Organoborane or organoboron compounds are chemical compounds of boron and carbon that are organic derivatives of BH3, for example trialkyl boranes. Organoboron chemistry or organoborane chemistry is the chemistry of these compounds. Organoboron compounds are important reagents in organic chemistry enabling many chemical transformations, the most important one called hydroboration.
Properties of the B-C bondEdit
The C-B bond has low polarity (the difference in electronegativity 2.55 for carbon and 2.04 for boron), and therefore alkyl boron compounds are in general stable though easily oxidized.
In part because its lower electronegativity, boron often forms electron-deficient compounds, such as the triorganoboranes. Vinyl groups and aryl groups donate electrons and make boron less electrophilic and the C-B bond gains some double bond character. Like the parent borane, diborane, organoboranes are classified in organic chemistry as strong electrophiles because boron is unable to gain a full octet of electrons. Unlike diborane however, most organoboranes do not form dimers.
From Grignard reagentsEdit
Simple organoboranes such as triethylborane or tris(pentafluorophenyl)boron can be prepared from trifluoroborane (as the ether complex) and the ethyl or pentafluorophenyl Grignard reagent. The borates (R4B− are generated via addition of R−-equivalents (RMgX, RLi, etc.) to R3B).
Alkenes insert into B-H bonds of boranes in a process called hydroboration. The process involves anti-Markovnikov addition. Hydroboration of alkenes or alkynes with borane (BH3) or borane equivalents leads to the conversion of only 33% of the starting olefin to product after oxidation or protonolysis—the remaining olefin is incorporated into boron-containing byproducts. One organoboron reagent that is often employed in synthesis is 9-BBN. Hydroborations take place stereospecifically in a syn mode, that is on the same face of the alkene. In this concerted reaction the transition state is represented as a square with the corners occupied by carbon, carbon, hydrogen and boron with maximum overlap between the two olefin p-orbitals and the empty boron orbital.
Metal-catalyzed C-H Borylation reactions are transition metal catalyzed organic reactions that produce an organoboron compound through functionalization of aliphatic and aromatic C-H bonds. A common reagent in this type of reaction is bis(pinacolato)diboron.
Boron–carbon bonds are polarized toward carbon. Thus, the carbon attached to boron is nucleophilic. This property is harnessed to transfer one of the R groups to an electrophilic center either inter- or (more often) intramolecularly.In the latter case, the nucleophilic R group is able to undergo 1,2-migration towards an electrophilic carbon attached to boron. The resulting reorganized borane can then be oxidized or subjected to protonolysis to afford organic products:
In organic synthesis the hydroboration reaction is taken further to generate other functional groups in the place of the boron group. The hydroboration-oxidation reaction offers a route to alcohols by oxidation of the borane with hydrogen peroxide or to the carbonyl group with the stronger oxidizing agent chromium oxide.
Carbon monoxide is found to react with trialkylboranes. What follows is a 1,2-rearrangement whereby an alkyl substituent migrates from boron to the carbon of the carbonyl group. Homologated primary alcohols result from the treatment of organoboranes with carbon monoxide and a hydride.
Asymmetric allylboration demonstrates another useful application of organoboranes in carbon–carbon bond formation. In this example from Nicolaou's synthesis of the epothilones, asymmetric allylboration (using an allylborane derived from chiral alpha-pinene) is used in conjunction with TBS protection and ozonolysis. Overall, this provides a two-carbon homologation sequence that delivers the required acetogenin sequence.
As reducing agentEdit
Borane hydrides such as 9-BBN and L-selectride (lithium tri-sec-butylborohydride) are reducing agents. An example of an asymmetric catalyst for carbonyl reductions is the CBS catalyst. This catalyst is also based on boron, the purpose of which is coordination to the carbonyl oxygen atom.
Trialkylboranes, BR3, can be oxidized to the corresponding borates, B(OR)3. One method for the determination of the amount of C-B bonds in a compound is by oxidation of R3B with trimethylamine oxide (Me3NO) to B(OR)3. The trimethylamine (Me3N) formed can then be titrated.
Boronic acids RB(OH)2 react with potassium bifluoride K[HF2] to form trifluoroborate salts K[RBF3] which are precursors to nucleophilic alkyl and aryl boron difluorides, ArBF2. The salts are more stable than the boronic acids themselves and used for instance in alkylation of certain aldehydes:[note 1]
Organoboron compounds also lend themselves to transmetalation reactions, especially with organopalladium compounds. This reaction type is exemplified in the Suzuki reaction, which involves coupling of aryl- or vinyl-boronic acid with an aryl- or vinyl-halide catalyzed by a palladium(0) complex,
This reaction is an important method for making carbon-carbon bonds.
Classes of organoboron compoundsEdit
Organoboranes and hydridesEdit
Among the most studied classes of organoboron compounds have the formula BRnH3−n. As discussed above, these compounds are used as catalysts, reagents, and synthetic intermediates. The trialkyl and triaryl derivatives feature trigonal planar boron center that is typically only weakly Lewis acidic. Except for a few very bulky derivatives, the hydrides (BRnH3−n for n = 1 or 2) exist as dimers, reminiscent of the structure of diborane itself. Trisubstituted derivatives, e.g. triethylboron are monomers.
Borinic and boronic acids and esters (BRn(OR)3-n)Edit
Compounds of the type BRn(OR)3-n are called borinic esters (n = 2), boronic esters (n = 1), and borates (n = 0). Boronic acids are used in Suzuki reaction. Trimethyl borate, which is debatably not an organoboron compound, is an intermediate in the production of sodium borohydride.
Boron is renowned for forming cluster compounds, e.g. dodecaborate [B12H12]2-. Many organic derivatives are known for such clusters. One example is [B12(CH3)12]2- and its radical derivative [B12(CH3)12]-. Related cluster compounds with carbon vertices are called carboranes are. The best known is orthocarborane, with the formula C2B10H12. Although they have few commercial applications, carboranes have attracted much attention because they are so structurally unusual. Anionic derivatives, dicarbollides, e.g., [C2B9H11]2− are ligands that behave like cyclopentadienide.
Bora-substituted aromatic compoundsEdit
In borabenzene, one CH center in benzene is replaced by boron. These compounds are invariably isolated as adducts, e.g., C5H5B-pyridine. The cyclic compound borole, a structural analog of pyrrole, has not been isolated, but substituted derivatives known as boroles are known. The cyclic compound borepin is aromatic.
Boryl anions have the formula R2B−. Nucleophilic anionic boryl compounds have long been elusive but a 2006 study described a boryllithium compound, which reacts as a nucleophile: Organometallic compounds with metal to boron bonds, (i.e., M–BR2), are known as boryl complexes. Related ligands are borylenes (M–B(R)–M).
The absence of lithium boryl compounds is notable because in other period 2 elements lithium salts are common e.g. lithium fluoride, lithium hydroxide lithium amide and methyllithium. The gap highlights the very low electronegativity of boron. Reaction of base with a borohydride R2BH does not result in deprotonation to the boryl anion R2B− but to formation of the boryl anion R2B−H(base)+. This reaction product has a complete octet. Instead the boryl compound is prepared by reductive heterolysis of a boron-bromide bond by lithium metal. The new boryl lithium compound is very similar to and isoelectronic with N-heterocyclic carbenes. It is designed to benefit from aromatic stabilization (6-electron system counting the nitrogen lone pairs and an empty boron p-orbital, see structure A) and from kinetic stabilization from the bulky 2,6-diisopropylphenyl groups. X-ray diffraction confirms sp2 hybridization at boron and its nucleophilic addition reaction with benzaldehyde gives further proof of the proposed structure.
Alkylideneboranes of the type RB=CRR with a boron – carbon double bond are rarely encountered. An example is borabenzene. The parent compound is HB=CH2 which can be detected at low temperatures. A fairly stable derivative is CH3B=C(SiMe3)2 but is prone to cyclodimerisation.
NHC adducts of boronEdit
NHCs and boranes form stable NHC borane adducts. Triethylborane adducts can be synthesised directly from the imidazolium salt and lithium triethylborohydride. Members of this compound class are investigated for use as reagent or catalyst.
Chemical compounds with boron to boron double bonds are rare. In 2007 the first neutral diborene (RHB=BHR) was presented by Gregory Robinson of the University of Georgia. Each boron atom has a proton attached to it and each boron atom is coordinated to a NHC carbene. The parent structure with the additional carbene ligands is diborane(2).
A reported diboryne is based on similar chemistry.
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