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Class of chemical compounds
Hybrids of boranes and hydrocarbons, the carboranes, are also a well developed class of compounds. The development of the chemistry of boranes led to innovations
Boranes
Chemical compound
Phosphine-boranes, with the formula R3−nHnPBH3, are adducts of organophosphines and borane. Borane adducts with amines are more widely used. Borane makes
Borane
Amine-boranes are a class of covalent compounds based on the ammonia borane parent structure. These compounds were once of some interest for hydrogen
Amine-boranes
Study of compounds containing a boron-carbon bond
and carbon; typically, they are organic derivatives of borane (BH3), as in the trialkyl boranes. Organoboranes and -borates enable many chemical transformations
Organoboron_chemistry
Chemical compound
secondary boranes are less common. Tert-butylamine borane (tBuNH2→BH3) Phosphine-borane (R3P→BH3) Borane dimethylsulfide ((CH3)2S→BH3) Borane–tetrahydrofuran
Ammonia_borane
Chemical compound
Borane carbonyl is the inorganic compound with the formula H3BCO. This colorless gas is the adduct of borane and carbon monoxide. It is usually prepared
Borane_carbonyl
Addition of a hydrogen-boron bond to C=C, C=N, C=O, or C≡C bonds
significant rate difference in producing di- and tri-alkyl boranes is useful in the synthesis of bulky boranes that can enhance regioselectivity. In terms of regiochemistry
Hydroboration
Chemical compound
range of alkyl-substituted boranes are specialty reagents in organic synthesis. Two such reagents closely related to Alpine borane are 9-BBN and diisopinocampheylborane
Alpine_borane
Typically phosphine-boranes are produced by treating the parent phosphine with a source of borane: PR3−nHn + BH3 → R3−nHnPBH3 Because borane solutions are expensive
Phosphine-borane
Chemical compound composed of boron and hydrogen atoms only
conjuncto-boranes, where the sub-units are joined by a B-B bond, can be made by ultra violet irradiation of nido-boranes. Some B-B coupled conjuncto-boranes can
Boron_hydride_clusters
Chemical element with atomic number 5 (B)
Like the volatile boranes, the alkyl boranes ignite spontaneously in air. In the 1950s, several studies examined the use of boranes as energy-increasing
Boron
Chemical rule used to calculate the structures of boranes
used to calculate the structures of boranes. It was developed by William Lipscomb in 1954. The rule defines boranes to have four types of bonds besides
Styx_rule
Chemical compound
organoborane compounds are useful intermediates in organic synthesis. Boranes add to alkenes in an anti-Markovnikov fashion and allow conversion of alkynes
Borane_dimethylsulfide
Any chemical compound having at least one boron atom
Boranes are chemical compounds of boron and hydrogen, with the generic formula of BxHy. These compounds do not occur in nature. Many of the boranes readily
Boron_compounds
the structures of condensed polyhedral boranes such as B20H16, which are obtained by condensing polyhedral boranes by sharing a triangular face, an edge
Jemmis_mno_rules
Radicals centered on boron atoms
xanthanes using NHC-boranes, which had previously been synthesized by Kuhn. They were able to isolate NHC-(methylthiocarbonylthio)borane as a solid product
Boryl_radicals
Chemical compound
Borane–tetrahydrofuran is an adduct derived from borane and tetrahydrofuran (THF). These solutions, which are colorless, are used for reductions and hydroboration
Borane–tetrahydrofuran
Chemical compound
William Nunn Lipscomb Jr. further confirmed the molecular structure of boranes using X-ray crystallography in the 1950s and developed theories to explain
Diborane
Chemical compound
2-substituted isomer compared to the use of borane. Organoboron chemistry Boron Brown, H. C. (1975). Organic Syntheses via Boranes. New York: John Wiley & Sons. ISBN 0-471-11280-1
9-Borabicyclo(3.3.1)nonane
Class of chemical compounds
C-alkyl and B-alkyl analogues are also known in a few cases. Carboranes and boranes adopt 3-dimensional cage (cluster) geometries in sharp contrast to typical
Carborane
Chemical compound
BCl3 BF BFO BF3 BI3 B2F4 B2Cl4 Acids B(NO3)3 B(OH)3 BPO4 B2(OH)4 BH3O Boranes BH3 B2H4 B2H6 BH3NH3 B4H10 B5H9 B5H11 B6H10 B6H12 B10H14 B18H22 [B12H12]2-
Boron_trifluoride
Laboratory technique for DNA methylation profiling
TET-assisted pyridine borane sequencing or TAPS is a laboratory technique in epigenetics for high-throughput profiling of DNA methylation at a single base-pair
TET-assisted pyridine borane sequencing
TET-assisted_pyridine_borane_sequencing
Technique for measuring a molecule's Lewis acidity
"frustrated Lewis pairs": facile formation of phosphine-boranes and cationic phosphonium-boranes", Dalton Trans., 2007, 3407–3414. doi: 10.1039/b704417h
Gutmann–Beckett_method
Chemical compound
H2: (C6F5)3B + PCy3 + H2 → (C6F5)3BH− + HPCy3+ Many related phosphines, boranes, and substrates participate in related reactions. (C6F5)3B was used to
Tris(pentafluorophenyl)borane
Indian theoretical chemist
for polyhedral boranes to macropolyhedral boranes and the Huckel 4n+2 Rule to three dimensions. The Jemmis mno rules for polyhedral boranes have found a
E._D._Jemmis
Chemical compound
and Brown in a pioneering demonstration of asymmetric synthesis using boranes. The reagent is mainly used for the synthesis of chiral secondary alcohols
Diisopinocampheylborane
Chemical reaction that converts an alkene to an alcohol
carboxylic acids instead of aldehydes for terminal alkenes. Aside from boranes, the oxidation of silanes and disilanes can also yield hydroxy groups.
Hydroboration–oxidation reaction
Hydroboration–oxidation_reaction
Pyrophoric liquid
(M = Li, Na) Triethylborane reacts with methanol to form diethyl(methoxy)borane, which is used as the chelating agent in the Narasaka–Prasad reduction for
Triethylborane
Electron-deficient chemical bond where three atoms share two electrons
compounds described by the polyhedral skeletal electron pair theory, such as boranes and carboranes. These molecules derive their stability from having a completely
Three-center two-electron bond
Three-center_two-electron_bond
Chemical catalyst
a mixture of tricyclohexylphosphine (PCy3) and tris(pentafluorophenyl)borane reacts with hydrogen to give the respective phosphonium and borate ions:
Frustrated_Lewis_pair
Chemical compound
catalyst is used along with borane-tetrahydrofuran (THF), borane-dimethylsulfide, borane-N,N-diethylaniline, or diborane as the borane source. Enantioselective
(R)-2-Methyl-CBS-oxazaborolidine
(R)-2-Methyl-CBS-oxazaborolidine
Chemical compound
composed of Na+ and H− ions, in contrast to molecular hydrides such as borane, silane, germane, ammonia, and methane. It is an ionic material that is
Sodium_hydride
Catalyzed organic reactions that produce an organoboron compound
Organoboron chemistry Reactions of organoborates and boranes Corey–Itsuno reduction Midland Alpine borane reduction Petasis reaction Suzuki reaction Boryl
Borylation
Term used in organic chemistry
stable nature of some spherical compounds such as fullerenes and polyhedral boranes. In 2000, Andreas Hirsch and coworkers in Erlangen, Germany, formulated
Spherical_aromaticity
Psychoactive drug, often called ecstasy
2004). "Reductive aminations of carbonyl compounds with borohydride and borane reducing agents". Organic Reactions. 59. Hoboken, New Jersey, United States:
MDMA
Chemical process of joining two molecular entities by bonds of any kind
dimers, even when the monomer is elusive. Diborane (B2H6) is an dimer of borane, which is elusive and rarely observed. Almost all compounds of the type
Dimerization
Alternate scientific theory of scent perception
original paper in the journal Chemical Senses, the well documented smell of borane compounds is sulfurous, though these molecules contain no sulfur. He proposes
Vibration_theory_of_olfaction
Chemical element with atomic number 1 (H)
and all react with water to liberate hydrogen. Covalent hydrides include boranes and polymeric aluminium hydride. Transition metals form metal hydrides
Hydrogen
Electron counting rules
clusters having about 4 electrons per vertex, as is the case for many boranes and carboranes. For such clusters, the structures are based on deltahedra
Polyhedral skeletal electron pair theory
Polyhedral_skeletal_electron_pair_theory
Chemical compound
MgH CaH SrH BaH Dihydrides BeH2 MgH2 CaH2 SrH2 BaH2 Group 13 hydrides Boranes BH3 BH B2H6 B2H2 B2H4 B4H10 B5H9 B5H11 B6H10 B6H12 B10H14 B18H22 Alanes
Tetraoxidane
Chemical compound
MgH CaH SrH BaH Dihydrides BeH2 MgH2 CaH2 SrH2 BaH2 Group 13 hydrides Boranes BH3 BH B2H6 B2H2 B2H4 B4H10 B5H9 B5H11 B6H10 B6H12 B10H14 B18H22 Alanes
Americium_trihydride
Fuels containing boranes for increased energy density
jet fuels containing additives in the form of hydro-boron compounds, or boranes. Zip fuels offer higher energy density than conventional fuels, helping
Zip_fuel
Chemical reaction
sodium borohydride, alkoxy borohydrides, alkoxy aluminium hydrides, and boranes. Although stoichiometric chiral reducing agents often afford products with
Enantioselective reduction of ketones
Enantioselective_reduction_of_ketones
Chemical compound
borirene products. Alternatively, photoinduced rearrangement of alkynyl-boranes provides another efficient pathway for borirene synthesis. Similar to other
Borirene
Oily organic chemical found in plants
been extensively examined. With borane-dimethylsulfide, two equivalents of α-pinene react to give (diisopinocampheyl)borane. Reaction with 9-BBN gives the
Pinene
High-strength glass, made of silica and boron trioxide
BCl3 BF BFO BF3 BI3 B2F4 B2Cl4 Acids B(NO3)3 B(OH)3 BPO4 B2(OH)4 BH3O Boranes BH3 B2H4 B2H6 BH3NH3 B4H10 B5H9 B5H11 B6H10 B6H12 B10H14 B18H22 [B12H12]2-
Borosilicate_glass
Hydrocarbon compound containing one or more C≡C bonds
across C≡C is general for silanes, boranes, and related hydrides. The hydroboration of alkynes gives vinylic boranes which oxidize to the corresponding
Alkyne
Chemical compound
doi:10.15227/orgsyn.053.0052. Michael W. Rathke; Alan A. Millard (1978). "Boranes in Functionalization of Olefins to Amines: 3-Pinanamine". Organic Syntheses
Diglyme
Chemical compound
derivative of catechol and a borane, having the formula C6H4O2BH. Traditionally catecholborane is produced by treating catechol with borane (BH3) in a cooled solution
Catecholborane
Chemical compound
Borane tert-butylamine is an amine borane complex derived from tert-butylamine and borane. It is a colorless solid. The compound is prepared by the reaction
Borane_tert-butylamine
Chemical compound
chemical suppliers. It can be synthesized by combining sodium cyanide and borane tetrahydrofuran. BH3·THF + NaCN → NaBH3CN + THF Since sodium cyanoborohydride
Sodium_cyanoborohydride
Chemical compound
chloride with the phosphine. The phosphine-borane H3BPMePh2 prepared by treating the phosphine with borane. Denniston, Michael L.; Martin, Donald R. (1977)
Methyldiphenylphosphine
Chemical naming suffix
hydrides of silicon are called silanes (SiH4); the hydrides of boron are boranes (B2H6). The final "-e" is dropped before a suffix that starts with a vowel
-ane
Chemical compound
Disiamylborane (bis(1,2-dimethylpropyl)borane) is an organoborane with the formula [((CH3)2CHCH(CH3))2BH]2 (abbreviation: Sia2BH). It is a colorless waxy
Disiamylborane
Healthcare company
1-methyl-3-nitro-1-nitrosoguanidine. 1966 – Aldrich's IPO 1972 – Subsidiary Aldrich-Boranes launched to manufacture hydroboration products 1975 – Merger of Sigma Chemical
Sigma-Aldrich
6-sided cyclic compound of oxygen and boron
temperature reaction of water and elemental boron or reaction of various boranes (B2H6 or B5H9) with O2. It is thermodynamically unstable with respect to
Boroxine
Chemical compound (C6H14)
MgH CaH SrH BaH Dihydrides BeH2 MgH2 CaH2 SrH2 BaH2 Group 13 hydrides Boranes BH3 BH B2H6 B2H2 B2H4 B4H10 B5H9 B5H11 B6H10 B6H12 B10H14 B18H22 Alanes
Hexane
Organic reaction
a hydrogen from the borane 3 to reform 4 and produce the alkane 6. Theoretical calculations suggest that O-H homolysis in a borane-water complex is endothermic
Barton–McCombie_deoxygenation
Molecule with a hydrogen bound to a more electropositive element or group
pub3. ISBN 978-3-527-30673-2. Brown, H. C. (1975). Organic Syntheses via Boranes. New York: John Wiley & Sons. ISBN 0-471-11280-1. Palladium hydride Züttel
Hydride
Flammable organic fuel (C4H10)
MgH CaH SrH BaH Dihydrides BeH2 MgH2 CaH2 SrH2 BaH2 Group 13 hydrides Boranes BH3 BH B2H6 B2H2 B2H4 B4H10 B5H9 B5H11 B6H10 B6H12 B10H14 B18H22 Alanes
Butane
Chemical compound
analogue of methyl violet. In organic synthesis, the complex diethylaniline·borane (DEANB) is used as a reducing agent. Diethylaniline and dimethylaniline
Diethylaniline
Chemical reaction
1981, Itsuno and coworkers first reported the use of chiral alkoxy-amine-borane complexes in reducing achiral ketones to chiral alcohols enantioselectively
Corey–Itsuno_reduction
Chemical compound
ISBN 9780470842898. Brown, H.C.; Zaidlewicz, M. (2001). Organic Syntheses Via Boranes, Vol. 2. Milwaukee, WI: Aldrich Chemical Co. ISBN 978-0-9708441-0-1. Ely
Pinacolborane
Product of a chemical reaction between elements of periodic groups 1–2 and groups 13–16
however the geometries Zintl ions can be well described by Wade’s rules of boranes. Wade’s rules offer an alternative model for the relationship between geometry
Zintl_phase
Cyclic chemical compound, (CH2)4O
basic than diethyl ether and forms stronger complexes with Li+, Mg2+, and boranes. It is a popular solvent for hydroboration reactions and for organometallic
Tetrahydrofuran
Aromatic alcohol
Furuta, Kyoji; Gao, Qing-Zhi; Yamamoto, Hisashi (1995). "Chiral (Acyloxy)borane Complex-Catalyzed Asymmetric Diels-Alder Reaction: (1R)-1,3
Benzyl_alcohol
Chemical bond theory
polarizable. typical hard acids: H+, alkali/alkaline earth metal cations, boranes, Zn2+ typical soft acids: Ag+, Mo(0), Ni(0), Pt2+ typical hard bases: ammonia
Lewis_acids_and_bases
Hydrocarbon compound with the formula C8H18
MgH CaH SrH BaH Dihydrides BeH2 MgH2 CaH2 SrH2 BaH2 Group 13 hydrides Boranes BH3 BH B2H6 B2H2 B2H4 B4H10 B5H9 B5H11 B6H10 B6H12 B10H14 B18H22 Alanes
Octane
Organic redox reaction
J. Jr.; Burkhardt, Elizabeth R.; Matos, Karl (2006). "Safe Handling of Boranes at Scale". Org. Process Res. Dev. 10 (6): 1292–1295. doi:10.1021/op068011l
Swern_oxidation
American chemist (1912–2004)
for producing sodium borohydride (NaBH4), which can be used to produce boranes, compounds of boron and hydrogen. His work led to the discovery of the
Herbert_C._Brown
American chemist (born 1928)
catalyst, with various boranes as the stoichiometric reductant. The Corey group first demonstrated the catalyst's synthesis using borane and the chiral amino
Elias_James_Corey
American inorganic chemist
polyhedral borane anions such as B12H122−. He was an inventor on some basic findings with the polyhedral borate anions. In addition to the polyhedral boranes, the
Earl_Muetterties
Chemical compound
Gas chromatography can be used to determine the amounts of the methyl boranes in a mixture. The order they elute are diborane, monomethyldiborane, trimethylborane
1,1-Dimethyldiborane
Hydrocarbon compound (H2C=CH2)
MgH CaH SrH BaH Dihydrides BeH2 MgH2 CaH2 SrH2 BaH2 Group 13 hydrides Boranes BH3 BH B2H6 B2H2 B2H4 B4H10 B5H9 B5H11 B6H10 B6H12 B10H14 B18H22 Alanes
Ethylene
Chemical compound
MgH CaH SrH BaH Dihydrides BeH2 MgH2 CaH2 SrH2 BaH2 Group 13 hydrides Boranes BH3 BH B2H6 B2H2 B2H4 B4H10 B5H9 B5H11 B6H10 B6H12 B10H14 B18H22 Alanes
Hydrogen_fluoride
Chemical reaction involving the removal of hydrogen
been developed. n PhSiH3 → [PhSiH]n + n H2 The dehydrogenation of amine-boranes is related reaction. This process once gained interests for its potential
Dehydrogenation
Topics referred to by the same term
where one vertex is missing. The descriptor nido- is typically applied boranes, derivatives such as carboranes, and deltahedral metal cluster compounds
Nido
Two-electron chemical bond where both electrons derive from the same atom
low ε inert solvent) is heterolytic rather than homolytic. The ammonia-borane adduct (H3N → BH3) is given as a classic example: the bond is weak, with
Coordinate_covalent_bond
Chemical compound
MgH CaH SrH BaH Dihydrides BeH2 MgH2 CaH2 SrH2 BaH2 Group 13 hydrides Boranes BH3 BH B2H6 B2H2 B2H4 B4H10 B5H9 B5H11 B6H10 B6H12 B10H14 B18H22 Alanes
1-Octene
Methods of storing hydrogen for later use
amine boranes, boron hydride ammoniates, hydrazine-borane complexes, and ammonium octahydrotriborates or tetrahydroborates. Of these, amine boranes (and
Hydrogen_storage
Chemical compound
"(S)-Tetrahydro-1-Methyl-3,3-Diphenyl-1H,3H-Pyrrolo-[1,2-c][1,3,2]Oxazaborole-Borane Complex". Organic Syntheses. 74: 50. 1997. doi:10.15227/orgsyn.074.0050
1-Indanone
Chemical compound
doi:10.1021/ja00895a046. Heřmánek, S.; Plešek, J. (1970). "Chemistry of boranes. XXI. Resolution of iso-octadecaborane to optical enantiomers". Collection
Octadecaborane
Pharmaceuticals to target cancerous cells
Miller, N. E.; Muetterties, E. L. (1964). "Chemistry of Boranes. XX. Syntheses of Polyhedral Boranes". Inorganic Chemistry. 3 (10): 1456–1463. doi:10.1021/ic50020a026
Boron neutron capture therapeutics
Boron_neutron_capture_therapeutics
Hydrocarbon compound (CH4) in natural gas
MgH CaH SrH BaH Dihydrides BeH2 MgH2 CaH2 SrH2 BaH2 Group 13 hydrides Boranes BH3 BH B2H6 B2H2 B2H4 B4H10 B5H9 B5H11 B6H10 B6H12 B10H14 B18H22 Alanes
Methane
Class of chemical compounds
adducts formed from phosphines and borane are useful reagents. These phosphine-boranes are air-stable, but the borane protecting group can be removed by
Organophosphine
Product of direct addition of two or more distinct molecules
bases. A good example is the formation of adducts between the Lewis acid borane and the oxygen atom in the Lewis bases, tetrahydrofuran (THF): BH3·O(CH2)4
Adduct
Organic compounds made of alkyl/aryl groups bound to oxygen (R–O–R')
For instance, diethyl ether forms a complex with boron trifluoride, i.e. borane diethyl etherate (BF3·O(CH2CH3)2). Ethers also coordinate to the Mg center
Ether
Weak acid with formula H3BO3
BCl3 BF BFO BF3 BI3 B2F4 B2Cl4 Acids B(NO3)3 B(OH)3 BPO4 B2(OH)4 BH3O Boranes BH3 B2H4 B2H6 BH3NH3 B4H10 B5H9 B5H11 B6H10 B6H12 B10H14 B18H22 [B12H12]2-
Boric_acid
Chemical compound
Borane(1), boron monohydride, hydridoboron or borylene is the molecule with the formula BH. It exists as a gas but rapidly degrades when condensed. By
Boron_monohydride
Chemical compound
MgH CaH SrH BaH Dihydrides BeH2 MgH2 CaH2 SrH2 BaH2 Group 13 hydrides Boranes BH3 BH B2H6 B2H2 B2H4 B4H10 B5H9 B5H11 B6H10 B6H12 B10H14 B18H22 Alanes
Hydrogen_polyoxide
Chemical compound
MgH CaH SrH BaH Dihydrides BeH2 MgH2 CaH2 SrH2 BaH2 Group 13 hydrides Boranes BH3 BH B2H6 B2H2 B2H4 B4H10 B5H9 B5H11 B6H10 B6H12 B10H14 B18H22 Alanes
1-Pentyne
Possible alternative biochemicals used by life forms
catalyse new carbon–silicon bonds between hydrosilanes and diazo compounds. Boranes are dangerously explosive in Earth's atmosphere, but would be more stable
Hypothetical types of biochemistry
Hypothetical_types_of_biochemistry
Chemical compound
inorganic compound with the chemical formula B10H14. It is classified as a borane and more specifically a boron hydride cluster. This white crystalline compound
Decaborane
Chemical compound
MgH CaH SrH BaH Dihydrides BeH2 MgH2 CaH2 SrH2 BaH2 Group 13 hydrides Boranes BH3 BH B2H6 B2H2 B2H4 B4H10 B5H9 B5H11 B6H10 B6H12 B10H14 B18H22 Alanes
Cyclohexasilane
Physical and chemical properties of pure water
MgH CaH SrH BaH Dihydrides BeH2 MgH2 CaH2 SrH2 BaH2 Group 13 hydrides Boranes BH3 BH B2H6 B2H2 B2H4 B4H10 B5H9 B5H11 B6H10 B6H12 B10H14 B18H22 Alanes
Properties_of_water
Extremely hard ceramic compound
BCl3 BF BFO BF3 BI3 B2F4 B2Cl4 Acids B(NO3)3 B(OH)3 BPO4 B2(OH)4 BH3O Boranes BH3 B2H4 B2H6 BH3NH3 B4H10 B5H9 B5H11 B6H10 B6H12 B10H14 B18H22 [B12H12]2-
Boron_carbide
Asymmetric catalyst derived from proline
condensed with a phenylboronic acid, or with borane (as shown below). The CBS catalyst then complexes in situ with borane to give the active catalyst. The general
CBS_catalyst
Organosulfur compound (CHSO2OH)
pharmaceutical preparations. Methanesulfonic acid can be used in the generation of borane (BH3) by reacting methanesulfonic acid with NaBH4 in an aprotic solvent
Methanesulfonic_acid
Heterocyclic aromatic organic compound
a sulfation agent used to convert alcohols to sulfate esters. Pyridine-borane (C5H5NBH3, melting point 10–11 °C) is a mild reducing agent. Transition
Pyridine
Polymer whose backbone does not contain carbon
S. Weller (2015). "The Catalytic Dehydrocoupling of Amine–Boranes and Phosphine–Boranes". Synthesis and Application of Organoboron Compounds. Topics
Inorganic_polymer
BORANES
BORANES
BORANES
BORANES
Girl/Female
Hindu, Indian, Kannada, Malayalam, Marathi, Tamil, Telugu
Prosperous
Girl/Female
German
Noble; Kind
Girl/Female
Indian, Marathi
Name of Goddess
Boy/Male
Biblical
Earthy; red; bloody.
Surname or Lastname
English
English : habitational name from a pair of villages in Northumbria named with Old English bēan ‘beans’ (a collective singular) or beonet ‘bent grass’ + tūn ‘enclosure’, ‘settlement’. The name is now most frequent in the West Midlands, however, so it may be that a place of the same name in that area should be sought as its origin.
Boy/Male
Indian, Sanskrit
The First Creator; Lord Brahma
Boy/Male
English Latin
Principal one; first. The rock musician Prince.
Boy/Male
Latin
Curly-haired.
Boy/Male
American, Anglo, British, English
From the Stony Hollow
Girl/Female
Tamil
Dee means Durga her means Shiv Shivas strength
BORANES
BORANES
BORANES
BORANES
BORANES