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The Pedersen Memorial Issue
springer.com Chemistry : Organic Chemistry The Pedersen Memorial Issue Foreword: Charles J. Pedersen (1904-1989), Nobel Laureate in Chemistry (1987) This issue is dedicated to the memory of the late Charles J. Pedersen in recognition of his outstanding contribution to scientific research, culminating in his discovery of crown ethers and their remarkable cation complexing properties and his receipt of the 1987 Nobel Prize in Chemistry. Charlie's origin and early years in Korea did not portend the creative work in chemistry which would characterize his later life. However, we can see in his early years the influence of his Norwegian father and Japanese mother who considered his formal education to be of utmost importance. At the age of eight, he was sent abroad to Japan for schooling, first at a convent school in Nagasaki, and two years later at a French-American preparatory school in Yokohama run by a Marianist order of Catholic priests and brothers. The latter group encouraged him to attend the order's University of Dayton in Ohio where he received a bachelors degree in Springer chemical engineering. Charlie's academic experiences, his employment with du Pont, and the Softcover reprint of the creative spark which he manifested at an early stage of his scientific career are detailed in the 1st original 1st ed. 1992, VI, paper in this issue by Herman Schroeder. Schroeder had a long-time association with Charlie at edition 406 p. du Pont as a co-worker, supervisor, and friend. His recollections provide insight into Charlie's creative mind. In addition, they make it clear that a long period of creative work preceded the accidental discovery of the first synthetic crown ether. -
The 2016 Nobel Prize in Chemistry
Pure Appl. Chem. 2016; 88(10-11): 917–918 Editorial Hugh D. Burrows* and Richard M. Hartshorn* The 2016 Nobel Prize in Chemistry DOI 10.1515/pac-2016-2005 Keywords: Ben L. Feringa; Jean-Pierre Sauvage; J. Fraser Stoddart; Nobel Prize in Chemistry; 2016. Pure and Applied Chemistry warmly congratulates Jean-Pierre Sauvage (University of Strasbourg, France), Sir J. Fraser Stoddart (Northwestern University, Evanston, IL, USA), and Bernard (Ben) L. Feringa (Univer- sity of Groningen, the Netherlands) on their award of the 2016 Nobel Prize in Chemistry. The citation from the Royal Swedish Academy of Sciences states that the award is “for the design and synthesis of molecu- lar machines”. Their work encompasses a broad spectrum of Chemistry, from elegant synthetic studies of catenanes, rotaxanes and other formerly considered exotic molecules, through coordination chemistry, and electron transfer reactions, to molecular switches and rotors driven by light and other external sources. They have all participated actively in IUPAC endorsed meetings and conference series, including the IUPAC World Congress in Chemistry, IUPAC International Conferences on Organic Synthesis (ICOS), Physical Organic Chemistry (ICPOC), and Coordination Chemistry (ICCC), and IUPAC International Symposia on Macrocyclic Chemistry (ISMC), Organometallic Chemistry Directed Towards Organic Synthesis (OMCOS), Novel Aromatic Compounds (ISNA), Carbohydrate Chemistry (ICS), the Chemistry of Natural Products ISCNP), and Photo- chemistry. Pure Appl. Chem. publishes collections of papers based upon authoritative lectures presented at such IUPAC endorsed events, in addition to IUPAC Recommendations, and Technical Reports. We are very pleased to highlight the following publications from these three Nobel Laureates that have been published in Pure and Applied Chemistry as a result of their involvement in these conferences. -
Pauling-Linus.Pdf
NATIONAL ACADEMY OF SCIENCES L I N U S C A R L P A U L I N G 1901—1994 A Biographical Memoir by J A C K D. D UNITZ Any opinions expressed in this memoir are those of the author(s) and do not necessarily reflect the views of the National Academy of Sciences. Biographical Memoir COPYRIGHT 1997 NATIONAL ACADEMIES PRESS WASHINGTON D.C. LINUS CARL PAULING February 28, 1901–August 19, 1994 BY JACK D. DUNITZ INUS CARL PAULING was born in Portland, Oregon, on LFebruary 28, 1901, and died at his ranch at Big Sur, California, on August 19, 1994. In 1922 he married Ava Helen Miller (died 1981), who bore him four children: Linus Carl, Peter Jeffress, Linda Helen (Kamb), and Edward Crellin. Pauling is widely considered the greatest chemist of this century. Most scientists create a niche for themselves, an area where they feel secure, but Pauling had an enormously wide range of scientific interests: quantum mechanics, crys- tallography, mineralogy, structural chemistry, anesthesia, immunology, medicine, evolution. In all these fields and especially in the border regions between them, he saw where the problems lay, and, backed by his speedy assimilation of the essential facts and by his prodigious memory, he made distinctive and decisive contributions. He is best known, perhaps, for his insights into chemical bonding, for the discovery of the principal elements of protein secondary structure, the alpha-helix and the beta-sheet, and for the first identification of a molecular disease (sickle-cell ane- mia), but there are a multitude of other important contri- This biographical memoir was prepared for publication by both The Royal Society of London and the National Academy of Sciences of the United States of America. -
The 2009 Lindau Nobel Laureate Meeting: Roger Y. Tsien, Chemistry 2008
Journal of Visualized Experiments www.jove.com Video Article The 2009 Lindau Nobel Laureate Meeting: Roger Y. Tsien, Chemistry 2008 Roger Y. Tsien1 1 URL: https://www.jove.com/video/1575 DOI: doi:10.3791/1575 Keywords: Cellular Biology, Issue 35, GFP, Green Fluorescent Protein, IFPs, jellyfish, PKA, Calmodulin Date Published: 1/13/2010 Citation: Tsien, R.Y. The 2009 Lindau Nobel Laureate Meeting: Roger Y. Tsien, Chemistry 2008. J. Vis. Exp. (35), e1575, doi:10.3791/1575 (2010). Abstract American biochemist Roger Tsien shared the 2008 Nobel Prize in Chemistry with Martin Chalfie and Osamu Shimomura for their discovery and development of the Green Fluorescent Protein (GFP). Tsien, who was born in New York in 1952 and grew up in Livingston New Jersey, began to experiment in the basement of the family home at a young age. From growing silica gardens of colorful crystallized metal salts to attempting to synthesize aspirin, these early experiments fueled what would become Tsien's lifelong interest in chemistry and colors. Tsien's first official laboratory experience was an NSF-supported summer research program in which he used infrared spectroscopy to examine how metals bind to thiocyanate, for which he was awarded a $10,000 scholarship in the Westinghouse Science Talent Search. Following graduation from Harvard in 1972, Tsien attended Cambridge University in England under a Marshall Scholarship. There he learned organic chemistry --a subject he'd hated as an undergraduate-- and looked for a way to synthesize dyes for imaging neuronal activity, generating BAPTA based optical calcium indicator dyes. Following the completion of his postdoctoral training at Cambridge in 1982, Tsien accepted a faculty position at the University of California, Berkeley. -
Otto Hahn Otto Hahn
R.N. 70269/98 Postal Registration No.: DL-SW-1/4082/15-17 ISSN : 0972-169X Date of posting: 26-27 of advance month Date of publication: 24 of advance month May 2017 Vol. 19 No. 8 Rs. 5.00 Otto Hahn Discoverer of Nuclear Fission Editorial: Consolidating 35 science communication activities in our country Otto Hahn: Discoverer of 34 Nuclear Fission Keep Your Eyes Healthy 31 Phenol: A Serious 30 Environmental Threat Accidental Discoveries in 28 Medical Science Cures for haemorrhoids— 24 Simple treatments and Surgeries Recent developments 21 in science and technology 36 Editorial Consolidating science communication activities in our country Dr. R. Gopichandran It is well known that the National Council of Science Museums of India’s leadership in science technology and innovation (STI) across the Ministry of Culture, Government of India, the National Institute the bilateral and multilateral framework also. The news feature service of Science Communication and Information Resources (NISCAIR) and the portal activity have well defined action plans to reach out to of CSIR, the National Council for Science and Technology fellow institutions and citizens with suitably embellished platform Communication (NCSTC) of the Department of Science and and opportunities for all to deliver together. Technology (DST), Government of India and Vigyan Prasar, also While these are interesting and extremely important, especially of DST, have been carrying out excellent science communication because they respond to the call to upscale and value add science activities over the years. It cannot be denied that the reach has been and technology communication, it is equally important to document quite significant collectively. -
2016 Nobel Prize in Chemistry
2016 NOBEL PRIZE IN CHEMISTRY The Nobel Prize in Chemistry 2016 was awarded to Jean-Pierre Sauvage, Sir Fraser Stoddart, and Bernard Feringa for the design and production of molecular machines with controllable movements. This year’s chemistry Nobel Prize is awarded for work on molecular machines which are a thousand times thinner than a human hair. The machines are formed from mechanically interlocked ring- shaped molecules which are able to move Ring-SHAPED MOLECULE 1 Ring-SHAPED MOLECULE 2 BINDING SITE relative to each other. UV 20˚C UV, 60˚C ORGANIC-BASED CORDINATING RINGS ‘SHUTLE’ Bulky Groups CENTRAL COPER ION ‘STATIONS’ REST OF MOLECULE DOUBLE BOND; ISOMERISATION DRIVES ROTATION Jean-Pierre Sauvage created a Fraser Stoddart made a ring-shaped Ben Feringa produced the pair of interlocking rings (called molecule attached to an axle (a first molecular motor by a catenane). One ring could rotaxane) which could shuttle up constructing a molecule that rotate around the other when and down. He also helped produce responded to light and heat and energy was added. a rotaxane-based computer chip. spun in a particular direction. WHY DOES THIS RESEARCH MATER? Research is investigating using molecular machines to transport and release drugs to specific cells in the body. They could also find future uses in ? electronic devices. The tasks they can accomplish are constantly expanding, so they may have further as yet unforeseen uses. Nobel Prize in Physics Press release: http://www.nobelprize.org/nobel_prizes/chemistry/laureates/2016/press.html © Compound Interest/Andy Brunning – compoundchem.com C COMPOUND INTEREST Shared under a CC Attribution-NonCommercial-NoDerivatives licence BY NC ND. -
Professor Ada Yonath, Weizmann Institute of Science, Rehovot, Israel, Nobel Laureate in Chemistry, 2009
1 Public Health Reviews, Vol. 34, No 2 Preface: Science and Public Health: Professor Ada Yonath, Weizmann Institute of Science, Rehovot, Israel, Nobel Laureate in Chemistry, 2009 Lore Leighton1 ABSTRACT Ribosomes are responsible for translating genetic code into protein and thus central components of cell life. Knowledge of their structure provided important potential applications in and understanding of the mode of action of antibiotics and resistance to antibiotics. The work of Professor Ada Yonath on the crystallography of ribosomes led to improvements in crystallization, crystallographic techniques, and x-ray diffraction detection procedures. In 2000 and 2001, Dr. Yonath published the three dimensional structures of the two subunits of bacterial ribosome. There are potential applications for this work, and hopefully science will use such tools to develop new methods to reduce the burden of many diseases. In 2009, Professor Ada Yonath was awarded the Nobel Prize in Chemistry for her structural work on the ribosome. Key Words: Nobel Prize Chemistry 2009, Professor Ada Yonath, Weizman Institute Israel, ribosome, x-ray crystallography, antibiotic resistance, science and public health Recommended Citation: Leighton, L. Science and Public Health: Professor Ada Yonath, Weizmann Institute of Science, Rehovot, Israel, Nobel Laureate in Chemistry, 2009. Public Health Reviews. 2013;34: epub ahead of print. BACKGROUND Professor Ada Yonath grew up in a poor family in Israel with a father who was quite ill. However, even as a young child she was always very curious about the world and despite their difficulties her parents sent her to a prestigious grammar school. Professor Yonath’s father passed away when she was 11 years old, and from that time onwards she had to help her struggling mother to meet the financial needs of the family with various 1 Public Health Reviews, Presses de l'EHESP, Paris and Rennes, France 2 Public Health Reviews, Vol. -
University Microfilms International 300 N
MOLECULAR BEAM KINETICS. Item Type text; Thesis-Reproduction (electronic) Authors Sentman, Judith Barlow. Publisher The University of Arizona. Rights Copyright © is held by the author. Digital access to this material is made possible by the University Libraries, University of Arizona. Further transmission, reproduction or presentation (such as public display or performance) of protected items is prohibited except with permission of the author. Download date 03/10/2021 03:47:31 Link to Item http://hdl.handle.net/10150/274898 INFORMATION TO USERS This reproduction was made from a copy of a document sent to us for microfilming. While the most advanced technology has been used to photograph and reproduce this document, the quality of the reproduction is heavily dependent upon the quality of the material submitted. The following explanation of techniques is provided to help clarify markings or notations which may appear on this reproduction. 1.The sign or "target" for pages apparently lacking from the document photographed is "Missing Page(s)". If it was possible to obtain the missing page(s) or section, they are spliced into the film along with adjacent pages. This may have necessitated cutting through an image and duplicating adjacent pages to assure complete continuity. 2. When an image on the film is obliterated with a round black mark, it is an indication of either blurred copy because of movement during exposure, duplicate copy, or copyrighted materials that should not have been filmed. For blurred pages, a good image of the page can be found in the adjacent frame. If copyrighted materials were deleted, a target note will appear listing the pages in the adjacent frame. -
Synthesis of Quinine
Synthesis of quinine Outstanding organic chemist Robert Burns Woodward over 30 years has carried out about 20 complex syntheses of natural compounds such as quinine, cholesterol, cortisone, strychnine, lysergic acid, reserpine, chlorophyll, cephalosporin, and colchicine that previously seemed unrealizable. For his contribution in organic chemistry he was awarded the Robert Burns Woodward Nobel Prize in Chemistry in 1965. The goal of one of the first in a series of April 10, 1917 – July 8, 1979 extremely complex and elegant syntheses he carried out was quinine, an alkaloid of the cinchona tree with a bitter taste. Quinine has antipyretic, analgesic, and antiarethmic properties and is still used in the treatment of malaria. Although the synthesis proved to be successful, it was too long and laborious to be applied on a practical scale. Later, E. Jacobsen and his co- workers were able to propose a much simpler enanteoselective synthesis of quinine using catalytic reactions. Steven E. Jacobsen MeO 1) Fe, HCl 1) HC C CO2Me Ph3PBr2 A B C o K H o 170 MW NO2 2) 2CO3, 2O 2) 250 C C, w(C) = 50.05% o O O O 1) BuLi, -78 C NC CO2Me H2, Ni Reney OEt D E F P o Ph N OEt (S,S)- ((salen)Al) O 44 atm, 80 C H 2 2) ee = 92% O OTBS Bpin Cbz LiAlH Cl CHBpin N 1) 4 1) Cbz2O, Et3N 1) Ph3P=CH2 NMO, TPAP 2 H I J G + - 2) H2O 2) NMO, TPAP 2) Bu4N F 4A MS CrCl2, LiI 4A MS X N OH H X, Pd(OAc)2 AD-mix-b CH3C(OMe)3 1) AcBr 1) Et2AlCl C K L M N MeO SPhos, K PO4 MeSO NH PPTS 2) K2CO3, MeOH 2) MeSPh 3 2 2 C H N O 31 36 2 6 o 3) 200 C, MW N Quinine Compound Brut formula Compound Brut formula Compound Brut formula Compound Brut formula A C7H9NO E C22H32N2O5Si I C17H23NO3 L C28H32N2O5 B C10H9NO2 F C15H29NO4Si J C17H21NO3 M C31H36N2O6 C C10H10BrNO G C14H31NO2Si X C18H22NO2 N C28H30N2O4 D C18H27NO3Si H C22H35NO4Si K C28H30N2O3 1. -
A Novel Crossed-Molecular-Beam Experiment for Investigating Reactions of State- and Conformationally Selected Strong-field-Seeking Moleculesa)
A novel CMB setup for strong-field-seeking molecules A novel crossed-molecular-beam experiment for investigating reactions of state- and conformationally selected strong-field-seeking moleculesa) L. Ploenes,1 P. Straňák,1 H. Gao,1, 2 J. Küpper,3, 4, 5, 6 and S. Willitsch1, b) 1)Department of Chemistry, University of Basel, Klingelbergstrasse 80, 4056 Basel, Switzerland 2)Present address: Beijing National Laboratory for Molecular Sciences (BNLMS), Institute of Chemistry, Chinese Academy of Sciences, Beijing 100190, People’s Republic of China 3)Center for Free-Electron Laser Science, Deutsches Elektronen-Synchrotron DESY, Notkestraße 85, 22607 Hamburg, Germany 4)Center for Ultrafast Imaging, Universität Hamburg, Luruper Chaussee 149, 22761 Hamburg, Germany 5)Department of Physics, Universität Hamburg, Luruper Chaussee 149, 22761 Hamburg, Germany 6)Department of Chemistry, Universität Hamburg, Martin-Luther-King-Platz 6, 20146 Hamburg, Germany (Dated: 14 May 2021) The structure and quantum state of the reactants have a profound impact on the kinetics and dynamics of chemical reactions. Over the past years, significant advances have been made in the control and manipulation of molecules with external electric and magnetic fields in molecular-beam experiments for investigations of their state-, structure- and energy-specific chemical reactivity. Whereas studies for neutrals have so far mainly focused on weak-field-seeking species, we report here progress towards investigating reactions of strong-field-seeking molecules by introducing a novel crossed-molecular-beam experiment featuring an electrostatic deflector. The new setup enables the characteri- sation of state- and geometry-specific effects in reactions under single-collision conditions. As a proof of principle, we present results on the chemi-ionisation reaction of metastable neon atoms with rotationally state-selected carbonyl sulfide (OCS) molecules and show that the branching ratio between the Penning and dissociative ionisation pathways strongly depends on the initial rotational state of OCS. -
Multistep Synthesis of Complex Carbogenic Molecules
THE LOGIC OF CHEMICAL SYNTHESIS: MULTISTEP SYNTHESIS OF COMPLEX CARBOGENIC MOLECULES Nobel Lecture, December 8, 1990 by E LIAS J AMES C OREY Department of Chemistry, Harvard University, Cambridge, Massachusetts, USA Carbogens, members of the family of carbon-containing compounds, can exist in an infinite variety of compositions, forms and sizes. The naturally occurring carbogens, or organic substances as they are known more tradi- tionally, constitute the matter of all life on earth, and their science at the molecular level defines a fundamental language of that life. The chemical synthesis of these naturally occurring carbogens and many millions of unnatural carbogenic substances has been one of the major enterprises of science in this century. That fact is affirmed by the award of the Nobel Prize in Chemistry for 1990 for the “development of the theory and methodology of organic synthesis”. Chemical synthesis is uniquely positioned at the heart of chemistry, the central science, and its impact on our lives and society is all pervasive. For instance, many of today’s medicines are synthetic and many of tomorrow’s will be conceived and produced by synthetic chemists. To the field of synthetic chemistry belongs an array of responsibilities which are crucial for the future of mankind, not only with regard to the health, material and economic needs of our society, but also for the attainment of an understanding of matter, chemical change and life at the highest level of which the human mind is capable. The post World War II period encompassed remarkable achievement in chemical synthesis. In the first two decades of this period chemical syntheses were developed which could not have been anticipated in the earlier part of this century. -
Induced Fluorescence Spectroscopy of Li (2 PJ-2 5 112, A.=670.7 Nm) Between 700 and 1000 K John M
A study of the reaction Li+ HCI by the technique of time-resolved laser 2 2 induced fluorescence spectroscopy of Li (2 PJ-2 5 112, A.=670.7 nm) between 700 and 1000 K John M. C. Plane and Eric S. Saltzman Rosenstiel School ofMarine and Atmospheric Science, University ofMiami, Miami, Florida 33149-1098 (Received 16 June 1987; accepted 9 July 1987) A kinetic study is presented of the reaction between lithium atoms and hydrogen chloride over the temperature range 700-1000 K. Li atoms are produced in an excess ofHCl and He bath gas by pulsed photolysis ofLiCl vapor. The concentration of the metal atoms is then monitored in real time by the technique of laser-induced fluorescence of Li atoms at A. = 670. 7 nm using a pulsed nitrogen-pumped dye laser and box-car integration of the fluorescence signal. Absolute second-order rate constants for this reaction have been measured at T = 700, 750, 800, and 900 K. At T = 1000 K the reverse reaction is sufficiently fast that equilibrium is rapidly established on the time scale of the experiment. A fit of the data between 700 and 900 K to the Arrhenius form, with 20' errors calculated from the absolute errors in the rate 10 3 1 constants, yields k(T) = (3.8 ± l.l) X 10- exp[ - (883 ± 218)/TJ cm molecule- • s- . This result is interpreted through a modified form of collision theory which is constrained to take account of the conservation of total angular momentum during the reaction. Thereby we 1 obtain an estimate for the reaction energy threshold, E0 = 8.2 ± 1.4 kJ mo1- (where the error arises from uncertainty in the exothermicity of the reaction), in very good agreement with a crossed molecular beam study of the title reaction, and substantially lower than estimates of E 0 from both semiempirical and ab initio calculations of the potential energy surface.