooyeon Hwang 1,* , Chao Xu 2 , Robert J. Agnew 3 , Shari Clifton 4 and Tara R. Malone 4 1 Department of Occupational and Environmental Health, Hudson College of Public Health, University of Oklahoma Health Sciences Center, Oklahoma City, OK 73104, USA 2 Department of Biostatistics and Epidemiology, Hudson College of Public Health, University of Oklahoma Health Sciences Center, Oklahoma City, OK 73104, USA; [email protected] 3 Fire Protection & Safety Engineering Technology Program, College of Engineering, Architecture and Technology, Oklahoma State University, Stillwater, OK 74078, USA; [email protected] 4 Department of Health Sciences Library and Information Management, Graduate College, University of Oklahoma Health Sciences Center, Oklahoma City, OK 73104, USA; [email protected] (S.C.); [email protected] (T.R.M.) * Correspondence: [email protected]; Tel.: +1-405-271-2070 (ext. 40415) Abstract: Firefighters have an elevated risk of cancer, which is suspected to be caused by occupational and environmental exposure to fire smoke. Among many substances from fire smoke contaminants, one potential source of toxic exposure is polycyclic aromatic hydrocarbons (PAH). The goal of this paper is to identify the association between PAH exposure levels and contributing risk factors to Citation: Hwang, J.; Xu, C.; Agnew, derive best estimates of the effects of exposure on structural firefighters’ working environment in R.J.; Clifton, S.; Malone, T.R. Health fire. We surveyed four databases (Embase, Medline, Scopus, and Web of Science) for this systematic Risks of Structural Firefighters from literature review. -
Chemistry and Hazards of Hazardous Materials and Weapons of Mass Destruction Chapter Contents
Chemistry and Hazards of Hazardous Materials and Weapons of Mass Destruction Chapter Contents Case History ................................145 Polymerization ...........................................................173 atoms ...........................................146 Decomposition ..........................................................174 Periodic table of elements ..................146 Synergistic Reactions ................................................174 Four significant Families ....................147 The Fundamentals of a Reaction ...............................175 Group I – The Alkali Metals .......................................153 Common Families of Hazardous Materials .....................................176 Group II – The Alkaline Earths ...................................154 Inorganic Compounds ...............................................176 Group VII – The Halogens .........................................155 Organic Compounds ..................................................176 Group VIII – The Noble Gases ...................................156 Oxidizers ....................................................................180 Matter ..........................................156 Reactive Materials .....................................................181 Elements ....................................................................158 Corrosives .................................................................185 Compounds ...............................................................160 special Hazards of Chemicals