Persistent carbene

In 1957, Ronald Breslow proposed that a relatively stable nucleophilic carbene, a thiazol-2-ylidene derivative of vitamin B₁ (thiamine), was the catalyst involved in the benzoin condensation that yields furoin from furfural.[2] [3] In this cycle, the vitamin's thiazolium ring exchanges a hydrogen atom (attached to carbon 2 of the ring) for a furfural residue. In deuterated water, the C2-proton was found to rapidly exchange for a deuteron in a statistical equilibrium.[4]

Deuterium exchange of the C2-proton of thiazolium salt.

This exchange was proposed to proceed via intermediacy of a thiazol-2-ylidene. In 2012 the isolation of the so-called Breslow intermediate was reported.[5][6]

In 1960, Hans-Werner Wanzlick and coworkers conjectured that carbenes derived from dihydroimidazol-2-ylidene were produced by vacuum pyrolysis of the corresponding 2-trichloromethyl dihydroimidazole compounds with the loss of chloroform.[7][8] [9] They conjectured that the carbene existed in equilibrium with its dimer, a tetraaminoethylene derivative, the so-called Wanzlick equilibrium. This conjecture was challenged by Lemal and coworkers in 1964, who presented evidence that the dimer did not dissociate;[10] and by Winberg in 1965.[11] However, subsequent experiments by Denk, Herrmann and others have confirmed this equilibrium, albeit in specific circumstances.[12][13]

In 1970, Wanzlick's group generated imidazol-2-ylidene carbenes by the deprotonation of an imidazolium salt.[14] Wanzlick as well as Roald Hoffmann,[9][15] proposed that these imidazole-based carbenes should be more stable than their 4,5-dihydro analogues, due to Hückel-type aromaticity. Wanzlick did not however isolate imidazol-2-ylidenes, but instead their coordination compounds with mercury and isothiocyanate:

Preparation and trapping of an imidazol-2-ylidene.[14]

In 1988, Guy Bertrand and others isolated a phosphinocarbene. These species can be represented as either a λ³-phosphinocarbene or λ⁵-phosphaacetylene:[16][17]

Alkyne and carbene resonances structures of Bertrand's carbene

These compounds were called "push-pull carbenes" in reference to the contrasting electron affinities of the phosphorus and silicon atoms. They exhibit both carbenic and alkynic reactivity. An X-ray structure of this molecule has not been obtained and at the time of publication some doubt remained as to their exact carbenic nature.

In 1991, Arduengo and coworkers crystallized a diaminocarbene by deprotonation of an imidazolium cation:[18]

Preparation of N,N′-diadamantyl-imidazol-2-ylidene

This carbene, the forerunner of a large family of carbenes with the imidazol-2-ylidene core, is indefinitely stable at room temperature in the absence of oxygen and moisture. It melts at 240–241 °C without decomposition. The ¹³C NMR spectrum shows a signal at 211 ppm for the carbenic atom.[19] The X-ray structure revealed longer N–C bond lengths in the ring of the carbene than in the parent imidazolium compound, indicating that there was very little double bond character to these bonds.[20]

The first air-stable ylidic carbene, a chlorinated member of the imidazol-2-ylidene family, was obtained in 1997.[21]

In 2000, Bertrand obtained additional carbenes of the phosphanyl type, including (phosphanyl)(trifluoromethyl)carbene, stable in solution at -30 °C[22] and a moderately stable (amino)(aryl)carbene with only one heteroatom adjacent to the carbenic atom.[23][24]

MO's of the allylic system.

In the modern understanding, the superficially unoccupied p-orbital on a (meta)stable carbene is not, in fact, fully empty. Instead, the carbene Lewis structures are in resonance with dative bonds toward adjacent lone-pair or pi-bond orbitals.

1,3,4,5-tetramethyl­imidazol-2-ylidene, a relatively unhindered carbene. (3D)

Early workers attributed the stability of Arduengo carbenes to the bulky N-adamantyl substituents, which prevent the carbene from dimerising. But replacement of the N-adamantyl groups with methyl groups also affords 1,3,4,5-tetramethylimidazol-2‑ylidene (Me₄ImC:), a thermodynamically stable unhindered NHC.[25]

Bis(diisopropylamino) carbene, the first acyclic stable carbene.

In 1995, Arduengo's group obtained a carbene derivative of dihydroimidazol-2-ylidene, proving that stability did not arise from the aromaticity of the conjugated imidazole backbone.[26] The following year, the first acyclic persistent carbene demonstrated that stability did not even require a cyclic backbone.[27] Unhindered derivatives of the hydrogenated[28][29] and acyclic[29][30][31] carbenes dimerized, suggesting that Me₄ImC: might be exceptional, rather than paradigmatic. But the behavior of the acyclic carbenes offered a tantalizing clue to the stabilization mechanism.

Unlike the cyclic derivatives, acyclic carbenes are flexible and bonds to the carbenic atom admit rotation. But bond rotation in the compound appeared hindered, suggesting a double bond character that would place the positive charge on adjacent nitrogen atoms while preserving the octet rule.[27] Indeed, most persistent carbenes are stabilized by two flanking nitrogen centers. The outliers include an aminothiocarbene and an aminooxycarbene, which use other heteroatoms,[32][33] and room-temperature-stable bis(diisopropylamino)cyclopropenylidene, in which the carbene atom is connected to two carbon atoms in a three-member, aromatic, cyclopropenylidene ring.[34]

Stable carbenes with oxygen or sulfur atoms bound to the carbenic atom (3D)

The first stable carbenes to be isolated were based on an imidazole ring, with the hydrogen in carbon 2 of the ring (between the two nitrogen atoms) removed, and other hydrogens replaced by various groups. These imidazol-2-ylidenes are still the most stable and the most well studied and understood family of persistent carbenes.

A considerable range of imidazol-2-ylidenes have been synthesised, including those in which the 1,3-positions have been functionalised with alkyl, aryl,[25] alkyloxy, alkylamino, alkylphosphino[35] and even chiral substituents:[35]

Stable imidazol-2-ylidenes

1,3-Dimesityl-4,5-dichloroimidazol-2-ylidene, the first air-stable carbene.
(View the 3D structure with external viewer.)

In particular, substitution of two chlorine atoms for the two hydrogens at ring positions 4 and 5 yielded the first air-stable carbene.[21] Its extra stability probably results from the electron-withdrawing effect of the chlorine substituents, which reduce the electron density on the carbon atom bearing the lone pair, via induction through the sigma-backbone.

Molecules containing two and even three imidazol-2-ylidene groups have also been synthesised.[36][37]

Imidazole-based carbenes are thermodynamically stable and generally have diagnostic ¹³C NMR chemical shift values between 210 and 230 ppm for the carbenic carbon. Typically, X-ray structures of these molecules show N–C–N bond angles of 101–102°.

Depending on the arrangement of the three nitrogen atoms in triazol-5-ylidene, there are two possible isomers, namely 1,2,3-triazol-5-ylidenes and 1,2,4-triazol-5-ylidenes.

Triazol-5-ylidene isomers.

The triazol-5-ylidenes based on the 1,2,4-triazole ring are pictured below and were first prepared by Enders and coworkers[38] by vacuum pyrolysis through loss of methanol from 2-methoxytriazoles. Only a limited range of these molecules have been reported, with the triphenyl substituted molecule being commercially available.

Examples of 1,2,4-triazol-5-ylidenes.

Triazole-based carbenes are thermodynamically stable and have diagnostic ¹³C NMR chemical shift values between 210 and 220 ppm for the carbenic carbon. The X-ray structure of the triphenyl substituted carbene above shows an N–C–N bond angle of around 101°. The 5-methoxytriazole precursor to this carbene was made by the treatment of a triazolium salt with sodium methoxide, which attacks as a nucleophile.[38] This may indicate that these carbenes are less aromatic than imidazol-2-ylidenes, as the imidazolium precursors do not react with nucleophiles due to the resultant loss of aromaticity.

The two families above can be seen as special cases of a broader class of compounds which have a carbenic atom bridging two nitrogen atoms. A range of such diaminocarbenes have been prepared principally by Roger Alder's research group. In some of these compounds, the N–C–N unit is a member of a five- or six-membered non-aromatic ring,[26][28][39] including a bicyclic example. In other examples, the adjacent nitrogens are connected only through the carbenic atom, and may or may not be part of separate rings.[27][30][31]

Synthesised cyclic and acyclic diaminocarbenes

Unlike the aromatic imidazol-2-ylidenes or triazol-5-ylidenes, these carbenes appear not to be thermodynamically stable, as shown by the dimerisation of some unhindered cyclic and acyclic examples.[28][30] Studies[29] suggest that these carbenes dimerise via acid catalysed dimerisation (as in the Wanzlick equilibrium).

Diaminocarbenes have diagnostic ¹³C NMR chemical shift values between 230 and 270 ppm for the carbenic atom. The X-ray structure of dihydroimidazole-2-ylidene shows a N–C–N bond angle of about 106°, whilst the angle of the acyclic carbene is 121°, both greater than those seen for imidazol-2-ylidenes.

There exist several variants of the stable carbenes above where one of the nitrogen atoms adjacent to the carbene center (the α nitrogens) has been replaced by an alternative heteroatom, such as oxygen, sulfur, or phosphorus.[16][17][32][33]

Synthesised heteroamino carbenes (top and bottom right) and Bertrand's carbenes (bottom left)

In particular, the formal substitution of sulfur for one of the nitrogens in imidazole would yield the aromatic heterocyclic compound thiazole. A thiazole based carbene (analogous to the carbene postulated by Breslow)[40] has been prepared and characterised by X-ray crystallography.[32] Other non-aromatic aminocarbenes with O, S and P atoms adjacent (i.e. alpha) to the carbene centre have been prepared, for example, thio- and oxyiminium based carbenes have been characterised by X-ray crystallography.[33]

Since oxygen and sulfur are divalent, steric protection of the carbenic centre is limited especially when the N–C–X unit is part of a ring. These acyclic carbenes have diagnostic ¹³C NMR chemical shift values between 250 and 300 ppm for the carbenic carbon, further downfield than any other types of stable carbene. X-ray structures have shown N–C–X bond angles of around 104° and 109° respectively.

Carbenes that formally derive from imidazole-2-ylidenes by substitution of sulfur, oxygen, or other chalcogens for both α-nitrogens are expected to be unstable, as they have the potential to dissociate into an alkyne (R¹C≡CR²) and a carbon dichalcogenide (X¹=C=X²).[41][42]

The reaction of carbon disulfide (CS₂) with electron deficient acetylene derivatives is proposed to give transient 1,3-dithiolium carbenes (i.e. where X¹ = X² = S), which then dimerise to give derivatives of tetrathiafulvene. Thus it is possible that the reverse of this process might be occurring in similar carbenes.[41][42]

In Bertrand's persistent carbenes, the unsaturated carbon is bonded to a phosphorus and a silicon.[43] However, these compounds seem to exhibit some alkynic properties, and when published the exact carbenic nature of these red oils was in debate.[17]

One stable N-heterocyclic carbene[44] has a structure analogous to borazine with one boron atom replaced by a methylene group. This results in a planar six-electron compound.

In the second step of this reaction sequence the proton is abstracted by LiTMP, while the two cyclohexyl groups shield the carbene.[44]

Another family of carbenes is based on a cyclopropenylidene core, a three-carbon ring with a double bond between the two atoms adjacent to the carbenic one. This family is exemplified by bis(diisopropylamino)cyclopropenylidene.[34]

In 2001, Hideo Tomioka and his associates were able to produce a comparatively stable triplet carbene (bis(9-anthryl)carbene, with a half-life of 19 minutes), by taking advantage of electron delocalization.[45][46]

Although the figure below shows the two parts of the molecule in one flat plane, molecular geometry puts the two aromatic parts in orthogonal positions with respect to each other.

Delocalization in a stable triplet carbene reported by Tomioka (2001)

In 2006 a triplet carbene was reported by the same group with a half-life of 40 minutes.[47] This carbene is prepared by a photochemical decomposition of a diazomethane precursor by 300 nm light in benzene with expulsion of nitrogen gas.

Again the figure below is not an adequate representation of the actual molecular structure: both phenyl rings are positioned orthogonal with respect to each other. The carbene carbon has an sp-hybridisation, the two remaining orthogonal p-orbitals each conjugating with one of the aromatic rings.

A persistent triplet carbene (right), synthesized by Itoh (2006)

Exposure to oxygen (a triplet diradical) converts this carbene to the corresponding benzophenone. The diphenylmethane compound is formed when it is trapped by cyclohexa-1,4-diene. As with the other carbenes, this species contains large bulky substituents, namely bromine and the trifluoromethyl groups on the phenyl rings, that shield the carbene and prevent or slow down the process of dimerization to a 1,1,2,2-tetra(phenyl)alkene. Based on computer simulations, the distance of the divalent carbon atom to its neighbors is claimed to be 138 picometers with a bond angle of 158.8°. The planes of the phenyl groups are almost at right angles to each other (the dihedral angle being 85.7°).

The imidazol-2-ylidenes are strong bases, having pK_a ≈ 24 for the conjugate acid in dimethyl sulfoxide (DMSO):[48]

Measurement of the pKa value for the conjugate acid of an imidazol-2-ylidene

However, further work showed that diaminocarbenes will deprotonate the DMSO solvent, with the resulting anion reacting with the resulting amidinium salt.

Using D6-DMSO as an NMR solvent can have unexpected results.

Reaction of imidazol-2-ylidenes with 1-bromohexane gave 90% of the 2-substituted adduct, with only 10% of the corresponding alkene, indicating that these molecules are also reasonably nucleophilic.

pK_a values for the conjugate acids of several NHC families have been examined in aqueous solution. pKa values of triazolium ions lie in the range 16.5–17.8,[49] around 3 pK_a units more acidic than related imidazolium ions.[50]

At one time, stable carbenes were thought to reversibly dimerise through the so-called Wanzlick equilibrium. However, imidazol-2-ylidenes and triazol-5-ylidenes are thermodynamically stable and do not dimerise, and have been stored in solution in the absence of water and air for years. This is presumably due to the aromatic nature of these carbenes, which is lost upon dimerisation. In fact imidazol-2-ylidenes are so thermodynamically stable that only in highly constrained conditions are these carbenes forced to dimerise.

Chen and Taton[51] made a doubly tethered diimidazol-2-ylidene by deprotonating the respective diimidazolium salt. Only the deprotonation of the doubly tethered diimidazolium salt with the shorter methylene bridge (–CH₂–) resulted in the dicarbene dimer:

Dimerisation of tethered diimidazol-2-ylidenes

If this dimer existed as a dicarbene, the electron lone pairs on the carbenic carbon would be forced into close proximity. Presumably the resulting repulsive electrostatic interactions would have a significant destabilising effect. To avoid this electronic interaction, the carbene units dimerise.

On the other hand, heteroamino carbenes (such as R₂N–C–OR or R₂N–C–SR) and non-aromatic carbenes such as diaminocarbenes (such as R₂N–C–NR₂) have been shown to dimerise,[52] albeit quite slowly. This has been presumed to be due to the high barrier to singlet state dimerisation:

"Least motion" (path A – not allowed) and "non-least motion" (path B) routes of carbene dimerisation.

Diaminocarbenes do not truly dimerise, but rather form the dimer by reaction via formamidinium salts, a protonated precursor species.[29] Accordingly, this reaction can be acid catalysed. This reaction occurs because unlike imidazolium based carbenes, there is no loss of aromaticity in protonation of the carbene.

Unlike the dimerisation of triplet state carbenes, these singlet state carbenes do not approach head to head ("least motion"), but rather the carbene lone pair attacks the empty carbon p-orbital ("non-least motion"). Carbene dimerisation can be catalyzed by both acids and metals.

The chemistry of stable carbenes has not been fully explored. However, Enders et al.[38][53][54] have performed a range of organic reactions involving a triazol-5-ylidene. These reactions are outlined below and may be considered as a model for other carbenes.

Reactions of triazol-5-ylidene[54]

a	3,6-diphenyl-1,2,4,5-tetrazine, toluene	92%		e	2 equiv., PhNCO, toluene, reflux	92%
b	RXH, RT	95–97%		f	CS2, toluene, or PhNCS, THF, RT	71–90%
c	O2, S8, or Se, toluene, reflux	54–68%		g	Maleimide, THF, RT	47–84%
d	R1CH=CHR2, THF, RT	25–68%		h	Dimethylacetylene dicarboxylate, THF, reflux	21%

These carbenes tend to behave in a nucleophilic fashion (e and f), performing insertion reactions (b), addition reactions (c), [2+1] cycloadditions (d, g and h), [4+1] cycloadditions (a) as well as simple deprotonations. The insertion reactions (b) probably proceed via deprotonation, resulting in the generation of a nucleophile (⁻XR) which can attack the generated salt giving the impression of a H–X insertion.

The reported stable isothiazole carbene (2b) derived from an isothiazolium perchlorate (1)[55] was questioned.[56] The researchers were only able to isolate 2-imino-2H-thiete (4). The intermediate 3 was proposed through a rearrangement reaction. The carbene 2b is no longer considered as stable.[57]

Isothiazole carbene (2b) was proved to be unstable.[56]

Imidazol-2-ylidenes, triazol-5-ylidenes (and less so, diaminocarbenes) have been shown to coordinate to a plethora of elements, from alkali metals, main group elements, transition metals and even lanthanides and actinides. A periodic table of elements gives some idea of the complexes which have been prepared, and in many cases these have been identified by single crystal X-ray crystallography.[39][58][59] Stable carbenes are believed to behave in a similar fashion to organophosphines in their coordination properties to metals. These ligands are said to be good σ-donors through the carbenic lone pair, but poor π-acceptors due to internal ligand back-donation from the nitrogen atoms adjacent to the carbene centre, and so are able to coordinate to even relatively electron deficient metals. Enders [60] and Hermann[61][62] have shown that these carbenes are suitable replacements for phosphine ligands in several catalytic cycles. Whilst they have found that these ligands do not activate the metal catalyst as much as phosphine ligands they often result in more robust catalysts. Several catalytic systems have been looked into by Hermann and Enders, using catalysts containing imidazole and triazole carbene ligands, with moderate success.[58][60][61][62] Grubbs [63] has reported replacing a phosphine ligand (PCy₃) with an imidazol-2-ylidene in the olefin metathesis catalyst RuCl₂(PCy₃)₂CHPh, and noted increased ring closing metathesis as well as exhibiting "a remarkable air and water stability". Molecules containing two and three carbene moieties have been prepared as potential bidentate and tridentate carbene ligands.[36][37]

Periodic table: Persistent carbene
Group →	1	2		3	4	5	6	7	8	9	10	11	12	13	14	15	16	17	18
↓ Period
1	1 H																		2 He
2	3 Li	4 Be												5 B	6 C	7 N	8 O	9 F	10 Ne
3	11 Na	12 Mg												13 Al	14 Si	15 P	16 S	17 Cl	18 Ar
4	19 K	20 Ca		21 Sc	22 Ti	23 V	24 Cr	25 Mn	26 Fe	27 Co	28 Ni	29 Cu	30 Zn	31 Ga	32 Ge	33 As	34 Se	35 Br	36 Kr
5	37 Rb	38 Sr		39 Y	40 Zr	41 Nb	42 Mo	43 Tc	44 Ru	45 Rh	46 Pd	47 Ag	48 Cd	49 In	50 Sn	51 Sb	52 Te	53 I	54 Xe
6	55 Cs	56 Ba		71 Lu	72 Hf	73 Ta	74 W	75 Re	76 Os	77 Ir	78 Pt	79 Au	80 Hg	81 Tl	82 Pb	83 Bi	84 Po	85 At	86 Rn
7	87 Fr	88 Ra		103 Lr	104 Rf	105 Db	106 Sg	107 Bh	108 Hs	109 Mt	110 Ds	111 Rg	112 Cn	113 Nh	114 Fl	115 Mc	116 Lv	117 Ts	118 Og
				57 La	58 Ce	59 Pr	60 Nd	61 Pm	62 Sm	63 Eu	64 Gd	65 Tb	66 Dy	67 Ho	68 Er	69 Tm	70 Yb
				89 Ac	90 Th	91 Pa	92 U	93 Np	94 Pu	95 Am	96 Cm	97 Bk	98 Cf	99 Es	100 Fm	101 Md	102 No

Legend

  Carbene complex with element known

  No carbene complex with element known

Carbenes can be stabilised as organometallic species. These transition metal carbene complexes fall into two categories:

• Fischer carbenes in which carbenes are tethered to a metal and an electron-withdrawing group (usually a carbonyl),
• Schrock carbenes; in which carbenes are tethered to a metal and an electron-donating group. The reactions that such carbenes participate in are very different from those in which organic carbenes participate.

Persistent triplet state carbenes are likely to have very similar reactivity as other non-persistent triplet state carbenes.

Deprotonation of carbene precursor salts with strong bases has proved a reliable route to almost all stable carbenes:

Deprotonation of precursor salts to give stable carbenes.

Imidazol-2-ylidenes and dihydroimidazol-2-ylidenes, such IMes, have been prepared by the deprotonation of the respective imidazolium and dihydroimidazolium salts. The acyclic carbenes[27][30] and the tetrahydropyrimidinyl[39] based carbenes were prepared by deprotonation using strong homogeneous bases.

Several bases and reaction conditions have been employed with varying success. The degree of success has been principally dependent on the nature of the precursor being deprotonated. The major drawback with this method of preparation is the problem of isolation of the free carbene from the metals ions used in their preparation.

One might believe that sodium or potassium hydride[26][32] would be the ideal base for deprotonating these precursor salts. The hydride should react irreversibly with the loss of hydrogen to give the desired carbene, with the inorganic by-products and excess hydride being removed by filtration. In practice this reaction is often too slow, requiring the addition of DMSO or t-BuOH.[18][25] These reagents generate soluble catalysts, which increase the rate of reaction of this heterogeneous system, via the generation of tert-butoxide or dimsyl anion. However, these catalysts have proved ineffective for the preparation of non-imidazolium adducts as they tend to act as nucleophiles towards the precursor salts and in so doing are destroyed. The presence of hydroxide ions as an impurity in the metal hydride could also destroy non-aromatic salts.

Deprotonation with sodium or potassium hydride in a mixture of liquid ammonia/THF at −40 °C has been reported[35] for imidazole-based carbenes. Arduengo and coworkers[32] managed to prepare a dihydroimidazol-2-ylidene using NaH. However, this method has not been applied to the preparation of diaminocarbenes. In some cases, potassium tert-butoxide can be employed without the addition of a metal hydride.[25]

The use of alkyllithiums as strong bases[18] has not been extensively studied, and have been unreliable for deprotonation of precursor salts. With non-aromatic salts, n-BuLi and PhLi can act as nucleophiles whilst t-BuLi can on occasion act as a source of hydride, reducing the salt with the generation of isobutene:

Reduction of formamidinium salts with tert-butyllithium

Lithium amides like the diisopropylamide (LDA) and the (tetramethylpiperidide (LiTMP))[27][30] generally work well for the deprotonation of all types of salts, providing that not too much LiOH is present in the n-butyllithium used to make the lithium amide. Titration of lithium amide can be used to determine the amount of hydroxide in solution. The deprotonation of precursor salts with metal hexamethyldisilazides[39] works very cleanly for the deprotonation of all types of salts, except for unhindered formamidinium salts, where this base can act as a nucleophile to give a triaminomethane adduct.

Stable carbenes readily coordinate to metals; in this case a diaminocarbene coordinates to KHMDS to form a complex.

The preparation of stable carbenes free from metal cations has been keenly sought to allow further study of the carbene species in isolation from these metals. Separating a carbene from a carbene-metal complex can be problematic due to the stability of the complex. Accordingly, it is preferable to make the carbene free from these metals in the first place. Indeed, some metal ions, rather than stabilising the carbene, have been implicated in the catalytic dimerisation of unhindered examples.

Shown right is an X-ray structure showing a complex between a diaminocarbene and potassium HMDS. This complex was formed when excess KHMDS was used as a strong base to deprotonate the formamidinium salt. Removing lithium ions resulting from deprotonation with reagents such as lithium diisopropylamide (LDA) can be especially problematic. Potassium and sodium salt by-products tend to precipitate from solution and can be removed. Lithium ions may be chemically removed by binding to species such as cryptands or crown ethers.

Metal free carbenes have been prepared in several ways as outlined below:

Another approach of preparing carbenes has relied on the desulfurisation of thioureas with potassium in THF.[28][70] A contributing factor to the success of this reaction is that the byproduct, potassium sulfide, is insoluble in the solvent. The elevated temperatures suggest that this method is not suitable for the preparation of unstable dimerising carbenes. A single example of the deoxygenation of a urea with a fluorene derived carbene to give the tetramethyldiaminocarbene and fluorenone has also been reported:[71]

Preparation of carbenes by dechalcogenation

The desulfurisation of thioureas with molten potassium to give imidazol-2-ylidenes or diaminocarbenes has not been widely used. The method was used to prepare dihydroimidazole carbenes.[28]

Vacuum pyrolysis, with the removal of neutral volatile byproducts i.e. methanol or chloroform, has been used to prepare dihydroimidazole and triazole based carbenes. Historically the removal of chloroform by vacuum pyrolysis of adducts A was used by Wanzlick[8] in his early attempts to prepare dihydroimidazol-2-ylidenes but this method is not widely used. The Enders laboratory[38] has used vacuum pyrolysis of adduct B to generate a triazol-5-ylidene.

Preparation of carbenes via vacuum pyrolysis.

Bis(trimethylsilyl)mercury (CH₃)₃Si-Hg-Si(CH₃)₃ reacts with chloro-iminium and chloro-amidinium salts to give a metal-free carbene and elemental mercury.[72] For example:

(CH₃)₃Si−Hg−Si(CH₃)₃ + R₂N=C(Cl)−NR⁺
₂Cl⁻ → R₂N−C−NR₂ + Hg_(l) + 2(CH₃)₃SiCl

Persistent triplet state carbenes have been prepared by photochemical decomposition of a diazomethane product via the expulsion of nitrogen gas, at a wavelength of 300 nm in benzene.

Sublimation of a carbene.

Stable carbenes are very reactive, and so the minimum amount of handling is desirable using air-free techniques. However, provided rigorously dry, relatively non-acidic and air-free materials are used, stable carbenes are reasonably robust to handling per se. By way of example, a stable carbene prepared from potassium hydride can be filtered through a dry celite pad to remove excess KH (and resulting salts) from the reaction. On a relatively small scale, a suspension containing a stable carbene in solution can be allowed to settle and the supernatant solution pushed through a dried membrane syringe filter. Stable carbenes are readily soluble in non-polar solvents such as hexane, and so typically recrystallisation of stable carbenes can be difficult, due to the unavailability of suitable non-acidic polar solvents. Air-free sublimation as shown right can be an effective method of purification, although temperatures below 60 °C under high vacuum are preferable as these carbenes are relatively volatile and also could begin to decompose at these higher temperatures. Indeed, sublimation in some cases can give single crystals suitable for X-ray analysis. However, strong complexation to metal ions like lithium will in most cases prevent sublimation.