Cyclosilane
Silanes are saturated chemical compounds with the empirical formula . They are hydrosilanes, a class of compounds that includes compounds with and other bonds. All contain tetrahedral silicon and terminal hydrides. They only have and single bonds. The bond lengths are 146.0 pm for a bond and 233 pm for a bond. The structures of the silanes are analogues of the alkanes, starting with silane, , the analogue of methane, continuing with disilane , the analogue of ethane, etc. They are mainly of theoretical or academic interest. Inventory 132px, cyclopentane.html" ;"title="Cyclopentasilane is structurally similar to cyclopentane">Cyclopentasilane is structurally similar to cyclopentane, just larger. The simplest isomer of a silane is the one in which the silicon atoms are arranged in a single chain with no branches. This isomer is sometimes called the ''n''-isomer (''n'' for "normal", although it is not necessarily the most common). However the chain of silicon atoms m ... [...More Info...]       [...Related Items...]     OR:     [Wikipedia]   [Google]   [Baidu]   |
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Disilane
Disilane is a chemical compound with general chemical formula Si2R6 that was first identified in 1902 by Henri Moissan and Samuel Smiles (1877–1953) where R = H. Moissan and Smiles reported disilane as being among the products formed by the action of dilute acids on metal silicides. Although these reactions had been previously investigated by Friedrich Woehler and Heinrich Buff between 1857 and 1858, Moissan and Smiles were the first to explicitly identify disilane. They referred to disilane as ''silicoethane''. Higher members of the homologous series formed in these reactions were subsequently identified by Carl Somiesky (sometimes spelled "Karl Somieski") and Alfred Stock. At standard temperature and pressure, disilane is a colourless, acrid gas. Disilane and ethane have similar structures, although disilane is much more reactive. Other compounds of the general formula (X = hydrogen, halogen, alkyl, aryl, and mixtures of these groups) are called disilanes. Disilane is a group ... [...More Info...]       [...Related Items...]     OR:     [Wikipedia]   [Google]   [Baidu]   |
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Isobutane
Isobutane, also known as ''i''-butane, 2-methylpropane or methylpropane, is a chemical compound with molecular formula HC(CH3)3. It is an isomer of butane. Isobutane is a colorless, odorless gas. It is the simplest alkane with a tertiary carbon atom. Isobutane is used as a precursor molecule in the petrochemical industry, for example in the synthesis of isooctane. Production Isobutane is obtained by isomerization of butane. Uses Isobutane is the principal feedstock in alkylation units of refineries. Using isobutane, gasoline-grade "blendstocks" are generated with high branching for good combustion characteristics. Typical products created with isobutane are 2,4-dimethylpentane and especially 2,2,4-trimethylpentane. Solvent In the Chevron Phillips slurry process for making high-density polyethylene, isobutane is used as a diluent. As the slurried polyethylene is removed, isobutane is "flashed" off, and condensed, and recycled back into the loop reactor for this purpose. Prec ... [...More Info...]       [...Related Items...]     OR:     [Wikipedia]   [Google]   [Baidu]   |
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Alkane
In organic chemistry, an alkane, or paraffin (a historical trivial name that also has other meanings), is an acyclic saturated hydrocarbon. In other words, an alkane consists of hydrogen and carbon atoms arranged in a tree structure in which all the carbon–carbon bonds are single. Alkanes have the general chemical formula . The alkanes range in complexity from the simplest case of methane (), where ''n'' = 1 (sometimes called the parent molecule), to arbitrarily large and complex molecules, like hexacontane () or 4-methyl-5-(1-methylethyl) octane, an isomer of dodecane (). The International Union of Pure and Applied Chemistry (IUPAC) defines alkanes as "acyclic branched or unbranched hydrocarbons having the general formula , and therefore consisting entirely of hydrogen atoms and saturated carbon atoms". However, some sources use the term to denote ''any'' saturated hydrocarbon, including those that are either monocyclic (i.e. the cycloalkanes) or polycycl ... [...More Info...]       [...Related Items...]     OR:     [Wikipedia]   [Google]   [Baidu]   |
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Polysilicon Hydride
Polysilicon hydrides are polymers containing only silicon and hydrogen. They have the formula (SiH_)_ where 0.2 ≤ ''n'' ≤ 2.5 and ''x'' is the number of monomer units. The polysilicon hydrides are generally colorless or pale-yellow/ocher powders that are easily hydrolyzed and ignite readily in air. The surfaces of silicon prepared by MOCVD using silane (SiH4) consist of a polysilicon hydride. Synthesis Polysilicon hydrides are much less thermally stable than the corresponding alkanes (CnH2n+2). They are kinetically labile, with their decomposition reaction rate increasing with increases in the number of silicon atoms in the molecule. Consequently, the preparation and isolation of polysilicon hydrides is difficult for species containing more than a few silicon atoms. Greater catenation of the Si atoms can be obtained with the halides (Sin''X''2n+2 with n = 14) for the fluorides. Thus the polymeric silicon hydrides are formed along with smaller s ... [...More Info...]       [...Related Items...]     OR:     [Wikipedia]   [Google]   [Baidu]   |
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Latin Language
Latin ( or ) is a classical language belonging to the Italic languages, Italic branch of the Indo-European languages. Latin was originally spoken by the Latins (Italic tribe), Latins in Latium (now known as Lazio), the lower Tiber area around Rome, Italy. Through the expansion of the Roman Republic, it became the dominant language in the Italian Peninsula and subsequently throughout the Roman Empire. It has greatly influenced many languages, Latin influence in English, including English, having contributed List of Latin words with English derivatives, many words to the English lexicon, particularly after the Christianity in Anglo-Saxon England, Christianization of the Anglo-Saxons and the Norman Conquest. Latin Root (linguistics), roots appear frequently in the technical vocabulary used by fields such as theology, List of Latin and Greek words commonly used in systematic names, the sciences, List of medical roots, suffixes and prefixes, medicine, and List of Latin legal terms ... [...More Info...]       [...Related Items...]     OR:     [Wikipedia]   [Google]   [Baidu]   |
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IUPAC Numerical Multiplier
The numerical multiplier (or multiplying affix) in IUPAC nomenclature indicates how many particular atoms or functional groups are attached at a particular point in a molecule. The affixes are derived from both Latin and Greek. Compound affixes The prefixes are given from the least significant decimal digit up: units, then tens, then hundreds, then thousands. For example: :548 → octa- (8) + tetraconta- (40) + pentacta- (500) = ''octatetracontapentacta-'' :9267 → hepta- (7) + hexaconta- (60) + dicta- (200) + nonalia- (9000) = ''heptahexacontadictanonalia-'' The numeral one While the use of the affix ''mono-'' is rarely necessary in organic chemistry, it is often essential in inorganic chemistry to avoid ambiguity: carbon oxide could refer to either ''carbon monoxide'' or ''carbon dioxide''. In forming compound affixes, the numeral one is represented by the term ''hen-'' except when it forms part of the number eleven (''undeca-''): hence :241 → hen- (1) + tetraconta- (40 ... [...More Info...]       [...Related Items...]     OR:     [Wikipedia]   [Google]   [Baidu]   |
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Affix
In linguistics, an affix is a morpheme that is attached to a word stem to form a new word or word form. The main two categories are Morphological derivation, derivational and inflectional affixes. Derivational affixes, such as ''un-'', ''-ation'', ''anti-'', ''pre-'' etc., introduce a semantic change to the word they are attached to. Inflectional affixes introduce a syntactic change, such as singular into plural (e.g. ''-(e)s''), or present simple grammatical tense, tense into present continuous or past tense by adding ''-ing'', ''-ed'' to an English word. All of them are bound morphemes by definition; prefixes and suffixes may be separable affixes. Affixes, infixes and their variations Changing a word by adding a morpheme at its beginning is called ''prefixation'', in the middle is called ''infixation'', and at the end is called ''suffixation''. ''Prefix'' and ''suffix'' may be subsumed under the term ''adfix'', in contrast to ''infix.'' When marking text for interlinear gl ... [...More Info...]       [...Related Items...]     OR:     [Wikipedia]   [Google]   [Baidu]   |
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Hexane
Hexane () or ''n''-hexane is an organic compound, a straight-chain alkane with six carbon atoms and the molecular formula C6H14. Hexane is a colorless liquid, odorless when pure, and with a boiling point of approximately . It is widely used as a cheap, relatively safe, largely unreactive, and easily evaporated non-polar solvent, and modern gasoline blends contain about 3% hexane. The term hexanes refers to a mixture, composed largely (>60%) of ''n''-hexane, with varying amounts of the isomeric compounds 2-methylpentane and 3-methylpentane, and possibly, smaller amounts of nonisomeric C5, C6, and C7 (cyclo)alkanes. These "hexanes" mixtures are cheaper than pure hexane and are often used in large-scale operations not requiring a single isomer (e.g., as cleaning solvent or for chromatography). Isomers Uses In industry, hexanes are used in the formulation of adhesive, glues for shoes, leather products, and roofing. They are also used to extract cooking oils (such as canola oil ... [...More Info...]       [...Related Items...]     OR:     [Wikipedia]   [Google]   [Baidu]   |
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Hexasilane
Silanes are saturated chemical compounds with the empirical formula . They are hydrosilanes, a class of compounds that includes compounds with and other bonds. All contain tetrahedral silicon and terminal hydrides. They only have and single bonds. The bond lengths are 146.0 pm for a bond and 233 pm for a bond. The structures of the silanes are analogues of the alkanes, starting with silane, , the analogue of methane, continuing with disilane , the analogue of ethane, etc. They are mainly of theoretical or academic interest. Inventory 132px, cyclopentane.html" ;"title="Cyclopentasilane is structurally similar to cyclopentane">Cyclopentasilane is structurally similar to cyclopentane, just larger. The simplest isomer of a silane is the one in which the silicon atoms are arranged in a single chain with no branches. This isomer is sometimes called the ''n''-isomer (''n'' for "normal", although it is not necessarily the most common). However the chain of silicon atoms m ... [...More Info...]       [...Related Items...]     OR:     [Wikipedia]   [Google]   [Baidu]   |
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Neopentane
Neopentane, also called 2,2-dimethylpropane, is a double-branched-chain alkane with five carbon atoms. Neopentane is a flammable gas at room temperature and pressure which can condense into a highly volatile liquid on a cold day, in an ice bath, or when compressed to a higher pressure. Neopentane is the simplest alkane with a quaternary carbon, and has achiral tetrahedral symmetry. It is one of the three structural isomers with the molecular formula C5H12 (pentanes), the other two being ''n''-pentane and isopentane. Out of these three, it is the only one to be a gas at standard conditions; the others are liquids. It was first synthesized by Russian chemist in 1870. Nomenclature The traditional name neopentane, coined by William Odling in 1876, was still retained in the 1993 IUPAC recommendations, but is no longer recommended according to the 2013 recommendations. The preferred IUPAC name is the systematic name 2,2-dimethylpropane, but the substituent numbers are su ... [...More Info...]       [...Related Items...]     OR:     [Wikipedia]   [Google]   [Baidu]   |
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Isopentane
Isopentane, also called methylbutane or 2-methylbutane, is a branched-chain saturated hydrocarbon (an alkane) with five carbon atoms, with formula or . Isopentane is a volatile and flammable liquid. It is one of three structural isomers with the molecular formula C5H12, the others being pentane (''n''-pentane) and neopentane (2,2-dimethylpropane). Isopentane is commonly used in conjunction with liquid nitrogen to achieve a liquid bath temperature of −160 °C. Natural gas typically contains 1% or less isopentane, but it is a significant component of natural gasoline.Ivan F. Avery, L. V. Harvey (1958): Natural-gasoline and Cycling Plants in the United States', Information circular, U.S. Department of the Interior, Bureau of Mines. 12 pages. History Although the mixture of pentanes was first isolated from the destructive distillation (pyrolysis) products of the boghead coal by Charles Greville Williams in 1862. In 1864–1865 two chemists tried to extract same hydro ... [...More Info...]       [...Related Items...]     OR:     [Wikipedia]   [Google]   [Baidu]   |