Ammonia Borane
Ammonia borane (also systematically named ammoniotrihydroborate), also called borazane, is the chemical compound with the formula . The colourless or white solid is the simplest molecular boron-nitrogen-hydride compound. It has attracted attention as a source for hydrogen fuel, but is otherwise primarily of academic interest. Synthesis Reaction of diborane with ammonia mainly gives the diammoniate salt (diammoniodihydroboronium tetrahydroborate). Ammonia borane is the main product when an adduct of borane is employed in place of diborane: : It can also be synthesized from sodium borohydride. Properties and structure The molecule adopts a structure similar to that of ethane, with which it is isoelectronic. The B−N distance is 1.58(2) Å. The B−H and N−H distances are 1.15 and 0.96 Å, respectively. Its similarity to ethane is tenuous since ammonia borane is a solid and ethane is a gas: their melting points differing by 284 °C. This difference is consistent with the high ... [...More Info...]       [...Related Items...]     OR:     [Wikipedia]   [Google]   [Baidu]   |
|
Sodium Borohydride
Sodium borohydride, also known as sodium tetrahydridoborate and sodium tetrahydroborate, is an inorganic compound with the formula (sometimes written as ). It is a white crystalline solid, usually encountered as an aqueous basic solution. Sodium borohydride is a reducing agent that finds application in papermaking and dye industries. It is also used as a reagent in organic synthesis. The compound was discovered in the 1940s by H. I. Schlesinger, who led a team seeking volatile uranium compounds.Hermann I Schlesinger and Herbert C Brown (1945)Preparation of alkali metal compounds. US Patent 2461661. Granted on 1949-02-15; expired on 1966-02-15. Results of this wartime research were declassified and published in 1953. Properties The compound is soluble in alcohols, certain ethers, and water, although it slowly hydrolyzes. Sodium borohydride is an odorless white to gray-white microcrystalline powder that often forms lumps. It can be purified by recrystallization from warm ... [...More Info...]       [...Related Items...]     OR:     [Wikipedia]   [Google]   [Baidu]   |
|
Acetylene
Acetylene (Chemical nomenclature, systematic name: ethyne) is a chemical compound with the formula and structure . It is a hydrocarbon and the simplest alkyne. This colorless gas is widely used as a fuel and a chemical building block. It is unstable in its pure form and thus is usually handled as a solution. Pure acetylene is odorless, but commercial grades usually have a marked odor due to impurities such as divinyl sulfide and phosphine.Compressed Gas Association (1995Material Safety and Data Sheet – Acetylene As an alkyne, acetylene is Saturated and unsaturated compounds, unsaturated because its two carbon atoms are Chemical bond, bonded together in a triple bond. The carbon–carbon triple bond places all four atoms in the same straight line, with CCH bond angles of 180°. The triple bond in acetylene results in a high energy content that is released when acetylene is burned. Discovery Acetylene was discovered in 1836 by Edmund Davy, who identified it as a "new carburet ... [...More Info...]       [...Related Items...]     OR:     [Wikipedia]   [Google]   [Baidu]   |
|
Ethylene
Ethylene (IUPAC name: ethene) is a hydrocarbon which has the formula or . It is a colourless, flammable gas with a faint "sweet and musky" odour when pure. It is the simplest alkene (a hydrocarbon with carbon–carbon bond, carbon–carbon double bonds). Ethylene is widely used in the chemical industry, and its worldwide production (over 150 million tonnes in 2016) exceeds that of any other organic compound. Much of this production goes toward creating polyethylene, which is a widely used plastic containing polymer chains of ethylene units in various chain lengths. Production greenhouse gas emissions, emits greenhouse gases, including methane from feedstock production and carbon dioxide from any non-sustainable energy used. Ethylene is also an important natural plant hormone and is used in agriculture to induce ripening of fruits. The hydrate of ethylene is ethanol. Structure and properties This hydrocarbon has four hydrogen atoms bound to a pair of carbon atoms that are con ... [...More Info...]       [...Related Items...]     OR:     [Wikipedia]   [Google]   [Baidu]   |
|
Iminoborane
Iminoboranes comprise a group of organoboron compounds with the formula RB=NR'. They are electronically related to acetylenes but are usually more reactive due to the polarity. Structure and bonding The parent iminoborane, HB=NH, is produced by the photodissociation, photolysis of H3BNH3. Bonding in iminoboranes can be described by two Resonance (chemistry), resonance structures: :R-\overset\overset-R R-B=\ddot-R The stability is dramatically affected by bulky substituents. One isolable iminoborane is . Synthesis Elimination of fluoro- or chlorosilanes provides a well-tested route. Bulky substituents such as tris(trimethylsilyl)silane, (Me3Si)3Si stabilize the iminoborane with respect to oligomerization: :(Me3Si)3SiB(F)-N(SiMe3)2 → (Me3Si)3Si-B=N-SiMe3 + F-SiMe3 Thermal decomposition of azidoboranes induces migration of R from boron to the nascent nitrene gives iminoboranes: :R2B-N3 → RB=NR + N2 Reactivity Oligomerization Iminoboranes tend to oligomerize ... [...More Info...]       [...Related Items...]     OR:     [Wikipedia]   [Google]   [Baidu]   |
|
Amine-borane
Ammonia borane (also systematically named ammoniotrihydroborate), also called borazane, is the chemical compound with the formula . The colourless or white solid is the simplest molecular boron-nitrogen-hydride compound. It has attracted attention as a source for hydrogen fuel, but is otherwise primarily of academic interest. Synthesis Reaction of diborane with ammonia mainly gives the diammoniate salt (diammoniodihydroboronium tetrahydroborate). Ammonia borane is the main product when an adduct of borane is employed in place of diborane: : It can also be synthesized from sodium borohydride. Properties and structure The molecule adopts a structure similar to that of ethane, with which it is isoelectronic. The B−N distance is 1.58(2) Å. The B−H and N−H distances are 1.15 and 0.96 Å, respectively. Its similarity to ethane is tenuous since ammonia borane is a solid and ethane is a gas: their melting points differing by 284 °C. This difference is consistent with the high ... [...More Info...]       [...Related Items...]     OR:     [Wikipedia]   [Google]   [Baidu]   |
|
Iminoborane
Iminoboranes comprise a group of organoboron compounds with the formula RB=NR'. They are electronically related to acetylenes but are usually more reactive due to the polarity. Structure and bonding The parent iminoborane, HB=NH, is produced by the photodissociation, photolysis of H3BNH3. Bonding in iminoboranes can be described by two Resonance (chemistry), resonance structures: :R-\overset\overset-R R-B=\ddot-R The stability is dramatically affected by bulky substituents. One isolable iminoborane is . Synthesis Elimination of fluoro- or chlorosilanes provides a well-tested route. Bulky substituents such as tris(trimethylsilyl)silane, (Me3Si)3Si stabilize the iminoborane with respect to oligomerization: :(Me3Si)3SiB(F)-N(SiMe3)2 → (Me3Si)3Si-B=N-SiMe3 + F-SiMe3 Thermal decomposition of azidoboranes induces migration of R from boron to the nascent nitrene gives iminoboranes: :R2B-N3 → RB=NR + N2 Reactivity Oligomerization Iminoboranes tend to oligomerize ... [...More Info...]       [...Related Items...]     OR:     [Wikipedia]   [Google]   [Baidu]   |
|
Journal Of Molecular Spectroscopy
''Journal of Molecular Spectroscopy'' is a peer-reviewed scientific journal that deals with experimental and theoretical articles on all subjects relevant to molecular spectroscopy and its modern applications. Indexing and abstracting According to the ''Journal Citation Reports'', the journal has a 2020 impact factor of 1.507. The journal in indexing in the following bibliographic databases: * AGRICOLA * Chemical Abstracts * Current Contents/Physics, Chemical, & Earth Sciences * Research Alert * Science Abstracts * Science Citation Index * Biological Abstracts * Scopus Scopus is a scientific abstract and citation database, launched by the academic publisher Elsevier as a competitor to older Web of Science in 2004. The ensuing competition between the two databases has been characterized as "intense" and is c ... References External links * Optics journals {{spectroscopy-journal-stub ... [...More Info...]       [...Related Items...]     OR:     [Wikipedia]   [Google]   [Baidu]   |
|
The Journal Of Chemical Physics
''The Journal of Chemical Physics'' is a scientific journal published by the American Institute of Physics that carries research papers on chemical physics."About the Journal" from the ''Journal of Chemical Physics'' website. Two volumes, each of 24 issues, are published annually. It was established in 1933 when '''' editors refused to publish theoretical works. The editors have been: *2019–present: Tim Lian *2008–2018: Marsha I. Lester *2007–2008: [...More Info...]       [...Related Items...]     OR:     [Wikipedia]   [Google]   [Baidu]   |