Carbon–hydrogen bond activation

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Carbon–hydrogen bond activation or C–H activation is a reaction that cleaves a carbon–hydrogen bond.[1][2][3][4][5][6][7][8][9][10][11] The term is often restricted to reactions that involve organometallic complexes and transformations that proceed by coordination of a hydrocarbon to the inner-sphere of a metal, either via an intermediate “alkane or arene complex” or as a transition state leading to a "M−C" intermediate.[12][13][14] Important to this definition is the requirement that during the C–H cleavage event, the hydrocarbyl species remains associated in the inner-sphere and under the influence of “M”.

Theoretical studies as well as experimental investigations indicate that C–H bonds, which are traditionally considered unreactive, can be cleaved by coordination. Much research effort has been devoted to the design and synthesis of new reagents and catalysts that can affect C–H activation. A significant driver for this type of research is the prospect that C–H activation could enable the conversion of cheap and abundant alkanes into valuable functionalized organic compounds and the efficient structural editing of already complex molecules.[15]

Historic overview[edit]

The first C–H activation reaction is often attributed to Otto Dimroth, who in 1902, reported that benzene reacted with mercury(II) acetate (See: organomercury), but some scholars[who?] do not view this reaction as being true C–H activation. As observed by Goldman & Goldberg[12] C–H activation resembles aspects of H−H activation: both can be achieved by electrophilic or oxidative addition.

From a modern organometallic perspective, the first true C–H activation reaction was reported by Joseph Chatt in 1965[16] with insertion of a ruthenium atom ligated to dmpe in the C–H bond of naphthalene. In 1969, A.E. Shilov reported that potassium tetrachloroplatinate induced isotope scrambling between methane and heavy water. The pathway was proposed to involve binding of methane to Pt(II). In 1972, the Shilov group was able to produce methanol and methyl chloride in a similar reaction involving a stoichiometric amount of potassium tetrachloroplatinate, catalytic potassium hexachloroplatinate, methane and water. Due to the fact that Shilov worked and published in the Soviet Union during the Cold War era, his work was largely ignored by Western scientists. This so-called Shilov system is today one of the few true catalytic systems for alkane functionalizations.[12]

On the other side of the spectrum, oxidative addition, M. L. H. Green in 1970 reported on the photochemical insertion of tungsten (as a Cp2WH2 complex) in a benzene C–H bond[17] and George M. Whitesides in 1979 was the first to carry out an intramolecular aliphatic C–H activation[18]

The next breakthrough was reported independently by two research groups in 1982. R. G. Bergman reported the first transition metal-mediated intermolecular C–H activation of unactivated and completely saturated hydrocarbons by oxidative addition. Using a photochemical approach, photolysis of Cp*Ir(PMe3)H2, where Cp* is a pentamethylcyclopentadienyl ligand, led to the coordinatively unsaturated species Cp*Ir(PMe3) which reacted via oxidative addition with cyclohexane and neopentane to form the corresponding hydridoalkyl complexes, Cp*Ir(PMe3)HR, where R = cyclohexyl and neopentyl, respectively.[19] W.A.G. Graham found that the same hydrocarbons react with Cp*Ir(CO)2 upon irradiation to afford the related alkylhydrido complexes Cp*Ir(CO)HR, where R = cyclohexyl and neopentyl, respectively.[20] In the latter example, the reaction is presumed to proceed via the oxidative addition of alkane to a 16-electron iridium(I) intermediate, Cp*Ir(CO), formed by irradiation of Cp*Ir(CO)2.

C–H activation by Bergman et al. (left) and Graham et al.

J.F. Hartwig reported a highly regioselective arene and alkane borylation catalyzed by a rhodium complex in 1999 and 2000. In the case of alkanes, exclusive terminal functionalization was observed.[21]

Hartwig Borylation 2000

Scope[edit]

The selective activation and functionalization of alkane C–H bonds was reported using a tungsten complex outfitted with pentamethylcyclopentadienyl, nitrosyl, allyl and neopentyl ligands, Cp*W(NO)(η3-allyl)(CH2CMe3).[22]

C–H activation of pentane, as seen in Ledgzdins et al., J. Am. Chem. Soc. 2007, 129, 5372–3.

In one example involving this system, the alkane pentane is selectively converted to the halocarbon 1-iodopentane. This transformation was achieved via the thermoloysis of Cp*W(NO)(η3-allyl)(CH2CMe3) in pentane at room temperature, resulting in elimination of neopentane by a pseudo-first-order process, generating an undetectable electronically and sterically unsaturated 16-electron intermediate that is coordinated by an η2-butadiene ligand. Subsequent intermolecular activation of a pentane solvent molecule then yields an 18-electron complex possessing an n-pentyl ligand. In a separate step, reaction with iodine at −60 °C liberates 1-iodopentane from the complex.

Arene C–H bonds can also be activated by metal complexes despite being fairly unreactive. One manifestation is found in the Murai olefin coupling.[23] In one reaction a ruthenium complex reacts with N,N-dimethylbenzylamine in a cyclometalation also involving C–H activation:[24]

Cyclometallation with a Substituted Benzylamine Chetcuti 2007

An alkene C–H bond activation with a rhodium catalyst is demonstrated in the synthesis of this strained bicyclic enamine:[25]

C–H bond activation Yotphan 2008

It has also been found by Prof. Roy A. Periana that reactions of late transition metal salts and complexes such of Pt, Pd, Au, and Hg react with methane (CH4), the major component of natural gas, in H2SO4 to yield methyl bisulfate in very low to high yields at very high selectivity.[26][27]

C–H Bond Activation Periana 1998

Reaction conditions[edit]

Most C–H bond activations proceed under rather harsh reaction conditions (high T, strongly acidic or basic conditions, strong oxidant), significantly lowering their attractiveness. However, more and more quite mild reactions have been developed, significantly expanding the scope of these exciting transformations.[28] Organocatalysis has recently been used as an important approach which has the advantage of being metal-free and cost-effective.[29]

Recently, Hashiguchi et al. discovered that M-hydroxides and aquo complexes can be utilized to carry out C–H activation on water soluble arenes in strongly basic conditions.[30] Specifically, they demonstrated a Ru precatalyst with an NNN-pincer ligand, 2,6-diimidizoylpyridine, (IPI), when dissolved in aqueous base generated the associated mixed hydroxide aquo complex, Ru(IPI(OH)n(H2O)m. This complex was then shown to catalyze H/D exchange between the arenes and aqueous base with increasing [KOH] upon initial reduction of Ru(III) to the Ru(II) complex. This was the first demonstrated report of base accelerated CH activation.

Base CH Activation 2010

Metal centers that contain a large number of electrons and are stable at high oxidation states, such as later transition metals, promote oxidative addition and are therefore ideal candidates to act as catalysts for C–H activation. Furthermore d8 metals that can undergo a square planar arrangement, are potential candidates catalysts as they have two vacant coordination sites and thus steric hindrance is limited.

See also[edit]

References[edit]

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  25. ^ The Stereoselective Formation of Bicyclic Enamines with Bridgehead Unsaturation via Tandem C–H Bond Activation/Alkenylation/ Electrocyclization Sirilata Yotphan, Robert G. Bergman, and Jonathan A. Ellman J. Am. Chem. Soc. 2008, 130, 2452–2453 doi:10.1021/ja710981b
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