Insights into the Composition and Structural Chemistry of Gallium(I) Triflate

Abstract “GaOTf” is a simple, convenient source of low‐valent gallium for synthetic chemistry and catalysis. However, little is currently known about its composition or reactivity. In this work, 71Ga NMR spectroscopy shows the presence of [Ga(arene)n]+ salts on oxidation of Ga metal with AgOTf in arene solvents. However, a more complex picture of speciation is uncovered by X‐ray diffraction studies. In all cases, mixed‐valence compounds containing Ga‐arene and Ga‐OTf coordination motifs, in addition to an unusual “naked” [Ga]+ ion, are found. Addition of 18‐crown‐6 allows for the isolation of a discrete GaI crown complex. Evidence of a potential intermediate in the formation of “GaOTf” has been isolated in the form of the bimetallic silver(I)/gallium(I) cluster anion [Ag4{Ga(OTf)3}4(μ‐Ga)6(OTf)4]2−.

Abstract: "GaOTf" is a simple, convenient source of lowvalent gallium for synthetic chemistry and catalysis. However, little is currently known about its composition or reactivity. In this work, 71 Ga NMR spectroscopy shows the presence of [Ga(arene) n ] + salts on oxidation of Ga metal with AgOTf in arene solvents. However, a more complex picture of speciation is uncovered by X-ray diffraction studies. In all cases, mixedvalence compounds containing Ga-arene and Ga-OTf coordination motifs, in addition to an unusual "naked" [Ga] + ion, are found. Addition of 18-crown-6 allows for the isolation of a discrete Ga I crown complex. Evidence of a potential intermediate in the formation of "GaOTf" has been isolated in the form of the bimetallic silver(I)/gallium(I) cluster anion [Ag 4 {Ga(OTf) 3 } 4 (m-Ga) 6 (OTf) 4

] 2À .
Gallium occupies a fascinating position in Group 13. Much of its chemistry is dominated by the + 3 oxidation state, like the lighter elements, but it also displays an extensive range of low oxidation state compounds. There have been a number of breakthroughs in the development of starting materials for low-valent gallium chemistry, each of which has advantages and disadvantages. True Ga I halides are thermodynamically unstable, and while they can be trapped and utilized, this requires specialist equipment. [1] Ga 2 Cl 4 (formulated as Ga + -[GaX 4 ] À ) has been known for many years, and has an extensive coordination chemistry with arene ligands, [2] but often undergoes dis-or comproportionation on reaction with other species. "GaI" can be an excellent source of Ga I , but like Ga 2 Cl 4 also has a tendency towards unexpected behavior. [3] [Ga 2 C 5 Me 5 ][B(Ar F ) 4 ] salts are capable of delivering Ga + ions as ligands to suitable transition-metal complexes. [4] [Ga(arene) n ] + [Al(OC(CF 3 ) 3 ) 4 ] À (n = 2, 3) salts are wellbehaved sources of Ga I , but these anions are still not as widely used as simple weakly coordinating anions (WCAs) such as triflate. [5] More recently, Ga I species have been accessed via reductive elimination of H 2 from Ga III dihy-drides. [6] Furthermore, a family of Ga-based carbenoids, with differing charges and ring sizes, have emerged as important building blocks in low-valent Ga chemistry and have been used as ligands in coordination chemistry. [7] There are a growing number of reports of Ga I involvement in catalysis and the development of new, more accessible, well-behaved low-valent gallium sources is particularly important to allow this area to grow. [Ga(arene) n ] + salts catalyze the polymerization of alkenes, [5e,f, 6] and have been shown to be active catalysts for cycloisomerization, transfer hydrogenation, and reductive hydroarylation reactions. [9] There is also evidence for Ga I involvement in important mechanistic steps that underpin many catalytic reactions, for example, reductive elimination, suggesting exciting possibilities for the Ga I /Ga III redox couple in other catalytic reactions. [3c, 6] In related work, the use of Ga 0 in synthesis and materials chemistry has received attention. [10] Schneider et al. recently reported the preparation of a new low-valent gallium reagent "GaOTf" (OTf = [O 3 SCF 3 ] À ) using a similar route to the preparation of [Ga(arene) n ] + [Al(OC(CF 3 ) 3 ) 4 ] À salts, [5a] where gallium metal is oxidized by AgOTf in arene solvents, or dioxane in the presence of 18-crown-6. [8] "GaOTf" solutions were then used as ambiphilic catalysts for C À C bond forming reactions ( Figure 1). Control experiments with Ga III salts, Ag 0 or other metal triflates showed that the presence of low oxidation-state Ga was important for catalytic activity. 71 Ga NMR spectroscopy suggested the formation of a [Ga(18crown-6)][OTf].(dioxane) n complex under catalytic conditions and other stoichiometric studies allowed a catalytic cycle involving Ga I -alkoxide and -allyl intermediates to be proposed. However, speciation in "GaOTf", particularly in arene solvents, was not explored in detail. Given the potential wider uses of "GaOTf" as one of the most easily accessible sources of Ga I yet reported, herein we explore the composition and Figure 1. Low-valent-Ga catalyzed reaction between acetals, ketals, or aminals and allyl boronic esters reported by Schneider (top) [8] and this work (below). structural chemistry of the "GaOTf" system in detail for the first time.
Reaction of AgOTf and Ga metal in toluene under ultrasonic activation (see Figure 1 for summary) led to the immediate formation of a pale-yellow solution and after ca. 1.5 hours of ultrasonication a dense black precipitate. After filtration, 71 Ga NMR spectroscopy showed a single, relatively sharp peak at À692 ppm, which is characteristic of a gallium(I) arene complex. [2] Storage of the solution overnight at À20 8C led to the formation of pale brown crystals, which X-ray crystallography revealed to contain [Ga][Ga(C 6 H 5 Me) 2 ] 2 -[Ga 3 (OTf) 8 ] (1; Figure 2).
The counterions in 1 are not simple [OTf] À ions, but the previously unknown trianion [Ga 3 (OTf) 8 ] 3À . This is composed of a catenated [Ga 3 ] 5+ core, coordinated by eight [OTf] À and is related to the Ga 3 X 5 L 3 motif identified by Schnçckel in [Ga 3 I 5 (PEt 3 ) 3 ], [12] the monoanion [Ga 3 (OTf) 6 (GaCp*) 2 ] À reported by Linti [13] and Baines [Ga 3 Cl 4 (crypt-222)] + cation. [14] Indeed, these species can all be viewed as Ga 3 X 5 L 3 -type compounds, where X = I, Cl, or OTf and L is either a neutral (PEt 3 , GaCp* or crypt-222) or anionic ([OTf] À ) ligand. In Baines system one X À has been lost and the [Ga 3 ] 5+ core forms an additional bond to the cryptand to compensate for this. Comparing the structural parameters of [Ga 3 (OTf) 8 ] 3À with other Ga 3 X 5 L 3 -type compounds shows that the average Ga À Ga bond lengths are shorter in [Ga 3 -(OTf) 8 ] 3À (2.374 , compared to 2.456 in [Ga 3 I 5 (PEt 3 ) 3 ], 2.426 in [Ga 3 (OTf) 6 (GaCp*) 2 ] À and 2.416 in [Ga 3 Cl 4 (crypt-222)] + ). These species are all mixed-valence Ga compounds and different oxidation state models have been proposed. In [Ga 3 (OTf) 8 ] 3À a Ga II -Ga I -Ga II model, in analogy to [Ga 3 I 5 (PEt 3 ) 3 ], would seem appropriate. However, recent XAS studies suggest that assignment of formal oxidation states in such species is challenging and a Ga I -Ga III -Ga I model is also feasible. [14b] Other examples of catenated Ga and In species, some with quite extended structures, have been reported and are of note. [7e, 12, 13, 15] In an attempt to prevent disproportionation and the formation of higher oxidation state species, "GaOTf" was prepared as described above, but with the addition of four equivalents of hexamethylbenzene, as a more p-basic arene. [16] The 71 Ga NMR spectrum after ultrasonication and filtration featured a single peak at À707 ppm. Colorless crystals were grown by storage of the solution at À20 8C and X-ray diffraction studies showed these to have the composition [Ga(C 6 H 5 Me)(C 6 Me 6 )] 2 [Ga 2 (OTf) 6 ] (2; Figure 3).
It can now be seen that there are several isolable lowvalent-gallium-containing species, both cationic and anionic, within "GaOTf" solutions. The composition of the crystalline material is only a snapshot of some of the potential species present in solution. What is clear, however, is that "GaOTf" is more complex than it might initially appear and multiple Ga coordination environments and oxidation states are present. This realization is very important for the interpretation of catalytic studies involving "GaOTf", as the catalytically active species could involve several possible Ga oxidation states.
Schneider et al. showed that addition of 18-crown-6 to "GaOTf" improved the yields in their catalytic CÀC bond forming reactions. [8] To investigate the potential for lowvalent Ga-crown complex formation in this system, "GaOTf" solutions were prepared in toluene, as described above, filtered and the filtrate added to a solution containing 18crown-6. In suitably concentrated solutions, this led to the spontaneous formation of colorless, block-like crystals. This was encouraged by low temperature at the time of filtration. X-ray diffraction studies revealed these to contain [Ga(18crown-6)(OTf)] (3; Figure 4).
Compound 3 is only the second structurally authenticated Ga I -18-crown-6 complex, the first being [Ga (18- 4 ] displays no con-tacts between the gallium cation and the more weakly coordinating alkoxyaluminate anion. Instead, weak Ga-C 6 H 5 F interactions above and below the plane of the crown complete the coordination sphere around Ga. Coordination of [OTf] À to Ga in 3 appears to lead to a weakening of the Gacrown interactions, with average Ga-O(crown) distances of 2.840 and 2.800 for 3 and [Ga(18-crown-6)(C 6 H 5 F) 2 ][Al-(OC(CF 3 ) 3 ) 4 ] respectively. Complex 3 can be compared to the isostructural indium salt [In(18-crown-6)(OTf)]. [22] In this case, the average In À O(crown) distance is longer (2.874 ) than in 3, suggesting that the larger In + ion sits slightly above the crown, compared to Ga. The Ga-OTf distance in 3 (2.137 ) is 0.233 shorter than the InÀOTf distance in [In(18-crown-6)(OTf)], closely mirroring the difference between the ionic radii of gallium(I) and indium(I) (0.23 ). [23] A related [Ga (12-crown-4)] + salt has also been reported in a recent PhD thesis and coordination of Ga + by the tridentate PMDETA ligand, somewhat related to crown ethers, is also noted for comparison. [24] Unlike in 1 and 2, the presence of 18-crown-6 in 3 appears to facilitate the formation of a Ga I salt with a discrete [OTf] À anion, rather than a complex Ga-containing polyanion. This may be because the crown offers additional stability to Ga I towards disproportionation, which could explain its positive impact in Schneiders catalysis. [8] Indeed, in our hands 3 is considerably more stable than solutions from which 1 or 2 are isolated, which readily disproportionate over time or on removal of the solvent.
To explore the electronic structure of 3, DFT studies were performed (see the Supporting Information for details). The optimized structure of 3 (at the (RI-)BP86/SV(P) level) is shown in Figure 5. Comparisons between 3 and other gallium-(I) species, such as GaCp*, can be drawn from analysis of the DFT data. [4f] Natural bond orbital (NBO) calculations (at the (RI-)PBE0/def2-TZVPP//(RI-)BP86/SV(P) level) suggest that there is a small amount of sp character to the Ga I lone pair (3 % p character), which gives some directionality, as shown in Figure 5. This is very similar to the hybridization in GaCp* (4 % p character), which has an established coordination chemistry as a ligand to other metals, and suggests that 3 may prove to be an interesting new low-valent Ga-based ligand, an area under investigation in our laboratory.  To explore speciation during the formation of "GaOTf" at shorter time periods, a toluene solution of AgOTf and a bead of Ga was sonicated for less than one hour. Filtration produced an orange solution, from which block-like orange crystals were formed after storage at À20 8C for four days. Xray diffraction studies revealed these to be salt (4), which is composed of two [Ga(C 6 H 5 Me) 2 ] + ions, the novel and unusual Ga-Ag cluster ion [Ag 4 {Ga(OTf) 3 } 4 (m-Ga) 6 (OTf) 4 ] 2À ( Figure 6) and a toluene molecule of crystallization. In light of the presence of both Ag I and low-valent Ga species in 4, we speculate that this may represent an intermediate species present at short reaction times during the formation of 1 or related systems. It is also a compound of significant fundamental interest and will be discussed below.
Although the overall XRD data quality for 4 are relatively poor, due to extensive disorder in the [Ga(C 6 H 5 Me) 2 ] + ions and toluene of crystallization, they are sufficient to confirm the composition of the salt and some discussion of the cluster anion, which is quite well resolved, is reasonable. The [Ag 4 {Ga(OTf) 3 } 4 (m-Ga) 6 Figure 7.
Although uncommon, clusters based around a tetrahedral [Ag 4 ] 4+ core, with vertex-capping or bridging ligands are not without precedent (for example, [Ag 4 (m 3 -I) 4 I 4 ] 4À and [Ag 4 -(TeC 4 H 3 S) 6 ] 2À ). [25] Most are based around conventional donor ligands such as halides, S-or Te-based ligands, rather than the unusual low-valent Ga ligands seen here. However, low oxidation state main-group ligands based on stanna-closododecaborate dianions have been found to stabilize an [Ag 4 ] 4+ cluster in [{Ag(m 3 -SnB 11 H 11 )(PMe 3 )} 4 ] 4À . [26] The AgÀAg bonds within 4 (av. 2.87 ) are amongst the shortest found for structures of this type on the Cambridge Crystallographic Database (av. for ten structures containing [Ag 4 ] 4+ tetrahedra is 3.110 ). Compound 4 contains only the fourth example of structurally authenticated Ag À Ga bonds. The average Ag-[Ga(OTf) 3 ] 2À bond length of 2.47 is shorter than the AgÀGa bond lengths found in [Ag(GaCp*) 4 ] + (average 2.519 ), [27] but longer than those found within the complexes  [28] The Ga-containing N-heterocyclic carbene analogue [Ga( Dip DAB)] À is known to be a strong donor ligand, GaCp* less so, and so based on Ag-Ga bond lengths alone it appears that the donor properties of [Ga(OTf) 3 ] 2À lie in between that of GaCp* and [Ga- Only one example of a complex that could be considered to involve the [Ga(OTf) 3 ] 2À motif has previously been reported, [(Cp*Ga)Cu(m-GaCp*) 3 Cu{Ga(OTf) 3 }] (5; Figure 8). [29] The authors formulate this as a Lewis acid/base adduct between [(Cp*Ga)Cu(m-GaCp*) 3 Cu], comprising two Cu 0 centers, and Ga III triflate. An alternative view, in light of our analysis of compound 4, is that 5 could involve two Cu I centers, with the [(Cp*Ga)Cu(m-GaCp*) 3 Cu] 2+ ion coordinated by [Ga(OTf) 3 ] 2À . As noted above, for Ga 3 X 5 L 3 , it is challenging to unambiguously assign oxidation states to such species. [14b] However, some features of 5 suggest that a Ga I / Cu I model is a plausible alternative formulation. The Cu-{Ga(OTf) 3 } distance (2.2906 ) is shorter than the terminal Cu-GaCp* distance (2.3268 ). This is consistent with the shorter Ag À Ga distances in Ag-[Ga(OTf) 3 ] 2À complexes compared to Ag-GaCp* complexes, as described above. The average GaÀOTf distances for the "Ga(OTf) 3 " unit in 5 (1.975 ) are more similar to those in 4 (1.996 ) than to the shorter Ga-OTf distances in Ga III systems such as [Ga(OTf) 3 -(THF) 3 ] (1.945 ). [13] Finally, NBO calculations carried out on 5 and the dianionic cluster in 4 are consistent with a similar Ga I donor model for the "Ga(OTf) 3 " units in both. In particular, the gallium center contributes 72 % of the electron    (5). [29] Angewandte Chemie Communications density to the GaÀCu bond in 5 and 85 % to the GaÀAg bond in 4.
In conclusion, a number of low-valent gallium species have been isolated from "GaOTf" solutions in aromatic solvents. These suggest that "GaOTf" in toluene is best considered a mixed-valence compound, even in the presence of more p-basic arenes, such as hexamethybenzene. However, the reaction of "GaOTf" with [18]-crown-6 leads to the isolation of a relatively stable univalent gallium crown ether complex. This simplification in speciation, compared to the crown-free system, may be linked to improved catalytic behavior seen by Schneider et al. Additionally, the bimetallic silver(I)/gallium(I) cluster anion [Ag 4 {Ga(OTf) 3 } 4 (m-Ga) 6 -(OTf) 4 ] 2À has been identified at short reaction times. Thus, while "GaOTf" solutions are very promising reagents for the emerging field of low-valent Ga catalysis, care is required when considering catalytic mechanisms, as the complex speciation in these systems mean that it may not always be obvious what the catalytically active metal and/or oxidation state will be.