Cyclic phosphonium ionic liquids

Ionic liquids (ILs) incorporating cyclic phosphonium cations are a novel category of materials. We report here on the synthesis and characterization of four new cyclic phosphonium bis(trifluoromethylsulfonyl)amide ILs with aliphatic and aromatic pendant groups. In addition to the syntheses of these novel materials, we report on a comparison of their properties with their ammonium congeners. These exemplars are slightly less conductive and have slightly smaller self-diffusion coefficients than their cyclic ammonium congeners.


Introduction
The most widely investigated and commercially available ionic liquids (ILs) are composed primarily of nitrogen-centered (particularly imidazolium, pyridinium, pyrrolidinium, and related quaternary ammonium) cations with a wide range of anions [1].While a number of these ILs have been applied successfully to commercial processes [1], efforts are continu-ally underway to synthesize ILs with improved properties (such as viscosity, thermal stability, melting point, etc.) to expand their applications into larger scale processes in diverse areas.Along that vein, phosphonium ILs have been observed to have favorable characteristics, including lower costs [2][3][4][5][6], lower viscosity (by ~50%) [7][8][9][10][11], greater thermal stability (by ~100 °C) [10][11][12], and wider electrochemical windows compared to their ammonium congeners.The family of ILs bearing cyclic cations (pyrrolidinium, piperidinium, and azepanium) [13,14] have been shown to have better transport and physical properties than most acyclic tetraalkylammonium salts.While cyclic phosphonium salts have been noted in patent applications [15], their characteristics have not been reported therein nor in journals, even though the comparisons noted above suggest those properties might be advantageous.To address such questions, we report here on the synthesis and physical characterization of some phosphonium analogues to pyrrolidinium and piperidinium ILs, i.e. phospholanium and phosphinanium ILs respectively.
The favorable stability of phosphonium ILs makes them good choices for applications where the IL would be exposed to extreme conditions, such as environmental exposure to high temperatures or exposure to extreme electromagnetic radiation (as in a dye-sensitized solar cell or ionizing radiation as in the recycling of spent nuclear fuel).ILs can play important roles in both of these latter areas [16].While dialkylimidazolium ILs can be efficient extraction media for nuclear separations [17][18][19], the imidazolium cation is also a good acceptor of radiolytically produced excess electrons.The resultant radical participates in radiation damage mechanisms that alter the IL's properties [20].On the other hand, phosphonium ILs, known for their durability and already made in large quantities, can be optimized for extraction of specific species from radioactive spent nuclear fuel.Inclusion of phenyl groups, as in two of the new ILs reported here, can stabilize excess charges (electrons or holes) leading to a more durable extraction system.The question of whether cyclic phosphonium ILs would succeed in solar photoconversion or spent fuel processing depends not only on whether their properties can be tuned to the application, but also whether their reactivity under extreme conditions can be managed.
A major challenge for this work has been the handling of the tertiary phosphine precursors, which are pyrophoric and extremely air sensitive.1-n-Butylphospholane and 1-nbutylphosphinane were synthesized by the reaction of n-butyldichlorophosphine [21] with the appropriate bis-Grignard reagents, BrMg(CH 2 ) 4 MgBr and BrMg(CH 2 ) 5 MgBr respectively.The resultant cyclic phosphines are air sensitive and therefore were allowed to react with BH 3 •THF to provide the air-stable 1-n-butylphospholane-borane and 1-n-butylphosphinane-borane complexes that were purified by silica-gel chromatography.The pure compounds were then treated under nitrogen with 1,4-diazabicyclo[2.2.2]octane (DABCO) at 80 °C to remove the borane, and the resultant mixture was purified in a nitrogen-filled glove box on a short silica-gel column.The pure cyclic phosphines (1-n-butylphospholane and 1-n-butylphosphinane) were allowed to react immediately with iodomethane at room temperature to produce the 1-n-butyl-1-methylphospholanium iodide and 1-n-butyl-1-methylphosphinanium iodide, respectively.These materials were each mixed with an equivalent amount of lithium bis(trifluoromethylsulfonyl)amide (LiNTf 2 ) in water at room temperature to produce the water-insoluble salts, 1-n-butyl-1-methylphospholanium bis(trifluoromethylsulfonyl)amide and the corresponding 1-n-butyl-1-methylphosphinanium bis(trifluoromethylsulfonyl)amide.In a corresponding manner were prepared the 1-phenylphospholane and the 1-phenylphosphinane by the reaction of dichlorophenylphosphine with the appropriate bis-Grignard reagents, BrMg(CH 2 ) 4 MgBr and BrMg(CH 2 ) 5 MgBr, respectively.The resulting five-membered cyclic 1-phenylphospholane was isolated in the same manner as was the 1-n-butylphospholane: i.e. by conversion with BH 3 •THF to give the air-stable 1-phenylphospholane-borane complex, followed by silica-gel chromatography and then removal of the borane with DABCO, to give the pure 1-phenylphospholane.The six-membered cyclic phosphine, which appears to be less air sensitive than the 1-butylphosphinane species, was purified in open air using a short column of silica gel.Both cyclic phosphines were each allowed to react with 1-bromobutane at reflux under nitrogen to give the 1-n-butyl-1-phenylphospholanium bromide (4c) and the 1-n-butyl-1-phenylphosphinanium bromide (4d), respectively.Each of these salts was then mixed with aqueous LiNTf 2 to form the 1-n-butyl-1-phenylphospholanium bis(trifluoromethylsulfonyl)amide (5c) and the corresponding 1-n-butyl-1phenylphosphinanium bis(trifluoromethylsulfonyl)amide (5d).The overall synthetic route is summarized in Scheme 1.

Results and Discussion
The conductivities, viscosities, self-diffusion coefficients and thermal properties of the phosphonium ILs 5a-d and their ammonium congeners are given in Table 1.
Comparison of the five-membered cyclic cation ILs C 4 mPphol NTf 2 5a and C 4 mPyrr NTf 2 (butylmethylpyrrolidinium NTf 2 ) reveals that the viscosity of the phosphonium salt is one third higher than that of the ammonium salt (101 cP vs 75 cP at 25 °C).For the six-membered rings the phosphonium IL C 4 mPphin NTf 2 5b is slightly less viscous than C 4 mPip NTf 2 (butylmethylpiperidinium NTf 2 ), 171 cP vs 183 cP.Interestingly, the cyclic cations do not follow the common trend among Scheme 1: Reaction scheme for the preparation of cyclic phosphonium ionic liquids.c Value subject to dispute, either −25 °C [25] or just below 0 °C [27].
the quaternary tetra-n-alkylated cations wherein the room temperature viscosities of the phosphonium salts are approximately one-half of those of their ammonium congeners [7][8][9][10][11].This difference draws attention to the particular role that the cyclic alkyl functionality plays in IL fluid dynamics in contrast to two linear chains.This topic merits further exploration via molecular dynamics simulations [28] and physical studies such as NMR diffusion measurements, nuclear Overhauser effect spectroscopies, and quasi-elastic neutron scattering.As seen for instance for the cyclic ammonium salts, the viscosities of the cyclic phosphonium salts increase with increasing ring size for two of the compounds synthesized.As suggested by the viscosity results, the conductivities of the phosphonium ILs are lower than those for their ammonium congeners, and that for both families they decrease with increasing ring size.The conductivity of C 4 mPphol NTf 2 (2.2 mS/cm) is slightly smaller than that of the C 4 mPyrr (2.8 mS/cm) although not as much as expected from the viscosity difference.The self-diffusion coefficients of the anion (D − ) and the cation (D + ) are somewhat lower for the phosphonium salts than the ammonium ones.Interestingly, despite its slightly lower viscosity, C 4 mPphin IL has lower diffusion coefficients than C 4 mPip NTf 2 .
For the P-versus-N pairs where direct comparisons can be made, the glass-transition temperatures T g are very close, allowing for experimental differences.In contradiction to the trend for linear tetraalkyl cations, the melting temperatures (T m ) for the cyclic phosphonium salts are higher than those of their cyclic ammonium congeners.C 4 mPphol NTf 2 melts 23 °C higher than does C 4 mPyrr NTf 2 , and C 4 mPphin NTf 2 melts 31 °C higher than does C 4 mPip NTf 2 .Henderson and Passerini [29] showed that the often-cited T m of −18 °C for C 4 mPyrr NTf 2 was due to a metastable crystalline form by using an annealing process.The DSC scan of un-annealed C 4 mPphol NTf 2 shows all the thermal features exhibited by un-annealed C 4 mPyrr NTf 2 (glass transition, cold crystallization, solid-solid transition, and melting).When the recommended annealing method [24] was applied to C 4 mPphol NTf 2 the first three thermal features listed just above were eliminated, but the position of the melting point did not change.The apparent thermal decomposition temperature (T d ) of the cyclic phosphonium NTf 2 ILs are not particularly different from those of the cyclic ammonium NTf 2 ILs, which is similar to the situation of linear alkyl quaternary cation ILs [11].In some instances where the anion is nucleophilic, such as with dicyanamide [12], or the leaving group is resonance-stabilized, such as a benzyl radical [10], the phosphonium cations have greater thermal stability than the ammonium ones.One trend observed for both cation types is that the ILs with five-membered rings have greater thermal stability than those with six-membered rings.Further work will be required to determine if the observed TGA behaviors are due to actual decomposition or to volatility of the ILs [30].
While developing our synthetic approach to the aliphatic C 4 mPphol + and C 4 mPphin + cations, which requires the use of highly air-sensitive reagents and intermediates as described above, we refined our techniques using less reactive phenylphosphines.The resulting butylphenylphospholanium (C 4 PhPphol NTf 2 ) and butylphenylphosphinanium (C 4 PhPphin NTf 2 ) ionic liquids are examples of a rare class of ILs with direct attachment of the aryl group to the cationic center.We were unable to find any information on ILs containing analogous nitrogen-centered cations for comparison, although ILs with aryl groups attached directly to the nitrogen atoms of imidazolium cations are reported [31].The melting points of the phenylphosphonium ILs are both above room temperature (see Table 1), however C 4 PhPphol NTf 2 is persistently metastable as a supercooled liquid under ambient conditions.The most significant effects observed for the replacement of a methyl group with a phenyl ring in this family of cations are the substantial increases of 19 °C and 30 °C in the glass-transition temperatures for the 5-and 6-membered ring cations respectively.Similar effects on T g have been reported for other classes of ILs bearing benzyl groups [32].This family of cations may have the useful attributes for reducing radiation-induced damage of the IL owing to the stabilization of excess charges on the phenyl groups.

Conclusion
We have successfully prepared a series of new cyclic phosphonium ILs that are representatives of a wide class of potentially useful ILs.These exemplars are slightly less conductive and have slightly smaller self-diffusion coefficients than their cyclic ammonium congeners.Their viscosities are also lower than their ammonium congeners.In other instances, such as the peculiarities in melting point and viscosity trends of the C-2methylated imidazolium salts [33], ether-substituted ILs [34], and bis(oxalato)borate salts [35], detailed investigation into those intriguing behaviors led to deeper insights into the dynamical workings of ILs that have had important impacts on the field.For this reason we will continue to explore cyclic phosphonium ILs through synthesis of a wider variety of structural types and substituents, variation of anions, and more extensive characterization of their physical, structural, and dynamical properties.In particular, this family of ILs, by comparison with the more familiar cyclic ammonium ILs, should reveal the dynamical effects of cyclic vs linear alkyl chains on the physical properties of ionic liquids.Sciences Geosciences and Biosciences under contract # DE-AC02-98CH10886.