Acetonitrile Complex Research Articles

Carbodicarbene‐Stibenium Ion‐Mediated Functionalization of C(sp3)−H and C(sp)−H Bonds

AbstractMain‐group element‐mediated C−H activation remains experimentally challenging and the development of clear concepts and design principles has been limited by the increased reactivity of relevant complexes, especially for the heavier elements. Herein, we report that the stibenium ion [(pyCDC)Sb][NTf2]3 (1) (pyCDC=bis‐pyridyl carbodicarbene; NTf2=bis(trifluoromethanesulfonyl)imide) reacts with acetonitrile in the presence of the base 2,6‐di‐tert‐butylpyridine to enable C(sp3)−H bond breaking to generate the stiba‐methylene nitrile complex [(pyCDC)Sb(CH2CN)][NTf2]2 (2). Kinetic analyses were performed to elucidate the rate dependence for all the substrates involved in the reaction. Computational studies suggest that C−H activation proceeds via a mechanism in which acetonitrile first coordinates to the Sb center through the nitrogen atom in a κ1 fashion, thereby weakening the C−H bond which can then be deprotonated by base in solution. Further, we show that 1 reacts with terminal alkynes in the presence of 2,6‐di‐tert‐butylpyridine to enable C(sp)−H bond breaking to form stiba‐alkynyl adducts of the type [(pyCDC)Sb(CCR)][NTf2]2 (3 a–f). Compound 1 shows excellent specificity for the activation of the terminal C(sp)−H bond even across alkynes with diverse functionality. The resulting stiba‐methylene nitrile and stiba‐alkynyl adducts react with elemental iodine (I2) to produce iodoacetonitrile and iodoalkynes, while regenerating an Sb trication.

Au(I) complexes installed on a self-assembled peptide efficiently catalyze intramolecular cyclization reactions.

Self-assembled peptides are used for diverse applications in the biomedical and technological fields. The morphology and function of the assembled systems are dictated by the peptide sequence and length. In this work, a supramolecular catalyst was obtained upon self-assembly of the diphenylalanine peptide conjugated to a triphenylphosphine Au(I) complex in acetonitrile. The assembled molecules were characterized by spectroscopic techniques and by scanning electron microscopy. The activity of the catalyst was tested on two substrates in cyclization reactions. The morphology and the dimensions of the assembled systems vary depending on the presence of a carboxyl versus an amide C-terminal end. The catalyst efficiently promotes intramolecular cyclization reactions. Results obtained encourage the use of self-assembled peptides for the obtainment of new and efficient catalysts.

Photophysics and photochemistry of (n-Bu4N)2[Pt(NO3)6] in acetonitrile: ultrafast pump-probe spectroscopy and quantum chemical insight.

The ultrafast processes caused by photoexcitation of (n-Bu4N)2[Pt(NO3)6] complex in acetonitrile were studied by means of transient absorption (TA) pump-probe spectroscopy and verified by quantum chemical calculations. The primary photochemical process was found to be an inner-sphere electron transfer followed by an escape of an •NO3 radical to the bulk solution. The reaction occurs via the dissociative triplet excited LMCT state of the initial complex. Based on the experimental data and quantum chemical calculations, the mechanism of ultrafast photophysical and photochemical processes is proposed.

Carbodicarbene-Stibenium Ion-Mediated Functionalization of C(sp3)-H and C(sp)-H Bonds.

Main-group element-mediated C-H activation remains experimentally challenging, and the development of clear concepts and design principles have been limited by the increased reactivity of relevant complexes, especially for the heavier elements. Herein, we report that the stibenium ion [(pyCDC)Sb][NTf2]3(1) (pyCDC = bis-pyridyl carbodicarbene; NTf2= bis(trifluoromethanesulfonyl)imide) reacts with acetonitrile in the presence of the base 2,6-di-tert--butylpyridine to enable C(sp3)-H bond breaking to generate the stiba-methylene nitrile complex [(pyCDC)Sb(CH2CN)][NTf2]2(2). Kinetic analyses were performed to elucidate the rate dependence for all the substrates involved in the reaction. Computational studies suggest that C-H activation proceeds via a mechanism in which acetonitrile first coordinates to the Sb center through the nitrogen atom in aκ1fashion, thereby weakening the C-H bond which can then be deprotonated by base in solution. Further, we show that1reacts with terminal alkynes in the presence of 2,6-di-tert--butylpyridine to enable C(sp)-H bond breaking to form stiba-alkynyl adducts of the type [(pyCDC)Sb(CCR)][NTf2]2(3a-f). Compound1shows excellent specificity for the activation of the terminal C(sp)-H bond even across alkynes with diverse functionality. The resulting stiba-methylene nitrile and stiba-alkynyl adducts react with elemental iodine (I2) to produce iodoacetonitrile and iodoalkynes, while regenerating an Sb trication.

Concerning the structures of Lewis base adducts of titanium(IV) hexafluoroisopropoxide.

The reaction of titanium(IV) chloride with sodium hexafluoroisopropoxide, carried out in hexafluoroisopropanol, produces titanium(IV) hexafluoroisopropoxide, which is a liquid at room temperature. Recrystallization from coordinating solvents, such as acetonitrile or tetrahydrofuran, results in the formation of bis-solvate complexes. These compounds are of interest as possible Ziegler-Natta polymerization catalysts. The acetonitrile complex had been structurally characterized previously and adopts a distorted octahedral structure in which the nitrile ligands adopt a cis configuration, with nitrogen lone pairs coordinated to the metal. The low-melting tetrahydrofuran complex has not provided crystals suitable for single-crystal X-ray analysis. However, the structure of chloridotris(hexafluoroisopropoxido-κO)bis(tetrahydrofuran-κO)titanium(IV), [Ti(C3HF6O)3Cl(C4H8O)2], has been obtained and adopts a distorted octahedral coordination geometry, with a facial arrangement of the alkoxide ligands and adjacent tetrahydrofuran ligands, coordinated by way of metal-oxygen polar coordinate interactions.

Synthesis and Lewis Acid Properties of Neutral Silver(III) Adducts Containing the AgIII(CF3)3 Moiety.

The acetonitrile AgIII complex [AgIII(CF3)3(NCCH3)] (2) has been reported independently by Eujen and Naumann in the last century, albeit with intriguing NMR discrepancy. In their reports, 2 was claimed to be obtained starting from either [AgIII(CF3)3Cl]- (3⋅Cl) or [AgIII(CF3)4]- (1) via halide abstraction using AgNO3 or acidic treatment, resp. These two synthetic routes are herein reinvestigated. The feasibility of Naumann's method is demonstrated, thus providing 2 yet accompanied by its s-triazinyl derivative [AgIII(CF3)3(C6H9N3)] (2'). The formation of 2' is unprecedented and was thereby investigated. Both 2 and 2' were isolated in pure fashion and fully characterized. In turn, halide extraction from 3⋅Cl leads to the AgIII-ONO2 anion 5 instead of 2, as evidenced by NMR spectroscopy, EA and Sc-XRD.

Photorelease of Nitric Oxide (NO) in Mono- and Bimetallic Ruthenium Nitrosyl Complexes: A Photokinetic Investigation with a Two-Step Model.

Two monometallic and three bimetallic ruthenium acetonitrile (RuMeCN) complexes are presented and fully characterized. All of them are built from the same skeleton [FTRu(bpy)(MeCN)]2+, in which FT is a fluorenyl-substituted terpyridine ligand and bpy is the 2,2'-bipyridine. The crystal structure of [FTRu(bpy)(MeCN)](PF6)2 is presented. A careful spectroscopic analysis allows establishing that these 5 RuMeCN complexes can be identified as the product of the photoreaction of 5 related RuNO complexes, investigated as efficient nitric oxide (NO) donors. Based on this set of complexes, the mechanism of the NO photorelease of the bimetallic complexes has been established through a complete investigation under irradiations performed at 365, 400, 455, and 490 nm wavelength. A two-step (A → B → C) kinetic model specially designed for this purpose provides a good description of the mechanism, with quantum yields of photorelease in the range 0.001-0.029, depending on the irradiation wavelength. In the first step of release, the quantum yields (ϕAB) are always found to be larger than those of the second step (ϕBC), at any irradiation wavelengths.

Photochemistry of (n-Bu4N)2[Pt(NO3)6] in acetonitrile.

Photochemistry of the (n-Bu4N)2[Pt(NO3)6] complex in acetonitrile was studied by means of stationary photolysis and nanosecond laser flash photolysis. The primary photochemical process was found to be an intramolecular electron transfer followed by an escape of an •NO3 radical to the solution bulk. The spectra of two successive Pt(III) intermediates were detected in the microsecond time domain, and their spectral and kinetic characteristics were determined. These intermediates were identified as PtIII(NO3)52- and PtIII(NO3)4- complexes. Disproportionation of Pt(III) species resulted in formation of final Pt(II) products.

Tc(NO)(Cp)(PPh3)Cl] and [Tc(NO)(Cp)(PPh3)(NCCH3)](PF6), and Their Reactions with Pyridine and Chalcogen Donors.

Reactions of the technetium(I) nitrosyl complex [Tc(NO)(Cp)(PPh3)Cl] with triphenylphosphine chalcogenides EPPh3 (E = O, S, Se), and Ag(PF6) in a CH2Cl2/MeOH mixture (v/v, 2/1) result in an exchange of the chlorido ligand and the formation of [Tc(NO)(Cp)(PPh3)(EPPh3)](PF6) compounds. The cationic acetonitrile complex [Tc(NO)(Cp)(PPh3)(NCCH3)]+ is formed when the reaction is conducted in NCCH3 without additional ligands. During the isolation of the corresponding PF6- salt a gradual decomposition of the anion was detected in the solvent mixture applied. The yields and the purity of the product increase when the BF4- salt is used instead. The acetonitrile ligand is bound remarkably strongly to technetium and exchange reactions readily proceed only with strong donors, such as pyridine or ligands with 'soft' donor atoms, such as the thioether thioxane. Substitutions on the cyclopentadienyl ring do not significantly influence the ligand exchange behavior of the starting material. 99Tc NMR spectroscopy is a valuable tool for the evaluation of reactions of the complexes of the present study. The extremely large chemical shift range of this method allows the ready detection of corresponding ligand exchange reactions. The observed 99Tc chemical shifts depend on the donor properties of the ligands. DFT calculations support the discussions about the experimental results and provide explanations for some of the unusual findings.

Single-Crystal X-ray Structure Determination of Tris(pyrazol-1-yl)methane Triphenylphosphine Copper(I) Tetrafluoroborate, Hirshfeld Surface Analysis and DFT Calculations

The tetrafluoroborate salt of the cationic Cu(I) complex [Cu(CHpz3)(PPh3)]+, where CHpz3 is the tridentate N-donor ligand tris(pyrazol-1-yl)methane and PPh3 is triphenylphosphine, was synthesized through a displacement reaction on the acetonitrile complex [Cu(NCCH3)4][BF4]. The compound crystallizes in the monoclinic P21/c space group. The single-crystal X-ray diffraction revealed that the copper(I) centre is tetracoordinated, with a disposition of the donor atoms surrounding the metal centre quite far from the ideal tetrahedral geometry, as confirmed by continuous shape measures and by the τ4 parameter. The intermolecular interactions at the solid state were investigated through the Hirshfeld surface analysis, which highlighted the presence of several non-classical hydrogen bonds involving the tetrafluoroborate anion. The electronic structure of the crystal was modelled using plane-wave DFT methods. The computed band gap is around 2.8 eV and separates a metal-centred valence band from a ligand-centred conduction band. NMR spectroscopy indicated the fluxional behaviour of the complex in CDCl3 solution. The geometry of the compound in the presence of chloroform as implicit solvent was simulated by means of DFT calculations, together with possible mechanisms related to the fluxionality. The reversible dissociation of one of the pyrazole rings from the Cu(I) coordination sphere resulted in an accessible process.

Coordination and fragmentation chemistry of CyMe4-BTPhen complexes with lanthanides and actinides: A combined investigation by ESI-MS and DFT calculations.

To further understand the complexation and fragmentation during the extraction process, the formation of 2,9-bis(5,5,8,8-tetramethyl-5,6,7,8-tetrahydro-12,4-benzotriazin-3-yl)-1,10-phenanthroline (CyMe4-BTPhen) complexes with lanthanides (Ln = La, Ce, Nd, Sm, Eu, Yb) and actinides (UO22+, Th4+) was observed by electrospray ionization mass spectrometry (ESI-MS) technique and density functional theory (DFT) calculations. Mass spectrometry titrations showed the variation relationship of different complexes in acetonitrile. For lanthanides, the major complexes were 1:2 species ([Ln(L)2]3+ and [Ln(L)2(NO3)]2+) with a ratio of 1:2, which were observed at the initial addition of Ln3+, whereas the species ([Ln(L)(NO3)2]+) with a ratio of 1:1 was detected when the [Ln]/[L] concentration ratio reached 1.0. For UO22+ and Th4+ complexes, 1:1 or 1:2 species ([UO2L(NO3)]+, Th(L)2(NO3)3+ and Th(L)2(NO3)22+) were formed. The fragmentation chemistry of both the ligand and the complex cations was characterized in detail by collision-induced dissociation. The fragmentation process of CyMe4-BTPhen was unfolded sequentially on both sides of the ligand by cleavage of C-C and C-N bonds. DFT calculations provided a detailed analysis of the structures and thermodynamics of those complexes, which indicated that the stable complexes formed in acetonitrile solution were consistent with the ESI-MS results.

Closed Synthetic Cycle for Nickel-Based Dihydrogen Formation.

Dihydrogen evolution was observed in a two-step protonation reaction starting from a Ni0 precursor with a tripodal N-heterocyclic carbene (NHC) ligand. Upon the first protonation, a NiII monohydride complex was formed, which was isolated and fully characterized. Subsequent protonation yields H2 via a transient intermediate (INT) and an isolable NiII acetonitrile complex. The latter can be reduced to regenerate its Ni0 precursor. The mechanism of H2 formation was investigated by using a deuterated acid and scrutinized by 1 H NMR spectroscopy and gas chromatography. Remarkably, the second protonation forms a rare nickel dihydrogen complex, which was detected and identified in solution and characterized by 1 H NMR spectroscopy. DFT-based computational analyses were employed to propose a reaction profile and a molecular structure of the Ni-H2 complex. Thus, a dihydrogen-evolving, closed-synthetic cycle is reported with a rare Ni-H2 species as a key intermediate.

New Ruthenium Nitrosyl Complexes Combining Potentially Photoactive Nitrosyl Group with the Magnetic Nitroxide Radicals as Ligands.

Two ruthenium nitrosyl complexes of Na[RuNOCl4L] with nitronyl nitroxide radicals coordinated to ruthenium with N-donor pyridine rings were prepared and described. The crystal structure of both complexes is 1D or 2D polymeric, due to the additional coordination of sodium cation by bridging the chloride ligands or oxygen atoms of nitroxides. Partially, the oligomeric forms remain in the solutions of the complexes in acetonitrile. The magnetic measurements in the solid state demonstrate the presence of antiferromagnetic interactions through the exchange channels, with the distance between paramagnetic centers equal to 3.1-3.9 Å. The electrochemical behavior of the prepared complexes was investigated in acetonitrile solutions.

Silver(I) complexes with nitrile ligands: New materials with versatile applications

In the present study, the structure, thermal stability, conductive properties, and antimicrobial activity of silver(I) complexes with nitrile ligands were investigated. For the construction of the materials, 2‐cyanopyridine (2‐cpy), 4‐cyanopyridine (4‐cpy), 1,2‐dicyanobenzene (1,2‐dcb), and 1,3‐dicyanobenzene (1,3‐dcb) were used in addition to the silver nitrite and nitrate. Four new compounds were isolated and structurally characterized: one molecular complex [Ag4(1,2‐dcb)4(NO3)4], two 1‐D coordination polymers [Ag(2‐cpy)2(NO2)]∞, [Ag2(1,3‐dcb)2(NO3)2]∞, and one 3‐D coordination polymer [Ag(4‐cpy)(NO2)]∞. The results indicate that the nitrile complexes display good antimicrobial properties against the tested bacterial and fungal strains. The presence of weakly coordinating CN groups increases the release of silver ions into the bacterial and yeast cell environments. Moreover, these materials exhibit unusual electrical properties in thin‐layer devices. On the other hand, the nitrite and nitrate counterions give rise to the low thermal stability of the complexes.

Sulfonamido-Pincer Complexes of Cu(II) and the Electrocatalysis of O2 Reduction.

Heteroleptic copper complexes of an asymmetrical pincer ligand containing a central anionic sulfonamide donor (pyridine-2-yl-sulfonyl)(quinolin-8-yl)-amide (psq), which contains a central anionic sulfonamido donor have been prepared. Meridional κ3-N,N″,N‴ binding with the co-ligands acetate, chloride, or acetonitrile (MeCN), trans to the central sulfonamido N-donor, is revealed by the X-ray crystal structures of [Cu(OAc)(psq)(H2O)], [CuCl(psq)]2, and [Cu(psq)(MeCN)](PF6). Either overall distorted square pyramidal or octahedral geometries of the copper atom are satisfied by coordinated water in the case of the acetate complex or interactions with periphery sulfonamido oxygen atoms on adjacent molecules in the dimeric chloride and 1D polymeric acetonitrile complexes. The cyclic voltammogram (CV) of [Cu(OAc)(psq)(H2O)] shows a quasi-reversible CuII/CuI reduction at -0.930 V (vs Fc+/Fc0, MeCN), and an irreversible CuII/CuI reduction for [Cu(psq)(MeCN)](PF6) is seen at -0.838 V. This signal is split into two quasi-reversible redox processes on the addition of 2,2,2-trifluoroethanol (TFE). This suggests that TFE pushes a solution equilibrium toward a dimeric acetate complex analogous to [CuCl(psq)]2, which shows two quasi-reversible waves at -0.666 V and -0.904 V vs Fc+/Fc0 consistent with its dimeric solid-state structure. A comparison of the CVs of [Cu(OAc)(psq)(H2O)] under either a N2 or an O2 atmosphere revealed that this complex catalyzes turnover electro-reduction of O2 to H2O2 and H2O. The rate of reaction increases on addition of a weak organic acid, and a coulombic efficiency of 48% for H2O2 was determined by iodometric titration. We propose that a CuI complex formed on electroreduction binds O2 to yield an intermediate superoxide complex. On electron and proton transfer to this species, a bifurcated route back to the O2-activating CuI complex is feasible with either release of H2O2 or O-O cleavage resulting in the liberation of H2O. The CuI complex is regenerated by subsequent reduction and protonation to close the cycle.

2,3-Diarylquinoline -Based Iridium (III) Complexes: Synthesis, Photophysical Properties and DFT studies

Phosphorescent transition–metal complexes have received considerable interest in the development of efficient organic light-emitting diodes (OLEDs). Iridium complexes derived from heterocyclic ligands have brought a paradigm shift in the optoelectronic materials. Quinoline-based molecular architectures offer excellent materials for such applications due to their exceptional electronic properties, extended π-conjugation and strong ligand–metal binding. Iridium complexes of 2,3-diaryl quinolines with electron rich and electron deficient substituents were synthesized and their electronic properties were studied. Iridium complexes Ir1 and Ir2 bearing the electron withdrawing (-CF3) and electron donating (–OCH3) groups, respectively at the para position of the 2-phenyl ring of 2,3-diarylquinoline exhibited prominent absorption bands in the UV range. Further, the complex Ir3 with unsubstituted 2,3-diarylquinoline ligand and CF3 containing Ir1 showed intensive red phosphorescence near 603 and 611 nm, respectively due to metal-to-ligand and ligand-to-ligand (MLCT/LLCT) charge transfer characteristics. The photoluminescence (PL) spectra of the Ir4 complex derived from 2-phenylquinoline ligand exhibited a bright yellow phosphorescent emission at 589 nm. An additional C3 aryl group on the quinoline ring resulted in a red shift in the emission wavelength of Ir1 and Ir3 complexes compared to Ir4. The PL spectra of Ir2 on the other hand was weak, and blue-shifted to 489 nm, which can be attributed to a ligand-centered (LC) transition. The complexes showed photoluminescence quantum yield (PLQY) in the range of 0.004 to 0.17 and fluorescence lifetime ranged from 1.5 ns to 399 ns, implying the significant effect of the ligand structure on the properties of the complexes. Photophysical investigation of the complexed affirms these complexes to be potent materials for OLEDs fabrication. Cyclic voltammetry was used to investigate the electrochemical characteristics of Ir1-Ir4 complexes in acetonitrile. All of the complexes Ir1-Ir4 exhibited irreversible oxidation waves at 0.44 V, 0.23 V, 0.25 V, and 0.24 V respectively. Ir1-Ir4 complexes showed a reduction potential at −0.98 V, −0.96 V, −1.02 V and −0.97 V respectively. The DFT calculations were used to explore HOMO-LUMO energies, and NBO characteristics by B3LYP level of theory using ECP type double zeta (DZ) quality basis set LanL2DZ for metal and 6-311G(d) basis sets for non-metal atoms. The theoretical calculations were in significant agreement with the experimental studies of these complexes.

Binding of Nitriles and Isonitriles to V(III) and Mo(III) Complexes: Ligand vs Metal Controlled Mechanism.

The synthesis and structures of nitrile complexes of V(N[tBu]Ar)3, 2 (Ar = 3,5-Me2C6H3), are described. Thermochemical and kinetic data for their formation were determined by variable temperature Fourier transform infrared (FTIR), calorimetry, and stopped-flow techniques. The extent of back-bonding from metal to coordinated nitrile indicates that electron donation from the metal to the nitrile plays a less prominent role for 2 than for the related complex Mo(N[tBu]Ar)3, 1. Kinetic studies reveal similar rate constants for nitrile binding to 2, but the activation parameters depend critically on the nature of R in RCN. Activation enthalpies range from 2.9 to 7.2 kcal·mol-1, and activation entropies from -9 to -28 cal·mol-1·K-1 in an opposing manner. Density functional theory (DFT) calculations provide a plausible explanation supporting the formation of a π-stacking interaction between a pendant arene of the metal anilide of 2 and the arene substituent on the incoming nitrile in favorable cases. Data for ligand binding to 1 do not exhibit this range of activation parameters and are clustered in a small area centered at ΔH‡ = 5.0 kcal·mol-1 and ΔS‡ = -26 cal·mol-1·K-1. Computational studies are in agreement with the experimental data and indicate a stronger dependence on electronic factors associated with the change in spin state upon ligand binding to 1.

Artifact-free balanced detection for the measurement of circular dichroism with a sub-picosecond time resolution.

Here we present the development of a subpicosecond spectropolarimeter enabling high sensitivity balanced detection of time-resolved circular dichroism (TRCD) signals from chiral sample in solution. The signals are measured with a conventional femtosecond pump-probe set-up using the combination of a quarter-waveplate and a Wollaston prism. This simple and robust method allows access to TRCD signals with improved signal-to-noise ratio and very short acquisition times. We provide a theoretical analysis of the artifacts of such detection geometry and the strategy to eliminate them. We illustrate the potential of this new detection with the study of the [Ru(phen)3]·2PF6 complexes in acetonitrile.

Ligand Rigidity Steers the Selectivity and Efficiency of the Photosubstitution Reaction of Strained Ruthenium Polypyridyl Complexes.

While photosubstitution reactions in metal complexes are usually thought of as dissociative processes poorly dependent on the environment, they are, in fact, very sensitive to solvent effects. Therefore, it is crucial to explicitly consider solvent molecules in theoretical models of these reactions. Here, we experimentally and computationally investigated the selectivity of the photosubstitution of diimine chelates in a series of sterically strained ruthenium(II) polypyridyl complexes in water and acetonitrile. The complexes differ essentially by the rigidity of the chelates, which strongly influenced the observed selectivity of the photosubstitution. As the ratio between the different photoproducts was also influenced by the solvent, we developed a full density functional theory modeling of the reaction mechanism that included explicit solvent molecules. Three reaction pathways leading to photodissociation were identified on the triplet hypersurface, each characterized by either one or two energy barriers. Photodissociation in water was promoted by a proton transfer in the triplet state, which was facilitated by the dissociated pyridine ring acting as a pendent base. We show that the temperature variation of the photosubstitution quantum yield is an excellent tool to compare theory with experiments. An unusual phenomenon was observed for one of the compounds in acetonitrile, for which an increase in temperature led to a surprising decrease in the photosubstitution reaction rate. We interpret this experimental observation based on complete mapping of the triplet hypersurface of this complex, revealing thermal deactivation to the singlet ground state through intersystem crossing.

Complex formation of Zinc(II) ion with acetonitrile in ionic liquid [C2mim][TFSA] studied by 15N NMR spectroscopy and DFT calculation

In bis(trifluoromethylsulfonyl)amide (TFSA−)–based ionic liquid, 1-ethyl-3-methylimidazolium TFSA− ([C2mim][TFSA]), the complex formation equilibria of Zn2+ ion with acetonitrile (AN) molecules have been investigated using 15N NMR spectroscopy with a help of density functional theory (DFT) calculation. Based on a comparison of the experimental 15N NMR peak of the TFSA− N atom with the calculated ones, the structure of the Zn2+ solvation complex with TFSA− anions formed in [C2mim][TFSA] has been determined. Three TFSA− anions coordinate with Zn2+ as bidentate ligands to form the monovalent complex of [Zn(tfsa)3]−. To determine the structure of the Zn2+−AN complexes formed in the [C2mim][TFSA]–AN solutions, the numbers of the experimental 15N NMR peaks of AN molecules coordinated with Zn2+ were compared with those calculated by the DFT. The complexes of [Zn(tfsa)2(an)2], [Zn(tfsa)(an)4]+, and [Zn(an)6]2+ are formed in the solutions. Their stability constants were determined from the relationship between the chemical shift value of TFSA− anions isolated from Zn2+ and the concentration ratio of AN to Zn2+.