DOCSLIB.ORG

Copyrighted Material

Total Page：16

File Type：pdf, Size：1020Kb

Download full-text PDF Read full-text
Copyrighted Material Index ABM Treaty of 1972, 183, 190 Anti-missile shield (“Star Wars”), 8, 190 Absorbent powder, 35, 211–212 Antivirals, 129, 131, 143, 214, 215, 228–229 Acute pulmonary edema, 30 Apoptosis, 4, 193 Additional protocol to the Non-Proliferation Arak (production unit for heavy water), 185 Treaty (NPT), 177, 186 Arbovirus, 112 Affymetrix (company), 169 Army Health Service, 84, 120, 205 Afghanistan, 2, 4 Arsenic, 12, 14, 23, 83 Afl atoxin, 62 Asilomar, 170 Agents, 3–6, 11–21, 29–37, 59–63, 68, 73–75, Aspergillus, 62 107–114, 153, 159–173, 201, 205–215, Assault medications, 4, 12 218, 220 Atropine, 35, 38–39, 54–56, 214 asphyxiants (suffocants), 92 Attack drone, 182 BZ, 12, 25, 31, 92 Atypical pneumonia (SARS), 3, 108, 120, incapacitants, 30, 32 135–152 neurotoxicants, 24, 33, 38, 77, 89 Aum Shinrikyo (sect), 20, 187 orange (2,4,5-trichlorophenoxyacetic Australian group, 102 acid), 12, 15 purple, 15 Bacillus red anthracis (anthrax agent), 61, 96, 101, tranquilizers, 32 113, 115, 153–154, 156–157, vesicants, 12–13, 23, 25, 34, 36, 205 166–167, 169 Aging of phosphorylated globigii, 99, 216 acetylcholinesterases, 36–37, 39 subtilis, 216 Alamogordo (USA), 178 Bartonella quintana, 101 Al-Hakam (Iraqi site of), 100 Basson Wouter Alibek Ken (Alibejov Kanatjan), 97, 107, Batelle (foundation), 167–168 117, 118, 157, 166, 188 Bedson Henry, 118, 171 Al-Tuwaitha, 182 Berg Paul, 170, 174 Amantadine, 129, 228 Bhopal, 9, 34, 55, 74, 83, 204 Ames (strain of BacillusCOPYRIGHTED anthracis), 98, 154, Biopreparat MATERIAL (biological war complex), 97–98, 156, 164, 169–170, 172 107, 157, 166 Anthrax, 52, 68, 97, 100–102, 105, 108, 112, Biopreparedness Act, 173 114, 136, 153–157, 164, 167–170, 172, Biochips, 114, 206 204, 218 Bioreactors, 161–162 Antibiotics, 35, 43, 97, 153, 155–156, 161, Biotechnologies, 104, 159–174, 206 164–167, 170, 198, 214–215 Bioterrorism, 24, 49, 100, 117, 125, 208, 219 Antidotes, 39, 48, 56–57, 74, 77, 81, 85, 203, Biotox (plan), 122–123, 153, 204 214–215, 218, 227 Bin Laden, 187–188 Treating Victims of Mass Destruction Edited by Patrick Barriot and Chantal Bismuth © 2008 John Wiley & Sons, Ltd 232 INDEX Blix Hans, 16–17 Clostridium BLU-82, 2–3 botulinum, 19, 60, 167 Bomb, 3, 97, 154, 178, 181, 188, 191–192, perfringens, 101, 111 195, 221 Cluster bomb, 2 A, 8, 179, 191–192 CN (omega-chloroacetophenone), 24, BL 61–11 or mini-nuke, 3, 181 29–30 Bouchehr (nuclear center), 186, 189 Coccidomycetes (pulmonary mycosis agent), Daisy Cutter, 2 109 dirty or radiological, 2, 181–182, Combat (newspaper), 191 188, 217 Computer simulations, 104–105, 205, E (electromagnetic), 7, 182–183, 196 216–217 FAE (fuel air explosive), 2–3 Contact subjects, 122 fragmentation, 2 Contamination, 5, 11, 14, 19–20, 24, 35, 45, graphite, 7, 196 59, 61, 65–66, 80–81, 97, 108, 113, 118, hydrogen, 179 123, 125, 129–130, 139–141, 163, 188, intelligent virus, 168 194, 198–202, 204, 207, 208, 217 megaton thermonuclear, 1 Counter-proliferation, 7–8, 95, 189–190 neutron, 180, 182–183, 195 Counter-terrorism, 4, 19, 21, 28, 91–93 portable nuclear (“suitcase bomb”), 188 Convention for the Prohibition of Biological Brazil, 96, 111, 188, 196 Weapons, 5, 173 British Anti-Lewisite (BAL or dimercaprol), Convention for the Prohibition of Chemical 36, 199, 201, 214, 216 Weapons, 43, 218 Brucella melitensis, 109, 115 Corona virus, 108, 138 Burkholderia Coxiella brunetii (Q fever agent), 101, 109, mallei, 96, 109–110, 115 115 pseudo-mallei (glanders agent), 101, CS (chlorobenzylidene malononitrile), 12, 110, 115 29–30 BZ (quinuclidinol benzilate), 12, 25, Cyanides, 28, 36, 77, 92 31, 92 Dark Winter (exercise), 103–104, 216 Camus Albert, 191 Decontamination, 30, 35–36, 39, 43, 48–50, Carcinogenic, 62, 170, 194 56–57, 60, 75–81, 85–87, 114, 156, 170, CDC, Atlanta, USA, 121, 138, 152, 155, 188, 194, 196, 199–200, 204, 211–213, 173, 206–207, 228 217–218, 227, 230 Chernobyl, 9, 151, 187, 196–197, 201, 207, Defense secret, 205 213, 216 Defoliants, 7, 11, 15, 21, 27, 29, 181 Chlamydia, 101, 109, 136–138, 143, 164 Dengue, 4, 101, 110, 112, 163, 172 Chlorine, 12–14, 21, 23–24, 32–34, 45, 51, Detection, 40, 105, 109, 119, 128, 137–140, 83, 212 155–156, 165–166, 168–170, 184, 194, Cholera, 62, 101, 103, 112–113, 115, 145, 205–207, 211 162, 164, 166 Detrick (camp, fort), 98, 154, 157, 172 Churchill Winston, 52 Diabrotica virgifera, 104 Ciclofovir, 115, 123 Directed mutagens, 166 Civil defense, 81, 153, 203–205, 219 DM (Adamsite), 30–31 Civilian populations, 1–2, 6–7, 23, 27, DNA chip (biochip), 169, 206 84, 88, 124, 195, 218 Doxycycline, 113–115, 136, 155–156, Ciprofl oxacin, 113–115, 155–156, 214–215, 214–215 230 Dresden (“Dresden effect”), 6, 74, 224 INDEX 233 DTPA (diethylene-triamine-pentacetic acid), Fraser Claire, 160 199, 201, 214, 216 Fusarium, 62, 104 Dugway Proving Ground (Utah, USA), 154 Dumbell (Professor), 118, 171 Gallo Robert, 171 Dupuy Jean-Pierre, 221 Gas, 2–4, 14–15, 20, 24–25, 30–37, 45, 51–52, 69, 80, 91–92, 203–205, Ecocide, 29 208–210 Effects lachrimators, 30 carcinogenic, 194 mustard, 14, 24, 27, 34, 51–52, 57, 69, genetic, 99, 108, 118–119, 126, 130–133, 74, 92 159–174, 194, 220 suffocant, 23, 27 radiomimetic, 35, 62 vesicant, 12, 23, 34, 211 teratogenic, 194 Gas masks, 32–34, 36–37, 39, 52, Einstein Albert, 178 208–210 Ekaterinburg (Sverdlovsk), 97, 154 Gastrointestinal incapacitants, 32 Electromagnetic impulosion, 179 Genetic amplifi cation, 114, 119, 138 Encephalitis, 111–113, 118, 120–121, 128 Genetic engineering, 3, 8, 63, 97, 99, Endogenous porcine retrovirus (PERV), 163 101–102, 113, 118, 133, 144, 157, Enola Gay, 191 159, 165–167, 170–174, 220 Epidemics, 6, 84, 103, 117–118, 128–129, Genetic markers, 156 141, 145, 208, 215, 218 Genetic recombination, 97, 108, 126, Escherich Karl, 14 138, 161 Escherichia coli, 61, 101, 112, 161–162, 164 Genetic sequencing, 99 Euratox (European exercise), 204, 217 Genetic therapy, 168, 170 Glanders, 109 Falluja (site of), 5 GMO (genetically modifi ed organisms), 104 Fentanyl, 91 Goïana (Brazil), 188 Fermi Enrico, 178 Gruinard (island of), 97, 154, 157, Fevers, 97, 110–114 213, 218 aphthous, 103, 208 ebola virus, 4, 101, 103, 108, 110, 114, Haber Fritz Jacob, 14 118, 170 Hahn Otto, 178 equine, 101, 112, 118 Halabja (Iraqi Kurdistan), 15, 28 exanthemous, 110–113 Hablan Hans Heinrich von, 8, 178 hemorrhagic, 4, 60, 62, 97, 101, 103, 108, Halothane, 91 110, 112–115, 136, 172 Hase Albrecht, 14 Lassa, 101, 110, 115, 170 Heavy metals, 12, 162, 181, 195, 199, 201 Marburg virus, 101, 110, 170, 172 chelators, 201 Q, 101, 108–109, 111 Herbicides, 11–12, 15 typhoid and paratyphoid, 100, 103, Hiroshima, 3, 6, 105, 179, 181, 191, 192, 111–113 194–195, 202, 224 yellow, 101, 110, 112–113, 145, 163 Hitler Adolph, 97 Filtering cartridges, 209–211, 214 Hussein Kamel (Lieutenant General), 100 First World War (WWI), 12, 14, 21, 23, Hussein Sadam, 15–18, 61–62, 100 33–34, 51–52, 69, 74, 96, 127, 208 Hybrid, 118, 170–172 Fluoroquinolone, 114 Hydrocyanic acid, 12–14, 27, 45 Francisella tularensis (tularemia agent), 101, Hydroxocobalamin (Cyanokit), 47–49, 214 109, 111, 115 Hypermutability, 166 234 INDEX Identifi cation, 55, 61, 70, 75, 114, 118, LSD (lysergamide), 31 139, 143, 156, 165, 168, 169, 171, Lopinavir, 143 205, 206, 209 Los Alamos Scientifi c Laboratory, 178, 181, I.G. Farben (company), 14 187, 218 Infl uenza, 3, 62, 99, 103, 108, 125, 129, 132, 136, 142, 147, 215, 227 Mac Veigh (Timothy), 2 Insecticides, 14, 27, 36, 52, 68, 69, Manchuria, 96 102, 163 Manhattan Project, 178 Institute for Radioprotection and Nuclear Manuguerra Jean-Claude, 141 Safety, 124, 187, 188, 214 Markov Georgi, 20, 27, 60 Interferon, 144, 161 Mass sociogenic pathology, 220 Interleukin-4, 99, 171, 172 Massachusetts Institute of Technology International Atomic Energy Agency (IAEA) (MIT), 169, 206 177, 185 Matsumoto, 20, 54, 55, 56 International agreements, 1, 5, 11, 16, 20, Mérieux (Institute), 169, 170, 206 29, 51, 68, 93, 133, 145, 170, 189, Methyl isocyanate, 34, 55, 74, 83 206, 223 Missiles, 13, 28, 40, 45, 62, 98, 100, Iran, 13, 23, 27, 60, 69, 95, 98, 100, 118, 102, 179, 181, 183, 184, 186, 208 123, 183, 186, 189 Molecular hybridization, 168, 206 Iraq, 2, 6, 8, 13, 15, 17, 19, 23, 28, 60, 69 Mollaret Henri, 123, 205 Irradiation, 156, 192, 193, 194, 197–201, 213 Monoclonal antibodies, 162, 169, 206 Ishii Shiro (General), 96 Monsanto (company), 15, 104, 162 Ivanovsky (Institute), 118 Mortuaries Moscow theater (Doubrovka), 28, 91 Jackson Ronald, 171 Munition(s), 2, 7, 13, 24, 28, 40, 44, Joliot Frédéric, 45, 83 102, 181, 195,218 Joy Bill, 174, 220 binary, 4, 5, 42, 43 Mycobacterium, 101,164 Kaczynski Theodore, 220 leprae, 164 Kaffa (siege of), 96 tuberculosis, 164 Kamikazi, 2, 8 Mycoplasma genitalium, 160 Kosovo, 2, 182 Mycotoxin, 59, 62, 114 Kowarski Lew, 8, 178 Nagasaki, 179, 191, 194 Laboratory, 5, 47, 55, 117, 118, 122, Naloxone, 28, 91 144, 163, 171, 178, 200, 218, 230 Nanotechnologies, 220, 221 Lacrimator grenade, 29 Nantanz (facility for uranium enrichment), Langemarck (Ypres), 14 184, 185, 189 Launchers, 2, 184 Narcotics, 32 Laurence Livermore National Laboratory, National Institute for Health Surveillance, 206 173, 218 Legionella, 109 Neuroleptics, 27 Lellouche Pierre, 98, 107, 204 Neutrons, 178, 180, 192, 193, 194, 198 Le Monde (newspaper), 19, 123, 136, Nixon Richard, 98 146, 149, 191, 229 NMD (National Missile Defense) Lethal Dose 50% (LD50), 193 Non-Proliferation Treaty (NPT), 177 Lewisite, 15, 36, 51, 201 North Korea, 13, 95, 98, 118, 183, 185 Listeria monocytogenes, 101 Novossibirsk (site of), 97 INDEX 235 Oklahoma City (USA), 2 Proteins Opiates, 35 illusory,
Load more

Recommended publications
  • Aldrich Raman
    Aldrich Raman Library Listing – 14,033 spectra This library represents the most comprehensive collection of FT-Raman spectral references available. It contains many common chemicals found in the Aldrich Handbook of Fine Chemicals. To create the Aldrich Raman Condensed Phase Library, 14,033 compounds found in the Aldrich Collection of FT-IR Spectra Edition II Library were excited with an Nd:YVO4 laser (1064 nm) using laser powers between 400 - 600 mW, measured at the sample. A Thermo FT-Raman spectrometer (with a Ge detector) was used to collect the Raman spectra. The spectra were saved in Raman Shift format. Aldrich Raman Index Compound Name Index Compound Name 4803 ((1R)-(ENDO,ANTI))-(+)-3- 4246 (+)-3-ISOPROPYL-7A- BROMOCAMPHOR-8- SULFONIC METHYLTETRAHYDRO- ACID, AMMONIUM SALT PYRROLO(2,1-B)OXAZOL-5(6H)- 2207 ((1R)-ENDO)-(+)-3- ONE, BROMOCAMPHOR, 98% 12568 (+)-4-CHOLESTEN-3-ONE, 98% 4804 ((1S)-(ENDO,ANTI))-(-)-3- 3774 (+)-5,6-O-CYCLOHEXYLIDENE-L- BROMOCAMPHOR-8- SULFONIC ASCORBIC ACID, 98% ACID, AMMONIUM SALT 11632 (+)-5-BROMO-2'-DEOXYURIDINE, 2208 ((1S)-ENDO)-(-)-3- 97% BROMOCAMPHOR, 98% 11634 (+)-5-FLUORODEOXYURIDINE, 769 ((1S)-ENDO)-(-)-BORNEOL, 99% 98+% 13454 ((2S,3S)-(+)- 11633 (+)-5-IODO-2'-DEOXYURIDINE, 98% BIS(DIPHENYLPHOSPHINO)- 4228 (+)-6-AMINOPENICILLANIC ACID, BUTANE)(N3-ALLYL)PD(II) CL04, 96% 97 8167 (+)-6-METHOXY-ALPHA-METHYL- 10297 ((3- 2- NAPHTHALENEACETIC ACID, DIMETHYLAMINO)PROPYL)TRIPH 98% ENYL- PHOSPHONIUM BROMIDE, 12586 (+)-ANDROSTA-1,4-DIENE-3,17- 99% DIONE, 98% 13458 ((R)-(+)-2,2'- 963 (+)-ARABINOGALACTAN BIS(DIPHENYLPHOSPHINO)-1,1'-
    [Show full text]
  • C-Metalated Nitriles: Diastereoselective Alkylations and Arylations
    Duquesne University Duquesne Scholarship Collection Electronic Theses and Dissertations Fall 12-20-2019 C-Metalated Nitriles: Diastereoselective Alkylations and Arylations Robert John Mycka Duquesne University Follow this and additional works at: https://dsc.duq.edu/etd Part of the Organic Chemistry Commons Recommended Citation Mycka, R. J. (2019). C-Metalated Nitriles: Diastereoselective Alkylations and Arylations (Doctoral dissertation, Duquesne University). Retrieved from https://dsc.duq.edu/etd/1851 This Immediate Access is brought to you for free and open access by Duquesne Scholarship Collection. It has been accepted for inclusion in Electronic Theses and Dissertations by an authorized administrator of Duquesne Scholarship Collection. C-METALATED NITRILES: DIASTEREOSELECTIVE ALKYLATIONS AND ARYLATIONS A Dissertation Submitted to the Bayer School of Natural and Environmental Sciences Duquesne University In partial fulfillment of the requirements for the degree of Doctor of Philosophy By Robert J. Mycka December 2019 Copyright by Robert J. Mycka 2019 C-METALATED NITRILES: DIASTEREOSELECTIVE ALKYLATIONS AND ARYLATIONS By Robert J. Mycka Approved November 13, 2019 ________________________________ ________________________________ Dr. Bruce D. Beaver Dr. Jeffrey D. Evanseck Professor of Chemistry and Biochemistry Professor of Chemistry and Biochemistry (Committee Chair) (Committee Member) ________________________________ ________________________________ Dr. Shahed U. M. Khan Dr. Patrick T. Flaherty Associate Professor of Chemistry and
    [Show full text]
  • Chemical Resistance of Plastics
    (c) Bürkle GmbH 2010 Important Important information The tables “Chemical resistance of plastics”, “Plastics and their properties” and “Viscosity of liquids" as well as the information about chemical resistance given in the particular product descriptions have been drawn up based on information provided by various raw material manufacturers. These values are based solely on laboratory tests with raw materials. Plastic components produced from these raw materials are frequently subject to influences that cannot be recognized in laboratory tests (temperature, pressure, material stress, effects of chemicals, construction features, etc.). For this reason the values given are only to be regarded as being guidelines. In critical cases it is essential that a test is carried out first. No legal claims can be derived from this information; nor do we accept any liability for it. A knowledge of the chemical and mechanical Copyright This table has been published and updated by Bürkle GmbH, D-79415 Bad Bellingen as a work of reference. This Copyright clause must not be removed. The table may be freely passed on and copied, provided that Extensions, additions and translations If your own experiences with materials and media could be used to extend this table then we would be pleased to receive any additional information. Please send an E-Mail to [email protected]. We would also like to receive translations into other languages. Please visit our website at http://www.buerkle.de from time to Thanks Our special thanks to Franz Kass ([email protected]), who has completed and extended these lists with great enthusiasm and his excellent specialist knowledge.
    [Show full text]
  • Development of Palladium-Catalyzed Decarboxylative Allylation of Electron-Deficient Sulfones: Method Development and Mechanistic Studies
    Development of Palladium-Catalyzed Decarboxylative Allylation of Electron-Deficient Sulfones: Method Development and Mechanistic Studies by Monica Anne Gill A thesis submitted to the Faculty of Graduate and Postdoctoral Affairs in partial fulfillment of the requirements for the degree of Doctor of Philosophy in Chemistry Carleton University Ottawa, Ontario © 2015, Monica Anne Gill Abstract Palladium-catalyzed decarboxylative allylation is a powerful method of carbon-carbon bond construction. This methodology relies on an electron- withdrawing group to promote the reaction. The use of sulfones in decarboxylative allylation has been explored using the trifluoromethylsulfonyl (triflyl) group, as well as the bis(3,5-trifluoromethyl)phenylsulfonyl (BTMP) group. These substrates are highly reactive at room temperature (triflyl) and 50 oC (BTMP sulfones). A detailed mechanistic study using deuterium-labelled substrates was performed to understand the origin of the protonation side-product. It was proposed that a β- hydride elimination from the η1 allyl on palladium could generate a palladium hydride intermediate along with an allene. Although small amounts of deuterium incorporation were observed in the protonated products, the proposed mechanism could not be the major pathway. Using isotopically labelled ligand, however, all protonation was supressed. This suggests that the origin of the proton is actually from the ligand and that kinetic isotope effects may be responsible for inhibiting the protonation pathway with labelled ligand. ii Acknowledgments I would like to thank Dr. Jeff Manthorpe for giving me the chance to pursue my PhD in his lab. I always appreciated Jeff’s enthusiasm for organic chemistry as well as his vast knowledge of the subject.
    [Show full text]
  • Synthesis of Polycyclic Natural Products Tuan Hoang Nguyen Iowa State University
    Iowa State University Capstones, Theses and Retrospective Theses and Dissertations Dissertations 2003 Synthesis of polycyclic natural products Tuan Hoang Nguyen Iowa State University Follow this and additional works at: https://lib.dr.iastate.edu/rtd Part of the Medicinal and Pharmaceutical Chemistry Commons, Medicinal Chemistry and Pharmaceutics Commons, Medicinal-Pharmaceutical Chemistry Commons, and the Organic Chemistry Commons Recommended Citation Nguyen, Tuan Hoang, "Synthesis of polycyclic natural products " (2003). Retrospective Theses and Dissertations. 1452. https://lib.dr.iastate.edu/rtd/1452 This Dissertation is brought to you for free and open access by the Iowa State University Capstones, Theses and Dissertations at Iowa State University Digital Repository. It has been accepted for inclusion in Retrospective Theses and Dissertations by an authorized administrator of Iowa State University Digital Repository. For more information, please contact [email protected]. Synthesis of polycyclic natural products by Tuan Hoang Nguyen A dissertation submitted to the graduate faculty in partial fulfillment of the requirements for the degree of DOCTOR. OF PHILOSOPHY Major: Organic Chemistry Program of Study Committee: George A. Kraus (Major Professor) Richard C. Larock Valerie V. Sheares-Ashby Jacob W. Petrich Earl G. Hammond Iowa State University Ames, Iowa 2003 UMI Number: 3105095 UMI UMI Microform 3105095 Copyright 2003 by ProQuest Information and Learning Company. All rights reserved. This microform edition is protected against unauthorized copying under Title 17, United States Code. ProQuest Information and Learning Company 300 North Zeeb Road P.O. Box 1346 Ann Arbor, Ml 48106-1346 ii Graduate College Iowa State University This is to certify that the doctoral dissertation of Tuan Hoang Nguyen has met the requirements of Iowa State University Signature was redacted for privacy.
    [Show full text]
  • ABSTRACT ZOU, YAN. Applications of [2+2+2] Cyclotrimerization
    ABSTRACT ZOU, YAN. Applications of [2+2+2] Cyclotrimerization Reactions and Light-Cleavable Groups in the Generation of Biologically Active Molecules. (Under the direction of Dr. Alexander Deiters). [2+2+2] Cyclotrimerization reactions are a versatile tool for constructing the poly- substituted carbo- and hetero- cyclic ring systems. A number of transition metal catalysts, such as Co, Ru, Rh, Ni and Pd complexes, have been applied. However, there are still regio- and chemo- selectivity issues present in [2+2+2] cyclotrimerization reactions, and only few applications of cyclotrimerization reactions in the synthesis of natural products have been reported. We aimed to develop cyclotrimerization reactions for the assembly of benzene and pyridine core structures found in natural products and for applications in the synthesis of fluorophores. Microwave irradiation, a more recent method used to assist organic reactions, was employed in various cyclotrimerization reactions. In order to obtain greater control over the chemoselectivity of these reactions, we developed a solid-supported method of cyclotrimerization reactions through the immobilization of an alkyne or diyne onto a polymer backbone. This methodology was applied to the assembly of poly-substituted pyridines. Furthermore, the microwave mediated cyclotrimerization methodology was utilized to synthesize various anthracene and azaanthracene fluorophores. Additionally, a cyclotrimerization reaction was used in key steps of the total synthesis of the natural products cryptoacetalide and the pyridine core of cyclothiazomycin. Currently, the cyclotrimerization reaction is being utilized in the ongoing synthesis of petrosasponglide L. Photolabile protecting groups (caging groups) have attracted considerable attention in the field of chemical biology. These caging groups are installed on biomolecules of interest to control their function with light.
    [Show full text]
  • Studies in Meroterpenoid Synthesis
    Studies in Meroterpenoid Synthesis A thesis presented by Jonathan W. Lockner to The Scripps Research Institute Graduate Program in partial fulfillment of the requirements for the degree of Doctor of Philosophy in the subject of Chemistry for The Scripps Research Institute La Jolla, California November 2011 1 UMI Number: 3507067 All rights reserved INFORMATION TO ALL USERS The quality of this reproduction is dependent on 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. UMI 3507067 Copyright 2012 by ProQuest LLC. All rights reserved. This edition of the work is protected against unauthorized copying under Title 17, United States Code. ProQuest LLC. 789 East Eisenhower Parkway P.O. Box 1346 Ann Arbor, MI 48106 - 1346 © 2011 by Jonathan W. Lockner All rights reserved. 2 Thesis Acceptance Form 3 Acknowledgements As a high school student in Plainfield, Illinois, I had the benefit of learning chemistry from Mr. Hill. He supplemented my experience with “Semi-Micro Qualitative Analysis” – allowing me to perform simple chemistry experiments after school. As an undergraduate at the University of Illinois at Urbana-Champaign, I had the opportunity to carry out synthetic organic chemistry research in the laboratory of Professor Robert M. Coates. I am indebted to him, as well as Dr. Chad Davis (then a graduate student and my mentor), for their influence in setting me on the path of scientific research. My first employment was at Pharmacia in Kalamazoo, Michigan.
    [Show full text]
  • Acutely Toxic Chemicals Chemical Class Standard Operating Procedure
    Acutely Toxic Chemicals Chemical Class Standard Operating Procedure Acutely Toxic Chemicals (ATCs) H300 H301 H304 H310 H311 H330 H331 H370 H372 Areas with blue text indicate that information must be provided or modified by researcher prior to the SOP approval. This SOP is not a substitute for hands-on training. Print a copy and insert into your laboratory SOP binder. Department: Chemistry Date SOP was written: Monday, October 24, 2016 Date SOP was approved by PI/lab supervisor: Name: R. Sarpong Principal Investigator: Signature: ______________________________ Name: Melissa Hardy/Justin Jurczyk Internal Lab Safety Coordinator or Lab Manager: Lab Phone: 406-696-1225/412-728-1952 Office Phone: 510-642-6312 Name: Melissa Hardy/Justin Jurczyk Emergency Contact: Lab Phone: 406-696-1225/412-728-1952 Latimer Hall Location(s) covered by this SOP: 831,832,834,836,837,838,839,842,844,847,849 1. Purpose This SOP covers the precautions and safe handling procedures for the use of Acutely Toxic Chemicals (ATCs). For a list of ATCs covered by this SOP and their use(s), see “List of Chemicals”. Procedures described in Section 12 apply to all materials covered in this SOP. If you have questions concerning the applicability of any recommendation or requirement listed in this procedure, contact the Principal Investigator/Laboratory Supervisor or the campus Chemical Hygiene Officer at [email protected]. Rev. Date: 09Sept2016 1 Acutely Toxic Chemicals Chemical Class Standard Operating Procedure 2. Acutely Toxic Chemicals Information Acute toxicity refers to those adverse effects occurring following oral or dermal administration of a single dose of a substance, or multiple doses within 24 hours, or an inhalation exposure of 4 hours as defined by the Globally Harmonized System (GHS).
    [Show full text]
  • Asymmetric Synthesis Using a Camphene-Derived Chiral Auxiliary
    Asymmetric Synthesis Using a Camphene-Derived Chiral Auxiliary Paul Thorburn B.Sc. Thesis presented for the degree of Doctor of Philosophy The University of Edinburgh 1997 Declaration I declare that this thesis is my own composition, that the work of which it is a record has been carried out by myself, and that it has not been submitted in any previous application for a higher degree. The thesis describes the results of research carried out in the Department of Chemistry of The University of Edinburgh, under the supervision of Dr. I. Gosney since the 14th of January 1992, the date of my admission as a reseach student. Paul Thorburn To Malcolm and both lans Acknowledgements I would like to thank Dr. Ian Gosney for his supervision and encouragement, Dr. Malcolm Banks for his advice and expertise, and Dr Ian Dawson for the inspiration to carry on. I would also like to thank all the departmental technical staff for the services that - they have provided over the years. Particular thanks must go to John R. Miller for his patience and provision of a working NMR service despite the pressure on it. And finally, I must thank my comrades who have accompanied me on this odyssey, Suneel Gaur, Keith Grant, Derek Kilgour, Douglas McDougall, Allan Doyle, Laurence Joly, Jamie Mayo and last and least Stuart Gebbie. Courses Attended The following is a statement of the courses attended during the period of research:- 1 Current Topics in Organic Chemistry, various speakers, Department of Chemistry, University of Edinburgh, 3 years attendance. 2 Organic Research Seminars, various speakers, Department of Chemistry, University of Edinburgh, 3 years attendance.
    [Show full text]
  • Acetic Acid Toxic
    Chemical Waste Name or Mixtures: Listed Characteristic Additional Info Disposal Notes (-)-B- bromodiisopropinocampheyl (-)-DIP-Bromide Non Hazardous None liquid: sanitary sewer/ solid: trash borane (-)-B- chlorodiisopropinocampheylb (-)-DIP-Chloride Non Hazardous None liquid: sanitary sewer/ solid: trash orane [(-)-2-(2,4,55,7-tetranitro-9- fluorenyodeneaminooxy)pro (-)-TAPA Non Hazardous None liquid: sanitary sewer/ solid: trash pionic acid] (+)-B- bromodiisopropinocampheyl (+)-DIP-Bromide Non Hazardous None liquid: sanitary sewer/ solid: trash borane (+)-B- chlorodiisopropinocampheylb (+)-DIP-Chloride Non Hazardous None liquid: sanitary sewer/ solid: trash orane [(+)-2-(2,4,55,7-tetranitro-9- fluorenylideneaminooxy)prop (+)-TAPA Non Hazardous None liquid: sanitary sewer/ solid: trash ionic acid] (2,4,5-Trichlorophenoxy) Acetic Acid Toxic None EHS NA (2,4-Dichlorophenoxy) Acetic Acid Toxic None EHS NA trans-8,trans-10-dodecadien- (E,E)-8,10-DDDA Non Hazardous None liquid: sanitary sewer/ solid: trash 1-ol trans-8,trans-10-dodecadien- (E,E)-8,10-DDDOL Non Hazardous None liquid: sanitary sewer/ solid: trash 1-yl acetate trans-7,cis-9-dodecadien-yl (E,Z)-7,9-DDDA Non Hazardous None liquid: sanitary sewer/ solid: trash acetate (Hydroxypropyl)methyl Cellulose Non Hazardous None liquid: sanitary sewer/ solid: trash NA ammonium phosphate (NH4)2HPO4 Non Hazardous None liquid: sanitary sewer/ solid: trash (dibasic) (NH4)2SO4 Non Hazardous None liquid: sanitary sewer/ solid: trash ammonium sulfate ammonium phosphate (NH4)3PO4 Non Hazardous None
    [Show full text]
  • The War Gases
    THE WAR GASES CHEMISTRY AND ANALYSIS BY DR. MARIO SARTORI Chemist of the Italian Chemical Warfare Service Preface by PROFESSOR G. BARGELLINI of Rome University Translated from the Second Enlarged Italian Edition by L. W. MARRISON, B.Sc., A.I.C. With 20 Figures and 15 Tables NEW YORK D. VAN NOSTRAND CO., INC. 250 FOURTH AVENUE 1939 PREFACE TO THE FIRST ITALIAN EDITION THE world conflict of 1914-18 opened a new field of study in the Chemistry of War : that of the war gases. Thus the Chemistry of War, which had for its cradle the chemical laboratory in Turin where Ascanio Sobrero discovered nitroglycerine and which for 60 years was confined to the study of explosives, underwent a new development and a new orientation when substances which had an offensive action on the human and animal organism were first used on the field of battle. Then commenced the study of war gases which has become one of the most complex and important departments of chemistry. Our present knowledge of most of these asphyxiating gases is very superficial and even inexact, which is the reason that while some merit the importance given to them, others tend to be overvalued. Books are therefore necessary to give information as to what has been published of the constitution, the methods of preparation and the properties of these substances. While many German, American and Russian treatises elucidate this subject, which is of such great and present interest, in a wide and complete manner, few publications exist on the subject in the Italian language.
    [Show full text]
  • Flammable Liquids and Solids Chemical Class Standard Operating Procedure
    Flammable Liquids and Solids Chemical Class Standard Operating Procedure Flammable Liquids and Solids H224 H225 H226 H227 H228 Areas with blue text indicate that information must be provided or modified by researcher prior to the SOP approval. This SOP is not a substitute for hands-on training. Print a copy and insert into your laboratory SOP binder. Department: Chemistry Date SOP was written: Monday, October 24, 2016 Date SOP was approved by PI/lab supervisor: Name: R. Sarpong Principal Investigator: Signature: ______________________________ Name: Melissa Hardy/Justin Jurczyk Internal Lab Safety Coordinator or Lab Manager: Lab Phone: 406-696-1225/412-728-1952 Office Phone: 510-642-6312 Name: Melissa Hardy/Justin Jurczyk Emergency Contact: Lab Phone: 406-696-1225/412-728-1952 Latimer Hall Location(s) covered by this SOP: 831,832,834,836,837,838,839,842,844,847,849 1. Purpose This SOP covers the precautions and safe handling procedures for the use of Flammable Liquids and Solids. For a list of Flammable Liquids and Solids covered by this SOP and their use(s), see “List of Chemicals”. Procedures described in Section 12 apply to all materials covered in this SOP. If you have questions concerning the applicability of any recommendation or requirement listed in this procedure, contact the Principal Investigator/Laboratory Supervisor or the campus Chemical Hygiene Officer at [email protected]. Rev. Date: 09Sept2016 1 Flammable Liquids and Solids Chemical Class Standard Operating Procedure 2. Physical & Chemical Properties/Definition of Chemical Group Flammable liquid means a liquid having a flash point1 of not more than 199.4 °F (93 °C).
    [Show full text]