Silicon-fluorine chemistry: from the preparation of SiF 2 to C–F bond activation using silylenes and its heavier congeners †

This feature article is intended to provide a background to the history of the isolation of silicon( II ) fluorides and the diﬀerent synthetic methodologies used to generate them. Although first detected in the 1970s, the chemistry of silicon( II ) fluorides has not encountered serious research eﬀorts for a rather long period of time. This is somewhat surprising given the fact that the chemistry of compounds with divalent silicon has undergone a renaissance during last three decades. Recently, the interest in silicon( II ) fluorides have been resparked with tremendous progress being achieved in this area, in particular, with respect to their synthesis and structural characterisation. The successful isolation of cyclic alkyl amino carbene (cAAC) stabilized silicon difluoride has completed the classic progression of SiF 2 , from a transient intermediate to spectroscopically detected molecule to a stable compound. The related germanium( II ), tin( II ), and lead( II ) fluoride chemistry will also be discussed. Apart from the isolation of tetrel( II ) fluorides, the use of compounds with low valent group 14 elements for the selective activation and functionalisation of C–F bonds has witnessed some remarkable advances, which will also be summarized in this feature article.


Introduction
''Oh threats of hell and hopes of paradise!One thing at least is certain -This Life flies'' -Omar Khayya ´m, Rubaiyat of Omar Khayyam The austere insight of Khayya ´m about life bears a striking resemblance to the present day silicon chemistry.Despite the ever-looming threat of instability and high reactivity of organosilicon compounds, especially in the low oxidation state, and the hope of taming them using chemical tricks (bulky ligands, donor-acceptor approach), the only certain thing is that the present day silicon chemistry is propelling in fifth gear.Starting from the seminal report on the synthesis of a compound with a SiQSi double bond by West and co-workers 1 that toppled the then much venerated ''double bond rule'', to a stable silanone, 2 which was ''F.S. Kipping's dream'', organosilicon chemistry has traversed a long journey, witnessing a catalogue of esteemed discoveries made across the world. 3Such realisation of novel organosilicon compounds has allowed us to analyze their structures, elucidate their bonding properties and study their reactivities, which eventually revealed the marked differences between silicon and carbon, and led W. Kutzelnigg to comment ''the heavier main-group elements, Si to Pb, actually exhibit 'normal' chemical behaviour while carbon should be considered the 'unusual' member of the group 14 elements rather than the prototype''. 4The remarkable progress of organosilicon chemistry over the last three decades has been closely monitored by the chemistry community, which has resulted in numerous elegant reviews. 5ven before the beginning of the chemistry of compounds with multiple-bonds between silicon atoms, the chemistry of silicon(II) halides has attracted considerable attention.The confirmation of the: CCl 2 intermediate in the Reimer-Tiemann reaction, 6a as well as Nef's pioneering work 6b,c on divalent carbon compounds have led silicon chemists to undertake the synthesis of dihalosilylenes.Another impetus originated from the realisation that silicon(II) halides are the intermediates in many important reactions, such as the Rochow Mu ¨ller process, 7a where methylchlorosilanes are prepared from methyl chloride in an easy and inexpensive way.The Rochow Mu ¨ller process has resulted in the huge growth of the silicone polymer area.Spectral evidence has been obtained in the formation of unstable silylenes (SiCl 2 and MeSiCl) during the reaction.Such silicon(II) compounds can be used as synthons to prepare new compounds, which are otherwise inaccessible.In their recent feature article on the readily available SiCl 2 /[SiCl 3 ] À system, Teichmann and Wagner elegantly highlighted the classical high-temperature protocols used for the generation of SiCl 2 and their utility as synthons for making unusual silicon compounds.7b Following the syntheses of [SiBr 2 ] x and [SiCl 2 ] x by the Schmeißer group, 8 chemists have turned their attention towards [SiF 2 ] x .The interest has been stimulated by the fact that the divalent fluoride of carbon is more stable than its parent carbene.For example, carbene (:CH 2 ) has a half-life of 1 ms in the gas phase, while carbon difluoride has a half-life of 1 s.9a,b The halflife of gaseous SiF 2 is 150 s at 0.2 Torr and ambient temperature.9c Moreover, neither CF 4 nor SiF 4 react with glass, which is a usual problem for other fluorides.The preparation of SiF 2 from magnesium and dibromofluorosilane by Schmeißer goes back as early as 1954. 10Since then, the divalent fluorides of silicon have become a major research area especially at Rice University, USA where the Timms and Margrave groups have performed an extensive and systematic study of the properties of silicon difluoride. 11Nevertheless, no monomeric SiF 2 has been isolated under synthetically useful conditions until very recently, when we reported cyclic alkyl amino carbene (cAAC) coordinated silicon difluoride from the reduction of cAACÁSiF 4 with KC 8 . 12In this review, we provide a comprehensive coverage of the synthesis and reactions of silicon(II) fluorides.The fluorides of other heavier group 14 elements such Ge(II), Sn(II) and Pb(II) will be covered.It will also summarize the recent efforts, by our group and others, on the activation of the C-F bond using compounds with low valent silicon atoms.We extend into other classes of reactivity that are closely related and of particular interest such as germylene and stannylene assisted C-F activation.Finally, the recent studies on the hydrodefluorination of CÀF bonds using silylium cations are also presented.

Early preparations of silicon difluoride
Table 1 lists some key milestones in the development of group 14-fluoride chemistry.Although the groups of Timms and Margrave at Rice University, Houston, USA are generally credited for preparing SiF 2 for the first time, Schmeißer prepared polymeric silicon(II) fluoride from the reaction of dibromofluorosilane and magnesium in 1954. 10In 1958, Pease found that silicon difluoride could be formed from the reaction of SiF 4 and Si at high temperature, which condenses below À80 1C. 13 Another effort from Schmeißer and Ehlers involved the cleavage of the Si-Si bond in Si 2 F 6 at 700 1C that led to the formation of SiF along with SiF 2 , 14 which condensed as a yellow solid in liquid air.Above À80 1C, SiF 2 polymerizes to yield a colorless, rubbery solid [SiF 2 ] x , which catches fire in moist air.
All the aforementioned reactions in fact deal with polymeric silicon difluoride but indicate the formation of monomeric SiF 2 as an intermediate.Moreover, no physical properties of SiF 2 were measured.To unequivocally prove the existence of monomeric SiF 2 , Timms et al. constructed a special apparatus (Fig. 1).SiF 4 was passed into a reservoir and subsequently, using the needle valves, passed over chunks of heated silicon at 1200 1C, which afforded 50% SiF 2 . 15To avoid the disproportionation reaction, as soon as the SiF 2 is formed, it is swept through the vacuum line to a point where it's physical properties or chemical reactivities could be measured.
Ehlert and Margrave performed a mass spectrometric experiment of SiF 2 .16a  This journal is © The Royal Society of Chemistry 2018 polymeric species of SiF 2 were observed.It was estimated that SiF 2 has a half-life of 120 seconds.The infrared spectrum of gaseous SiF 2 has been recorded from 1050 to 400 cm À1 .Two absorption bands centered at 855 and 872 cm À1 were assigned to the symmetric and anti-symmetric stretching modes, respectively.16b The relatively easy generation of SiF 2 by the Timms' group saw a flurry of research activity into their properties and reactivity in the early 1970s.The reactivity of polymeric SiF 2 was investigated with various substrates such as BF 3 , benzene, hexafluorobenzene, and water (Scheme 1). 17The general strategy of the reactions was to condense the reactant and SiF 4 -SiF 2 mixture together and characterize the condensate.Multi-nuclear NMR spectroscopy, IR spectroscopy, mass spectrometry, and elemental analysis were performed to characterize the condensates.As none of the product was characterized by single crystal X-ray diffraction, the structural authentication of the SiF 2 unit remained elusive.In the following years, publications on silicon difluoride trickled out and there were not many significant advances.In fact, the research interest in silicon difluoride never again reached the heights that were attained in the 1960s and 70s.
The efforts to prepare stable compounds with an Si(II)-F bond: structural validation The facile isolation of stable silicon(II) chlorides 18 such as [LSi(II)Cl, L = {PhC(NtBu) 2 } À ] (1) and N-heterocyclic carbene (NHC)-stabilized dichlorosilylene (L 0 Si(II)Cl 2 , L 0 = 1,3-bis(2,6-iPr 2 C 6 H 3 )imidazol-2-ylidene) (2) renewed the interest in making a compound with a Si(II)-F bond.However, due to the high propensity of silicon(II) fluoride toward polymerization or disproportionation, attempts to isolate ''[PhC(NtBu) 2 ]SiF'' or ''IDippÁSiF 2 '' were not successful.In line with our observations, Jutzi and co-workers also found that Me 5 C 5 SiF was unstable and dimerized into the corresponding disilene, Me 5 C 5 (F)SiQSi(F)C 5 Me 5 .The latter was also found to be unstable and underwent a [2+2]cycloaddition to form cyclotetrasilane. 19 ''We must accept finite disappointment, but never lose infinite hope.''-Martin Luther King, Jr.We imagined that the presence of the stereoactive lone pair of electrons on the silicon atom of silicon difluoride impedes its isolation.To prevent this feisty nature of silicon(II) difluoride, we reacted 1 with BH 3 to coordinate the lone pair of electrons of silicon to the electron deficient boron center (Scheme 2). 20he reaction led to the formation of an adduct, 3. The latter was subsequently reacted with L 1 PbF, [L 1 = CH{(CMe)(2,6-iPr 2 C 6 H 3 N)} 2 ] (4), 20 which resulted in the formation of compound 5 along with the formation of L 1 PbCl (6). 5 features a formal Si(II)-F bond.The 19 F NMR spectrum displayed a resonance at d À121.59 ppm accompanied by 29 Si satellite signals ( J = 438.17Hz).The 29 Si NMR spectrum revealed a doublet of quartets (d 23.63 ppm and J (29Si-11B) = 66.78 Hz), which underpinned the presence of Si-B and Si-F bonds.Although the spectroscopic data unambiguously affirmed the formation of a compound with a Si(II)-F bond, its structural characterization by X-ray diffraction was still missing.
Fig. 1 The apparatus used for the preparation and reaction of SiF 2 .Reproduced with permission from ref. 17.
Scheme 1 The reactions of a SiF 4 -SiF 2 mixture with various substrates.
Table 1 The important milestones in the chemistry of silicon fluorides

Year Comment
The unraveling of an efficient synthetic pathway to access formal Si(II) fluorides using a donor-acceptor approach furthered us to bring transition metals into play instead of borane.A very common strategy that has often been applied in organometallic chemistry for isolating reactive compounds is to bind those species to transition metals. 21Moreover, the presence of a transition metal in a compound usually allows the growth of better quality single crystals suitable for X-ray analysis.Silylenes are known to coordinate with transition metals.Prior to us Rivard and co-workers described the generation of stable M(II)H 2 (M = Si, Ge, and Sn) and H 2 SiEH 2 (E = Ge and Sn) under the coordination sphere of late transition metals. 22By applying the same synthetic protocol, we prepared three silicon(II) fluoride compounds, PhC(NtBu) 2 (F)SiÁM(CO) 5 {M = Cr (10), Mo (11), and W(12)}, 23 using a metathesis reaction of the corresponding chlorides (7-9) with Me 3 SnF, a versatile fluorinating agent (Scheme 3). 10 and 12 were structurally characterized.There is a small variation in the Si-M bond lengths in 10 (2.3398(4) Å) and 12 (2.4990(8)Å) when compared to the corresponding chloride analogues 7 (2.3458(7)Å) and 9 (2.5086(11)Å).The Si-F bond lengths in 10 and 12 are 1.6168(8) and 1.6245( 14) Å, respectively.A comparison of the SiÀF bond lengths in 10 and 12 with that in gaseous SiF 2 (1.59 Å) indicates an increase in the bond length by only 0.03 Å.
''It's kind of fun to do the impossible.''-Walt Disney Although, 5 and 10-12 possess a formal Si(II)-F bond, access to a silicon difluoride that is stable at room temperature remained elusive.Therefore, the question arose whether it is viable to isolate a stable compound featuring a silicon(II) difluoride moiety.Since NHCs were found inappropriate for stabilizing the silicon(II) difluoride moiety, we turned our attention towards cAAC.According to the calculations, 24 the singlet-triplet energy gap of cAAC (46 kcal mol À1 ) is much smaller than that of NHC (68 kcal mol À1 ), and as a result, the HOMO of cAAC (À5.0 eV) is higher in energy than that of NHC (À5.2 eV).Following the isolation of stable cAAC by the Bertrand group, 25 it has been widely used for the stabilisation of a plethora of unprecedented silicon compounds that could be prepared in no other way. 26The attempts to synthesize cAAC supported SiF 2 from the reactions of (cAAC) 2 SiCl 2 with various fluorinating agents (Me 3 SnF, CsF, and C 5 F 5 N) were unsuccessful.Hence, a conventional reduction method was employed.The reduction of the cAAC-SiF 4 adduct (13) with KC 8 in the presence of another equivalent of cAAC resulted in (cAAC) 2 SiF 2 ( 14) as a purple solid (Scheme 4). 12The 29 Si and 19 F NMR spectra of 14 display no resonance at room temperature due to their rapid exchange on the NMR timescale.However, a low temperature NMR experiment exhibited a triplet at d 29.73 ppm in the 29 Si NMR spectrum and a broad singlet at d À123.47 ppm in the 19 F NMR spectrum.The UV-vis spectrum of 14 showed an absorption band at 529 nm that was in good accordance with the TD-DFT calculations.This absorption can be attributed to ligand to silicon charge transfer.An X-ray crystal structure of 14 (Fig. 2) revealed that the SiF 2 unit was coordinated by two cAAC moieties with Si-F bond lengths of 1.592(1) and 1.593(1) Å, which are within the range of those reported for 10.Subsequent theoretical studies showed that 14 possesses an open shell singlet configuration, which is 4.9 kcal mol À1 lower in energy than the triplet configuration and 10.2 kcal mol À1 lower in energy than the closed-shell singlet configuration.The large energy difference between the open shell singlet configuration and the triplet configuration underpins why 14 was EPR silent.
''There is no end.There is only the infinite passion of life'' -Federico Fellini (Italian Film Director) Once we accomplished the isolation of a compound with a silicon(II) difluoride moiety, we wished to prepare a compound with a SiF 3 radical unit.Gratifyingly, the reduction of 13 with one equivalent of KC 8 in the absence of any free cAAC resulted in a monoradical product, (cAAC)SiF 3 (15), which was the first stable radical containing a SiF 3 group (Scheme 5). 12The monomeric nature of 15 was characterized using a single crystal X-ray diffraction study (Fig. 3).The EPR spectrum of 15 was recorded in n-hexane at room temperature (Fig. 4), which showed a very large 19 F coupling parameter.According to the McConnell spin polarisation model, this high coupling parameter is due to the high polarity of the Si-F bond and its interaction with the carbon radical center.

Germanium, tin and lead(II) fluorides
Due to the inert-pair effect, GeF 2 and SnF 2 are more stable than their lower homologues.GeF 2 is a strongly fluorine-bridged chain polymer in which the parallel chains are cross-linked by weak fluorine bridges.SnF 2 exists as a tetramer containing a puckered eight-membered ring in which the Sn and F atoms are alternately arranged.SnF 2 has been widely used in toothpaste as a source of fluoride to harden the dental enamel.However, due to their polymeric structures GeF 2 and SnF 2 have low solubilities in common organic solvents and hence, it is difficult to study their reactions in the solution state.
We have mentioned the use of Pb(II) fluoride before (vide supra, Scheme 2) as a fluorinating agent for the metathesis reaction of Si(II) chloride to fluoride.However, the preparation of Pb(II) fluoride was found to be more challenging than its lighter congeners, which could be attributed to the insolubility associated with the lead compounds.The synthetic strategies applied for the preparation of Ge(II) and Sn(II) fluorides did not furnish the analogous Pb(II) fluoride, and instead, the formation of metallic lead was observed in each reaction.These findings left an impression that Me 3 SnF should be substituted by another mild fluorinating agent.Moreover, the by-product formed while using Me 3 SnF as a fluorinating agent is Me 3 SnCl, which is highly toxic.Therefore, pentafluoropyridine was chosen as a fluorinating agent and reacted with L 1 Pb(II)NMe (33)

Activation of C-F bonds using compounds with a low valent silicon atom
The activation of C-F bonds in fluorinated hydrocarbons is of fundamental interest from the standpoint of the potential application of organofluorine compounds in synthetic organic chemistry, pharmacy and agrochemistry, 41 as well as the everincreasing environmental concerns related to fluorinated compounds. 42Fluorinated hydrocarbons are not only contributing to global warming but cause the depletion of the ozone layer. 42As a result, there is a need to develop new synthetic strategies for the activation of C-F bonds.Owing to the strength and the resulting high activation barrier of the C-F bonds in fluorocarbons, a strong Lewis acid with high fluoride affinity is sought-after for C-F bond activation.4][45] For example, the groups of Kuhn, Bertrand, Turner, Lee, Baker, Chaplin, Radius, and many others have demonstrated the activation of aromatic C-F bonds using various carbenes. 43Studer and co-workers have described C-F bond activation in perfluoroarenes using aryl and alkyl isonitriles under UV irradiation. 44The groups of Mikami, Nikonov, and Stephan have independently reported the respective use of boryl lithium, Al(I) compound and phosphonium cations for C-F bond activation. 45ompounds with low valent silicon atoms are especially appealing for CÀF bond activation because they can integrate both Lewis acidity and fluoride affinity.The propensity of compounds with low valent silicon atom towards oxidative addition reactions can be tapped for cleaving inert bonds such as C-F bonds.Although never accredited, it was the groups of Timms and Margrave who noted that the reaction of hexafluorobenzene and in situ generated SiF 2 gave pentafluorophenyltrifluorosilane (C 6 F 5 SiF 3 ) as the major product arising from the oxidative addition of one of the C-F bonds at the Si(II) center (Scheme 1, eqn (g)).They were also able to trace the formation of C 6 F 4 (SiF 3 ) 2 as minor products in an o : m : p ratio of B1 : 9 : 6.This was perhaps the first example of C-F bond activation using a compound with a low valent silicon atom.
We embarked our investigation upon the reaction of 1 with C 6 F 6 , which led to the oxidative addition of the Si(II) center with the simultaneous cleavage of one of the C-F bonds in C 6 F 6 (Scheme 13). 46Similar activation of the aromatic C-F bond was achieved with C 6 F 5 CF 3 and C 6 F 5 N. 46 The resonances of the Si-F moiety present in 35, 36, and 37 arise at d À63.4,À63.7, and À64.4 ppm in their respective 19 F NMR spectra.The 29 Si NMR spectra of 35, 36, and 37 show doublets (d À91.9, À97.2, and À97.9 ppm) with a coupling constant of 1 J (29Si-19F) 282.9, 283.6, and 282.7 Hz, respectively.
The introduction of C-H bonds into the fluorinated substrate often slows down the reactions and generates competition between the C-F and C-H oxidative addition reactions.For example, the Johnson group described the reaction of Ni(PEt 3 ) 2 with C 6 F 5 H, where the C-H activated species was formed as the kinetic product, while C-F oxidative addition led to the thermodynamic product. 47The reaction of 1 with partially fluorinated benzene, C 6 F 5 H, yielded exclusively the product of C-F oxidative addition, 38 (Scheme 13).The formation of the Si-F bond in the product is assumed to drive the C-F bond activation. 46he reactions of the analogous silylene, LSiN(SiMe 3 ) 2 (L = PhC(NtBu) 2 ) (39), with hexafluorobenzene and octafluorotoluene follow an analogous oxidative addition pathway (Scheme 14) leading to 40 and 41. 48In the 19  Of particular importance is the preference for the activation of the C-F bond para to the CF 3 moiety in octafluorotoluene.In a subsequent paper, Koley and co-workers computationally demonstrated that the activation energy barrier for the para C-F bond is lower than the ortho and meta C-F bonds by 5.2 kcal mol À1 and 8.0 kcal mol À1 , respectively. 49Moreover, the overall distortion energy for the para C-F bond activation (25.4 kcal mol À1 ) was found to be significantly smaller than those for the ortho (56.6 kcal mol À1 ) and meta (63.8 kcal mol À1 ) C-F bonds.The fact that the activation of the C-F bond in hexafluorobenzene occurs at elevated temperature while in octafluorotoluene its takes place at room temperature can be ascribed to the diminishing strength of the C-F bond upon increasing the fluorination and thereby lowering the energy barriers for the C-F bond activation in the more fluorinated substrates.
Apart from functionalized three coordinate silylenes, such as 1 and 39, typical N-heterocyclic silylene, CH[{(CQCH 2 )(CMe)-(2,6-iPr 2 C 6 H 3 N) 2 }]Si (42), was also reported for the activation of the aromatic C-F bonds. 46All these aforementioned reactions with fluorinated substrates were investigated with 42 (Scheme 15).The oxidative addition of the C-F bond at the Si(II) atom takes place in the reactions with hexafluorobenzene, octafluorotoluene and pentafluoropyridine leading to the formation of 43-45, respectively.However, the reaction of 42 with C 6 F 5 H exclusively led to the C-H activated product 46 instead of the C-F activated product observed in the case of 38.No activation of the C-F bond was observed even at low temperature.These differences are likely to be due to the lower coordination number of the Si(II) atom in 42 than that in 1. Usually, silicon hydrides with a high coordinate silicon atom are less stable than those of the corresponding fluoride analogues, which could be the underlying rationality for the preferred formation of low coordinate silicon with hydrides and not with fluorides.
The selective activation of the aliphatic C(sp 3 )ÀF bonds, such as the functionalization of the trifluoromethyl group, was not known for a long time. 50Recently, we have shown that silylene 39 selectively activates one of the C-F bonds in 1,1,1 trifluoro acetophenone leading to a difluorinated alkene (47)  featuring both the Si-O and Si-F bond (Scheme 16). 48The DFT calculations revealed that the reaction goes through an Si-O bond formation with an energy barrier (DG) of 16.2 kcal mol À1 .Subsequently, the reaction proceeded through a five-membered transition state with a corresponding energy barrier of 6.8 kcal mol À1 , where a Si-F bond and CQC bond are formed.The final product, 47, is very thermodynamically stable (À41.7 kcal mol À1 ), which, along with the low barriers obtained, indicates that this reaction is both kinetically and thermodynamically viable at room temperature.Insertion of a Si(II) atom into the CF 3 group of hexafluoroacetimine was also reported.The reactions of 1 and 42 with PhNQC(CF 3 ) 2 led to the facile C-F activation of one of the CF 3 substituents and the formation of difluorinated alkenes, such as 48 and 49 (Scheme 17). 51Such selective activation of one of the C-F bonds This journal is © The Royal Society of Chemistry 2018 rather than complete defluorination of the CF 3 group by compounds with low valent silicon atoms was not known beforehand.

Activation of C-F bonds using compounds with low valent germanium and tin atoms
In addition to silylenes, germylenes and stannylenes have also been found to activate aromatic C-F bonds.In an early example, we showed that both {PhC(NtBu) 2 }GeNiPr 2 (50) and {PhC(NtBu) 2 }-SnNMe 2 (51) can activate the C-F bond in pentafluoropyridine, however, divergent behavior was observed regarding their reactivities. 52Like in the cases of silylenes, the C-F bond of pentafluoropyridine underwent an oxidative addition reaction at the Ge(II) atom leading to the formation of 52.However, no oxidative addition product was formed with 51 and instead the substitution of the NMe 2 group by the fluoride ion occurred at the Sn(II) atom resulting in 53 (Scheme 18).Single crystal X-ray diffraction studies on 53 revealed that it exists as a dimer in which the two molecules are connected by weak intermolecular SnÁ Á ÁF bonds.
In a subsequent theoretical paper, Koley and co-workers explained the dichotomous reactivity pattern of germylene 50 and stannylene 51 towards pentafluoropyridine. 49In 50, the electron density is located on the Ge atom and due to the presence of the NiPr 2 substituent on Ge, the transition state for the oxidative addition pathway was found to be more favored than the metathesis pathway by 32.1 kcal mol À1 .However, they predicted that substitution on the Ge atom plays a part in determining which product will be formed.For example, they calculated that the replacement of the NiPr 2 substituent with an NMe 2 group may lead to a competition between the oxidative addition and metathesis pathways as the electronic and steric environments support both the transition states.An experimental verification of this prediction is deemed desirable and may open up a new avenue for C-F bond activation using functionalized germylenes.However, in case of 51, the HOMO-LUMO energy gap increases due to the larger s-p gap.Therefore, the metathesis reaction was found to be more favored over the oxidative addition reaction by 13.3 kcal mol À1 .The same group also demonstrated the lower HOMO-LUMO energy gap is required for para C-F bond activation than the corresponding ortho or meta C-F bond activations and thereby explained the penchant for the para C-F bond activation of pentafluoropyridine.
Tin(II) hydride 54 was also found to activate the C-F bond of C 6 F 6 under ambient conditions and resulted in tin(II) fluoride 30 along with the tin(II) pentafluorophenyl compound, 55, and C 6 F 5 H (Scheme 19). 53A closer look at this reaction revealed that stoichiometric hydrodefluorination of C 6 F 6 to C 6 F 5 H takes place during the reaction.The reaction is likely to occur via the metathesis between hydride and fluoride as well as hydride and the pentafluorophenyl substituent.The formation of 55 during the reaction was indicated by the 119 Sn NMR resonance at d À176.4 ppm, which is significantly high-field shifted with respect to that of 54 (d À4.5 ppm, 1 J Sn-H = 64 Hz) 54 and 30 (d À371.5 ppm, 1 J Sn-F = 3100 Hz).To unequivocally prove the formation of 55 during the reaction, 28 was reacted with C 6 F 5 Li, which exclusively led to 55 and the resulting NMR spectra were compared.

Silylium ion in the hydrodefluorination reaction
Hydrodefluorination is a reaction in which a C-F bond is replaced by a C-H bond.The removal of fluorines from fluorocarbons compounds and replacement with hydrogen is an important goal, in order to convert them into more biodegradable compounds.Usually, transition metal catalysts are used for this conversion. 55Ozerov and co-workers showed that a silylium-borane catalyst, Et 3 Si + [B(C 6 F 5 ) 4 ] À , can catalyze the selective hydrodefluorination of C 6 F 5 CF 3 to C 6 F 5 CH 3 , although with a poor turn over number (TON = 19). 56By varying the counter-anion with a carborane catalyst, Et 3 Si + [CHB 11 H 5 Cl 6 ] À , the TON of the same reaction was found to increase up to 2700 (Scheme 20). 57The mechanism has been assumed to proceed via a silylium ion-mediated fluoride abstraction from the substrate with subsequent hydride transfer from the organosilane to the intermediate carbenium ion.The driving force for the overall reaction is the formation of Si-F and C-H bonds that counterbalance the cleavage of the C-F and Si-H bonds by 45.4 kcal mol À1 , thereby enabling the metathesis.
Parallel to Ozerov's findings, Mu ¨ller and co-workers reported the hydrodefluorination of trifluorotoluene to give toluene using a hydride-bridged disilyl cation as the catalyst (Scheme 21). 58The specialty of this case is that the cation combines the silicon electrophile as well as the hydride source.Both hydride (I) and fluoride (II) bridged silylium cations were observed as intermediates, structurally characterized and found to be interconvertible in the reaction with alkylfluorides or silanes.The tentative catalytic cycle is shown in Scheme 21, however, the cycle operates with a moderate TON.

Conclusions
While the basis of silicon(II) difluoride chemistry dates back into the 1970s, most progress in this area has been made during the last few years.The first stable silicon(II) difluoride ( 14) was made accessible using cyclic alkyl amino carbene (cAAC) ligand.The synthesis of the first compound containing an SiF 3 radical (15) has also been recently accomplished.The lion's share of the credit must go to the cAAC ligand due to its high lying HOMO and low lying LUMO, which not only donates electron density to the Si(II) center but unlike NHC, can accept electron density from the Si-F bonds.Structural analysis of these complexes in tandem with DFT calculations has significantly enhanced the understanding of their electronic properties.The reactivities of both 14 and 15 have yet to be reported but promise rich further chemistry.And of course, the success of cAAC and the failure of NHC (so far!!) for stabilizing the SiF 2 moiety will encourage synthetic chemists to make newer neutral ligands with tunable electronic properties.The chemistry of silicon(II) fluorides can be best described in Churchill's words ''. ..it is not even the beginning of the end. ..''.The game is on!Of equal importance are the recent achievements in the activation of C-F bonds using compounds with low valent silicon atoms.Progress in the use of silylenes to activate both alkyl and aryl C-F bonds was also detailed.The formation of a strong Si-F bond is likely to be the driving impetus of these reactions.In addition to the commonly observed stoichiometric C-F bond activation, silylium ion catalyzed hydrodefluorination has been discovered with remarkable turn over numbers, which was previously considered the exclusive domain of transition metal complexes.Apart from the hydrodefluorination reactions, silylium cations have been recently employed in the Friedel Crafts reactions of fluoroarenes 59 and C-C coupling reactions, 60 which have not been discussed in this feature article.As a consequence, the focus in silicon fluorine chemistry will likely tilt from fundamental to application-oriented research in the near future.As part of a natural progression, the heavier congeners of silylenes, such as germylenes and stannylenes, have also been reported for C-F bond activation but their examples are still very scant.Nevertheless, we hold great hopes for studying these riveting molecules in the future.
SiF 4 was passed through a Si column at very high temperature and subsequently passed into a mass spectrometer, which detected only SiF 4 and monomeric SiF 2 ; no Sakya S. Sen Sakya S. Sen received his PhD from the University of Go ¨ttingen, Germany under the supervision of Professor Herbert W. Roesky and subsequently joined the laboratory of Professor Holger Braunschweig at the University of Wu ¨rzburg, Germany as an AvH postdoctoral fellow.Since 2014 he has worked in the CSIR-NCL, Pune, India as a senior scientist.His research interests are the synthesis and application of compounds with low valent main group elements.Sakya is the recipient of the CSIRyoung scientist award in 2017 and young associate of Indian Academy of Sciences.Herbert W. Roesky Herbert W. Roesky obtained his doctorate from the University of Go ¨ttingen.After working at DuPont in the United States, he returned to Go ¨ttingen and finished his habilitation.He then became a Professor at the Johann-Wolfgang-Goethe-Universita ¨t, Frankfurt am Main in 1971.He moved to the University of Go ¨ttingen in and was the director of the Institute for Inorganic Chemistry until 2004.He is primarily known for his pioneering work on fluorides of both transition and main group elements.His current research interest is focused on the synthesis and reactivity of compounds with heavier group 13 and 14 elements in low oxidation states.More than 1250 peer-reviewed papers, articles, patents, and books record his research activities in the areas of inorganic chemistry and materials science.He is also the recipient of several prizes, i.e.Gottfried Wilhelm Leibniz Prize, the Alfred Stock Memorial Prize, the Grand Prix de la Foundation de la Maison de la Chimie, the Wilkinson Prize, Moissan award and ACS awards in Inorganic and Fluorine Chemistry.

19 F
to afford the b-diketiminatolead(II) monofluoride, L 1 Pb(II)F (4), together with 4-dimethylaminotetrafluoropyridine (Scheme 11).The driving force of this reaction is the formation of a C-N bond, which compensated the energy required for the C-F bond cleavage.The Pb-F bond length in 4 (2.088(17)Å) is expectedly longer than those of Ge-F (1.805(17) Å) in 18 and Sn-F (1.988(2) Å) in 30.The low temperature 19 F NMR spectrum of 20 exhibits a resonance at This journal is © The Royal Society of Chemistry 2018 d 102.7 ppm, accompanied by two 207 Pb satellites (d 106.4 and 99.0 ppm).The low temperature 207 Pb NMR spectrum shows a doublet at d 787.4 ppm with a coupling constant of 1 J (19F-207Pb) = 2792 Hz.When the measurements were performed at room temperature, the satellite signals and coupling constants of the and 207 Pb NMR spectra were not observed, reflecting the kinetically labile nature of the Pb-F bond at room temperature.The reactive nature of the Pb-F bond was further confirmed when 4 was treated with trifluoroacetophenone to yield a homoleptic Pb(II) compound(34) along with the formation of insoluble PbF 2 (Scheme 12).20 The solid-state structure of 34 shows a spirocyclic structure where the two six-membered C 3 ONPb rings are interconnected by the common Pb atom.