Ionization Potentials, Appearance Potentials, and Heats of Formation of Gaseous Positive Ions
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Monoamine Oxydases Et Athérosclérose : Signalisation Mitogène Et Études in Vivo
UNIVERSITE TOULOUSE III - PAUL SABATIER Sciences THESE Pour obtenir le grade de DOCTEUR DE L’UNIVERSITE TOULOUSE III Discipline : Innovation Pharmacologique Présentée et soutenue par : Christelle Coatrieux le 08 octobre 2007 Monoamine oxydases et athérosclérose : signalisation mitogène et études in vivo Jury Monsieur Luc Rochette Rapporteur Professeur, Université de Bourgogne, Dijon Monsieur Ramaroson Andriantsitohaina Rapporteur Directeur de Recherche, INSERM, Angers Monsieur Philippe Valet Président Professeur, Université Paul Sabatier, Toulouse III Madame Nathalie Augé Examinateur Chargé de Recherche, INSERM Monsieur Angelo Parini Directeur de Thèse Professeur, Université Paul Sabatier, Toulouse III INSERM, U858, équipes 6/10, Institut Louis Bugnard, CHU Rangueil, Toulouse Résumé Les espèces réactives de l’oxygène (EROs) sont impliquées dans l’activation de nombreuses voies de signalisation cellulaires, conduisant à différentes réponses comme la prolifération. Les EROs, à cause du stress oxydant qu’elles génèrent, sont impliquées dans de nombreuses pathologies, notamment l’athérosclérose. Les monoamine oxydases (MAOs) sont deux flavoenzymes responsables de la dégradation des catécholamines et des amines biogènes comme la sérotonine ; elles sont une source importante d’EROs. Il a été montré qu’elles peuvent être impliquées dans la prolifération cellulaire ou l’apoptose du fait du stress oxydant qu’elles génèrent. Ce travail de thèse a montré que la MAO-A, en dégradant son substrat (sérotonine ou tyramine), active une voie de signalisation mitogène particulière : la voie métalloprotéase- 2/sphingolipides (MMP2/sphingolipides), et contribue à la prolifération de cellules musculaire lisses vasculaires induite par ces monoamines. De plus, une étude complémentaire a confirmé l’importance des EROs comme stimulus mitogène (utilisation de peroxyde d’hydrogène exogène), et a décrit plus spécifiquement les étapes en amont de l’activation de MMP2, ainsi que l’activation par la MMP2 de la sphingomyélinase neutre (première enzyme de la cascade des sphingolipides). -
A Guide to Export Controls
Foreign Affairs, Trade and Affaires étrangères, Commerce et Development Canada Développment Canada A Guide To CANADA’S EXPORT CONTROLS December 2012 Introduction The issuance of export permits is administered by the Export Controls Division (TIE) of Foreign Affairs, Trade and Development Canada (DFATD). TIE provides assistance to exporters in determining if export permits are required. It also publishes brochures and Notices to Exporters that are freely available on request and on our website www.exportcontrols.gc.ca. How to contact us: Export Controls Division (TIE) Foreign Affairs, Trade and Development Canada 111 Sussex Drive Ottawa, Ontario K1A 0G2 Telephone: (613) 996-2387 Facsimile: (613) 996-9933 Email: [email protected] For information on how to apply for an export permit and additional information on export controls please refer to our website. To enquire on the status of an export permit application: Recognized EXCOL users can check the status of an export permit application on-line. Non-recognized users can call (613) 996-2387 or email [email protected] and quote your export permit application identification (ref ID) number. Export Controls Division website: www.exportcontrols.gc.ca This Guide, at time of publication, encompasses the list of items enumerated on the Export Control List (ECL) that are controlled for export in accordance with Canadian foreign policy, including Canada’s participation in multilateral export control regimes and bilateral agreements. Unless otherwise specified, the export controls contained in this Guide apply to all destinations except the United States. Canada’s Export Control List can be found at the Department of Justice website at http://canada.justice.gc.ca/. -
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. -
Mechanistic Study of Methylbenzene Dealkylation in Methanol-To-Olefins
Journal of Catalysis 369 (2019) 86–94 Contents lists available at ScienceDirect Journal of Catalysis journal homepage: www.elsevier.com/locate/jcat Mechanistic study of methylbenzene dealkylation in methanol-to-olefins catalysis on HSAPO-34 ⇑ Andrew Hwang, Blake A. Johnson, Aditya Bhan Department of Chemical Engineering and Materials Science, University of Minnesota, Minneapolis, MN 55455, USA article info abstract Article history: Methylbenzenes entrained within the cavities of silicoaluminophosphate zeotype HSAPO-34 react with Received 14 June 2018 methanol in H+-mediated dealkylation to give ethylene and propylene in methanol-to-olefins catalysis. Revised 1 August 2018 Methylbenzenes dealkylation on solid acids is proposed to occur either via the side-chain mechanism, Accepted 14 October 2018 where an exocyclic C@C undergoes successive methylation prior to CAC cleavage for olefin elimination, or the paring mechanism, where ring contraction to a bicyclohexenyl cation precedes CAC cleavage for olefin elimination. Distinct dealkylation mechanisms prescribe distinct combinations of C atoms—from Keywords: aromatic methyl, aromatic ring, and methanol/dimethyl ether—to comprise the olefin product. Site- Methanol-to-olefins specific isotope tracing that distinguishes between isotope labels in aromatic methyl and aromatic ring Methylbenzenes dealkylation Isotope tracing positions for each methylbenzene shows that tetramethylbenzene gives ethylene via the side-chain Site-specific mechanism and penta- and hexamethylbenzene give propylene via the paring mechanism. The ratio of Quantitative 13C NMR propylene selectivity to ethylene selectivity increases in methanol reactions on HSAPO-34 entrained with HSAPO-34 a distribution of methylbenzenes deliberately manipulated towards increasing fractions of penta- and Methylbenzene flash chromatography hexamethylbenzene, corroborating the conclusion that aromatic precursors and dealkylation mecha- nisms for ethylene diverge from those for propylene. -
Cubane and Triptycene As Scaffolds in the Synthesis of Porphyrin Arrays
Cubane and Triptycene as Scaffolds in the Synthesis of Porphyrin Arrays Submitted by Gemma M. Locke B.A. (Mod.) Medicinal Chemistry Trinity College Dublin, Ireland A thesis submitted to the University of Dublin, Trinity College for the degree of Doctor of Philosophy Under the Supervision of Prof. Dr. Mathias O. Senge University of Dublin, Trinity College September 2020 Declaration I declare that this thesis has not been submitted as an exercise for a degree at this or any other university and it is entirely my own work. I agree to deposit this thesis in the University’s open access institutional repository or allow the Library to do so on my behalf, subject to Irish Copyright Legislation and Trinity College Library conditions of use and acknowledgement. I consent to the examiner retaining a copy of the thesis beyond the examining period, should they so wish. Furthermore, unpublished and/or published work of others, is duly acknowledged in the text wherever included. Signed: ____________________________________________ March 2020 Trinity College Dublin ii Summary The primary aim of this research was to synthesise multichromophoric arrays that are linked through rigid isolating units with the capacity to arrange the chromophores in a linear and fixed orientation. The electronically isolated multichromophoric systems could then ultimately be tested in electron transfer studies for their applicability as photosynthesis mimics. Initially, 1,4-diethynylcubane was employed as the rigid isolating scaffold and one to two porphyrins were reacted with it in order to obtain the coupled product(s). Pd-catalysed Sonogashira cross-coupling reactions were used to try and achieve these bisporphyrin complexes. -
Evaluated Gas Phase Basicities and Proton Affinities of Molecules; Heats of Formation of Protonated Molecules
Evaluated Gas Phase Basicities and Proton Affinities of Molecules; Heats of Formation of Protonated Molecules Cite as: Journal of Physical and Chemical Reference Data 13, 695 (1984); https://doi.org/10.1063/1.555719 Published Online: 15 October 2009 Sharon G. Lias, Joel F. Liebman, and Rhoda D. Levin ARTICLES YOU MAY BE INTERESTED IN Evaluated Gas Phase Basicities and Proton Affinities of Molecules: An Update Journal of Physical and Chemical Reference Data 27, 413 (1998); https:// doi.org/10.1063/1.556018 Density-functional thermochemistry. III. The role of exact exchange The Journal of Chemical Physics 98, 5648 (1993); https://doi.org/10.1063/1.464913 A consistent and accurate ab initio parametrization of density functional dispersion correction (DFT-D) for the 94 elements H-Pu The Journal of Chemical Physics 132, 154104 (2010); https://doi.org/10.1063/1.3382344 Journal of Physical and Chemical Reference Data 13, 695 (1984); https://doi.org/10.1063/1.555719 13, 695 © 1984 American Institute of Physics for the National Institute of Standards and Technology. Evaluated Gas Phase Basicities and Proton Affinities of Molecules; Heats of Formation of Protonated Molecules Sharon G. Lias Center for Chemical Physics, National Bureau of Standards, Gaithersburg, MD 20899 Joel F. Liebman Department of Chemistry, University of Maryland Baltimore County, Catonsville, MD 21228 and Rhoda D. Levin Center for Chemical Physics. National Bureau of Standards, Gaithersburg, MD 20899 The available data on gas phase basicities and proton affinities of molecules are compiled and evaluated. Tables giving the molecules ordered (1) according to proton affinity and (2) according to empirical formula, sorted alphabetically are provided. -
Silybum Marianum (Milk Thistle) Flower in Vitro and on Human Explants
Molecules 2015, 20, 3549-3564; doi:10.3390/molecules20033549 OPEN ACCESS molecules ISSN 1420-3049 www.mdpi.com/journal/molecules Article Anti-Glycation Activities of Phenolic Constituents from Silybum marianum (Milk Thistle) Flower in Vitro and on Human Explants Seoungwoo Shin, Jung-A Lee, Minkyung Kim, Hyunwoo Kum, Eunsun Jung * and Deokhoon Park * Biospectrum Life Science Institute, Eines Platz 11th FL, 442-13 Sangdaewon Dong, Seoungnam City, Gyunggi Do 462-807, Korea; E-Mails: [email protected] (S.S.); [email protected] (J.-A.L.); [email protected] (M.K.); [email protected] (H.K.) * Authors to whom correspondence should be addressed; E-Mails: [email protected] (E.J.); [email protected] (D.P.); Tel.: +82-31-750-9400 (E.J. & D.P.); Fax: +82-31-750-9494 (E.J. & D.P.). Academic Editor: Derek J. McPhee Received: 25 November 2014 / Accepted: 15 February 2015 / Published: 19 February 2015 Abstract: Glycation is an ageing reaction of naturally occurring sugars with dermal proteins, with clinical signs appearing in vivo around age 30, and increasing steadily/regularly with age. The suppleness of the dermis is affected by the formation of bridges between proteins and sugars (Maillard’s reaction). The accumulation of advanced glycation end products (AGEs) in skin plays a very important role in skin ageing. Therefore, natural compounds or extracts that possess antiglycation activities may have great anti-ageing potential. In the present study, Silybum marianum flower extract (SMFE) was demonstrated to possess antiglycation activity. We found that SMFE inhibits glycation reaction between BSA and glucose. In addition, antiglycation activity of SMFE was confirmed in a human skin explants model. -
Toxicological Profile for Hydrazines. US Department Of
TOXICOLOGICAL PROFILE FOR HYDRAZINES U.S. DEPARTMENT OF HEALTH AND HUMAN SERVICES Public Health Service Agency for Toxic Substances and Disease Registry September 1997 HYDRAZINES ii DISCLAIMER The use of company or product name(s) is for identification only and does not imply endorsement by the Agency for Toxic Substances and Disease Registry. HYDRAZINES iii UPDATE STATEMENT Toxicological profiles are revised and republished as necessary, but no less than once every three years. For information regarding the update status of previously released profiles, contact ATSDR at: Agency for Toxic Substances and Disease Registry Division of Toxicology/Toxicology Information Branch 1600 Clifton Road NE, E-29 Atlanta, Georgia 30333 HYDRAZINES vii CONTRIBUTORS CHEMICAL MANAGER(S)/AUTHOR(S): Gangadhar Choudhary, Ph.D. ATSDR, Division of Toxicology, Atlanta, GA Hugh IIansen, Ph.D. ATSDR, Division of Toxicology, Atlanta, GA Steve Donkin, Ph.D. Sciences International, Inc., Alexandria, VA Mr. Christopher Kirman Life Systems, Inc., Cleveland, OH THE PROFILE HAS UNDERGONE THE FOLLOWING ATSDR INTERNAL REVIEWS: 1 . Green Border Review. Green Border review assures the consistency with ATSDR policy. 2 . Health Effects Review. The Health Effects Review Committee examines the health effects chapter of each profile for consistency and accuracy in interpreting health effects and classifying end points. 3. Minimal Risk Level Review. The Minimal Risk Level Workgroup considers issues relevant to substance-specific minimal risk levels (MRLs), reviews the health effects database of each profile, and makes recommendations for derivation of MRLs. HYDRAZINES ix PEER REVIEW A peer review panel was assembled for hydrazines. The panel consisted of the following members: 1. Dr. -
And 5,10,15,20-Tetraalkylporphyrins: Implications For
336 J. Am. Chem. SOC.1988, 110, 336-342 values being Ai,(IH) = 127.2 G and gs0= 2.0042. Since these intermediates produced under reactive laser sputtering21and other results are very similar to those calculated from the neon data, high-energy condition^.^' The use of the neon ESR matrix namely, Ais0(lH) = 128.6 G and giso= 2.0038, it is reasonable technique for studying ion products formed injon-neutral reactions to conclude that these parameters are characteristic of the un- has also been demonstrated for the following reactions which are complexed cation irrespective of the nature of the matrix. Con- important in stratospheric chemistry: CO + CO' -+ C202+,42 sequently, the significantly different parameters observed for the N2 + N2+- N4+,43N2 + CO+ - N2CO+,'and O2 + 02+- cation above 120 K in the CFC1, matrix (Table 111) now become 04+.44 anomalous for a dissociated cation. On the other hand, these 120 K parameters are just what would be expected if the complex Acknowledgment. The neon matrix ESR experiments were persists and the loss of fine structure results simply from a motional conducted at Furman University with support from the National averaging of the 35Cl hyperfine tensor components. Science Foundation (CHE-8508085), the General Electric Except for a recent investigation of the cubane radical cation Foundation, the Amoco Foundation, and Research Corporation. (C8H8+),39the acetaldehyde ion is the largest cation studied to A new ESR spectrometer was made possible by a chemistry date by the neon matrix ESR method. Given the high resolution equipment grant to Furman University from the Pew Memorial that can be achieved in neon and the chance of preferential Trust. -
Supporting Information
Electronic Supplementary Material (ESI) for ChemComm. This journal is © The Royal Society of Chemistry 2015 Electronic Supplementary Information for Anodic aromatic C,C cross-coupling reaction using parallel laminar flow mode in a flow microreactor Toshihiro Arai, Hiroyuki Tateno, Koji Nakabayashi, Tsuneo Kashiwagi, and Mahito Atobe Department of Environment and System Sciences, Yokohama National University, 79-7 Tokiwadai, Hodogaya-ku, Yokohama 2408501, Japan. *To whom the correspondence should be addressed. E-mail: [email protected] This PDF file includes: Instrumentation Materials Experimental procedure Spectroscopic data S1 1. Instrumentation Nuclear magnetic resonance (1H NMR) spectra were measured on BRUKER DRX 300 1 1 spectrometer operating at 300 MHz ( H NMR) in CDCl3. All H NMR chemical shifts were reported in ppm relative to internal references of TMS at 0.00. Preparative electrolyses were carried out with a HOKUTO DENKO HABF-501A Potentiostat/Galvanostat. GCMS analyses were performed with a Shimadzu gas chromatograph mass spectrometer GCMS-QP2010. 2. Materials Acetonitrile, acetic acid, and naphthalene (1) were purchased from Kanto Chemical and used as received. Pentamethylbenzene (2), isodurene (5), mesitylene (6), 2-bromonaphthalene (8), and tetrabutylammonium tetrafluoroborate (Bu4NBF4) were purchased from Tokyo Chemical Industry and used as received. 3. Flow Microreactor Figure S1 shows construction procedure for the electrochemical two-inlet flow microreactor. The reactor was constructed from glass plates and two platinum (Pt) plates (3 cm width, 3 cm length each) (Step 1 of Figure S1). A spacer (20 m thickness double faced adhesive tape) was used to leave a rectangular channel exposed, and the two electrodes were simply sandwiched together (area of the two electrodes: 1 × 3 cm2). -
Revised Group Additivity Values for Enthalpies of Formation (At 298 K) of Carbon– Hydrogen and Carbon–Hydrogen–Oxygen Compounds
Revised Group Additivity Values for Enthalpies of Formation (at 298 K) of Carbon– Hydrogen and Carbon–Hydrogen–Oxygen Compounds Cite as: Journal of Physical and Chemical Reference Data 25, 1411 (1996); https://doi.org/10.1063/1.555988 Submitted: 17 January 1996 . Published Online: 15 October 2009 N. Cohen ARTICLES YOU MAY BE INTERESTED IN Additivity Rules for the Estimation of Molecular Properties. Thermodynamic Properties The Journal of Chemical Physics 29, 546 (1958); https://doi.org/10.1063/1.1744539 Critical Evaluation of Thermochemical Properties of C1–C4 Species: Updated Group- Contributions to Estimate Thermochemical Properties Journal of Physical and Chemical Reference Data 44, 013101 (2015); https:// doi.org/10.1063/1.4902535 Estimation of the Thermodynamic Properties of Hydrocarbons at 298.15 K Journal of Physical and Chemical Reference Data 17, 1637 (1988); https:// doi.org/10.1063/1.555814 Journal of Physical and Chemical Reference Data 25, 1411 (1996); https://doi.org/10.1063/1.555988 25, 1411 © 1996 American Institute of Physics for the National Institute of Standards and Technology. Revised Group Additivity Values for Enthalpies of Formation (at 298 K) of Carbon-Hydrogen and Carbon-Hydrogen-Oxygen Compounds N. Cohen Thermochemical Kinetics Research, 6507 SE 31st Avenue, Portland, Oregon 97202-8627 Received January 17, 1996; revised manuscript received September 4, 1996 A program has been undertaken for the evaluation and revision of group additivity values (GAVs) necessary for predicting, by means of Benson's group additivity method, thermochemical properties of organic molecules. This review reports on the portion of that program dealing with GAVs for enthalpies of formation at 298.15 K (hereinafter abbreviated as 298 K) for carbon-hydrogen and carbon-hydrogen-oxygen compounds. -
Handbook on the Management of Munitions Response Actions
United States Office of Solid Waste and EPA 505-B-01-001 Environmental Protection Emergency Response May 2005 Agency Washington, DC 20460 EPA Handbook on the Management of Munitions Response Actions Interim Final 000735 EPA Handbook on The Management of Munitions Response Actions INTERIM FINAL May 2005 000736 This page intentionally left blank. 000737 Disclaimer This handbook provides guidance to EPA staff. The document does not substitute for EPA’s statutes or regulations, nor is it a regulation itself. Thus, it cannot impose legally binding requirements on EPA, States, or the regulated community, and may not apply to a particular situation based upon the circumstances. This handbook is an Interim Final document and allows for future revisions as applicable. 000738 This page intentionally left blank. 000739 TABLE OF CONTENTS GLOSSARY OF TERMS ..................................................... xiii ACRONYMS ...............................................................xxv 1.0 INTRODUCTION ..................................................... 1-1 1.1 Overview...................................................... 1-1 1.2 The Common Nomenclature ....................................... 1-2 1.3 Organization of This Handbook .................................... 1-5 2.0 REGULATORY OVERVIEW ........................................... 2-1 2.1 Regulatory Overview............................................. 2-2 2.1.1 Defense Environmental Restoration Program .................... 2-2 2.1.2 CERCLA ...............................................