Effect of Dimethyl Carbonate on the Dynamic Properties and Ionicities of Ionic Liquids with [MIII(hfip)4]− (M=B,Al) Anions

Several ionic liquids (ILs) comprising [B(hfip)₄]^? [hfip=OCH(CF₃)₂] or [Al(hfip)₄]^? anions and imidazolium or ammonium cations were prepared and mixed with up to 270 mol % of dimethyl carbonate (DMC). The viscosities, conductivities, and self‐diffusion constants of these mixtures and, where possible, of the neat ILs were measured and compared with common [NTf₂]^? based ILs and their mixtures with DMC. A tremendous decrease of the viscosities and a likewise increase of the conductivities and diffusion constants can be achieved for all classes of ILs. However, the order of the conductivities is partially reversed in the diffusion data. This is probably due to the low dielectric constant of DMC and the, thus, favored ion pairing, as evidenced, for example, by the calculated ionicities. Altogether, our data show that the chemically robust, but high‐melting and more viscous [B(hfip)₄]^? ILs might be candidates for electrolytes when mixed with suitable molecular solvents.     

Size Matters! On the Way to Ionic Liquid Systems without Ion Pairing

Several, partly new, ionic liquids (ILs) containing imidazolium and ammonium cations as well as the medium‐sized [NTf₂]^? (0.230 nm³; Tf=CF₃SO₃^?) and the large [Al(hfip)₄]^? (0.581 nm³; hfip=OC(H)(CF₃)₂) anions were synthesized and characterized. Their temperature‐dependent viscosities and conductivities between 25 and 80 °C showed typical Vogel–Fulcher–Tammann (VFT) behavior. Ion‐specific self‐diffusion constants were measured at room temperature by pulsed‐gradient stimulated‐echo (PGSTE) NMR experiments. In general, self‐diffusion constants of both cations and anions in [Al(hfip)₄]^?‐based ILs were higher than in [NTf₂]^?‐based ILs. Ionicities were calculated from self‐diffusion constants and measured bulk conductivities, and showed that [Al(hfip)₄]^?‐based ILs yield higher ionicities than their [NTf₂]^? analogues, the former of which reach values of virtually 100 % in some cases.From these observations it was concluded that [Al(hfip)₄]^?‐based ILs come close to systems without any interactions, and this hypothesis is underlined with a Hirshfeld analysis. Additionally, a robust, modified Marcus theory quantitatively accounted for the differences between the two anions and yielded a minimum of the activation energy for ion movement at an anion diameter of slightly greater than 1 nm, which fits almost perfectly the size of [Al(hfip)₄]^?. Shallow Coulomb potential wells are responsible for the high mobility of ILs with such anions.     

Ionic liquids with perfluorinated alkoxyaluminates

Ionic liquids with the weakly coordinating perfluoroalkoxyaluminate anions, Al(ORF)4-, are obtained by a metathesis reaction of LiAl(ORF)4 and [bmim]Cl or [bmpyr]Cl in high yields. The compounds [bmim][Al(hfip)4] and [bmpyr][Al(hfip)4] have surprisingly low viscosities at elevated temperatures (60 degrees C) and an exceptionally high electrochemical window, which might render them useful for certain applications.     

Extending the coordination chemistry of molecular P(4)S(3): the polymeric Ag(P(4)S(3))(+) and Ag(P(4)S(3))(2)(+) cations

Upon reacting P(4)S(3) with AgAl(hfip)(4) and AgAl(pftb)(4) [hfip = OC(H)(CF(3))(2); pftb = OC(CF(3))(3)], the compounds Ag(P(4)S(3))Al(hfip)(4) 1 and Ag(P(4)S(3))(2)(+)[Al(pftb)(4)](-) 2 formed in CS(2) (1) or CS(2)/CH(2)Cl(2) (2) solution. Compounds 1 and 2 were characterized by single-crystal X-ray structure determinations, Raman and solution NMR spectroscopy, and elemental analyses. One-dimensional chains of [Ag(P(4)S(3))(x)](infinity) (x = 1, 1; x = 2, 2) formed in the solid state with P(4)S(3) ligands that bridge through a 1,3-P,S, a 2,4-P,S, or a 3,4-P,P eta(1) coordination to the silver ions. Compound 2 with the least basic anion contains the first homoleptic metal(P(4)S(3)) complex. Compounds 1 and 2 also include the long sought sulfur coordination of P(4)S(3). Raman spectra of 1 and 2 were assigned on the basis of DFT calculations of related species. The influence of the silver coordination on the geometry of the P(4)S(3) cage is discussed, additionally aided by DFT calculations. Consequences for the frequently observed degradation of the cage are suggested. An experimental silver ion affinity scale based on the solid-state structures of several weak Lewis acid base adducts of type (L)AgAl(hfip)(4) is given. The affinity of the ligand L to the silver ion increases according to P(4) < CH(2)Cl(2) < P(4)S(3) < S(8) < 1,2-C(2)H(4)Cl(2) < toluene.     

A remarkable anion effect on palladium nanoparticle formation and stabilization in hydroxyl-functionalized ionic liquids

Pd nanoparticles (NPs) with a small size and narrow size distribution were prepared from the decomposition of Pd(OAc)(2) in a series of hydroxyl-functionalized ionic liquids (ILs) comprising the 1-(2'-hydroxylethyl)-3-methylimidazolium cation and various anions, viz. [C(2)OHmim][OTf] (2.4 ± 0.5 nm), [C(2)OHmim][TFA] (2.3 ± 0.4 nm), [C(2)OHmim][BF(4)] (3.3 ± 0.6 nm), [C(2)OHmim][PF(6)] (3.1 ± 0.7 nm) and [C(2)OHmim][Tf(2)N] (4.0 ± 0.6 nm). Compared with Pd NPs isolated from the non-functionalized IL, [C(4)mim][Tf(2)N] (6.2 ± 1.1 nm), it would appear that the hydroxyl group accelerates the formation of the NPs, and also helps to protect the NPs from oxidation once formed. Based on the amount of Pd(OAc)(2) that remains after NP synthesis (under the given conditions) the ease of formation of the Pd NPs in the [C(2)OHmim](+)-based ILs follows the trend [Tf(2)N](-), [PF(6)](-) > [BF(4)](-) > [OTf](-) > [TFA](-). Also, the ability of the [C(2)OHmim](+)-based ILs to prevent the Pd NPs from undergoing oxidation follows the trend [Tf(2)N](-) > [PF(6)](-) > [TFA](-) > [OTf](-) > [BF(4)](-). DFT calculations were employed to rationalize the interactions between Pd NPs and the [C(2)OHmim](+) cation and the various anions.     

Isolated cationic crown ether complexes of gallium(I) and indium(I)

The recently reported homologous low-valent indium and gallium salts M(+)[Al(OR(F))(4)](-) (M = Ga, In; R(F) = C(CF(3))(3)) were used to extend the coordination chemistry of Ga(I) and In(I) to the isolated [18]crown-6 complexes [M([18]crown-6)(PhF)(2)](+)[Al(OR(F))(4)](-) in fluorobenzene solution (PhF = C(6)H(5)F). In contrast to known ion-paired compounds for M = In, our complexes are undisturbed and in the solid state free of contacts to the anion. A peculiar combination of very weak η(1)- and η(6)-coordination to the PhF-solvent was observed that allows speculation about the presence of a stereochemically active lone pair at M(I). Structure and energetics of these novel salts were rationalized on the basis of DFT calculations.     

Enhanced refolding of lysozyme with imidazolium-based room temperature ionic liquids: Effect of hydrophobicity and sulfur residue

The expression of recombinant proteins in microorganism frequently leads to the formation of insoluble aggregates, inclusion bodies (IBs). Thus, the additional in vitro protein refolding process is required to convert inactive IBs into water-soluble active proteins. This study investigated the effect of sulfur residue and hydrophobicity of imidazolium-based room temperature ionic liquids (RTILs) on the refolding of lysozyme as a model protein in the batch dilution method which is the most commonly used refolding method. When lysozyme was refolded in the refolding buffer containing [BF4]-based RTILs with a systematic variety of alkyl chain on cations varying from two to eight, less hydrophobic imidazolium cations having shorter alkyl chains were effective to facilitate lysozyme refolding. Compared to the conventional refolding buffer, 2 times higher lysozyme refolding yield was obtained in 1-ethyl-3-methylimidazolium tetrafluoroborate ([EMIM][BF4]) containing refolding buffer. The refolding yield of lysozyme was even more increased by 2.5 times when 1-butyl-3-methylimidazolium methylsulfate ([BMIM][MS]) containing sulfur residue on anion was used. The sulfur residue in [BMIM][MS] is supposed to improve the refolding yield of lysozyme which has 4 intramolecular disulfide bonds. For dilution-based refolding of lysozyme, the optimum concentrations of RTILs in refolding buffer were found to be 1.0 M [EMIM][BF4] and 0.5 M [BMIM][MS], respectively. The optimum temperate for dilution-based refolding of lysozyme with RTILs was 4 °C.     

Screening the extractability of some typical environmental pollutants by ionic liquids in liquid-phase microextraction

The extractability of some typical environmental pollutants in ionic liquids (ILs) was screened by using a simple one-step liquid phase microextraction procedure. It was demonstrated that 1-alkyl-3-methylimidazolium hexafluorophosphate ([CnMIM][PF6], n = 4, 8), two typical ILs, could effectively extract a set of 45 typical environmental pollutants including BTEX (benzene, toluene, ethylbenzene, and xylene), polycyclic aromatic hydrocarbons, phthalates, phenols, aromatic amines, herbicides, organotin, and organomecury. Analytes in 10 mL sample solution held in a 15 mL vial were extracted by a 5 microL drop of ILs suspended on the needle of a high-performance liquid chromatography (HPLC) microsyringe; this was followed by HPLC, atomic absorption spectrometry, or cold-vapor atomic fluorescence spectrometry determination. The enrichment factors determined were in the range of 5-168 for 15 min extraction by [C4MIM][PF6] and 4-178 for 30 min extraction by [C8MIM][PF6], respectively, which indicates that ILs might be considered as potential environmentally benign alternative recyclable solvents for the enrichment of environmental pollutants.     

Thermally triggered reductive elimination of bromine from Au(III) as a path to Au(I)-based coordination polymers

Four new [AuBr(2)(CN)(2)](-)-based coordination polymers, Zn(pyz)(NCMe)(2)[AuBr(2)(CN)(2)](2) (1; pyz = pyrazine), Co(pyz)[AuBr(2)(CN)(2)](2)·H(2)O (2) and [M(bipy)(2)(AuBr(2)(CN)(2))][(n)Bu(4)N][AuBr(2)(CN)(2)](2) (bipy = 4,4'-bipyridine), where M = Co (5) and Zn (6), were synthesized and three of them structurally characterized. 1 forms 1-D chains connected by pyz ligands while isostructural 5 and 6 form 3-D frameworks via [AuBr(2)(CN)(2)](-) and bipy linkers. Aqueous suspensions of 2, 5 and 6 or their precursors in situ (preferred) were heated hydrothermally to 125 °C, triggering the reductive elimination of bromine from the Au(III) centres, which yielded the [Au(CN)(2)](-)-based coordination polymers M(pyz)[Au(CN)(2)](2), where M = Zn (3) or Co (4) and Zn(bipy)[Au(CN)(2)][Au{Br(0.68)(CN)(0.32)}CN] (7), or a mixture of cyanoaurate(I)-containing products in the case of 5 and 6. The structural characterization of 3 revealed a [Au(CN)(2)](-)/pyz-based framework similar to previously reported Cu(pyz)[Au(CN)(2)](2), whereas 7 formed an intricate network consisting of individual 2-D networks held together by AuAu interactions and featuring the rare [AuBrCN](-) unit. The kinetics of the thermally-induced reductive elimination of Br(2) from K[AuBr(2)(CN)(2)] in 1-BuOH yielded a t(?) of approx. 10 min to 4 h from 98 to 68 °C, and activation parameters of ΔH(?) = 131(15) kJ mol(-1) and ΔS(?) = 14.97(4) kJ K(-1)mol(-1), indicating that the elimination of the halogen provides the highest barrier to activation.     

Synthesis, reactivity, electrochemical behavior, and crystal structure of a family of multivalent metal carbido-carbonyl clusters based on the rh(10)(c)(2)au(4-6) framework

Six metal carbido-carbonyl clusters have been isolated and recognized as members of a multivalent family based on the dioctahedral Rh(10)(C)(2) frame, with variable numbers of CO ligands, AuPPh(3) moieties, and anionic charge: [Rh(10)(C)(2)(CO)(x)(AuPPh(3))(y)](n-) (x = 18, 20; y = 4, 5, 6; n = 0, 1, 2). Anions [Rh(10)(C)(2)(CO)(18)(AuPPh(3))(4)](-) ([2](-)) and [Rh(10)(C)(2)(CO)(18)(AuPPh(3))(4)](2-) ([2](2-)) have been obtained by the reduction of [Rh(10)(C)(2)(CO)(18)(AuPPh(3))(4)] (2) under N(2), while [Rh(10)(C)(2)(CO)(18)(AuPPh(3))(5)](-) ([3](-)) was obtained from [Rh(10)(C)(2)(CO)(20)(AuPPh(3))(4)] (1) by reduction under a CO atmosphere. [3](-) can be better obtained by the addition of AuPPh(3)Cl to [2](2-). [Rh(10)(C)(2)(CO)(18)(AuPPh(3))(6)] (4) is obtained from [3](-) and 2 as well by the reduction and subsequent addition of AuPPh(3)Cl. The molecular structures of [2](2-) ([NBu(4)](+) salt), [3](-) ([NMe(4)](+) salt), and 4 have been determined by single-crystal X-ray diffraction. The redox activities of complexes 1, 2 and [3](-) have been investigated by electrochemical and electron paramagnetic resonance (EPR) techniques. The data from EPR spectroscopy have been accounted for by theoretical calculations.     

CCl3(+) and CBr3(+) salts with the [Al(OR(F))4]- and [((F)RO)3Al-F-Al(OR(F))3]- anions (R(F) = C(CF3)3)

The CX3(+) salts [CCl(3)](+)[Al(OR(F))(4)](-)1, [CCl(3)](+)[(R(F)O)(3)Al-F-Al(OR(F))(3)](-)2, [CBr(3)](+)[Al(OR(F))(4)](-)3, [CBr(3)](+)[(R(F)O)(3)Al-F-Al(OR(F))(3)](-)4 (R(F) = C(CF(3))(3)) were prepared in 56 to 85% yield from CX(4) (X = Cl, Br) and the corresponding silver salts (weight balance, NMR, IR, X-ray structure of 1). The most convenient solvent for the preparation of 1 and 2 is SO(2)ClF but for 3 and 4 it is SO(2). The reactions are complete after about three days stirring at -30 to -40 °C. The salts are stable for weeks in solution at -40 °C and stable for a few hours at RT in the solid state. In SO(2)ClF (1, 2) or SO(2) (3, 4) solution they decompose slowly at -20 °C and within several hours at RT; in general the CBr3(+) salts are more stable than the CCl3(+) homologues. The decomposition products were assigned as CCl(3)F and primarily CBr(2)F(2) (which likely forms as a Lewis acid induced disproportionation product of the initial CBr(3)F). The C-X vibrations of the salts were found in the expected range and the assignments were made based on experimental and calculated data. The IR spectrum of a CBr3(+) salt is for the first time reported here.     

Ionic liquid-based liquid-phase microextraction, a new sample enrichment procedure for liquid chromatography

Room temperature ionic liquids (RTILs) were used as extraction solvent in liquid-phase microextraction (LPME) coupled with liquid chromatography. Using 1-hexyl-3-methylimidazolium hexafluorophosphate ([C6MIM][PF6]) as extraction solvent, some parameters related to LPME of 4-nonylphenol (4-NP) and 4-tert-octylphenol (4-t-OP) were optimized. Although [C6MIM][PF6] can suspend a much larger volume of drop on the needle of the microsyringe than the conventional solvents such as 1-octanol and carbon tetrachloride, the method sensitivity was analyte dependent because of the different partition coefficients and the relatively large viscosity of [C6MIM][PF6]. The proposed procedure has a detection limit and enrichment factor of 0.3 microg l(-1) and 163 for 4-NP, and 0.7 microg l(-1) and 130 for 4-t-OP, respectively. Aqueous samples including tap water, river water, and effluent from sewage treatment plant were analyzed by the proposed method and the recoveries at 10 microg l(-1) spiked level were in the range of 90-113%.     

Cyclometallated Pt(II) and Pd(II) complexes with a trithiacrown ligand

We report the synthesis and full characterization for a series of cyclometallated complexes of Pt(II) and Pd(II) incorporating the fluxional trithiacrown ligand 1,4,7-trithiacyclononane ([9]aneS3). Reaction of [M(C insertion mark N)(micro-Cl)]2 (M = Pt(II), Pd(II); C insertion mark N = 2-phenylpyridinate (ppy) or 7,8-benzoquinolinate (bzq)) with [9]aneS3 followed by metathesis with NH4PF6 yields [M(C insertion mark N)([9]aneS3)](PF6). The complexes [M(C insertion mark P)([9]aneS3)](PF6) (M = Pt(II), Pd(II); Cinsertion markP = [CH2C6H4P(o-tolyl)2-C,P]-) were synthesized from their respective [Pt(C insertion mark P)(micro-Cl)]2 or [Pd(C insertion mark P)(micro-O2CCH3)]2 (C insertion mark P) starting materials. All five new complexes have been fully characterized by multinuclear NMR, IR and UV-Vis spectroscopies in addition to elemental analysis, cyclic voltammetry, and single-crystal structural determinations. As expected, the coordinated [9]aneS3 ligand shows fluxional behavior in its NMR spectra, resulting in a single 13C NMR resonance despite the asymmetric coordination environment of the cyclometallating ligand. Electrochemical studies reveal irreversible one-electron metal-centered oxidations for all Pt(II) complexes, but unusual two-electron reversible oxidations for the Pd(II) complexes of ppy and bzq. The X-ray crystal structures of each complex indicate an axial M-S interaction formed by the endodentate conformation of the [9]aneS3 ligand. The structure of [Pd(bzq)([9]aneS3)](PF6) exhibits disorder in the [9]aneS3 conformation indicating a rare exodentate conformation as the major contributor in the solid-state structure. DFT calculations on [Pt([9]aneS3)(ppy)](PF6) and [Pd([9]aneS3)(ppy)](PF6) indicate the HOMO for both complexes is primarily dz2 in character with a significant contribution from the phenyl ring of the ppy ligand and p orbital of the axial sulfur donor. In contrast, the calculated LUMO is primarily ppy pi* in character for [Pt([9]aneS3)(ppy)](PF6), but dx2-y2 in character for [Pd([9]aneS3)(ppy)](PF6).     

Synthesis and characterization of the dimercury(I)-linked compound [PPn]4[(Re7C(CO)21Hg)2]. Oxidative cleavage of the mercury-mercury bond leading to carbidoheptarhenate complexes of mercury(II), including [PPN][Re7C(CO)21Hg(S=C(NME2)2)

The reaction of [PPN](3)[Re(7)C(CO)(21)] with Hg(2)(NO(3))(2).2H(2)O in dichloromethane formed the complex [PPN](4)[(Re(7)C(CO)(21)Hg)(2)] ([PPN](4)[1]), isolated in 60% yield. Analogous salts of [1](4-) with [PPh(4)](+) and [NEt(4)](+) were also prepared. The crystal structure of [PPN](4)[1] showed that two carbidoheptarhenate cores are linked by a dimercury(I) unit (d(Hg-Hg) = 2.610(4) A), with each individual mercury atom face-bridging. Oxidative cleavage of the Hg-Hg bond in [1](4-) was effected by 4-bromophenyl disulfide to form [Re(7)C(CO)(21)HgSC(6)H(4)Br](2-) ([4](2-)), by I(2) to form [Re(7)C(CO)(21)HgI](2-) ([5](2-)), and by Br(2) to form [Re(7)C(CO)(21)HgBr](2-) ([6](2-)). Oxidation of [1](4-) by ferrocenium ion (2 equiv) in the presence of tetramethylthiourea resulted in the derivative [Re(7)C(CO)(21)HgSC(NMe(2))(2)](-) ([7](-)). The molecular structure of [PPN][7] was determined by X-ray crystallography. This is the first example of a carbidoheptarhenate-mercury complex with a neutral ligand on mercury, and ligand exchange was demonstrated by displacement with triethylphosphine. Complex [7](-) can also be prepared by protonating [Re(7)C(CO)(21)HgO(2)CCH(3)](2-) in the presence of tetramethylthiourea. Cyclic voltammetry data to calibrate and compare the redox properties of compounds [1](4-) and [7](-) have been measured.     

Interactions of 1-butyl-3-methylimidazolium carboxylate ionic liquids with glucose in water: a study of volumetric properties, viscosity, conductivity and NMR

Extensive applications of ionic liquids (ILs) may result in their accumulation in the ecological environment and organisms. Although ILs are popularly called "green solvents", their toxicity, in fact, has been exhibited. Therefore the interaction of ILs with biomolecules is a cutting-edge research subject. Herein, the interactions of 1-butyl-3-methylimidazolium carboxylate ionic liquids ([C(4)mim][HCOO], [C(4)mim][CH(3)COO] and [C(4)mim][CH(3)CH(2)COO]) with glucose in water were studied for their volumetric properties, viscosity, conductivity and NMR spectra. Limiting apparent molar volumes (V(Φ, IL)(0)), viscosity B-coefficients, limiting molar conductivities (Λ(0)) and Walden products (Λ(0)η(0)) were evaluated for the ILs in glucose + water solutions. Volumetric interaction parameters were also obtained from the transfer volumes of the ionic liquids. The contributions of the solvent properties (B(1)) and the ionic liquid-solvent interactions (B(2)) to the B-coefficient were extracted, together with molar activation energies (Δμ(IL)(0≠)) of the ionic liquids for viscous flow of the aqueous glucose + IL solution. In addition, the (13)C and (1)H NMR spectra of methyl β-D-glucopyranoside and ILs in β-D-glucopyranoside + IL + D(2)O were studied. The NMR results show that no special and strong interactions were observed between glucopyranoside and the ILs. However, it was confirmed that the H2 on the imidazolium ring has more activity (acidity) than atoms H4 and H5. The macro-properties and their changes were also discussed in terms of the size, structure and solvation of the ILs and glucose.     

Why are viscosities lower for ionic liquids with -CH2Si(CH3)3 vs -CH2C(CH3)3 substitutions on the imidazolium cations?

We have prepared novel room temperature ionic liquids (RTILs) with trimethylsilylmethyl (TMSiM)-substituted imidazolium cations and compared the properties of these liquids with those for which the TMSiM group is replaced by the analogous neopentyl group. The ionic liquids are prepared with both tetrafluoroborate (BF(4)(-)) and bis(trifluoromethylsulfonyl)imide (NTf(2)(-)) anions paired with the imidazolium cations. At 22 degrees C, the TMSiM-substituted imidazolium ILs have shear viscosities that are reduced by a factor of 1.6 and 7.4 relative to the alkylimidazolium ILs for the NTf(2)(-) and BF(4)(-) anions, respectively. To understand the effect of silicon substitution on the viscosity, the charge densities have been calculated by using density functional theory electronic structure calculations. The ultrafast intermolecular, vibrational, and orientational dynamics of these RTILs have been measured by using femtosecond optical heterodyne-detected Raman-induced Kerr effect spectroscopy (OHD-RIKES). The intermolecular dynamical spectrum provides an estimate of the strength of interactions between the ions in the RTILs, and provides a qualitative explanation for the observed reduction in viscosity for the silicon-substituted RTILs.     

Unusual Anions [LAl(SH)(S)]- and [LAl(S)2]2- stabilized by weakly coordinating imidazolium cations. synthesis of LAl(SSiMe2)2O (L = HC[C(Me)N(Ar)]2, Ar = 2,6-iPr2C6H3)

Deprotonation of an Al-SH moiety has been achieved easily by using N-heterocyclic carbene as the base. Monomeric mono- and bis-imidazolium salts [C(t)H(+)][LAl(SH)(S)](-) ([C(t)H(+)] = N,N'-bis-tert-butylimidazolium), [C(m)H(+)][LAl(SH)(S)](-), and [C(m)H(+)](2)[LAl(S)(2)](2-) ([C(m)H(+)] = N,N'-bismesitylimidazolium), containing unusual anions [LAl(SH)(S)](-) and [LAl(S)(2)](2-), have been synthesized in nearly quantitative yields. Furthermore, [C(m)H(+)](2)[LAl(S)(2)](2-) has been successfully used for the preparation of LAl(SSiMe(2))(2)O containing the [O(Me(2)SiS)(2)](2-) ligand.     

Estimation of physicochemical properties of ionic liquids 1-alkyl-3-methylimidazolium chloroaluminate

The density and surface tension of ionic liquids [C(2)mim][AlCl(4)] (1-ethlyl-3-methyl imidazolium chloroaluminate) and [C(6)mim][AlCl(4)] (1-hexyl-3-methylimidazolium chloroaluminate) were measured in the temperature range from 283.15 to 338.15 +/- 0.05 K. In terms of these experimental results, the estimation of physicochemical properties of 1-alkyl-3-methylimidazolium chloroaluminate ([C(n)mim][AlCl(4)], n = 1-6) was carried out. With the use of the parachor, the values of surface tension of the ILs were predicted. In terms of Glasser's theory, the standard molar entropy, lattice energy, and surface properties of the ILs were estimated. With the use of Kabo's method and Rebelo's method, the molar enthalpy of vaporization of the ILs, Delta(l)(g)H(m)(0), was predicted. According to the interstice model, the values of the thermal expansion coefficient of the ILs were also estimated. Since the magnitude order of the thermal expansion coefficient estimated by the model is in good agreement with that measured experimentally, this result means that the interstice model is reasonable.     

Effect of imidazolium-based ionic liquids on the aggregation behavior of twin-tailed cationic gemini surfactant in aqueous solution

Micellization behavior of the twin-tailed surfactants can be modulated by the addition of various modifiers. Ionic liquids (ILs) are one of them and are documented here. The beauty of these environmentally benign neoteric molecules lies in their structural versatility. Here, we have investigated the effect of three ILs: 1-butyl-3-methylimidazolium bromide ([C₄mim][Br]), 1-hexyl-3-methylimidazolium bromide ([C₆mim][Br]), and 1-octyl-3-methylimidazolium bromide ([C₈mim][Br]) on the aggregation and surface adsorption behavior of cationic gemini surfactant, bis(hexadecyldimethyl ammonium)propane dibromide (16-3-16) through experimentally measured electrical conductivities, surface tensions, and by spectral methods (UV-vis absorbance and fluorescence measurements). The main focus of the study is to observe the effect of added ILs on the critical micelle concentration (cmc), various surface parameters, aggregation number, and size of the aggregates of gemini surfactant. The results show that the more hydrophobic ILs, that is, [C₆mim][Br] and [C₈mim][Br] behave as electrolyte at lower concentration and cosurfactant at higher concentration, whereas moderately hydrophobic IL [C₄mim][Br] acts as an electrolyte at all concentration ranges studied. The modulating effects of ILs were also compared with conventional electrolyte (NaBr) at similar conditions.