среда, 30 ноября 2016 г.

Halogen Compounds of Chlorine, Bromine, Iodine and Astatine

A majority of the halides of the pretransition metals in groups 1 and 2 of the periodic table, as well as those of the lanthanides and actinides at the valence states of +2 and +3, are usually ionic compounds - http://www.science-chemistry.com/halogen-compounds-of-chlorine-bromine-iodine-and-astatine

Properties of Chlorine, Bromine, Iodine and Astatine

Chlorine was the first halogen to be isolated and sodium chloride, common salt, has been known from early times as being essential to the human diet; as such it has been mentioned in the Bible - http://www.science-chemistry.com/molecular-properties-of-chlorine-bromine-iodine-and-astatine

Chlorine, Bromine, Iodine and Astatine: Atomic Structure

The elements of group 17, fluorine, chlorine, bromine, iodine, and astatine, are collectively called the halogens and these are the most representative nonmetals in the periodic table - http://www.science-chemistry.com/chlorine-bromine-iodine-and-astatine-atomic-structure

Carbon-Based Molecular Ladders

Structures resembling a ladder are encountered in the chemistry (e.g. Zintl phases) of many elements, but among group IV elements are found only in the case of carbon. The molecular ladders of carbon chemistry are [n]-ladderanes - http://www.science-chemistry.com/carbon-based-molecular-ladders

Cyanides and Related Compounds

Cyanogen, N≡C–C≡N, is a flammable and toxic gas, mp −28 ◦C, bp −21 ◦C, which is kinetically stable but endothermic (297 kJ mol−1). It has a linear structure with a sufficiently weak C–C bond to allow dissociation into •CN radicals - http://www.science-chemistry.com/cyanides-and-related-compounds

вторник, 29 ноября 2016 г.

Carbon–Sulfur Derivatives

The raw material for much of carbon–sulfur chemistry is carbon disulfide, CS2, a very flammable and reactive liquid, mp −109 ◦C, bp +46 ◦C, which can be synthesized from elemental carbon or methane and sulfur at high temperatures - http://www.science-chemistry.com/carbon-sulfur-derivatives

Carbon Oxyacids and Oxyanions

Carbon dioxide is the anhydride of carbonic acid but hydrolyzes only slowly at pH 7 to H2CO3. In aqueous solution, CO2 is physically dissolved and only loosely solvated so that only - http://www.science-chemistry.com/carbon-oxyacids-and-oxyanions

Carbon Halides

Carbon tetrafluoride, CF4, mp−185 ◦C, bp−128 ◦C, which is the end product of the fluorination of carbon compounds, is a very stable gas. It can also be made by the fluorination of silicon carbide - http://www.science-chemistry.com/carbon-halides

Carbon Isotopes and Elemental Carbon

Table 1 summarizes some of the important properties of the carbon isotopes. Note that only the rare (≈1%), naturally occurring, stable carbon isotope, namely, 13C, has a nuclear spin and is observable by NMR - http://www.science-chemistry.com/carbon-isotopes-and-elemental-carbon

понедельник, 28 ноября 2016 г.

Boron-Halogen Compounds

Boron-halogen compounds, or boron halides, can be divided into three major categories that are defined by the ratios of halogens to borons. The boron trihalides (halogen: boron ratio = 3) were discovered and characterized first and represent the most common and thoroughly investigated boron halide category - http://www.science-chemistry.com/boron-halogen-compounds

Boron–Phosphorus Compounds

The chemistry of boron–phosphorus compounds has been reviewed. Numerous boron–phosphorus derivatives have been reported, but relatively few boron–arsenic or boron–antimony compounds have been described - http://www.science-chemistry.com/boron-phosphorus-compounds

Boron–Sulfur Compounds

The detailed chemistry of boron–sulfur and related boron–selenium compounds has emerged only slowly because of a lack of suitable experimental techniques to handle these highly reactive compounds until recently - http://www.science-chemistry.com/boron-sulfur-compounds

Boric Acid Esters

Ebelman and Bouquet prepared the first examples of boric acid esters in 1846 from boron trichloride and alcohols. Literature reviews of this subject are available - http://www.science-chemistry.com/boric-acid-esters

воскресенье, 27 ноября 2016 г.

Nonmetal Borates

Ammonia, alkylamines, and other proton acceptor species can react with boric acid in aqueous or alcoholic solutions to form a wide range of crystalline nonmetal borate salts - http://www.science-chemistry.com/nonmetal-borates

Metal Borates

Metal borates can be divided into two broad classes: hydrated and anhydrous. So-called hydrated borates, which have the general formula aMxO·bB2O3·CH2O, contain B-OH groups, sometimes interstitial OH−, and may also contain interstitial water. Anhydrous borates do not contain water, OH−, or B-OH groups, and have the general formula aMxO·bB2O3 - http://www.science-chemistry.com/metal-borates

Boric Oxides, Boric Acids, and Metal Borates

Boric oxides, boric acids, and metal borates are of primary importance in any discussion of boron chemistry since these include essentially all boron minerals and the vast majority of boron compounds produced and used worldwide on a weight basis - http://www.science-chemistry.com/boric-oxides-boric-acids-and-metal-borates


Elemental Boron and Refractory Boron Compounds

Elemental boron is a refractory material that is usually isolated either as a shiny black crystalline solid or a softer, browner, more impure amorphous solid. Reduction of readily available boron compounds containing boron–oxygen bonds to elemental boron is energy intensive and costly - http://www.science-chemistry.com/elemental-boron-and-refractory-boron-compounds

Boron

The fifth element in the periodic table, boron, is usually grouped with the nonmetallic elements but has some metallic properties and is sometimes labeled a metalloid. Unlike the other group 13 elements, it is a semiconductor rather than a metallic conductor - http://www.science-chemistry.com/boron

суббота, 26 ноября 2016 г.

Periodic Table: Historical Aspects

The periodic table is one of the great classifications of the natural world and ranks on a par with several other major classifications, including the classification of plant species by Linnaeus in the 1750s, the classification of stars by Hertzsprung and Russell in 1913, and the classification of subnuclear particles by Gell-Mann and Ne’eman in the 1950s.
The periodic table has for its primary purpose the classification of the chemical elements, the basis for this being the analogies they exhibit in their physical and chemical properties. As the story of the periodic table is closely entwined with that of the elements, we shall explore these two concepts concomitantly here. From this broad perspective, some of the most colorful events that have occurred in chemical history over the past 2600 years are encompassed. In developing our theme, we shall endeavor to stimulate a greater interest in and bring a new awareness of the very rich legacy bequeathed to us by our pioneering predecessors. It is our hope that such an approach may in some way compensate for the often rather cursory treatment afforded our theme in elementary chemistry textbooks and foundational courses.
Because there can be no periodic table without an understanding of the nature of the elements, we shall start by delving into the history of the chemical elements. First, we mention the somewhat ironic fact that around nine genuine elements were known in ancient times, these being carbon, sulfur, copper, iron, lead, tin, mercury, silver, gold, and possibly antimony, though none of them was recognized as an element. Like everything else that was material, these true elements were thought to be composed of metaphysical entities such as essences or principles. The notion that all material objects consisted of essences or principles was a remarkably enduring one that was to persist for well over 2000 years.
In fact, this notion remained dominant until the end of the alchemical era was reached toward the end of the eighteenth century. In the Western World, the conception of meta physical elements is usually traced back to and considered to originate from certain of the natural philosophers of ancient Greece.
However, it is important to point out that all of the other major civilizations of the past paid homage to the idea that physical reality manifests itself in terms of metaphysical entities that were regarded as elements. There was even substantial overlap in these entities in different civilizations. Thus, virtually all of the early civilizations conceived of air and fire as elements.

Before probing further into the history of the elements, a brief comment on the etymological derivation of the word element seems appropriate. The first usage of the term element was made by the Greek philosopher Plato (427–347 BCE) in the fifth century BCE. The Latin equivalent of this Greek term is elementum, and this was first used by the Roman poet Lucretius in his famous poem De Rerum Natura (On the Nature of Things) extolling the virtues of an atomic conception of the world. While on the subject of words, we mention in passing the origin of the word quintessence. It was thought by the ancient Greeks that four elements comprised all of the matter on Earth whereas the celestial sphere was constituted from only one transcendent element referred to as the ether or the quinta essentia, the fifth essence, from which our modern word quintessence is derived. Interestingly, the ether turned out to be by far the longest lived of the Greek elements, for it was not until the dawn of the twentieth century that belief in the ether was finally abandoned.

Reactions of Boranes

The syntheses of the heteroboranes often involves the addition of heteromolecules to nido-boranes, in so called cage expansion reactions - http://www.science-chemistry.com/reactions-of-boranes

Syntheses of Boron Hydrides

The heteroboranes are derived ultimately from boranes, which, in turn, can be built up from lower molecular weight boron hydrides, the simplest of which is diborane, B2H6 - http://www.science-chemistry.com/syntheses-of-boron-hydrides

Nomenclature of the Heteroboranes

The IUPAC nomenclature of the heteroboranes takes the name of the unsubstituted borane as the parent, with the number of hydrogens given in parentheses, that is, B5H9 is pentaborane(9) - http://www.science-chemistry.com/nomenclature-of-the-heteroboranes

Boron Hydrides

Boranes are mixed hydrides of boron and hydrogen. The unusual properties of these compounds arise from the fact that in forming compounds, boron can furnish four orbitals (s, px, py, pz) but only three electrons for bonding - http://www.science-chemistry.com/boron-hydrides

Properties and Applications of Borides

Characteristic properties of borides are high chemical inertness, high thermal stability, and great hardness. Magnetic and electrical properties vary strongly within the boride group of compounds - http://www.science-chemistry.com/properties-and-applications-of-borides

Band Structure and Bonding of Borides

The nature of the chemical bonding in borides was in early work described by simplified models emphasizing the role of M–M, M–B, and B–B bonding. The question of magnitude and direction of charge transfer has been much debated - http://www.science-chemistry.com/band-structure-and-bonding-of-borides

пятница, 25 ноября 2016 г.

Synthesis of Borides

The synthesis of borides often requires high temperatures, involving difficulties in obtaining pure products while simultaneously using simple methods - http://www.science-chemistry.com/synthesis-of-borides

Occurence and Crystal Chemistry of Borides

Preparation and phase characterization of a great number of binary borides were carried out in the period 1950 to 1980, while interest was focused on ternary borides in the time that followed - http://www.science-chemistry.com/occurence-and-crystal-chemistry-of-borides

Pentavalent Organobismuth Compounds

Triarylorganobismuth complexes are easily oxidized to bismuth(V) complexes by treatment with chlorine or bromine, giving Ar3BiX2 (X = Cl, Br) - http://www.science-chemistry.com/pentavalent-organobismuth-compounds

Trivalent Organobismuth Compounds

Triethylbismuth, the first known organobismuth compound, was prepared in 1850 by Lowig and Schweizer from iodoethane and a potassium–bismuth alloy - http://www.science-chemistry.com/trivalent-organobismuth-compounds


четверг, 24 ноября 2016 г.

Optical Properties of Borates

Broad-band laser emission has been observed from Cr3+– doped ScBO3. The luminescence band extends from 700 to 1000 nm, with a peak at 810 nm - http://www.science-chemistry.com/optical-properties-of-borates


Synthesis of Borates

Anhydrous metal borates are conveniently prepared by heating hydrated salts or by direct fusion or firing of one or more metal oxides with H3BO3 or B2O3. Because the melting points of most borates fall well below 1500 ◦C, heating suitable reagents for only a few hours near 1000 ◦C generally produces homogeneous microcrystalline powders - http://www.science-chemistry.com/synthesis-of-borates

Borates: Crystal Structure

The known structural chemistry of anhydrous borates through 1985 has been summarized, and those borate minerals containing fused octahedra and triangles have been classified according to selected fundamental building blocks - http://www.science-chemistry.com/borates-crystal-structure

Borates: Electronic Structure

A wide range of borate structures contain the isolated triangular BO33− group (1), while a fewer number contain the isolated tetrahedral BO45− group (2) - http://www.science-chemistry.com/borates-electronic-structure


Borates

Borates are unique among the oxoanion compounds of the second-row elements in forming anhydrous substances that are both chemically and thermally stable - http://www.science-chemistry.com/borates

среда, 23 ноября 2016 г.

Compounds of Bismuth

Less reduced intermetallic phases with the alkali metals and alkaline-earth metals are also known. Examples include MBi (M = Li, Na), MBi2 (M = K, Rb, Cs), and MʹBi3 (M = Mg, Ca, Sr, Ba). The compounds MʹBi3 (Mʹ = Ca, Sr, or Ba) superconduct at low temperatures. Some of these intermetallic phases have been extracted with amine solvents to yield anionic bismuth clusters in solution - http://www.science-chemistry.com/compounds-of-bismuth

Bismuth

Bismuth, element 83, is a soft gray naturally oc curring metal. It is most commonly found as bismite (Bi2O3), bismutite ((BiO)2CO3), or bismuthinite (Bi2S3) - http://www.science-chemistry.com/bismuth

понедельник, 21 ноября 2016 г.

Applications of Biominerals and Biomineralization

The strict control of the organism on its skeletal units and their arrangement allows us to use the microstructure and composition as taxonomical and phylogenetical criteria. The example of the nacreous layer of the mollusk shells - http://www.science-chemistry.com/applications-of-biominerals-and-biomineralization

Modes of Biomineralization

Biomineralization involves the formation of minerals by organisms, and two different modes are summarized by Lowenstam and Weiner. In the biologically induced mineralization, an organism modifies its local microenvironment - http://www.science-chemistry.com/modes-of-biomineralization

Biominerals: Structure and Composition

Biominerals: Structure and Composition

Biomineralization

Biomineralization
Biomineralization is widespread in the biosphere (more than 60 different minerals are produced by 55 phyla, from bacteria to humans).

Preparation of Magnesium and Beryllium

The classical method for formation of a Grignard reagent, as originally described by Victor Grignard in 1900, is the reaction of an organic halide in ether solution with magnesium metal - http://www.science-chemistry.com/preparation-of-magnesium-and-beryllium

Organoberyllium and -Magnesium Spectroscopy

A variety of spectroscopic techniques has made invaluable contributions to understanding the structure and reactions of organoberyllium and -magnesium compounds. In this section, general spectroscopic - http://www.science-chemistry.com/organoberyllium-and-magnesium-spectroscopy

Beryllium & Magnesium: Organometallic Chemistry

Victor Grignard found in 1900 that solutions of organomagnesium halides may be prepared easily by the reaction of an organic halide with magnesium metal in diethyl ether, and that these solutions undergo useful reactions - http://www.science-chemistry.com/beryllium-magnesium-organometallic-chemistry

воскресенье, 20 ноября 2016 г.

Beryllium and Magnesium: Bonding and Structure

Beryllium and magnesium have a formal oxidation state of +2 in their compounds (see Oxidation Number); other oxidation states appear to exist only as transient reaction intermediates. Therefore, organometallic compounds of general formula R2M and RMY may exist, in addition to the nonorganometallic MY - http://www.science-chemistry.com/beryllium-and-magnesium-bonding-and-structure

Nontraditional Approaches to Asymmetric Catalysis

The utility of the traditional approach to asymmetric catalysis, involving synthesis and screening of chiral ligands and complexes in catalytic reactions is a powerful method for the development and optimization of catalytic asymmetric processes - http://www.science-chemistry.com/nontraditional-approaches-to-asymmetric-catalysis

суббота, 19 ноября 2016 г.

Asymmetric Synthesis by Homogeneous Catalysis

The field of asymmetric catalysis hasmoved to the forefront of organic chemistry, culminating with the award of the 2001 Nobel Prize in Chemistry to Knowles, Noyori, and Sharpless - http://www.science-chemistry.com/asymmetric-synthesis-by-homogeneous-catalysis


Organoarsenic Compounds Containing As–O Bonds

The synthesis and reactivity of organoarsenic compounds that contain As–O bonds has been extensively reviewed. Because of space limitations, the extensive chemistry associated with As–O bonded systems cannot be covered - http://www.science-chemistry.com/organoarsenic-compounds-containing-as-o-bonds

Organoarsenic Compounds Containing As–Group 15 Bonds

There have been several reviews that provide a comprehensive coverage of the synthesis and reactivity of organoarsenic compounds that contain tricoordinate arsenic with an As–N bond - http://www.science-chemistry.com/organoarsenic-compounds-containing-as-group-15-bonds

Organoarsenic Compounds Containing As–Group 14 Bonds

Several references review the chemistry associated with organoarsines that contain the As–Si bond. Silylation of the alkali metal organoarsenide leads to salt elimination and the formation of the silylarsines - http://www.science-chemistry.com/organoarsenic-compounds-containing-as-group-14-bonds

четверг, 17 ноября 2016 г.

Organoarsenic Compounds Containing As–Group 13 Bonds

Relatively few organoarsenic compounds that contain an As–B bond are known. In most cases, these are synthesized by the straightforward reaction of the primary, secondary, and tertiary arsine with diborane or BH3·THF - http://www.science-chemistry.com/organoarsenic-compounds-containing-as-group-13-bonds

Organoarsenic Compounds Containing As–Halogen Bonds

The haloarsines are most commonly prepared from the reduction of the arsonic or arsinic acids by sulfur dioxide in the presence of a hydrogen halide and a trace of KI - http://www.science-chemistry.com/organoarsenic-compounds-containing-as-halogen-bonds

Organoarsenic Containing As–H Bonds

Organoarsines containing the As–H bond are limited to the primary and secondary organoarsines. Both the alkyl and aryl derivatives are usually synthesized by the reduction of the arsinous acid - http://www.science-chemistry.com/organoarsenic-containing-as-h-bonds

Fully Substituted Organoarsenic Compounds

Tertiary arsines comprise the most common class of tricoordinate, fully organosubstituted arsenic compounds - http://www.science-chemistry.com/fully-substituted-organoarsenic-compounds


Arsenic: Organoarsenic Chemistry

The organometallic chemistry of arsenic has a long history that dates back to the synthesis and discovery in 1760 of the first 
organometallic compound, Me2AsAsMe2, by L. C. Cadet de Gassicourt http://www.science-chemistry.com/arsenic-organoarsenic-chemistry