1.
Jmol
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Jmol is computer software for molecular modelling chemical structures in 3-dimensions. Jmol returns a 3D representation of a molecule that may be used as a teaching tool and it is written in the programming language Java, so it can run on the operating systems Windows, macOS, Linux, and Unix, if Java is installed. It is free and open-source software released under a GNU Lesser General Public License version 2.0, a standalone application and a software development kit exist that can be integrated into other Java applications, such as Bioclipse and Taverna. A popular feature is an applet that can be integrated into web pages to display molecules in a variety of ways, for example, molecules can be displayed as ball-and-stick models, space-filling models, ribbon diagrams, etc. Jmol supports a range of chemical file formats, including Protein Data Bank, Crystallographic Information File, MDL Molfile. There is also a JavaScript-only version, JSmol, that can be used on computers with no Java, the Jmol applet, among other abilities, offers an alternative to the Chime plug-in, which is no longer under active development. While Jmol has many features that Chime lacks, it does not claim to reproduce all Chime functions, most notably, Chime requires plug-in installation and Internet Explorer 6.0 or Firefox 2.0 on Microsoft Windows, or Netscape Communicator 4.8 on Mac OS9. Jmol requires Java installation and operates on a variety of platforms. For example, Jmol is fully functional in Mozilla Firefox, Internet Explorer, Opera, Google Chrome, fast and Scriptable Molecular Graphics in Web Browsers without Java3D
2.
ChEMBL
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ChEMBL or ChEMBLdb is a manually curated chemical database of bioactive molecules with drug-like properties. It is maintained by the European Bioinformatics Institute, of the European Molecular Biology Laboratory, based at the Wellcome Trust Genome Campus, Hinxton, the database, originally known as StARlite, was developed by a biotechnology company called Inpharmatica Ltd. later acquired by Galapagos NV. The data was acquired for EMBL in 2008 with an award from The Wellcome Trust, resulting in the creation of the ChEMBL chemogenomics group at EMBL-EBI, the ChEMBL database contains compound bioactivity data against drug targets. Bioactivity is reported in Ki, Kd, IC50, and EC50, data can be filtered and analyzed to develop compound screening libraries for lead identification during drug discovery. ChEMBL version 2 was launched in January 2010, including 2.4 million bioassay measurements covering 622,824 compounds and this was obtained from curating over 34,000 publications across twelve medicinal chemistry journals. ChEMBLs coverage of available bioactivity data has grown to become the most comprehensive ever seen in a public database, in October 2010 ChEMBL version 8 was launched, with over 2.97 million bioassay measurements covering 636,269 compounds. ChEMBL_10 saw the addition of the PubChem confirmatory assays, in order to integrate data that is comparable to the type, ChEMBLdb can be accessed via a web interface or downloaded by File Transfer Protocol. It is formatted in a manner amenable to computerized data mining, ChEMBL is also integrated into other large-scale chemistry resources, including PubChem and the ChemSpider system of the Royal Society of Chemistry. In addition to the database, the ChEMBL group have developed tools and these include Kinase SARfari, an integrated chemogenomics workbench focussed on kinases. The system incorporates and links sequence, structure, compounds and screening data, the primary purpose of ChEMBL-NTD is to provide a freely accessible and permanent archive and distribution centre for deposited data. July 2012 saw the release of a new data service, sponsored by the Medicines for Malaria Venture. The data in this service includes compounds from the Malaria Box screening set, myChEMBL, the ChEMBL virtual machine, was released in October 2013 to allow users to access a complete and free, easy-to-install cheminformatics infrastructure. In December 2013, the operations of the SureChem patent informatics database were transferred to EMBL-EBI, in a portmanteau, SureChem was renamed SureChEMBL. 2014 saw the introduction of the new resource ADME SARfari - a tool for predicting and comparing cross-species ADME targets
3.
ChemSpider
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ChemSpider is a database of chemicals. ChemSpider is owned by the Royal Society of Chemistry, the database contains information on more than 50 million molecules from over 500 data sources including, Each chemical is given a unique identifier, which forms part of a corresponding URL. This is an approach to develop an online chemistry database. The search can be used to widen or restrict already found results, structure searching on mobile devices can be done using free apps for iOS and for the Android. The ChemSpider database has been used in combination with text mining as the basis of document markup. The result is a system between chemistry documents and information look-up via ChemSpider into over 150 data sources. ChemSpider was acquired by the Royal Society of Chemistry in May,2009, prior to the acquisition by RSC, ChemSpider was controlled by a private corporation, ChemZoo Inc. The system was first launched in March 2007 in a release form. ChemSpider has expanded the generic support of a database to include support of the Wikipedia chemical structure collection via their WiChempedia implementation. A number of services are available online. SyntheticPages is an interactive database of synthetic chemistry procedures operated by the Royal Society of Chemistry. Users submit synthetic procedures which they have conducted themselves for publication on the site and these procedures may be original works, but they are more often based on literature reactions. Citations to the published procedure are made where appropriate. They are checked by an editor before posting. The pages do not undergo formal peer-review like a journal article. The comments are moderated by scientific editors. The intention is to collect practical experience of how to conduct useful chemical synthesis in the lab, while experimental methods published in an ordinary academic journal are listed formally and concisely, the procedures in ChemSpider SyntheticPages are given with more practical detail. Comments by submitters are included as well, other publications with comparable amounts of detail include Organic Syntheses and Inorganic Syntheses
4.
PubChem
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PubChem is a database of chemical molecules and their activities against biological assays. The system is maintained by the National Center for Biotechnology Information, a component of the National Library of Medicine, PubChem can be accessed for free through a web user interface. Millions of compound structures and descriptive datasets can be downloaded via FTP. PubChem contains substance descriptions and small molecules with fewer than 1000 atoms and 1000 bonds, more than 80 database vendors contribute to the growing PubChem database. PubChem consists of three dynamically growing primary databases, as of 28 January 2016, Compounds,82.6 million entries, contains pure and characterized chemical compounds. Substances,198 million entries, contains also mixtures, extracts, complexes, bioAssay, bioactivity results from 1.1 million high-throughput screening programs with several million values. PubChem contains its own online molecule editor with SMILES/SMARTS and InChI support that allows the import and export of all common chemical file formats to search for structures and fragments. In the text search form the database fields can be searched by adding the name in square brackets to the search term. A numeric range is represented by two separated by a colon. The search terms and field names are case-insensitive, parentheses and the logical operators AND, OR, and NOT can be used. AND is assumed if no operator is used, example,0,5000,50,10 -5,5 PubChem was released in 2004. The American Chemical Society has raised concerns about the publicly supported PubChem database and they have a strong interest in the issue since the Chemical Abstracts Service generates a large percentage of the societys revenue. To advocate their position against the PubChem database, ACS has actively lobbied the US Congress, soon after PubChems creation, the American Chemical Society lobbied U. S. Congress to restrict the operation of PubChem, which they asserted competes with their Chemical Abstracts Service
5.
International Chemical Identifier
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Initially developed by IUPAC and NIST from 2000 to 2005, the format and algorithms are non-proprietary. The continuing development of the standard has supported since 2010 by the not-for-profit InChI Trust. The current version is 1.04 and was released in September 2011, prior to 1.04, the software was freely available under the open source LGPL license, but it now uses a custom license called IUPAC-InChI Trust License. Not all layers have to be provided, for instance, the layer can be omitted if that type of information is not relevant to the particular application. InChIs can thus be seen as akin to a general and extremely formalized version of IUPAC names and they can express more information than the simpler SMILES notation and differ in that every structure has a unique InChI string, which is important in database applications. Information about the 3-dimensional coordinates of atoms is not represented in InChI, the InChI algorithm converts input structural information into a unique InChI identifier in a three-step process, normalization, canonicalization, and serialization. The InChIKey, sometimes referred to as a hashed InChI, is a fixed length condensed digital representation of the InChI that is not human-understandable. The InChIKey specification was released in September 2007 in order to facilitate web searches for chemical compounds and it should be noted that, unlike the InChI, the InChIKey is not unique, though collisions can be calculated to be very rare, they happen. In January 2009 the final 1.02 version of the InChI software was released and this provided a means to generate so called standard InChI, which does not allow for user selectable options in dealing with the stereochemistry and tautomeric layers of the InChI string. The standard InChIKey is then the hashed version of the standard InChI string, the standard InChI will simplify comparison of InChI strings and keys generated by different groups, and subsequently accessed via diverse sources such as databases and web resources. Every InChI starts with the string InChI= followed by the version number and this is followed by the letter S for standard InChIs. The remaining information is structured as a sequence of layers and sub-layers, the layers and sub-layers are separated by the delimiter / and start with a characteristic prefix letter. The six layers with important sublayers are, Main layer Chemical formula and this is the only sublayer that must occur in every InChI. The atoms in the formula are numbered in sequence, this sublayer describes which atoms are connected by bonds to which other ones. Describes how many hydrogen atoms are connected to each of the other atoms, the condensed,27 character standard InChIKey is a hashed version of the full standard InChI, designed to allow for easy web searches of chemical compounds. Most chemical structures on the Web up to 2007 have been represented as GIF files, the full InChI turned out to be too lengthy for easy searching, and therefore the InChIKey was developed. With all databases currently having below 50 million structures, such duplication appears unlikely at present, a recent study more extensively studies the collision rate finding that the experimental collision rate is in agreement with the theoretical expectations. Example, Morphine has the structure shown on the right, as the InChI cannot be reconstructed from the InChIKey, an InChIKey always needs to be linked to the original InChI to get back to the original structure
6.
Simplified molecular-input line-entry system
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The simplified molecular-input line-entry system is a specification in form of a line notation for describing the structure of chemical species using short ASCII strings. SMILES strings can be imported by most molecule editors for conversion back into two-dimensional drawings or three-dimensional models of the molecules, the original SMILES specification was initiated in the 1980s. It has since modified and extended. In 2007, a standard called OpenSMILES was developed in the open-source chemistry community. Other linear notations include the Wiswesser Line Notation, ROSDAL and SLN, the original SMILES specification was initiated by David Weininger at the USEPA Mid-Continent Ecology Division Laboratory in Duluth in the 1980s. The Environmental Protection Agency funded the project to develop SMILES. It has since modified and extended by others, most notably by Daylight Chemical Information Systems. In 2007, a standard called OpenSMILES was developed by the Blue Obelisk open-source chemistry community. Other linear notations include the Wiswesser Line Notation, ROSDAL and SLN, in July 2006, the IUPAC introduced the InChI as a standard for formula representation. SMILES is generally considered to have the advantage of being slightly more human-readable than InChI, the term SMILES refers to a line notation for encoding molecular structures and specific instances should strictly be called SMILES strings. However, the term SMILES is also used to refer to both a single SMILES string and a number of SMILES strings, the exact meaning is usually apparent from the context. The terms canonical and isomeric can lead to confusion when applied to SMILES. The terms describe different attributes of SMILES strings and are not mutually exclusive, typically, a number of equally valid SMILES strings can be written for a molecule. For example, CCO, OCC and CC all specify the structure of ethanol, algorithms have been developed to generate the same SMILES string for a given molecule, of the many possible strings, these algorithms choose only one of them. This SMILES is unique for each structure, although dependent on the algorithm used to generate it. These algorithms first convert the SMILES to a representation of the molecular structure. A common application of canonical SMILES is indexing and ensuring uniqueness of molecules in a database, there is currently no systematic comparison across commercial software to test if such flaws exist in those packages. SMILES notation allows the specification of configuration at tetrahedral centers, and these are structural features that cannot be specified by connectivity alone and SMILES which encode this information are termed isomeric SMILES
7.
Chemical formula
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These are limited to a single typographic line of symbols, which may include subscripts and superscripts. A chemical formula is not a name, and it contains no words. Although a chemical formula may imply certain simple chemical structures, it is not the same as a full chemical structural formula. Chemical formulas can fully specify the structure of only the simplest of molecules and chemical substances, the simplest types of chemical formulas are called empirical formulas, which use letters and numbers indicating the numerical proportions of atoms of each type. Molecular formulas indicate the numbers of each type of atom in a molecule. For example, the formula for glucose is CH2O, while its molecular formula is C6H12O6. This is possible if the relevant bonding is easy to show in one dimension, an example is the condensed molecular/chemical formula for ethanol, which is CH3-CH2-OH or CH3CH2OH. For reasons of structural complexity, there is no condensed chemical formula that specifies glucose, chemical formulas may be used in chemical equations to describe chemical reactions and other chemical transformations, such as the dissolving of ionic compounds into solution. A chemical formula identifies each constituent element by its chemical symbol, in empirical formulas, these proportions begin with a key element and then assign numbers of atoms of the other elements in the compound, as ratios to the key element. For molecular compounds, these numbers can all be expressed as whole numbers. For example, the formula of ethanol may be written C2H6O because the molecules of ethanol all contain two carbon atoms, six hydrogen atoms, and one oxygen atom. Some types of compounds, however, cannot be written with entirely whole-number empirical formulas. An example is boron carbide, whose formula of CBn is a variable non-whole number ratio with n ranging from over 4 to more than 6.5. When the chemical compound of the consists of simple molecules. These types of formulas are known as molecular formulas and condensed formulas. A molecular formula enumerates the number of atoms to reflect those in the molecule, so that the formula for glucose is C6H12O6 rather than the glucose empirical formula. However, except for very simple substances, molecular chemical formulas lack needed structural information, for simple molecules, a condensed formula is a type of chemical formula that may fully imply a correct structural formula. For example, ethanol may be represented by the chemical formula CH3CH2OH
8.
Conjugate acid
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A conjugate acid, within the Brønsted–Lowry acid–base theory, is a species formed by the reception of a proton by a base—in other words, it is a base with a hydrogen ion added to it. On the other hand, a base is merely what is left after an acid has donated a proton in a chemical reaction. Hence, a base is a species formed by the removal of a proton from an acid. A proton is a particle with a unit positive electrical charge, it is represented by the symbol H+ because it constitutes the nucleus of a hydrogen atom, that is. A cation can be an acid, and an anion can be a conjugate base, depending on which substance is involved. In an acid-base reaction, an acid plus a base reacts to form a conjugate base plus a conjugate acid, refer to the following figure, We say that the water molecule is the conjugate acid of the hydroxide ion after the latter received the hydrogen proton donated by ammonium. On the other hand, ammonia is the base for the acid ammonium after ammonium has donated a hydrogen ion towards the production of the water molecule. The strength of an acid is directly proportional to its dissociation constant. If a conjugate acid is strong, its dissociation will have an equilibrium constant. The strength of a base can be seen as the tendency of the species to pull hydrogen protons towards itself. If a conjugate base is classified as strong, it will hold on to the hydrogen proton when in solution, if a chemical species is classified as a weak acid, its conjugate base will be strong in nature. This can be observed in ammonias reaction with water, the reaction proceeds until most of the ammonia has been transformed to ammonium. This shift to the right in the equilibrium of the reaction means that ammonium does not dissociate easily in water. On the other hand, if a species is classified as a strong acid, an example of this case would be the dissociation of Hydrochloric acid HCl in water. Since HCl is an acid, its conjugate base will be a weak conjugate base. Therefore, in system, most H+ will be in the form of a Hydronium ion H 3O+ instead of attached to a Cl anion. To summarize, the stronger the acid or base, the weaker the conjugate, the acid and conjugate base as well as the base and conjugate acid are known as conjugate pairs. When finding a conjugate acid or base, it is important to look at the reactants of the chemical equation, to identify the conjugate acid, look for the pair of compounds that are related
9.
Standard enthalpy of formation
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Its symbol is ΔHo f or ΔfHo. The superscript Plimsoll on this symbol indicates that the process has occurred under standard conditions at the specified temperature. One exception is phosphorus, for which the most stable form at 1 atm is black phosphorus and this is true for all enthalpies of formation. In physics the energy per particle is expressed in electronvolts. All elements in their states have a standard enthalpy of formation of zero. The formation reaction is a constant pressure and constant temperature process, since the pressure of the standard formation reaction is fixed at 1 atm, the standard formation enthalpy or reaction heat is a function of temperature. For tabulation purposes, standard formation enthalpies are all given at a temperature,298 K. The standard enthalpy of formation is equivalent to the sum of separate processes included in the Born–Haber cycle of synthesis reactions. This is because enthalpy is a state function, in the example above the standard enthalpy change of formation for sodium chloride is equal to the sum of the standard enthalpy change of formation for each of the steps involved in the process. This is especially useful for very long reactions with many intermediate steps, chemists may use standard enthalpies of formation for a reaction that is hypothetical. That it is shows that the reaction, if it were to proceed, would be exothermic. It is possible to heat of formations for simple unstrained organic compounds with the Heat of formation group additivity method. Standard enthalpies of formation are used in thermochemistry to find the enthalpy change of any reaction. This implies that the reaction is exothermic, the converse is also true, the standard enthalpy of reaction will be positive for an endothermic reaction. When a reaction is reversed, the magnitude of ΔH stays the same, when the balanced equation for a reaction is multiplied by an integer, the corresponding value of ΔH must be multiplied by that integer as well. Allotropes of an element other than the state generally have non-zero standard enthalpies of formation. Standard enthalpy of sublimation, or heat of sublimation, is defined as the required to sublime one mole of the substance under standard conditions. Standard enthalpy of solution is the change associated with the dissolution of a substance in a solvent at constant pressure under standard conditions
10.
Pharmacokinetics
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Pharmacokinetics, sometimes abbreviated as PK, is a branch of pharmacology dedicated to determining the fate of substances administered to a living organism. The substances of interest include any chemical xenobiotic such as, pharmaceutical drugs, pesticides, food additives, cosmetic ingredients, etc. It attempts to analyze chemical metabolism and to discover the fate of a chemical from the moment that it is administered up to the point at which it is eliminated from the body. Pharmacokinetics is the study of how an organism affects a drug, both together influence dosing, benefit, and adverse effects, as seen in PK/PD models. Pharmacokinetic properties of chemicals are affected by the route of administration and these may affect the absorption rate. Models have been developed to simplify conceptualization of the processes that take place in the interaction between an organism and a chemical substance. The various compartments that the model is divided into are commonly referred to as the ADME scheme, absorption - the process of a substance entering the blood circulation. Distribution - the dispersion or dissemination of substances throughout the fluids, metabolism – the recognition by the organism that a foreign substance is present and the irreversible transformation of parent compounds into daughter metabolites. Excretion - the removal of the substances from the body, in rare cases, some drugs irreversibly accumulate in body tissue. The two phases of metabolism and excretion can also be grouped together under the title elimination, the study of these distinct phases involves the use and manipulation of basic concepts in order to understand the process dynamics. All these concepts can be represented through mathematical formulas that have a graphical representation. The model outputs for a drug can be used in industry or in the application of pharmacokinetic concepts. Clinical pharmacokinetics provides many performance guidelines for effective and efficient use of drugs for human-health professionals, in practice, it is generally considered that steady state is reached when a time of 4 to 5 times the half-life for a drug after regular dosing is started. Noncompartmental methods estimate the exposure to a drug by estimating the area under the curve of a concentration-time graph, compartmental methods estimate the concentration-time graph using kinetic models. Noncompartmental methods are more versatile in that they do not assume any specific compartmental model. The final outcome of the transformations that a drug undergoes in an organism, a number of functional models have been developed in order to simplify the study of pharmacokinetics. These models are based on a consideration of an organism as a number of related compartments, the simplest idea is to think of an organism as only one homogenous compartment. However, these models do not always reflect the real situation within an organism
11.
Ion
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An ion is an atom or a molecule in which the total number of electrons is not equal to the total number of protons, giving the atom or molecule a net positive or negative electrical charge. Ions can be created, by chemical or physical means. In chemical terms, if an atom loses one or more electrons. If an atom gains electrons, it has a net charge and is known as an anion. Ions consisting of only a single atom are atomic or monatomic ions, because of their electric charges, cations and anions attract each other and readily form ionic compounds, such as salts. In the case of ionization of a medium, such as a gas, which are known as ion pairs are created by ion impact, and each pair consists of a free electron. The word ion comes from the Greek word ἰόν, ion, going and this term was introduced by English physicist and chemist Michael Faraday in 1834 for the then-unknown species that goes from one electrode to the other through an aqueous medium. Faraday also introduced the words anion for a charged ion. In Faradays nomenclature, cations were named because they were attracted to the cathode in a galvanic device, arrhenius explanation was that in forming a solution, the salt dissociates into Faradays ions. Arrhenius proposed that ions formed even in the absence of an electric current, ions in their gas-like state are highly reactive, and do not occur in large amounts on Earth, except in flames, lightning, electrical sparks, and other plasmas. These gas-like ions rapidly interact with ions of charge to give neutral molecules or ionic salts. These stabilized species are commonly found in the environment at low temperatures. A common example is the present in seawater, which are derived from the dissolved salts. Electrons, due to their mass and thus larger space-filling properties as matter waves, determine the size of atoms. Thus, anions are larger than the parent molecule or atom, as the excess electron repel each other, as such, in general, cations are smaller than the corresponding parent atom or molecule due to the smaller size of its electron cloud. One particular cation contains no electrons, and thus consists of a single proton - very much smaller than the parent hydrogen atom. Since the electric charge on a proton is equal in magnitude to the charge on an electron, an anion, from the Greek word ἄνω, meaning up, is an ion with more electrons than protons, giving it a net negative charge. A cation, from the Greek word κατά, meaning down, is an ion with fewer electrons than protons, there are additional names used for ions with multiple charges
12.
Chloride
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The chloride ion /ˈklɔəraɪd/ is the anion Cl−. It is formed when the element chlorine gains an electron or when a compound such as chloride is dissolved in water or other polar solvents. Chloride salts such as sodium chloride are often soluble in water. It is an essential electrolyte located in all body fluids responsible for maintaining acid/base balance, transmitting nerve impulses and regulating fluid in, less frequently, the word chloride may also form part of the common name of chemical compounds in which one or more chlorine atoms are covalently bonded. For example, methyl chloride, with the standard name chloromethane is a compound with a covalent C−Cl bond in which the chlorine is not an anion. A chloride ion is much larger than an atom,167 and 99 pm. The ion is colorless and diamagnetic, in aqueous solution, it is highly soluble in most cases, however, some chloride salts, such as silver chloride, lead chloride, and mercury chloride are slightly soluble in water. In aqueous solution, chloride is bound by the end of the water molecules. Some chloride-containing minerals include the chlorides of sodium, potassium, and magnesium, called serum chloride, the concentration of chloride in the blood is regulated by the kidneys. A chloride ion is a component of some proteins, e. g. it is present in the amylase enzyme. The chlor-alkali industry is a consumer of the worlds energy budget. This process converts sodium chloride into chlorine and sodium hydroxide, which are used to make many other materials and chemicals, in the petroleum industry, the chlorides are a closely monitored constituent of the mud system. An increase of the chlorides in the mud system may be an indication of drilling into a high-pressure saltwater formation and its increase can also indicate the poor quality of a target sand. Chloride is also a useful and reliable chemical indicator of river / groundwater fecal contamination, as chloride is a non-reactive solute, many water regulating companies around the world utilize chloride to check the contamination levels of the rivers and potable water sources. Chloride salts such as sodium chloride are used to preserve food, chloride is an essential electrolyte, trafficking in and out of cells through chloride channels and playing a key role in maintaining cell homeostasis and transmitting action potentials in neurons. Characteristic concentrations of chloride in model organisms are, in both E. coli and budding yeast are 10-200mM, in mammalian cell 5-100mM and in blood plasma 100mM, chloride can be oxidized but not reduced. The first oxidation, as employed in the process, is conversion to chlorine gas. Chlorine can be oxidized to other oxides and oxyanions including hypochlorite, chlorine dioxide, chlorate
13.
Ligand
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In coordination chemistry, a ligand is an ion or molecule that binds to a central metal atom to form a coordination complex. The bonding with the metal generally involves formal donation of one or more of the electron pairs. The nature of bonding can range from covalent to ionic. Furthermore, the bond order can range from one to three. Ligands are viewed as Lewis bases, although rare cases are known to involve Lewis acidic ligand, metals and metalloids are bound to ligands in virtually all circumstances, although gaseous naked metal ions can be generated in high vacuum. Ligands in a complex dictate the reactivity of the atom, including ligand substitution rates, the reactivity of the ligands themselves. Ligand selection is a consideration in many practical areas, including bioinorganic and medicinal chemistry, homogeneous catalysis. Ligands are classified in many ways, including, charge, size, the identity of the atom. The size of a ligand is indicated by its cone angle, the composition of coordination complexes have been known since the early 1800s, such as Prussian blue and copper vitriol. The key breakthrough occurred when Alfred Werner reconciled formulas and isomers and he showed, among other things, that the formulas of many cobalt and chromium compounds can be understood if the metal has six ligands in an octahedral geometry. The first to use the term ligand were Alfred Stock and Carl Somiesky, the theory allows one to understand the difference between coordinated and ionic chloride in the cobalt ammine chlorides and to explain many of the previously inexplicable isomers. He resolved the first coordination complex called hexol into optical isomers, in general, ligands are viewed as electron donors and the metals as electron acceptors. This is because the ligand and central metal are bonded to one another, bonding is often described using the formalisms of molecular orbital theory. The HOMO can be mainly of ligands or metal character, ligands and metal ions can be ordered in many ways, one ranking system focuses on ligand hardness. Metal ions preferentially bind certain ligands, in general, soft metal ions prefer weak field ligands, whereas hard metal ions prefer strong field ligands. According to the orbital theory, the HOMO of the ligand should have an energy that overlaps with the LUMO of the metal preferential. Metal ions bound to strong-field ligands follow the Aufbau principle, whereas complexes bound to weak-field ligands follow Hunds rule. Binding of the metal with the results in a set of molecular orbitals, where the metal can be identified with a new HOMO and LUMO
14.
Bromine
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Bromine is a chemical element with symbol Br and atomic number 35. It is the third-lightest halogen, and is a fuming red-brown liquid at room temperature that readily to form a similarly coloured gas. Its properties are intermediate between those of chlorine and iodine. Isolated independently by two chemists, Carl Jacob Löwig and Antoine Jérôme Balard, its name was derived from the Ancient Greek βρῶμος stench, referencing its sharp and disagreeable smell. Elemental bromine is very reactive and thus does not occur free in nature, while it is rather rare in the Earths crust, the high solubility of the bromide ion has caused its accumulation in the oceans. Commercially the element is easily extracted from brine pools, mostly in the United States, Israel, the mass of bromine in the oceans is about one three-hundredth of that of chlorine. At high temperatures, organobromine compounds readily convert to free bromine atoms and this effect makes organobromine compounds useful as fire retardants and more than half the bromine produced worldwide each year is put to this purpose. Unfortunately, the same property causes sunlight to convert volatile organobromine compounds to free bromine atoms in the atmosphere, as a result, many organobromide compounds—such as the pesticide methyl bromide—are no longer used. Bromine compounds are used in well drilling fluids, in photographic film. Bromine has sometimes been considered to be essential in humans, but with the support of only limited circumstantial evidence. As a pharmaceutical, the bromide ion has inhibitory effects on the central nervous system. They retain niche uses as antiepileptics, bromine was discovered independently by two chemists, Carl Jacob Löwig and Antoine Balard, in 1825 and 1826, respectively. Löwig isolated bromine from a water spring from his hometown Bad Kreuznach in 1825. Löwig used a solution of the mineral salt saturated with chlorine, after evaporation of the ether a brown liquid remained. With this liquid as a sample for his work he applied for a position in the laboratory of Leopold Gmelin in Heidelberg, the publication of the results was delayed and Balard published his results first. Balard found bromine chemicals in the ash of seaweed from the marshes of Montpellier. The seaweed was used to produce iodine, but also contained bromine, Balard distilled the bromine from a solution of seaweed ash saturated with chlorine. In his publication, Balard states that he changed the name from muride to brôme on the proposal of M. Anglada, brôme derives from the Greek βρωμος
15.
Electric charge
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Electric charge is the physical property of matter that causes it to experience a force when placed in an electromagnetic field. There are two types of charges, positive and negative. Like charges repel and unlike attract, an absence of net charge is referred to as neutral. An object is charged if it has an excess of electrons. The SI derived unit of charge is the coulomb. In electrical engineering, it is common to use the ampere-hour. The symbol Q often denotes charge, early knowledge of how charged substances interact is now called classical electrodynamics, and is still accurate for problems that dont require consideration of quantum effects. The electric charge is a conserved property of some subatomic particles. Electrically charged matter is influenced by, and produces, electromagnetic fields, the interaction between a moving charge and an electromagnetic field is the source of the electromagnetic force, which is one of the four fundamental forces. 602×10−19 coulombs. The proton has a charge of +e, and the electron has a charge of −e, the study of charged particles, and how their interactions are mediated by photons, is called quantum electrodynamics. Charge is the property of forms of matter that exhibit electrostatic attraction or repulsion in the presence of other matter. Electric charge is a property of many subatomic particles. The charges of free-standing particles are integer multiples of the charge e. Michael Faraday, in his electrolysis experiments, was the first to note the discrete nature of electric charge, robert Millikans oil drop experiment demonstrated this fact directly, and measured the elementary charge. By convention, the charge of an electron is −1, while that of a proton is +1, charged particles whose charges have the same sign repel one another, and particles whose charges have different signs attract. The charge of an antiparticle equals that of the corresponding particle, quarks have fractional charges of either −1/3 or +2/3, but free-standing quarks have never been observed. The electric charge of an object is the sum of the electric charges of the particles that make it up. An ion is an atom that has lost one or more electrons, giving it a net charge, or that has gained one or more electrons
16.
Caesium bromide
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Caesium bromide, is an ionic compound of caesium and bromine. It has simple cubic p-type cubic crystallic structure, comparable to that of caesium chloride type with space group Pm3m, the distance between Cs+ and Br− ions is 0.37198 nm. Due to its high cost, it is not used for preparation, caesium bromide is sometimes used in optics as a beamsplitter component in wide-band spectrophotometers
17.
Ionic compound
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In chemistry, an ionic compound is a chemical compound composed of ions held together by electrostatic forces termed ionic bonding. The compound is overall, but consists of positively charged ions called cations. These can be simple ions such as the sodium and chloride in sodium chloride, or polyatomic species such as the ammonium, Ionic compounds containing hydrogen ions are classified as acids, and those containing basic ions hydroxide or oxide are classified as bases. Ionic compounds without these ions are known as salts and can be formed by acid–base reactions. Ionic compounds typically have high melting and boiling points, and are hard, as solids they are almost always electrically insulating, but when melted or dissolved they become highly conductive, because the ions are mobilized. The word ion is the Greek ἰόν, ion, going and this term was introduced by English physicist and chemist Michael Faraday in 1834 for the then-unknown species that goes from one electrode to the other through an aqueous medium. In 1913 the crystal structure of sodium chloride was determined by William Henry Bragg, many other inorganic compounds were also found to have similar structural features. Principal contributors to the development of a treatment of ionic crystal structures were Max Born, Fritz Haber, Alfred Landé, Erwin Madelung, Paul Peter Ewald. Born predicted crystal energies based on the assumption of ionic constituents, Ionic compounds can be produced from their constituent ions by evaporation, precipitation, or freezing. Reactive metals such as the alkali metals can react directly with the highly electronegative halogen gases to form an ionic product and they can also be synthesized as the product of a high temperature reaction between solids. If the ionic compound is soluble in a solvent, it can be obtained as a compound by evaporating the solvent from this electrolyte solution. This process occurs widely in nature, and is the means of formation of the evaporite minerals, insoluble ionic compounds can be precipitated by mixing two solutions, one with the cation and one with the anion in it. Because all solutions are neutral, the two solutions mixed must also contain counterions of the opposite charges. To ensure that these do not contaminate the precipitated ionic compound, if the two solutions have hydrogen ions and hydroxide ions as the counterions, they will react with one another in what is called an acid–base reaction or a neutralization reaction to form water. Alternately the counterions can be chosen to ensure that even when combined into a solution they will remain soluble as spectator ions. Molten salts will solidify on cooling to below their freezing point and this is sometimes used for the solid-state synthesis of complex ionic compounds from solid reactants, which are first melted together. In other cases the solid reactants do not need to be melted, other synthetic routes use a solid precursor with the correct stoichiometric ratio of non-volatile ions, which is heated to drive off other species. There is also an additional attractive force from van der Waals interactions which contributes only around 1–2% of the cohesive energy for small ions
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Oxidation state
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The oxidation state, often called the oxidation number, is an indicator of the degree of oxidation of an atom in a chemical compound. This is never exactly true for real bonds, the term oxidation was first used by Lavoisier to signify reaction of a substance with oxygen. Much later, it was realized that the substance, upon being oxidized, loses electrons, oxidation states are typically represented by integers. In some cases, the oxidation state of an element is a fraction. It is predicted that even a +10 oxidation state may be achieveable by platinum in the platinum tetroxide dication, the increase in oxidation state of an atom, through a chemical reaction, is known as an oxidation, a decrease in oxidation state is known as a reduction. Such reactions involve the transfer of electrons, a net gain in electrons being a reduction. For pure elements, the state is zero. There are various methods for determining oxidation states, in inorganic nomenclature, the oxidation state is determined and expressed as an oxidation number, and is represented by a Roman numeral placed after the element name. In coordination chemistry, oxidation number is defined differently from oxidation state, a “Comprehensive definition of oxidation state ” has been published with free access. This article is a distillation of an IUPAC technical report Toward a comprehensive definition of oxidation state. Exceptions to this are that hydrogen has a state of −1 in hydrides of active metals, e. g. LiH. There are two different methods for determining the state of elements in chemical compounds. First a method based on the rules in the IUPAC definition, second, a method based on the relative electronegativity of the elements in the compound, where the more electronegative element is assumed to take the negative charge. Any pure element—even if it forms diatomic molecules like chlorine —has an oxidation state of zero, examples of this are Cu or O2. For monatomic ions, the state is the same as the charge of the ion. For example, the anion has an oxidation state of −2. The sum of oxidation states for all atoms in a molecule or polyatomic ion is equal to the charge of the molecule or ion, thus, the oxidation state of one element can be calculated from the oxidation states of the other elements. An application of this rule is that the sum of the states of all atoms in a neutral molecule must be zero
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Covalent bond
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A covalent bond, also called a molecular bond, is a chemical bond that involves the sharing of electron pairs between atoms. These electron pairs are known as shared pairs or bonding pairs, for many molecules, the sharing of electrons allows each atom to attain the equivalent of a full outer shell, corresponding to a stable electronic configuration. Covalent bonding includes many kinds of interactions, including σ-bonding, π-bonding, metal-to-metal bonding, agostic interactions, bent bonds, the term covalent bond dates from 1939. In the molecule H2, the atoms share the two electrons via covalent bonding. Covalency is greatest between atoms of similar electronegativities, thus, covalent bonding does not necessarily require that the two atoms be of the same elements, only that they be of comparable electronegativity. Covalent bonding that entails sharing of electrons more than two atoms is said to be delocalized. The term covalence in regard to bonding was first used in 1919 by Irving Langmuir in a Journal of the American Chemical Society article entitled The Arrangement of Electrons in Atoms and Molecules. Langmuir wrote that we shall denote by the term covalence the number of pairs of electrons that an atom shares with its neighbors. The idea of covalent bonding can be traced several years before 1919 to Gilbert N. Lewis and he introduced the Lewis notation or electron dot notation or Lewis dot structure, in which valence electrons are represented as dots around the atomic symbols. Pairs of electrons located between atoms represent covalent bonds, multiple pairs represent multiple bonds, such as double bonds and triple bonds. An alternative form of representation, not shown here, has bond-forming electron pairs represented as solid lines, Lewis proposed that an atom forms enough covalent bonds to form a full outer electron shell. In the diagram of methane shown here, the atom has a valence of four and is, therefore, surrounded by eight electrons, four from the carbon itself. Each hydrogen has a valence of one and is surrounded by two electrons – its own one electron plus one from the carbon, walter Heitler and Fritz London are credited with the first successful quantum mechanical explanation of a chemical bond in 1927. Their work was based on the valence bond model, which assumes that a bond is formed when there is good overlap between the atomic orbitals of participating atoms. Atomic orbitals have specific directional properties leading to different types of covalent bonds, sigma bonds are the strongest covalent bonds and are due to head-on overlapping of orbitals on two different atoms. A single bond is usually a σ bond, pi bonds are weaker and are due to lateral overlap between p orbitals. A double bond between two given atoms consists of one σ and one π bond, and a bond is one σ. Covalent bonds are also affected by the electronegativity of the atoms which determines the chemical polarity of the bond
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Sulfur dibromide
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Sulfur dibromide is the chemical compound with the formula Br2S. Sulfur dibromide readily decomposes into S2Br2 and elemental bromine, in analogy to sulfur dichloride, it hydrolyzes in water to give hydrogen bromide, sulfur dioxide and elemental sulfur. SBr2 can be prepared by reacting SCl2 with HBr, but due to its rapid decomposition it cannot be isolated at standard conditions, instead the more stable S2Br2 is obtained
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Seawater
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Seawater, or salt water, is water from a sea or ocean. On average, seawater in the oceans has a salinity of about 3. 5% This means that every kilogram of seawater has approximately 35 grams of dissolved salts. Average density at the surface is 1.025 kg/l, seawater is denser than both fresh water and pure water because the dissolved salts increase the mass by a larger proportion than the volume. The freezing point of seawater decreases as salt concentration increases, at typical salinity, it freezes at about −2 °C. The coldest seawater ever recorded was in 2010, in a stream under an Antarctic glacier, seawater pH is typically limited to a range between 7.5 and 8.4. However, there is no universally accepted reference pH-scale for seawater, although the vast majority of seawater has a salinity of between 31 g/kg and 38 g/kg, seawater is not uniformly saline throughout the world. Where mixing occurs with fresh water runoff from river mouths, near melting glaciers or vast amounts precipitation, the most saline open sea is the Red Sea, where high rates of evaporation, low precipitation and low river run-off, and confined circulation result in unusually salty water. The salinity in isolated bodies of water can be considerably greater still, historically, several salinity scales were used to approximate the absolute salinity of seawater. A popular scale was the Practical Salinity Scale where salinity was measured in practical salinity units, the current standard for salinity is the Reference Salinity scale with the salinity expressed in units of g/kg. The density of surface seawater ranges from about 1020 to 1029 kg/m3, depending on the temperature, at a temperature of 25 °C, salinity of 35 g/kg and 1 atm pressure, the density of seawater is 1023.6 kg/m3. Deep in the ocean, under pressure, seawater can reach a density of 1050 kg/m3 or higher. The density of seawater also changes with salinity, brines generated by seawater desalination plants can have salinities up to 120 g/kg. The density of typical seawater brine of 120 g/kg salinity at 25 °C, seawater pH is limited to the range 7.5 to 8.4. The speed of sound in seawater is about 1,500 m/s, and varies with temperature, salinity. The thermal conductivity of seawater is 0.6 W/mK at 25 °C, the thermal conductivity decreases with increasing salinity and increases with increasing temperature. Seawater contains more dissolved ions than all types of freshwater, however, the ratios of solutes differ dramatically. Bicarbonate ions also constitute 48% of river water solutes but only 0. 14% of all seawater ions, differences like these are due to the varying residence times of seawater solutes, sodium and chlorine have very long residence times, while calcium tends to precipitate much more quickly. The most abundant dissolved ions in seawater are sodium, chloride, magnesium, sulfate and its osmolarity is about 1000 mOsm/l
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Salinity
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Salinity is the saltiness or amount of salt dissolved in a body of water. This is usually measured in g salt k g sea water, a contour line of constant salinity is called an isohaline – or sometimes isohale. Salinity in rivers, lakes, and the ocean is conceptually simple, conceptually the salinity is the quantity of dissolved salt content of the water. Salts are compounds like sodium chloride, magnesium sulfate, potassium nitrate, the concentration of dissolved chloride ions is sometimes referred to as chlorinity. Operationally, dissolved matter is defined as that which can pass through a fine filter. Salinity can be expressed in the form of a mass fraction, Seawater typically has a mass salinity of around 35 g/kg, although lower values are typical near coasts where rivers enter the ocean. Rivers and lakes can have a range of salinities, from less than 0.01 g/kg to a few g/kg. The Dead Sea has a salinity of more than 200 g/kg, whatever pore size is used in the definition, the resulting salinity value of a given sample of natural water will not vary by more than a few percent. A bottled seawater product known as IAPSO Standard Seawater is used by oceanographers to standardize their measurements with enough precision to meet this requirement, measurement and definition difficulties arise because natural waters contain a complex mixture of many different elements from different sources in different molecular forms. The chemical properties of some of these depend on temperature and pressure. Many of these forms are difficult to measure with high accuracy, different practical definitions of salinity result from different attempts to account for these problems, to different levels of precision, while still remaining reasonably easy to use. For many purposes this sum can be limited to a set of eight major ions in natural waters, the major ions dominate the inorganic composition of most natural waters. Exceptions include some pit lakes and waters from some hydrothermal springs, the concentrations of dissolved gases like oxygen and nitrogen are not usually included in descriptions of salinity. However, carbon dioxide gas, which when dissolved is partially converted into carbonates and bicarbonates, is often included. Silicon in the form of acid, which usually appears as a neutral molecule in the pH range of most natural waters. The term salinity is, for oceanographers, usually associated with one of a set of measurement techniques. As the dominant techniques evolve, so do different descriptions of salinity, the distinctions between these different descriptions are important to physical oceanographers but are obscure and confusing to nonspecialists. Salinities were largely measured using titration-based techniques before the 1980s, titration with silver nitrate could be used to determine the concentration of halide ions to give a chlorinity
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Salt
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Salt is present in vast quantities in seawater, where it is the main mineral constituent. The open ocean has about 35 grams of solids per litre, Salt is essential for life in general, and saltiness is one of the basic human tastes. The tissues of animals contain larger quantities of salt than do plant tissues, Salt is one of the oldest and most ubiquitous food seasonings, and salting is an important method of food preservation. Salt was also prized by the ancient Hebrews, the Greeks, the Romans, the Byzantines, the Hittites, Egyptians, and the Indians. Salt became an important article of trade and was transported by boat across the Mediterranean Sea, along specially built salt roads, the scarcity and universal need for salt has led nations to go to war over it and use it to raise tax revenues. Salt is used in ceremonies and has other cultural significance. Salt is processed from salt mines, or by the evaporation of seawater or mineral-rich spring water in shallow pools. Its major industrial products are caustic soda and chlorine, and is used in industrial processes including the manufacture of polyvinyl chloride, plastics, paper pulp. Of the annual production of around two hundred million tonnes of salt, only about 6% is used for human consumption. Other uses include water conditioning processes, de-icing highways, and agricultural use, edible salt is sold in forms such as sea salt and table salt which usually contains an anti-caking agent and may be iodised to prevent iodine deficiency. As well as its use in cooking and at the table, sodium is an essential nutrient for human health via its role as an electrolyte and osmotic solute. Excessive salt consumption can increase the risk of diseases, such as hypertension, in children. Such health effects of salt have long been studied, accordingly, numerous world health associations and experts in developed countries recommend reducing consumption of popular salty foods. The World Health Organization recommends that adults should consume less than 2,000 mg of sodium, humans have always tended to build communities either around sources of salt, or where they can trade for it. All through history the availability of salt has been pivotal to civilization, the word salary comes from the Latin word for salt because the Roman Legions were sometimes paid in salt. The Natron Valley was a key region that supported the Egyptian Empire to its north, because it supplied it with a kind of salt that came to be called by its name, natron. Even before this, what is now thought to have been the first city in Europe is Solnitsata, in Bulgaria, even the name Solnisata means salt works. A very ancient salt-works operation has been discovered at the Poiana Slatinei archaeological site next to a spring in Lunca, Neamț County
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Silver nitrate
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Silver nitrate is an inorganic compound with chemical formula AgNO3. This compound is a precursor to many other silver compounds. It is far less sensitive to light than the halides and it was once called lunar caustic because silver was called luna by the ancient alchemists, who believed that silver was associated with the moon. In solid silver nitrate, the ions are three-coordinated in a trigonal planar arrangement. Albertus Magnus, in the 13th century, documented the ability of nitric acid to separate gold, Magnus noted that the resulting solution of silver nitrate could blacken skin. Silver nitrate can be prepared by reacting silver, such as a silver bullion or silver foil, with acid, resulting in silver nitrate, water. Reaction byproducts depend upon the concentration of acid used. 3 Ag +4 HNO3 →3 AgNO3 +2 H2O + NO Ag +2 HNO3 → AgNO3 + H2O + NO2 This is performed under a fume hood because of nitrogen oxide evolved during the reaction. A typical reaction with silver nitrate is to suspend a rod of copper in a solution of silver nitrate, silver nitrate is the least expensive salt of silver, it offers several other advantages as well. It is non-hygroscopic, in contrast to silver fluoroborate and silver perchlorate and it is relatively stable to light. Finally, it dissolves in solvents, including water. The nitrate can be replaced by other ligands, rendering AgNO3 versatile. Treatment with solutions of halide ions gives a precipitate of AgX, similarly, silver nitrate is used to prepare some silver-based explosives, such as the fulminate, azide, or acetylide, through a precipitation reaction. This reaction is used in inorganic chemistry to abstract halides, Ag+ + X− → AgX where X− = Cl−, Br−. Other silver salts with non-coordinating anions, namely silver tetrafluoroborate and silver hexafluorophosphate are used for demanding applications. Similarly, this reaction is used in chemistry to confirm the presence of chloride, bromide. Samples are typically acidified with nitric acid to remove interfering ions, e. g. carbonate ions. This step avoids confusion of silver sulfide or silver carbonate precipitates with that of silver halides, the color of precipitate varies with the halide, white, pale yellow/cream, yellow
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Silver bromide
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Silver bromide, a soft, pale-yellow, water-insoluble salt well known for its unusual sensitivity to light. This property has allowed silver halides to become the basis of modern photographic materials, AgBr is widely used in photographic films and is believed by some to have been used for making the Shroud of Turin. The salt can be found naturally as the mineral bromargyrite, modern preparation of a simple, light-sensitive surface involves forming an emulsion of silver halide crystals in a gelatine, which is then coated onto a film or other support. The crystals are formed by precipitation in an environment to produce small. The coordination geometry for AgBr in the NaCl structure is unexpected for Ag which typically forms linear, unlike the other silver halides, iodargyrite contains a hexagonal zincite lattice structure. The silver halides have a range of solubilities. The solubility of AgF is about 6 ×107 times that of AgI and these differences are attributed to the relative solvation enthalpies of the halide ions, the enthalpy of solvation of fluoride is anomalously large. Although photographic processes have been in development since the mid-1800s, there were no suitable theoretical explanations until 1938 with the publication of a paper by R. W. Gurney and N. F. This paper triggered a large amount of research in fields of chemistry and physics. Further research into this mechanism revealed that the properties of silver halides were a result of deviations from an ideal crystal structure. What is unique about AgBr Frenkel pairs is that the interstitial Agi+ are exceptionally mobile, the formation energy of the Frenkel pair is low at 1.16 eV, and the migration activation energy is unusually low at 0.05 eV. These low energies result in large concentrations, which can reach near 1% near the melting point. The low activation energy in silver bromide can be attributed the silver ions’ high quadrupolar polarizability and this property, a result of the d9 electronic configuration of the silver ion, facilitates migration in both the silver ion and in silver-ion vacancies, thus giving the unusually low migration energy. Studies have demonstrated that the concentrations are strongly affected by crystal size. Most defects, such as interstitial silver ion concentration and surface kinks, are proportional to crystal size. This phenomenon is attributed to changes in the surface chemistry equilibrium, impurity concentrations can be controlled by crystal growth or direct addition of impurities to the crystal solutions. After this point, only silver-ion vacancy defects, which increase by several orders of magnitude, are prominent. When a photoelectron is mobilized, a photohole h• is also formed, the lifetime of a photohole, however, does not correlate with that of a photoelectron
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Potassium bromide
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Potassium bromide is a salt, widely used as an anticonvulsant and a sedative in the late 19th and early 20th centuries, with over-the-counter use extending to 1975 in the US. Its action is due to the bromide ion, potassium bromide is used as a veterinary drug, as an antiepileptic medication for dogs. Under standard conditions, potassium bromide is a crystalline powder. It is freely soluble in water, it is not soluble in acetonitrile, in a dilute aqueous solution, potassium bromide tastes sweet, at higher concentrations it tastes bitter, and tastes salty when the concentration is even higher. These effects are due to the properties of the potassium ion—sodium bromide tastes salty at any concentration. In high concentration, potassium bromide strongly irritates the mucous membrane, causing nausea. Potassium bromide, an ionic salt, is fully dissociated. It serves as a source of bromide ions, bromide can be regarded as the first effective medication for epilepsy. At the time, it was thought that epilepsy was caused by masturbation. Locock noted that bromide calmed sexual excitement and thought this was responsible for his success in treating seizures, there was not a better epilepsy drug until phenobarbital in 1912. Bromides exceedingly long life in the body made it difficult to dose without side effects. Medical use of bromides in the US was discontinued at this time, as many better, use of bromide in cats is limited because it carries a substantial risk of causing lung inflammation in them. Potassium bromide is not approved by the US Food and Drug Administration for use in humans to control seizures, in Germany, it is still approved as an antiepileptic drug for humans, particularly children and adolescents. These indications include severe forms of generalized tonic-clonic seizures, early-childhood-related Grand-Mal-seizures, adults who have reacted positively to the drug during childhood/adolescence may continue treatment. Potassium bromide tablets are sold under the brand name Dibro-Be mono, the drug has almost complete bioavailability, but the bromide ion has a relatively long half life of 12 days in the blood, making bromide salts difficult to adjust and dose. The therapeutic index for bromide is small, as with other antiepileptics, sometimes even therapeutic doses may give rise to intoxication. Often indistinguishable from expected side-effects, these include, Bromism These are central nervous system reactions, rarely, tongue disorder, aphten, bad breath, and obstipation occur. Potassium bromide is transparent from the ultraviolet to long-wave infrared wavelengths and has no significant optical absorption lines in its high transmission region
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Bromo-Seltzer
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Bromo-Seltzer, was a brand of antacid to relieve pain occurring together with heartburn, upset stomach, or acid indigestion. The product took its name from a component of the original formula, each dose contained 3.2 mEq/teaspoon of this active ingredient. Bromides are a class of tranquilizers that were withdrawn from the U. S. market in 1975 due to their toxicity and their sedative effect probably accounted for Bromo-Seltzers popularity as a remedy for hangovers. Early formulas also used, as the ingredient, acetanilide. Bromo-Seltzers main offices and main factory were located in downtown Baltimore, Maryland, at the corner of West Lombard, the factorys most notable feature was the clock tower, built in 1911, which featured BROMOSELTZER in place of the numbers on all four clock faces. The tower was patterned on the Palazzo Vecchio in Florence, Italy, the tower originally had a 51 ft Bromo-Seltzer bottle, glowing blue and rotating. The sign weighed 20 tons, included 314 incandescent light bulbs, the sign was removed in 1936 because of structural concerns. Bromo-Seltzer at drugs. com Emerson Bromo-Seltzer Tower website
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Antiepileptic
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Anticonvulsants are a diverse group of pharmacological agents used in the treatment of epileptic seizures. Anticonvulsants suppress the rapid and excessive firing of neurons during seizures, anticonvulsants also prevent the spread of the seizure within the brain. Some investigators have observed that anticonvulsants themselves may cause reduced IQ in children, conventional antiepileptic drugs may block sodium channels or enhance γ-aminobutyric acid function. Several antiepileptic drugs have multiple or uncertain mechanisms of action, next to the voltage-gated sodium channels and components of the GABA system, their targets include GABAA receptors, the GAT-1 GABA transporter, and GABA transaminase. Additional targets include voltage-gated calcium channels, SV2A, and α2δ, by blocking sodium or calcium channels, antiepileptic drugs reduce the release of excitatory glutamate, whose release is considered to be elevated in epilepsy, but also that of GABA. This is probably an effect or even the actual mechanism of action for some antiepileptic drugs, since GABA can itself, directly or indirectly. Another potential target of antiepileptic drugs is the peroxisome proliferator-activated receptor alpha, the drug class was the 5th-best-selling in the US in 2007. Some anticonvulsants have shown antiepileptogenic effects in animal models of epilepsy and that is, they either prevent the development of epilepsy or can halt or reverse the progression of epilepsy. However, no drug has shown in human trials to prevent epileptogenesis. The usual method of achieving approval for a drug is to show it is effective when compared against placebo, in monotherapy it is considered unethical by most to conduct a trial with placebo on a new drug of uncertain efficacy. This is because untreated epilepsy leaves the patient at significant risk of death, therefore, almost all new epilepsy drugs are initially approved only as adjunctive therapies. Patients whose epilepsy is currently uncontrolled by their medication are selected to see if supplementing the medication with the new leads to an improvement in seizure control. Any reduction in the frequency of seizures is compared against a placebo, the lack of superiority over existing treatment, combined with lacking placebo-controlled trials, means that few modern drugs have earned FDA approval as initial monotherapy. In contrast, Europe only requires equivalence to existing treatments, and has approved many more, despite their lack of FDA approval, the American Academy of Neurology and the American Epilepsy Society still recommend a number of these new drugs as initial monotherapy. In the following list, the dates in parentheses are the earliest approved use of the drug and it is still used to treat status epilepticus, particularly where there are no resuscitation facilities. Indicated for the treatment of Dravet syndrome, barbiturates are drugs that act as central nervous system depressants, and by virtue of this they produce a wide spectrum of effects, from mild sedation to anesthesia. The following are classified as anticonvulsants, Phenobarbital, see also the related drug primidone. Known as mephobarbital in the US, no longer marketed in the UK Barbexaclone
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Cerebrospinal fluid
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Cerebrospinal fluid is a clear, colorless body fluid found in the brain and spine. It is produced in the choroid plexuses of the ventricles of the brain and it acts as a cushion or buffer for the brains cortex, providing basic mechanical and immunological protection to the brain inside the skull. The CSF also serves a function in cerebral autoregulation of cerebral blood flow. The CSF occupies the space and the ventricular system around and inside the brain. It constitutes the content of the ventricles, cisterns, and sulci of the brain, there is also a connection from the subarachnoid space to the bony labyrinth of the inner ear via the perilymphatic duct where the perilymph is continuous with the cerebrospinal fluid. The brain produces roughly 500 mL of cerebrospinal fluid per day and this transcellular fluid is constantly reabsorbed, so that only 100–160 mL is present at any one time. Ependymal cells of the choroid plexus produce more than two thirds of CSF, the choroid plexus is a venous plexus contained within the four ventricles of the brain, hollow structures inside the brain filled with CSF. The remainder of the CSF is produced by the surfaces of the ventricles, ependymal cells secrete sodium into the lateral ventricles. This creates osmotic pressure and draws water into the CSF space, chloride, with a negative charge, moves with the positively charged sodium and a neutral charge is maintained. As a result, CSF contains a concentration of sodium and chloride than blood plasma. CSF circulates within the system of the brain. The ventricles are a series of cavities filled with CSF, inside the brain, the majority of CSF is produced from within the two lateral ventricles. From here, the CSF passes through the interventricular foramina to the third ventricle, the fourth ventricle is an outpouching on the posterior part of the brainstem. From the fourth ventricle, the passes through three openings to enter the subarachnoid space – these are the median aperture, and the lateral apertures. The subarachnoid space covers the brain and spinal cord, there is connection from the subarachnoid space to the bony labyrinth of the inner ear making the cerebrospinal fluid continuous with the perilymph. The team concluded that the term circulation should be avoided and an appropriate term movement of CSF would be advisable. The CSF moves in a pulsatile manner throughout the CSF system with a zero net flow. It had been thought that CSF returns to the system by entering the dural venous sinuses via the arachnoid granulations
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