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Chemical compound
Trimethylborane (TMB) is a toxic, pyrophoric gas with the formula B(CH3)3 (which can also be written as Me3B, with Me representing methyl). As a liquid
Trimethylborane
Product of direct addition of two or more distinct molecules
non-aqueous solvents to form adducts have been examined in the ECW model. Trimethylborane, trimethyltin chloride and bis(hexafluoroacetylacetonato)copper(II)
Adduct
Chemical bond theory
is a Lewis base, because it can donate its lone pair of electrons. Trimethylborane [(CH3)3B or Me3B] is a Lewis acid as it is capable of accepting a lone
Lewis_acids_and_bases
Chemical compound
methods to form methyldiboranes include heating trimethylborane with hydrogen. Alternatively trimethylborane reacts with borohydride salts with in the presence
1,1-Dimethyldiborane
Chemical compound
1,2-dimethyldiborane, trimethyldiborane, tetramethyldiborane, and trimethylborane (which is not a dimer). At room temperature the substance is at equilibrium
Methyldiborane
Chemical compound
including methyldiborane, trimethyldiborane, tetramethyldiborane. Trimethylborane exists as a monomer. Methylboranes were first prepared by H. I. Schlesinger
1,2-Dimethyldiborane
Salt formed by a Lewis acid-base reaction where the acid atom loses formal charge
example, the ate complex of a boron compound is called a borate. Thus trimethylborane and methyllithium react to form the ate compound Li+B(CH3)−4, lithium
Ate_complex
Chemical compound
Lewis acids. Because of its compact structure, quinuclidine binds to trimethylborane more tightly than does triethylamine. Quinuclidine is structurally
Quinuclidine
Chemical compound
Schlesinger and A. O. Walker in the 1930s. Trimethylborane is formed by the reaction of diborane and trimethylborane. This reaction produces four different
Trimethyldiborane
Chemical theory about acids and bases
comparison. Borderline cases are also identified: borderline acids are trimethylborane, sulfur dioxide and ferrous Fe2+, cobalt Co2+ caesium Cs+ and lead
HSAB_theory
Class of chemical substituents
resulting in an increased Lewis acidity of boron trifluoride relative to trimethylborane. This effect of EWG has been quantified in many of ways. The Tolman
Electron-withdrawing_group
Chemical compound
monomethyldiborane, trimethyldiborane, 1,2-dimethylborane, 1,1-dimethylborane and trimethylborane. At room temperature the substance is at equilibrium between these
Tetramethyldiborane
Organic compound with at least one hydroxyl (–OH) group
alcohol is deoxygenated to an alkane with tributyltin hydride or a trimethylborane-water complex in a radical substitution reaction. Meanwhile, the oxygen
Alcohol_(chemistry)
Pyrophoric liquid
Related compounds Tetraethyllead Diborane Sodium tetraethylborate Trimethylborane Triethylaluminium Triethylgallium Triethylindium Except where otherwise
Triethylborane
Topics referred to by the same term
a village in County Tipperary, Ireland Tour du Mont Blanc, a walk Trimethylborane Tumor mutational burden 3,3',5,5'-Tetramethylbenzidine, a chemical
TMB
Exchange of ligands and metalloid centers
monomethyldiborane rapidly converts at room temperature to diborane and trimethylborane: 6 MeB2H5 → 5 B2H6 + 2 Me3B Useful redistribution reactions are found
Redistribution_(chemistry)
Chemical compound
release methane Related compounds Related compounds Triethylgallium Trimethylborane Trimethylaluminium Trimethylindium Except where otherwise noted, data
Trimethylgallium
Organic reaction
anhydrous conditions) the borane itself. Typically the reagents are trimethylborane or triethylborane contaminated with small amounts of water. The catalytic
Barton–McCombie_deoxygenation
Chemical compound
4 °F; 256.1 K) Related compounds Related compounds Triethylaluminium Trimethylborane Trimethylgallium Trimethylindium Except where otherwise noted, data
Trimethylaluminium
Solar-cell architecture
layers. Examples of dopant gases include phosphine (PH3) for n-type and trimethylborane (B(CH3)3) or diborane (B2H6) for p-type. Due to its defective nature
Heterojunction_solar_cell
Chemical compound
InCl + CpLi → CpIn + LiCl InCp reacts with BF3, BCl3, BBr3, BI3 and trimethylborane B(CH3)3 to form adducts, e.g.: CpIn + BF3 → CpIn·BF3 In these adducts
Cyclopentadienylindium(I)
373-80-8 Chlorotrifluorogermane GeClF3 −20.3 −66.2 165.5 14188-40-0 Trimethylborane (CH3)3B −20.2 −159.93 56 593-90-8 Dimethylsilane (CH3)2SiH2 −20 −150
List_of_gases
Chemical compound
P405, P422, P501 Related compounds Related compounds Triethylindium Trimethylborane Trimethylaluminium Trimethylgallium Except where otherwise noted, data
Trimethylindium
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