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
среда, 30 ноября 2016 г.
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 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
вторник, 22 ноября 2016 г.
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
Biomineralization
Biomineralization
Biomineralization is widespread in the biosphere (more than 60 different minerals are produced by 55 phyla, from bacteria to humans).
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
organometallic compound, Me2AsAsMe2, by L. C. Cadet de Gassicourt http://www.science-chemistry.com/arsenic-organoarsenic-chemistry
среда, 16 ноября 2016 г.
Transition-Metal Complexes with Sbn Ligands
The coordination of ‘naked’ antimony atoms Sbn is achieved in complexes with Sb, Sb2, cyclo-Sb3, and cyclo-Sb5 ligands - http://www.science-chemistry.com/transition-metal-complexes-with-sbn-ligands
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