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Synthesis of Polycyclic Natural Products Jianmin Shi Iowa State University
Iowa State University Capstones, Theses and Retrospective Theses and Dissertations Dissertations 1990 Synthesis of polycyclic natural products Jianmin Shi Iowa State University Follow this and additional works at: https://lib.dr.iastate.edu/rtd Part of the Organic Chemistry Commons Recommended Citation Shi, Jianmin, "Synthesis of polycyclic natural products " (1990). Retrospective Theses and Dissertations. 9891. https://lib.dr.iastate.edu/rtd/9891 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]. JLÎMI MICROFILMED 1991 INFORMATION TO USERS The most advanced technology has been used to photograph and reproduce this manuscript from the microfihn master. UMI films the text directly from the original or copy submitted. Thus, some thesis and dissertation copies are in typewriter face, while others may be from any type of computer printer. The quality of this reproduction is dependent upon the quality of the copy submitted. Broken or indistinct print, colored or poor quality illustrations and photographs, print bleedthrough, substandard margins, and improper alignment can adversely affect reproduction. In the unlikely event that the author did not send UMI a complete manuscript and there are missing pages, these will be noted. Also, if unauthorized copyright material had to be removed, a note will indicate the deletion. Oversize materials (e.g., maps, drawings, charts) are reproduced by sectioning the original, beginning at the upper left-hand corner and continuing from left to right in equal sections with small overlaps. -
A Novel Route to Synthesis of Lead Glycolate and Perovskite Lead Titanate, Lead Zirconate, and Lead Zirconate Titanate (PZT)
36 «“√ “√«‘®—¬ ¡¢. (∫».) 7 (1) : ¡.§. - ¡’.§. 2550 A Novel Route to Synthesis of Lead Glycolate and Perovskite Lead Titanate, Lead Zirconate, and Lead Zirconate Titanate (PZT) via Sol-Gel Process π«—µ°√√¡¢Õß°√–∫«π°“√ —߇§√“–Àå‡≈¥‰°≈‚§‡≈µ·≈–‚§√ß √â“ß·∫∫ ‡æÕ√Õø ‰°µå¢Õ߇≈¥‰∑∑“‡πµ ‡≈¥‡´Õ√傧‡πµ ·≈– ‡≈¥‡´Õ√傧‡πµ‰∑∑“‡πµ ºà“π°√–∫«π°“√‚´≈-‡®≈ Nuchnapa Tangboriboon (πÿ™π¿“ µ—Èß∫√‘∫Ÿ√≥å)* Dr. Sujitra Wongkasemjit (¥√. ÿ®‘µ√“ «ß»å‡°…¡®‘µµå)** Dr. Alexander M. Jameison (¥√. Õ‡≈Á°´“π‡¥Õ√å ‡ÕÁ¡ ‡®¡‘ —π)*** Dr. Anuvat Sirivat (¥√. Õπÿ«—≤πå »‘√‘«—≤πå)**** ABSTRACT The reaction of lead acetate trihydrate Pb(CH3COO)2.3H2O and ethylene glycol, using triethylenetetramine (TETA) as a catalyst, provides, in one step, an access to a polymer-like precursor of lead glycolate [-PbOCH2CH2O-] via oxide one pot synthesis (OOPS). The lead glycolate precursor has superior electrical properties than lead acetate trihydrate, suggesting that the lead glycolate precursor can possibly be used as a starting material mixed with other precursors such as titanium glycolate and sodium tris (glycozirconate) to produce lead titanate, lead zirconate, and lead zirconate titanate by sol-gel transition process. ∫∑§¥¬— àÕ ß“π«‘®—¬π’ȉ¥â»÷°…“°“√‡°‘¥ªØ‘°‘√‘¬“√–À«à“߇≈¥Õ–´’‡µ¥‰µ√‰Œ‡¥√µ ·≈–‡Õ∑‘≈’π‰°≈§Õ≈‚¥¬„™â “√ ‰µ√‡Õ∑‘≈’π‡µµ√–¡’π‡ªìπ§–µ–≈’ µå‡æ◊ËÕ„™â„π°“√º≈‘µ “√µ—Èßµâπ‚æ≈‘‡¡Õ√å§◊Õ‡≈¥‰°≈‚§‡≈µ [-PbOCH2CH2O-] ∑ ”§’Ë ≠™π— ¥Àπ‘ ßµ÷Ë Õ¢∫«π°“√𔉪„™à „π°“√ â ߇§√“–À— å “√‰¥Õ‡≈§µ√‘ °™π‘ ¥µ‘ “ßÊà ‰¥·°â à “√‡øÕ√‚√‰¥Õå ‡≈§µ√‘ °‘ “√·Õπ‰∑‡øÕ√å‚√Õ‘‡≈§µ√‘°·≈– “√‡æ’¬‚´‰¥Õ‘‡≈§µ√‘°®“°°“√ —߇§√“–Àå¥â«¬ “√ª√–°Õ∫ÕÕ°‰´¥å‡æ’¬ß ¢—ÈπµÕπ‡¥’¬«∑’ˇ√’¬°«à“ Oxide One Pot Synthesis (OOPS) ∑”„À≥⠓√µ—Èßµâπ‡≈¥‰°≈‚§‡≈µ¡’ ¡∫—µ‘∑“߉øøÑ“ ¥’°«à“‡≈¥Õ–´’‡µ¥‰µ√‰Œ‡¥√µ πÕ°®“°π’Ȭ—ß “¡“√∂𔉪„™âº ¡°—∫ “√µ—Èßµâπ™π‘¥Õ◊ËπÊ ‡™àπ ‰∑∑“‡π’¬¡ ‰°≈‚§‡≈µ·≈–‚´‡¥’¬¡∑√’ ‰°≈‚§‡´Õ√傧‡πµ‡æ◊ËÕº≈‘µ‡≈¥‰∑∑“‡πµ ‡≈¥‡´Õ√傧‡πµ·≈–‡≈¥‡´Õ√傧‡πµ ‰∑∑“‡πµ ‚¥¬ºà“π°√–∫«π°“√‚´≈-‡®≈∑√“π ‘™—Ëπ Key Words : OOPS, Sol-gel process, Dielectric materials §” ”§—≠ : OOPS °√–∫«π°“√‚´≈-‡®≈ «— ¥ÿ‰¥Õ‘‡≈§µ√‘° * Ph.D. -
The Titanium Industry: a Case Study in Oligopoly and Public Policy
THE TITANIUM INDUSTRY: A CASE STUDY IN OLIGOPOLY AND PUBLIC POLICY DISSERTATION Presented in Partial Fulfillment of the Requirements for the Degree Doctor of Philosophy In the Graduate School of the Ohio State University by FRANCIS GEORGE MASSON, B.A., M.A. The Ohio State University 1 9 5 k Content* L £MR I. INTRODUCTION............................................................................................... 1 II. THE PRODUCT AND ITS APPLICATIONS...................................... 9 Consumption and Uses ................................. 9 Properties ........................................................ ...... 16 III. INDUSTRY STRUCTURE................................................................................ 28 Definition of the I n d u s t r y ............................................ 28 Financial Structure. ..••••••.••. 32 Alloys and Carbide Branch. ........................... 3 k Pigment Branch .............................................................................. 35 Primary Metal Branch ................................. 1*0 Fabrication Branch ................................. $0 IT. INDUSTRY STRUCTURE - CONTINUED............................................. $2 Introduction ................................ $2 World Production and Resources ................................. $3 Nature of the Demand for Ram Materials . $8 Ores and Concentrates Branch. ••••••• 65 Summary.................................................................. 70 V. TAXATION. ANTITRUST AND TARIFF POLICY............................ -
Perfluoroalkyl-Iodo Norbornane Compounds and Their Use As
Europâisches Patentamt (g) ÛJ)) European Patent Office (0) Publication number: O 002 74 1 Office européen des brevets Bl © EUROPEAN PATENT SPECIFICATION @ Date of publication of patent spécification: 18.11.81 @© Int.lnt.CI.3: Cl.3: C 07 C 61/12, C07C 103/19, number: 78101696.9 @ Application CC07C 07 C 103/737,103/737 @ Date offiling: 15.12.78 C 07 D 209/76, C07B 29/04, C07C 69/74, C 07 D 307/77, B 01 F 17/00 (54) Perfluoroaikyl-iodo norbornane compounds and their use as surfactants. (§) Priority: 27.12.77 US 865060 @ Proprietor: CIBA-GEIGY AG Patentabteilung Postfach CH-4002 Basel (CH) (43) Date of publication of application: 11.07.79 Bulletin 79/14 (72) Inventor: Brace, Neal O. 1 022 East North Path (45) Publication of the grant of the European patent: Wheaton Illinois 60187 (US) 18.11.81 Bulletin 81/46 (84) Designated Contracting States: CH DE FR GB (56) References cited: NL - A - 68 08078 Note: Within nine months from the publication of the mention of the grant of the European patent, any person may give notice to the European Patent Office of opposition to the European patent granted. Notice of opposition shall be filed in a written reasoned statement. It shall not be deemed to have been filed until the opposition fee has been paid. (Art. 99(1 ) European patent convention). Courier Press, Leamington Spa, England. The compounds of this invention are perfluoroalkyliodo norbornane derivatives of the formula wherein Y is independently oxygen or the group >NR, R is independently hydrogen or alkyl of 1 to 24 carbon atoms or each group - YR is independently halogen with the proviso that if two halogen atoms are present these are identical and Rf is a straight or branched chain perfluoroalkyl of 1 to 18 carbon atoms or said perfluoroalkyl substituted by a perfluoroalkoxy group of 2 to 6 carbon atoms. -
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. -
NXP Semiconductors NXP List of Hazardous Substances in Products
NXP Semiconductors NX3-00119 NXP List of Hazardous Substances Sustainability 01-October-2012 in Products and Packaging Sustainability Page 1 of 7 Supersedes: NX3-00119 01-October-2010 Table of contents 1 Objectives ............................................................................................................................. 2 2 Scope ................................................................................................................................... 2 3 Responsibilities, Records & Risks......................................................................................... 2 3.1 Roles and Responsibilities .................................................................................................... 2 3.2 Records ................................................................................................................................ 2 3.3 Risks .................................................................................................................................... 3 4 References ........................................................................................................................... 3 5 Definitions/Abbreviations ...................................................................................................... 3 5.1 Definitions ............................................................................................................................. 3 5.2 Abbreviations ....................................................................................................................... -
Circular of the Bureau of Standards No. 539 Volume 5: Standard X-Ray
: :;.ta^4aya9 . Bl.ig NBS CIRCULAR 539 VOLUME V Reference taken Standard X-ray Diffraction Powder Patterns UNITED STATES DEPARTMENT OF COMMERCE NATIONAL BUREAU OF STANDARDS Standard X-ray Diffraction Powder Patterns The four previously issued volumes in this series are avail- able from the Superintendent of Documents, U. S. Govern- ment Printing Office, Washington 25, D. C., as follows: NBS Circular 539, Volume I, Standard X-ray Diffraction Powder Patterns (Data for 54 inorganic substances) NBS Circular 539, Volume II, Standard X-ray Diffraction Powder Patterns (Data for 30 inorganic substances) NBS Circular 539, Volume III, Standard X-ray Diffraction Powder Patterns (Data for 34 inorganic substances) NBS Circular 539, Volume IV, Standard X-ray Diffraction Powder Patterns (Data for 42 inorganic substances) The price of each volume is 45 cents. Send orders with remittance to: Superintendent of Documents, Government Printing Office, Washington 25, D. C. UNITED STATES DEPARTMENT OF COMMERCE • Sinclair Weeks, Secretary NATIONAL BUREAU OF STANDARDS • A. V. Astin, Director Standard X-ray Diffraction Powder Patterns Howard E. Swanson, Nancy T. Gilfrich, and George M. Ugrinic National Bureau of Standards Circular 539 Volume V, Issued October 21, 1955 For sale by the Superintendent of Documents, U. S. Government Printing Office, Washington 25, D. C. Price 45 cents CONTENTS Page Page Introduction 1 Standard X-ray powder patterns—Continued Standard X-ray powder patterns: Lead titanate, PbTi0 3 39 Ammonium chloroplatinate, (NH 4 ) 2 PtCl 6 3 Magnesium tin, Mg 2 Sn 41 Ammonium chlorostannate, (NH 4 ) 2 SnCl 6 4 Magnesium titanate (geikielite), MgTi0 3 43 Ammonium fluosilicate (cryptohalite), Manganese (II) oxide, (manganosite) MnO._ 45 (NH 4 ) 2 SiF6 5 Molybdenum disulfide (molybdenite), MoS 2 _. -
D.GR.EHS-09E.07 AT&S Guidelines for the Regulation of Environmental
Guidelines for the regulation of environmental related substances D.GR.EHS-09E.09 Guidelines for the regulation of environmental related substances Scope................................................................................................................................................................ 2 Definition ......................................................................................................................................................... 2 Demands on supplier ....................................................................................................................................... 3 Revisions.......................................................................................................................................................... 3 List of banned substances ................................................................................................................................ 5 List of restricted substances ............................................................................................................................. 8 Annex A......................................................................................................................................................... 12 Annex B ......................................................................................................................................................... 12 Annex C ........................................................................................................................................................ -
The Photochemistry of Some Substituted 2-Cyclohexenones and the Excited States Involved
PHOTOCHEMISTRY OF SUBSTITUTi':D 2... CYCLOHE:XE;NONES THE PHOTOCHEMISTRY OF S0~1E SUBSTITUTED 2~CYCLOHEXENONES AND THE EXCITED STATES INVOLVED By FLOlTI FP~ERICK SNYDER, B.Sce .A Thesis Submitted to the Faculty of Graduate Studies in Partial Fulfilment of the Requirements for the Degree Master of Science McMaster University October 1969 To MOM and DAD on Your 25th Anniversary MASTER OF SCIENCE (1969) McMASTER UNIVERSITY (Ghemi stry) Hamilton, Ontario. TITLE: The Photochemistry of some Substituted 2-Cyclohexenones and the Excited States Involved AUTHOR: Floyd Frederick Snyder, B.Sc. '(University of Alberta) SUPERVISOR: Dr. J. J. McCullough NUMBER OF PAGES: viii, 87 SCOPE AND CONTENTS: The photoadditions of 3~phenyl-2-cyclohexenone to bicyclo [2.2.1] hepta-2,5-diene, bicyclo [2.2.1] hept-2mene and cyclopentene have been studied. In all cases £.!1! fused cyclobutane products were obtained. Quenching and sensitization experiments indicated a singlet excited state to be active in photocycloaddition. Phosphorescence and fluorescence emission were observed from 3-phenyl-2-cyclohexenoneo Energy transfer to the lo~.rest triplet of 3-phenyl-2-cyclohexenone was evident from the quenching of Michler's ketone phosphorescence. Two norbornene dimers were detected in the photolysis of 3-phenyl-2-cyclo hexenone and norbornene giving evidence for a higher triplet excited state of the enone. The photoaddition of 3-methyl-2-cyclohexenone to cyclopentene l.ras studied for comparison and both .£!..! and !.r..!.U! fused adducts l-Tere obtained. In photolyses with bicyclo [2e2el] hepta-2,5 diene or cyclopentene, 2-phenyl... 2-cyclohexenone lvas unreactive. iii ACKNOWLEDGEMENTS It is a pleasure to express my gratitude to Dr. -
Structure and Properties of Lead Zirconate Titanate Thin Films by Pulsed Laser Deposition GOH WEI CHUAN
Structure and Properties of Lead Zirconate Titanate Thin Films by Pulsed Laser Deposition GOH WEI CHUAN (B.Sc (Hons), NUS) A THESIS SUBMITTED FOR THE DEGREE OF Doctoral of Philosophy Department of Physics National University of Singapore 2005 Acknowledgements I would like to express my deepest gratitude to my supervisors, Prof. Ong Chong Kim and Dr. Yao Kui. I would like to thank Prof. Ong for giving me the opportunity to study and perform research work in the Center of Superconducting and Magnetic Materials (CSMM). His passion and enthusiasm in the search for understanding the underlying physics of the experiments have deeply influenced my mindset in conducting experiments and will continue to be my source of inspiration and guidance. Without Prof. Ong’s constant guidance and criticism, I would have lost my bearing in the vast sea of knowledge, and would not have reached this far. I would also like to express my greatest appreciation to Dr. Yao Kui in Institute of Material Research and Engineering (IMRE). His constant advice and meticulous attention to the theoretical and experimental details had deeply influenced my way of research both in designing experiments and interpreting the results. Without his supervision and encouragements in countless hours of his time, it would not be possible for me to complete my publications and thesis. For that I am in debt to him and will forever remember his advice when pursuing my future endeavors. I am indebted to my fellow colleagues in CSMM, IMRE and Department of Physics, NUS, including A/P Sow Chorng Haur, Xu Sheng Yong, Wang Shi Jie, Li Jie, Yang Tao, Tan Chin Yaw, Rao Xue Song, Chen Lin Feng, Yan Lei, Kong Lin Bing, Liu Hua Jun, Lim Poh Chong, Yu Shu Hui, Gan Bee Keen and all those have shared their time helping me and discussing with me in this project. -
Dielectric and Electrical Properties of Lead Zirconate Titanate
Available online a t www.derpharmachemica.com Scholars Research Library Der Pharma Chemica, 2015, 7(10):175-185 (http://derpharmachemica.com/archive.html) ISSN 0975-413X CODEN (USA): PCHHAX Dielectric and electrical properties of lead zirconate titanate R. Balusamy a, P. Kumaravel b and N. G. Renganathan c* aDepartment of Mechanical Engineering, Al-Ameen Engineering College, Erode bDepartment of Mechanical Engineering, Institute of Road and Transport Technology, Erode c School of Basic Sciences, Vel Tech University, Chennai _____________________________________________________________________________________________ ABSTRACT o Lead zirconate titanate (PZT) (P bZrO3- PbTiO3) were prepared by mixed oxide method at 1100 C. Crystalline nature of the synthesized PZT has been confirmed by X-ray powder diffraction studies. The particle size and strain is calculated from X-ray peak broadening analysis by using Williamson-Hall plot. The crystallite size is also calculated using Debye-Scherrer’s formula. Also, the surface morphology and particle size of the samples were imaged using scanning electron microscopy (SEM). Dielectric measurement demonstrates that decrease in dielectric constant with increase in temperature. The temperature dependence of the ac conductivity indicated that the conduction process is due to singly ionized (in ferroelectric region) and doubly ionized (in paraelectric region). Key words : PZT ceramics, dielectric spectroscopy, dielectric losses, SEM. _____________________________________________________________________________________________ INTRODUCTION Lead zirconate titanate (PZT) – a ferroelectric ceramic material has piezoelectric properties and reciprocal behavior. This material is used to convert electrical energy into mechanical energy and vice-versa. The material properties of PZT have been the subject for significant research in recent years due to its excellent applications in micro- electromechanical (MEMS) and nano-electromechanical (NEMS) devices. -
Status of Numerical Modeling of Halocarbon Impacts on Stratospheric Ozone
THE STATUS OF NUMERICAL MODELING OF HALOCARBON IMPACTS ON STRATOSPHERIC OZONE Donald J. Wuebbles Department of Atmospheric Sciences University of Illinois, Urbana, IL 61801 Tel: 217-244-1568; Fax: 217-244-4393 [email protected] INTRODUCTION Numerical models of the chemistry and physics of the global atmosphere have played a key role in the scientific understanding of past, current and potential future effects of human-related emissions of halocarbons, including Halons, other brominated compounds and various replacement compounds on stratospheric ozone and climate change. As a result, these models have led directly to the Montreal Protocol and other national and international policy decisions regarding halocarbon controls due to their effects on stratospheric ozone. The purpose of this paper is to provide a perspective on atmospheric models, the role they have played in studies of the effects of Halons and other halocarbons on ozone, and to discuss what role models will likely play in future studies of stratospheric ozone THE COMPLEXITY OF STRATOSPHERIC OZONE It is important to recognize that the stratospheric ozone layer is a naturally occurring phenomenon that has great benefits to life on Earth. In fact, the formation of the ozone layer is generally believed to have played an important role in the development of life here on Earth. The accumulation of oxygen molecules in the atmosphere allowed for the production of ozone. Gradually the increasing levels of ozone led to the formation of the stratosphere, a region of the upper atmosphere where temperature increases with altitude largely as a result of the absorption of solar radiation by ozone.