On the Potential of Silicon As a Building Block for Life
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Regulated Substance List
INSTRUCTIONS FOR THE UNIFIED PROGRAM (UP) FORM REGULATED SUBSTANCE LIST CHEMICAL NAME CAS # TQ Listing CHEMICAL NAME CAS # TQ Listing (Lbs) Basis (Lbs) Basis Acetaldehyde 75-07-0 10,000 g Cantharidin 56-25-7 100/10,0001 * Acetone Cyanohydrin 75-86-5 1,000 Carbachol Chloride 51-83-2 500/10,0001 Acetone Thiosemicarbazide 1752-30-3 1,000/10,0001 Acetylene (Ethyne) 74-86-2 10,000 f Carbamic Acid, Methyl-,o- Acrolein (2-Propenal) 107-02-8 500 b (((2,4-Dimethyl-1,3-Dithiolan- Acrylamide 79-06-1 1,000/10,0001 2-YL) Methylene)Amino)- 26419-73-8 100/10,0001 Acrylonitrile (2- Propenenitrile) 107-13-1 10,000 b Carbofuran 1563-66-2 10/10,0001 Acrylyl Chloride Carbon Disulfide 75-15-0 10,000 b (2-Propenoyl Chloride) 814-68-6 100 b Carbon Oxysulfide Aldicarb 116-06-3 100/10,0001 (Carbon Oxide Sulfide (COS)) 463-58-1 10,000 f Aldrin 309-00-2 500/10,0001 Chlorine 7782-50-5 100 a,b Allyl Alcohol (2-Propen-1-ol) 107-18-6 1,000 b Chlorine Dioxide Allylamine (2-Propen-1-Amine) 107-11-9 500 b (Chlorine Oxide (ClO2)) 10049-04-4 1,000 c Aluminum Phosphide 20859-73-8 500 Chlorine Monoxide (Chlorine Oxide) 7791-21-1 10,000 f Aminopterin 54-62-6 500/10,0001 Chlormequat Chloride 999-81-5 100/10,0001 Amiton Oxalate 3734-97-2 100/10,0001 Chloroacetic Acid 79-11-8 100/10,0001 Ammonia, Anhydrous 2 7664-41-7 500 a,b Chloroform 67-66-3 10,000 b Ammonia, Aqueous Chloromethyl Ether (conc 20% or greater) 7664-41-7 20,000 a,b (Methane,Oxybis(chloro-) 542-88-1 100 b * Aniline 62-53-3 1,000 Chloromethyl Methyl Ether Antimycin A 1397-94-0 1,000/10,0001 (Chloromethoxymethane) -
Comparison of Sulfur to Oxygen*
OpenStax-CNX module: m34977 1 Comparison of Sulfur to Oxygen* Andrew R. Barron This work is produced by OpenStax-CNX and licensed under the Creative Commons Attribution License 3.0 1 Size Table 1 summarizes the comparative sizes of oxygen and sulfur. Element Atomic radius Covalent radius Ionic radius (Å) van der Waal ra- (Å) (Å) dius (Å) Oxygen 0.48 0.66 1.40 1.52 Sulfur 0.88 1.05 1.84 1.80 Table 1: Comparison of physical characteristics for oxygen and sulfur. 2 Electronegativity Sulfur is less electronegative than oxygen (2.4 and 3.5, respectively) and as a consequence bonds to sulfur are less polar than the corresponding bonds to oxygen. One signicant result in that with a less polar S-H bond the subsequent hydrogen bonding is weaker than observed with O-H analogs. A further consequence of the lower electronegativity is that the S-O bond is polar. 3 Bonds formed Sulfur forms a range of bonding types. As with oxygen the -2 oxidation state prevalent. For example, sulfur forms analogs of ethers, i.e., thioethers R-S-R. However, unlike oxygen, sulfur can form more than two covalent (non-dative) bonds, i.e., in compounds such as SF4 and SF6. Such hypervalent compounds were originally thought be due to the inclusion of low energy d orbitals 3 2 in hybrids (e.g., sp d for SF6); however, a better picture involves a combination of s and p ortbitals in bonding (Figure 1). Any involvement of the d orbitals is limited to the polarization of the p orbitals rather than direct hydridization. -
Thermodynamic Hydricity of Small Borane Clusters and Polyhedral Closo-Boranes
molecules Article Thermodynamic Hydricity of Small Borane Clusters y and Polyhedral closo-Boranes Igor E. Golub 1,* , Oleg A. Filippov 1 , Vasilisa A. Kulikova 1,2, Natalia V. Belkova 1 , Lina M. Epstein 1 and Elena S. Shubina 1,* 1 A. N. Nesmeyanov Institute of Organoelement Compounds and Russian Academy of Sciences (INEOS RAS), 28 Vavilova St, 119991 Moscow, Russia; [email protected] (O.A.F.); [email protected] (V.A.K.); [email protected] (N.V.B.); [email protected] (L.M.E.) 2 Faculty of Chemistry, M.V. Lomonosov Moscow State University, 1/3 Leninskiye Gory, 119991 Moscow, Russia * Correspondence: [email protected] (I.E.G.); [email protected] (E.S.S.) Dedicated to Professor Bohumil Štibr (1940-2020), who unfortunately passed away before he could reach the y age of 80, in the recognition of his outstanding contributions to boron chemistry. Academic Editors: Igor B. Sivaev, Narayan S. Hosmane and Bohumír Gr˝uner Received: 6 June 2020; Accepted: 23 June 2020; Published: 25 June 2020 MeCN Abstract: Thermodynamic hydricity (HDA ) determined as Gibbs free energy (DG◦[H]−) of the H− detachment reaction in acetonitrile (MeCN) was assessed for 144 small borane clusters (up 2 to 5 boron atoms), polyhedral closo-boranes dianions [BnHn] −, and their lithium salts Li2[BnHn] (n = 5–17) by DFT method [M06/6-311++G(d,p)] taking into account non-specific solvent effect (SMD MeCN model). Thermodynamic hydricity values of diborane B2H6 (HDA = 82.1 kcal/mol) and its 2 MeCN dianion [B2H6] − (HDA = 40.9 kcal/mol for Li2[B2H6]) can be selected as border points for the range of borane clusters’ reactivity. -
Towards a Classification System of Terrestrial Planets
7RZDUGVD&ODVVL¿FDWLRQ6\VWHPRI7HUUHVWULDO3ODQHWV Charles H. Lineweaver and Jose A. Robles Planetary Science Institute, Research School of Astronomy and Astrophysics, Research School of Earth Sciences, The Australian National University, Canberra ACT 0200 Australia. Abstract: The focus of extrasolar planet searches has become the detection of habitable terrestrial planets. Planetary mass and orbit have large and obvious effects on habitability. Since the chemical compositions of terrestrial planets also play an important role in habitability, we propose the creation RIDFODVVL¿FDWLRQV\VWHPIRU(DUWKOLNHSODQHWVEDVHGRQWKHDEXQGDQFHVRIHOHPHQWVPRVWLPSRUWDQW IRUKDELWDELOLW\:HGHVFULEHWKHPHWKRGRORJ\IRUWKHFUHDWLRQRIVXFKDFODVVL¿FDWLRQV\VWHPEDVHG on the observed chemical abundances of stars. Keywords: Terrestrial planet formation, Solar system, chemical composition Introduction %DFNJURXQGIRUWKH&UHDWLRQRID3ODQHW&ODVVL¿FDWLRQ6\VWHP 6FLHQWL¿FXQGHUVWDQGLQJRIDJURXSRIQHZREMHFWVEHJLQVZLWKDXVHIXOFODVVL¿FDWLRQVFKHPH)RU a century astronomers have relied on the Hertzsprung-Russell diagram to classify stars according to their colour and magnitude. In the Hertzsprung-Russell diagram the Sun is seen to be part of the PDLQVHTXHQFHRIK\GURJHQEXUQLQJVWDUV$QDQDORJRXVFODVVL¿FDWLRQV\VWHPIRUSODQHWVKDV\HWWR emerge. In our Solar System we have: small rocky planets close to the Sun (Mercury, Venus, Earth, Mars, asteroids), the gas giants (Jupiter and Saturn), then the ice giants (Uranus and Neptune) and ¿QDOO\DVZDUPRIVPDOOGLUW\VQRZEDOOV 3OXWRDQGFRPSDQ\ 7KLVUXGLPHQWDU\RUELWDOUDGLXV -
A Facile Approach to Prepare Multiple Heteroatom-Doped Carbon
www.nature.com/scientificreports OPEN A Facile Approach to Prepare Multiple Heteroatom-Doped Carbon Materials from Imine- Received: 17 November 2017 Accepted: 19 February 2018 Linked Porous Organic Polymers Published: xx xx xxxx Juan Yang, Min Xu, Jingyu Wang , Shangbin Jin & Bien Tan In this paper, we proposed a new strategy to prepare multiple heteroatom doped (N, P-doped) porous carbon materials with high surface area of ~1,535 m2 g−1 simply by pyrolysis of imine-linked porous organic polymers (POPs) synthesized via Schif base condensation. The strategy is simple without any post-processing and various heteroatoms could be involved. Scanning electron microscopy, Raman spectra, Nitrogen gas adsorption-desorption, X-ray photoelectron spectroscopy have been used to characterize the morphology, the structure and the composition of the materials. The multiple heteroatom doped porous carbon materials also display high electrocatalytic performance as exampled by the application in oxygen reduction, which showed the catalyst favors 4-electron transfer during the process, along with superior stability and higher tolerance to methanol as compared to the Pt/C. These results indicate the present method is promising for the preparation of multi-heteroatom doped carbon materials in the application of electrocatalysis. Porous organic polymers (POPs) are a type of organic polymers with large surface area, tunable skeleton and high stability1,2. Tey have attracted extensive attentions for broad applications in the felds of gas storage and separations, catalysis and energy storage3–5. Tere are many methodologies reported for the preparation of porous polymers6–10. Among them, Schif base reaction is one of the most versatile ways due to the facile, one-pot, catalyst-free, quantitative synthesis11. -
FIRE-SAFE POLYMERS and POLYMER COMPOSITES September 2004 6
DOT/FAA/AR-04/11 Fire-Safe Polymers and Polymer Office of Aviation Research Washington, D.C. 20591 Composites September 2004 Final Report This document is available to the U.S. public through the National Technical Information Service (NTIS), Springfield, Virginia 22161. U.S. Department of Transportation Federal Aviation Administration NOTICE This document is disseminated under the sponsorship of the U.S. Department of Transportation in the interest of information exchange. The United States Government assumes no liability for the contents or use thereof. The United States Government does not endorse products or manufacturers. Trade or manufacturer's names appear herein solely because they are considered essential to the objective of this report. This document does not constitute FAA certification policy. Consult your local FAA aircraft certification office as to its use. This report is available at the Federal Aviation Administration William J. Hughes Technical Center’s Full-Text Technical Reports page: actlibrary.act.faa.gov in Adobe Acrobat portable document format (PDF). Technical Report Documentation Page 1. Report No. 2. Government Accession No. 3. Recipient's Catalog No. DOT/FAA/AR-04/11 4. Title and Subtitle 5. Report Date FIRE-SAFE POLYMERS AND POLYMER COMPOSITES September 2004 6. Performing Organization Code 7. Author(s) 8. Performing Organization Report No. Huiqing Zhang 9. Performing Organization Name and Address 10. Work Unit No. (TRAIS) Polymer Science and Engineering University of Massachusetts Amhurst, MA 01003 11. Contract or Grant No. 12. Sponsoring Agency Name and Address 13. Type of Report and Period Covered U.S. Department of Transportation Federal Aviation Administration Office of Aviation Research 14. -
Aldrichimica Acta
VOLUME 51, NO. 1 | 2018 ALDRICHIMICA ACTA The Spectacular Resurgence of Electrochemical Redox Reactions in Organic Synthesis Carbon–Carbon π Bonds as Conjunctive Reagents in Cross-Coupling The life science business of Merck KGaA, Darmstadt, Germany operates as MilliporeSigma in the U.S. and Canada. MakInG sTrIDes In Genome EDITInG: THe DIGITaL, CHemIcaL, anD BIoLogIcaL Dear Fellow Researchers: You may not know that MilliporeSigma can make DNA from scratch, using 100% synthetic chemical methods—no living cells and no fermentation necessary. Our DNA synthesis facilities in The Woodlands (Texas) and Haverhill (U.K.) receive thousands of DNA orders daily from scientists all over the world. A small piece of DNA, one hundred bases long, gives scientists 4100 possibilities using only the fundamental letters of our genetic code (A,C,G,T). Included within these options is the opportunity for a researcher to open a common text editor on his or her PC and design a 100-base piece of DNA. This piece of DNA could help study diseases ranging from sickle cell anemia and blindness to cystic fibrosis by using CRISPR. To get started, scientists cut this 100-base DNA text from the text editor and paste it into MilliporeSigma’s online ordering system. The corresponding DNA piece that likely has never existed before is then delivered to them in 24–48 hours. Once received, this piece of DNA is mixed with CRISPR and living cells, and, with a “blast” of electricity, these synthetic chemical pieces activate the cell to edit the genome. Learn more about our CRISPR gene editing portfolio at SigmaAldrich.com/CRISPR Sincerely yours, Udit Batra, Ph.D. -
The Search for Another Earth – Part II
GENERAL ARTICLE The Search for Another Earth – Part II Sujan Sengupta In the first part, we discussed the various methods for the detection of planets outside the solar system known as the exoplanets. In this part, we will describe various kinds of exoplanets. The habitable planets discovered so far and the present status of our search for a habitable planet similar to the Earth will also be discussed. Sujan Sengupta is an 1. Introduction astrophysicist at Indian Institute of Astrophysics, Bengaluru. He works on the The first confirmed exoplanet around a solar type of star, 51 Pe- detection, characterisation 1 gasi b was discovered in 1995 using the radial velocity method. and habitability of extra-solar Subsequently, a large number of exoplanets were discovered by planets and extra-solar this method, and a few were discovered using transit and gravi- moons. tational lensing methods. Ground-based telescopes were used for these discoveries and the search region was confined to about 300 light-years from the Earth. On December 27, 2006, the European Space Agency launched 1The movement of the star a space telescope called CoRoT (Convection, Rotation and plan- towards the observer due to etary Transits) and on March 6, 2009, NASA launched another the gravitational effect of the space telescope called Kepler2 to hunt for exoplanets. Conse- planet. See Sujan Sengupta, The Search for Another Earth, quently, the search extended to about 3000 light-years. Both Resonance, Vol.21, No.7, these telescopes used the transit method in order to detect exo- pp.641–652, 2016. planets. Although Kepler’s field of view was only 105 square de- grees along the Cygnus arm of the Milky Way Galaxy, it detected a whooping 2326 exoplanets out of a total 3493 discovered till 2Kepler Telescope has a pri- date. -
This Ubiquitous Carbon…
Engineering Physics Department Presents Dr. Cristian Contescu Senior Research Staff, Materials Science and Technology Division Oak Ridge National Laboratory This ubiquitous carbon… Abstract: After Stone Age, Bronze Age, and Iron Age, and after the Silicon Age of the informational revolution, the technologies of 21st century are marked by the ubiquitous presence of various forms of carbon allotropes. For a very long time, diamond and graphite were the only known carbon allotropes, but that has changed with the serendipitous discovery of fullerenes, carbon nanotubes, and graphene. Every ten or fifteen years scientists unveil new forms of carbons with new and perplexing properties, while computations suggest that the carbon’s family still has members unknown to us today. At a dramatically accelerated pace, new carbon forms find their place at the leading edge of scientific and technological innovations. At the same time traditional forms of carbon are being used in new and exciting applications that make our life safer, healthier, and more enjoyable. The 21st century may soon be recognized as the Age of Carbon forms. This educational talk will show how carbon, the fourth most abundant element in the Galaxy and the basis of life on Earth, was the engine of most important technological developments throughout the history of civilization. It will emphasize the ability of carbon atoms to generate a variety of mutual combinations and with many other chemical elements. These properties have placed carbon at the core of numerous inventions that define our civilization, while emerging new technologies open a rich path for value-added products in today’s market. -
Properties of Carbon the Atomic Element Carbon Has Very Diverse
Properties of Carbon The atomic element carbon has very diverse physical and chemical properties due to the nature of its bonding and atomic arrangement. fig. 1 Allotropes of Carbon Some allotropes of carbon: (a) diamond, (b) graphite, (c) lonsdaleite, (d–f) fullerenes (C60, C540, C70), (g) amorphous carbon, and (h) carbon nanotube. Carbon has several allotropes, or different forms in which it can exist. These allotropes include graphite and diamond, whose properties span a range of extremes. Despite carbon's ability to make 4 bonds and its presence in many compounds, it is highly unreactive under normal conditions. Carbon exists in 2 main isotopes: 12C and 13C. There are many other known isotopes, but they tend to be short-lived and have extremely short half-lives. Allotropes The different forms of a chemical element. Cabon is the chemical element with the symbol C and atomic number 6. As a member of group 14 on the periodic table, it is nonmetallic and tetravalent—making four electrons available to form covalent chemical bonds. Carbon has 6 protons and 6 Source URL: https://www.boundless.com/chemistry/nonmetallic-elements/carbon/properties-carbon/ Saylor URL: http://www.saylor.org/courses/chem102#6.1 Attributed to: Boundless www.saylor.org Page 1 of 2 neutrons, and has a standard atomic weight of 12.0107 amu. Its electron configuration is denoted as 1s22s22p2. It is a solid, and sublimes at 3,642 °C. It's oxidation state ranges from 4 to -4, and it has an electronegativity rating of 2.55 on the Pauling scale. Carbon has several allotropes, or different forms in which it exists. -
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. -
Visualization of Chemical Space Using Principal Component Analysis
World Applied Sciences Journal 29 (Data Mining and Soft Computing Techniques): 53-59, 2014 ISSN 1818-4952 © IDOSI Publications, 2014 DOI: 10.5829/idosi.wasj.2014.29.dmsct.10 Visualization of Chemical Space Using Principal Component Analysis B. Firdaus Begam and J. Satheesh Kumar Department of Computer Applications, School of Computer Science and Engineering, Bharathiar University, Coimbatore, Tamilnadu, India Abstract: Principal component analysis is one of the most widely used multivariate methods to visualize chemical space in new dimension by the chemist for analysing data. In Multivariate data analysis, the relationship between two variables with more number of characteristics can be considered. PCA provides a compact view of variation in chemical data matrix which helps in creating better Quantitative Structure Activity Relationship (QSAR) model. It highlights the dominating pattern in the matrix through principal component and graphical representation. This paper focuses on mathematical aspects of principal components and role of PCA on Maybridge dataset to identify dominating hidden patterns of drug likeness based on Lipinski RO5. Key words: Principal Component Analysis Load p lot Score plot Biplot INTRODUCTION a new model of selected objects and variables with minimal loss of information. It can also be used for Principal Component Analysis (PCA) is a multivariate prediction model as PCA acts as exploratory tool for data statistical approach to analyze data in lower dimensional analysis by calculating the variance among the variables space. PCA used vector space transformation technique which are uncorrelated [8]. to view datasets from higher-dimensional space to lower Chemical space (drug space) is defined as dimensional space. PCA is an application of linear algebra number of descriptors calculated for each molecule [2] which was first coined by Karl Pearson during 1901 [1].