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1.
The salt, [F5TeN(H)Xe][AsF6], has been synthesized in the natural abundance and 99.5% 15N-enriched forms. The F5TeN(H)Xe+ cation has been obtained as the product of the reactions of [F5TeNH3][AsF6] with XeF2 (HF and BrF5 solvents) and F5TeNH2 with [XeF][AsF6] (HF solvent) and characterized in solution by 129Xe, 19F, 125Te, 1H, and 15N NMR spectroscopy at -60 to -30 degrees C. The orange [F5TeN(H)Xe][AsF6] and colorless [F5TeNH3][AsF6] salts were crystallized as a mixture from HF solvent at -35 degrees C and were characterized by Raman spectroscopy at -165 degrees C and by X-ray crystallography. The crystal structure of the low-temperature phase, alpha-F5TeNH2, was obtained by crystallization from liquid SO2 between -50 and -70 degrees C and is fully ordered. The high-temperature phase, beta-F5TeNH2, was obtained by sublimation at room temperature and exhibits a 6-fold disorder. Decomposition of [F5TeN(H)Xe][AsF6] in the solid state was rapid above -30 degrees C. The decomposition of F5TeN(H)Xe+ in HF and BrF5 solution at -33 degrees C proceeded by fluorination at nitrogen to give F5TeNF2 and Xe gas. Electronic structure calculations at the Hartree-Fock and local density-functional theory levels were used to calculate the gas-phase geometries, charges, Mayer bond orders, and Mayer valencies of F5TeNH2, F5TeNH3+, F5TeN(H)Xe+, [F5TeN(H)Xe][AsF6], F5TeNF2, and F5TeN2- and to assign their experimental vibrational frequencies. The F5TeN(H)Xe+ and the ion pair, [F5TeN(H)Xe][AsF6], systems were also calculated at the MP2 and gradient-corrected (B3LYP) levels. 相似文献
2.
The fields of sulfur-nitrogen-fluorine chemistry and noble-gas chemistry have been significantly extended by the syntheses and characterizations of four new Xe-N-bonded cations derived from N≡SF(3). The adduct-cation, F(3)S≡NXeF(+), has provided the entry point to a significant chemistry through HF solvolysis of the coordinated N≡SF(3) ligand and HF-catalyzed and solid-state rearrangements of F(3)S≡NXeF(+). The HF solvolyses of [F(3)S≡NXeF][AsF(6)] in anhydrous HF (aHF) and aHF/BrF(5) solutions yield the F(4)S═NXe(+) cation, which likely arises from an HF-catalyzed mechanism. The F(4)S═NXe(+) cation, in turn, undergoes HF displacement to form F(4)S═NH(2)(+) and XeF(2), as well as HF addition to the S═N bond to form F(5)SN(H)Xe(+). Both cations undergo further solvolyses in aHF to form the F(5)SNH(3)(+) cation. The F(4)S═NXe(+) and F(4)S═NH(2)(+) cations were characterized by NMR spectroscopy and single-crystal X-ray diffraction and exhibit high barriers to rotation about their S═N double bonds. They are the first cations known to contain the F(4)S═N- group and significantly extend the chemistry of this ligand. The solid-state rearrangement of [F(3)S≡NXeF][AsF(6)] at 22 °C has yielded [F(4)S═NXe][AsF(6)], which was characterized by Raman spectroscopy, providing the first examples of xenon bonded to an imido nitrogen and of the F(4)S═N- group bonded to a noble-gas element. The rearrangement of [F(3)S≡NXeF][AsF(6)] in a N≡SF(3) solution at 0 °C also yielded [F(4)S═NXe?N≡SF(3)][AsF(6)], which represents a rare example of a N?Xe?N linkage and the first to be characterized by X-ray crystallography. Solvolysis of N≡SF(3) in aHF was previously shown to give the primary amine F(5)SNH(2), whereas solvolysis in the superacid medium, AsF(5)/aHF, results in amine protonation to give [F(5)SNH(3)][AsF(6)]. Complete structural characterizations were not available for either species. Isolation of F(5)SNH(2)·nHF from the reaction of N≡SF(3) with HF has provided a structural characterization of F(5)SNH(2) by Raman spectroscopy. Crystal growth by sublimation of F(5)SNH(2)·nHF at -30 to -40 °C has resulted in the X-ray crystal structure of F(5)SNH(2)·2[F(5)SNH(3)][HF(2)]·4HF and structural characterizations of F(5)SNH(2) and F(5)SNH(3)(+). The redox decomposition of [F(4)S═NXe?N≡SF(3)][AsF(6)] in N≡SF(3) at 0 °C generated Xe, cis-N(2)F(2), and [F(3)S(N≡SF(3))(2)][AsF(6)]. 相似文献
3.
The salt, [F3S(triple bond)NXeF][AsF6], has been synthesized by the reaction of [XeF][AsF6] with liquid N(triple bond)SF3 at -20 degrees C. The Xe-N bonded cation provides a rare example of xenon bound to an inorganic nitrogen base in which nitrogen is formally sp-hybridized. The F3S(triple bond)NXeF+ cation was characterized by Raman spectroscopy at -150 degrees C and by 129Xe, 19F, and 14N NMR spectroscopy in HF solution at -20 degrees C and in BrF5 solution at -60 degrees C. Colorless [F3S(triple bond)NXeF][AsF6] was crystallized from HF solvent at -45 degrees C, and its low-temperature X-ray crystal structure was determined. The Xe-N bond is among the longest Xe-N bonds known (2.236(4) A), whereas the Xe-F bond length (1.938(3) A) is significantly shorter than that of XeF2 but longer than in XeF+ salts. The Xe-F and Xe-N bond lengths are similar to those of HC(triple bond)NXeF+, placing it among the most ionic Xe-N bonds known. The nonlinear Xe-N-S angle (142.6(3)o) contrasts with the linear angle predicted by electronic structure calculations and is attributed to close N...F contacts within the crystallographic unit cell. Electronic structure calculations at the MP2 and DFT levels of theory were used to calculate the gas-phase geometries, charges, bond orders, and valencies of F3S(triple bond)NXeF+ and to assign vibrational frequencies. The calculated small energy difference (7.9 kJ mol-1) between bent and linear Xe-N-S angles also indicates that the bent geometry is likely the result of crystal packing. The structural studies, natural bond orbital analyses, and calculated gas-phase dissociation enthalpies reveal that F3S(triple bond)NXeF+ is among the weakest donor-acceptor adducts of XeF+ with an Xe-N donor-acceptor interaction that is very similar to that of HC(triple bond)NXeF+, but considerably stronger than that of F3S(triple bond)NAsF5. Despite the low dissociation enthalpy of the donor-acceptor bond in F3S(triple bond)NXeF+, 129Xe, 19F, and 14N NMR studies reveal that the F3S(triple bond)NXeF+ cation is nonlabile at low temperatures in HF and BrF5 solvents. 相似文献
4.
The dependence of the 129Xe NMR chemical shift value of XeF2 on temperature and concentration was determined in a variety of prototypic media: in acidic (anhydrous HF, aHF), nonprotic but polar (dichloromethane), and basic (CD3CN-EtCN, 1:3 v/v) solvents. The 129Xe NMR spectra of a representative series of organoxenon(II) salts [RXe][Y] (R = C6F5, heptafluoro-1,4-cyclohexadien-1-yl (cyclo-1,4-C6F7), pentafluoro-1,4-cyclohexadien-3-on-1-yl (cyclo-3-O-1,4-C6F5), CF2=C(CF3), (CF3)2CFC[triple bond]C, C4H9C[triple bond]C; Y = BF4, AsF6) in aHF showed, compared with XeF2-aHF, a quantitatively less distinct but qualitatively related dependence of delta(129Xe) vs temperature. The dependence of their delta(129Xe) values on concentration in aHF is negligible. An explanation for the different behavior of [RXe][Y] and XeF2 is offered. 相似文献
5.
New examples of [C6F5Xe]+ salts of the weakly coordinating [BY4]- (Y = CN, CF3, or C6F5) anions were synthesized by metathesis of [C6F5Xe][BF4] with MI[BY4] (MI = K or Cs; Y = CN, CF3, or C6F5) in CH3CN at -40 degrees C, and were crystallized from CH2Cl2 or from a CH2Cl2/CH3CN solvent mixture. The low-temperature (-173 degrees C) X-ray crystal structures of the [C6F5Xe]+ cation and of the [C6F5XeNCCH3]+ adduct-cation are reported for [C6F5Xe][B(CF3)4], [C6F5XeNCCH3][B(CF3)4], [C6F5Xe][B(CN)4], and [C6F5XeNCCH3][B(C6F5)4]. The [C6F5Xe]+ cation, in each structure, interacts with either the anion or the solvent, with the weakest cation-anion interactions occurring for the [B(CF3)4]- anion. The solid-state Raman spectra of the [C6F5Xe]+ and [C6F5XeNCCH3]+ salts have been assigned with the aid of electronic structure calculations. Gas-phase thermodynamic calculations show that the donor-acceptor bond dissociation energy of [C6F5XeNCCH3]+ is approximately half that of [FXeNCCH3]+. Coordination of CH3CN to [C6F5Xe]+ is correlated with changes in the partial charges on mainly Xe, the ipso-C, and N, that is, the partial charge on Xe increases and those on the ipso-C and N decrease upon coordination, typifying a transition from a 2c-2e to a 3c-4e bond. 相似文献
6.
New examples of [C6F5Xe]+ salts of the weakly coordinating anions [B(CF3)4]-, [B(C6F5)4]-, [B(CN)4]-, and [B(OTeF5)4]- have been synthesized by metathesis reactions of [C6F5Xe][BF4] with the corresponding MI[BY4] salts (MI = K or Cs; Y = CF3, C6F5, CN, or OTeF5). The salts were characterized in solution by multi-NMR spectroscopy. Their stabilities in prototypic solvents (CH3CN and CH2Cl2) and decomposition products are reported. The influence of the coordinating nature of [BY4]- on the decomposition rate of [C6F5Xe]+ as well as the presence of the weakly nucleophilic [BF4]- ion has been studied. The electrophilic pentafluorophenylation of C6H5F by [C6F5Xe][BY4] in solvents of different coordinating abilities (CH3CN and CH2Cl2) and the effects of stronger nucleophiles (fluoride and water) on the pentafluorophenylation process have been investigated. Simulations of the 19F and 129Xe NMR spectra of [C6F5Xe]+ have provided the complete set of aryl 19F-19F and 129Xe-19F coupling constants and their relative signs. The 19F NMR parameters of the [C6F5Xe]+ cation in the present series of salts are shown to reflect the relative degrees of cation-solvent interactions. 相似文献
7.
Perfluoroalkynylxenonium salts, [RXe][BF(4)] (R = CF(3)C≡C, (CF(3))(2)CFC≡C), reacted with organyl iodides, R'I (R' = 3-FC(6)H(4), C(6)F(5), CF(2)═CF, CF(3)CH(2); no reaction with R' = CF(3)CF(2)CF(2)) in anhydrous HF to yield the corresponding asymmetric polyfluorinated iodonium salts, [RR'I][Y]. The action of the arylxenonium salt, [C(6)F(5)Xe][BF(4)], and the cycloalkenylxenonium salt, [cyclo-1,4-C(6)F(7)Xe][AsF(6)], on 4-FC(6)H(4)I gave [C(6)F(5)(4-FC(6)H(4))I][BF(4)] and [cyclo-1,4-C(6)F(7)(4-FC(6)H(4))I][AsF(6)], respectively, besides the symmetric iodonium salt, [(4-FC(6)H(4))(2)I][Y]. But the aryl-, as well as the cycloalkenylxenonium salt, did not react with C(6)F(5)I, CF(2)═CFI, and CF(3)CH(2)I. 相似文献
8.
Gerken M Kolb P Wegner A Mercier HP Borrmann H Dixon DA Schrobilgen GJ 《Inorganic chemistry》2000,39(13):2813-2824
The salts [AsX4][As(OTeF5)6] and [AsBr4][AsF(OTeF5)5] (X = Cl, Br) have been prepared by oxidation of AsX3 with XOTeF5 in the presence of the OTeF5 acceptors As(OTeF5)5 and AsF(OTeF5)4. The mixed salts [AsCl4][Sb(OTeF5)6-nCl(n-2)] and [AsCl4][Sb(OTeF5)6-nCl(n)] (n > or = 2) have also been prepared. The AsBr4+ cation has been fully structurally characterized for the first time in SO2ClF solution by 75As NMR spectroscopy and in the solid state by a single-crystal X-ray diffraction study of [AsBr4][AsF(OTeFs)5]: P1, a = 9.778(4) A, b = 17.731(7) A, c = 18.870(8) A, alpha = 103.53(4)degrees, beta = 103.53(4) degrees, gamma = 105.10(4) degrees, V = 2915(2) A3, Z = 4, and R1 = 0.0368 at -183 degrees C. The crystal structure determination and solution 75As NMR study of the related [AsCl4][As(OTeF5)6] salt have also been carried out: [AsCl4][As(OTeF5)6], R3, a = 9.8741(14) A, c = 55.301(11) A, V= 4669(1) A3, Z = 6, and R1 = 0.0438 at -123 degrees C; and R3, a = 19.688(3) A, c = 55.264(11) A, V= 18552(5) A3, Z = 24, and R1 = 0.1341 at -183 degrees C. The crystal structure of the As(OTeF5)6- salt reveals weaker interactions between the anion and cation than in the previously known AsF6- salt. The AsF(OTeF5)5- anion is reported for the first time and is also weakly coordinating with respect to the AsBr4+ cation. Both cations are undistorted tetrahedra with bond lengths of 2.041(5)-2.056(3) A for AsCl4+ and 2.225(2)-2.236(2) A for AsBr4+. The Raman spectra are consistent with undistorted AsX4+ tetrahedra and have been assigned under Td point symmetry. The 35Cl/37Cl isotope shifts have been observed and assigned for AsCl4+, and the geometrical parameters and vibrational frequencies of all known and presently unknown PnX4+ (Pn = P, As, Sb, Bi; X = F, Cl, Br, I) cations have been calculated using density functional theory methods. 相似文献
9.
Reactions of XeO2F2 with the strong fluoride ion acceptors, AsF5 and SbF5, in anhydrous HF solvent give rise to alpha- and beta-[XeO2F][SbF6], [XeO2F][AsF6], and [FO2XeFXeO2F][AsF6]. The crystal structures of alpha-[XeO2F][SbF6] and [XeO2F][AsF6] consist of trigonal-pyramidal XeO2F+ cations, which are consistent with an AXY2E VSEPR arrangement, and distorted octahedral MF6- (M = As, Sb) anions. The beta-phase of [XeO2F][SbF6] is a tetramer in which the xenon atoms of four XeO2F+ cations and the antimony atoms of four SbF6- anions are positioned at alternate corners of a cube. The FO2XeFXeO2F+ cations of [FO(2)XeFXeO2F][AsF6] are comprised of two XeO2F units that are bridged by a fluorine atom, providing a bent Xe- - -F- - -Xe arrangement. The angle subtended by the bridging fluorine atom, a xenon atom, and the terminal fluorine atom of the XeO2F group is bent toward the valence electron lone-pair domain on xenon, so that each F- - -XeO2F moiety resembles the AX(2)Y(2)E arrangement and geometry of the parent XeO2F2 molecule. Reaction of XeF6 with [H3O][SbF6] in a 1:2 molar ratio in anhydrous HF predominantly yielded [XeF5][SbF6].XeOF4 as well as [XeO2F][Sb2F11]. The crystal structure of the former salt was also determined. The energy-minimized, gas-phase MP2 geometries for the XeO2F+ and FO2XeFXeO2F+ cations are compared with the experimental and calculated geometries of the related species IO2F, TeO2F-, XeO2(OTeF5)+, XeO2F2, and XeO2(OTeF5)2. The bonding in these species has been described by natural bond orbital and electron localization function analyses. The standard enthalpies and Gibbs free energies for reactions leading to XeO2F+ and FO2XeFXeO2F+ salts from MF5 (M = As, Sb) and XeO2F2 were obtained from Born-Haber cycles and are mildly exothermic and positive, respectively. When the reactions are carried out in anhydrous HF at low temperatures, the salts are readily formed and crystallized from the reaction medium. With the exception of [XeO2F][AsF6], the XeO2F+ and FO2XeFXeO2F+ salts are kinetically stable toward dissociation to XeO2F2 and MF5 at room temperature. The salt, [XeO2F][AsF6], readily dissociates to [FO2XeFXeO2F][AsF6] and AsF5 under dynamic vacuum at 0 degree C. The decompositions of XeO2F+ salts to the corresponding XeF+ salts and O2 are exothermic and spontaneous but slow at room temperature. 相似文献
10.
Osmium dioxide tetrafluoride, cis-OsO(2)F(4), reacts with the strong fluoride ion acceptors AsF(5) and SbF(5) in anhydrous HF and SbF(5) solutions to form orange salts. Raman spectra are consistent with the formation of the fluorine-bridged diosmium cation F(cis-OsO(2)F(3))(2)(+), as the AsF(6)(-) and Sb(2)F(11)(-) salts, respectively. The (19)F NMR spectra of the salts in HF solution are exchange-averaged singlets occurring at higher frequency than those of the fluorine environments of cis-OsO(2)F(4). The F(cis-OsO(2)F(3))(2)(+)Sb(2)F(11)(-) salt crystallizes in the orthorhombic space group Imma. At -107 degrees C, a = 12.838(3) ?, b = 10.667(2) ?, c = 11.323(2) ?, V = 1550.7(8) ?(3), and Z = 4. Refinement converged with R = 0.0469 [R(w) = 0.0500]. The crystal structure consists of discrete fluorine-bridged F(cis-OsO(2)F(3))(2)(+) and Sb(2)F(11)(-) ions in which the fluorine bridge of the F(cis-OsO(2)F(3))(2)(+) cation is trans to an oxygen atom (Os-O 1.676 ?) of each OsO(2)F(3) group. The angle at the bridge is 155.2(8) degrees with a bridging Os---F(b) distance of 2.086(3) ?. Two terminal fluorine atoms (Os-F 1.821 ?) are cis to the two oxygen atoms (Os-O 1.750 ?), and two terminal fluorine atoms of the OsO(2)F(3) group are trans to one another (1.813 ?). The OsO(2)F(3)(+) cation was characterized by (19)F NMR and by Raman spectroscopy in neat SbF(5) solution but was not isolable in the solid state. The NMR and Raman spectroscopic findings are consistent with a trigonal bipyramidal cation in which the oxygen atoms and a fluorine atom occupy the equatorial plane and two fluorine atoms are in axial positions. Density functional theory calculations show that the crystallographic structure of F(cis-OsO(2)F(3))(2)(+) is the energy-minimized structure and the energy-minimized structures of the OsO(2)F(3)(+) cation and ReO(2)F(3) are trigonal bipyramidal having C(2)(v)() point symmetry. Attempts to prepare the OsOF(5)(+) cation by oxidative fluorination of cis-OsO(2)F(4) with KrF(+)AsF(6)(-) in anhydrous HF proved unsuccessful. 相似文献
11.
The interactions of BrO3F and ClO3F with the strong Lewis acids AsF5 and SbF5 were investigated. Although ClO3F is unreactive toward AsF5 and SbF5, BrO3F undergoes fluoride ion abstraction and O2 elimination, accompanied by central halogen reduction, to form [BrO2][Sb(n)F(5n+1)] (n > or = 1), rather than simple fluoride ion abstraction to form BrO3(+) salts. The geometric parameters of the BrO2(+) cation have been obtained in the solid state for the first time by a single-crystal X-ray diffraction study of [BrO2][SbF6] at -173 degrees C and are compared with those of ClO2(+) salts. Quantum-chemical calculations have been used to arrive at the geometries and vibrational frequencies of XO2(+) and XO3(+) (X = Cl, Br) and have been compared with the experimental values for XO2(+). The calculations have also been used to account for the contrasting behaviors of ClO3F and BrO3F toward central halogen reduction in the presence of liquid SbF5. The thermochemical stabilities of ClO3(+) and BrO3(+) salts of the AsF6(-), SbF6(-), Sb2F11(-), and Sb3F16(-) were also investigated, which provided the fluoride ion affinities of AsF5, SbF5, Sb2F10, and Sb3F15 up to and including the CCSD(T) level of theory. These values are compared with the current literature values. Thermochemical studies indicate that XO3(+) formation by fluoride ion abstraction from XO3F is not spontaneous under standard conditions whereas a concerted fluoride abstraction and O2 elimination to give the XO2(+) cations is spontaneous to near thermally neutral. Failure to observe reactivity between ClO3F and any of the aforementioned Lewis acid fluoride ion acceptors is attributed to a significant kinetic barrier to fluoride ion abstraction. 相似文献
12.
The crystal structures of alpha-KrF(2) and salts containing the KrF(+) and Kr(2)F(3)(+) cations have been investigated for the first time using low-temperature single-crystal X-ray diffraction. The low-temperature alpha-phase of KrF(2) crystallizes in the tetragonal space group I4/mmm with a = 4.1790(6) A, c = 6.489(1) A, Z = 2, V = 113.32(3) A(3), R(1) = 0.0231, and wR(2) = 0.0534 at -125 degrees C. The [KrF][MF(6)] (M = As, Sb, Bi) salts are isomorphous and isostructural and crystallize in the monoclinic space group P2(1)/c with Z = 4. The unit cell parameters are as follows: beta-[KrF][AsF(6)], a = 5.1753(2) A, b = 10.2019(7) A, c = 10.5763(8) A, beta = 95.298(2) degrees, V = 556.02(6) A(3), R(1) = 0.0265, and wR(2) = 0.0652 at -120 degrees C; [KrF][SbF(6)], a = 5.2922(6) A, b = 10.444(1) A, c = 10.796(1) A, beta = 94.693(4) degrees, V = 594.73(1) A(3), R(1) = 0.0266, wR(2) = 0.0526 at -113 degrees C; [KrF][BiF(6)], a = 5.336(1) A, b = 10.513(2) A, c = 11.046(2) A, beta = 94.79(3) degrees, V = 617.6(2) A(3), R(1) = 0.0344, and wR(2) = 0.0912 at -130 degrees C. The Kr(2)F(3)(+) cation was investigated in [Kr(2)F(3)][SbF(6)].KrF(2), [Kr(2)F(3)](2)[SbF(6)](2).KrF(2), and [Kr(2)F(3)][AsF(6)].[KrF][AsF(6)]. [Kr(2)F(3)](2)[SbF(6)](2).KrF(2) crystallizes in the monoclinic P2(1)/c space group with Z = 4 and a = 8.042(2) A, b = 30.815(6) A, c = 8.137(2) A, beta = 111.945(2) degrees, V = 1870.1(7) A(3), R(1) = 0.0376, and wR(2) = 0.0742 at -125 degrees C. [Kr(2)F(3)][SbF(6)].KrF(2) crystallizes in the triclinic P1 space group with Z = 2 and a = 8.032(3) A, b = 8.559(4) A, c = 8.948(4) A, alpha = 69.659(9) degrees, beta = 63.75(1) degrees, gamma = 82.60(1) degrees, V = 517.1(4) A(3), R(1) = 0.0402, and wR(2) = 0.1039 at -113 degrees C. [Kr(2)F(3)][AsF(6)].[KrF][AsF(6)] crystallizes in the monoclinic space group P2(1)/c with Z = 4 and a = 6.247(1) A, b = 24.705(4) A, c = 8.8616(6) A, beta = 90.304(6) degrees, V = 1367.6(3) A(3), R(1) = 0.0471 and wR(2) = 0.0958 at -120 degrees C. The terminal Kr-F bond lengths of KrF(+) and Kr(2)F(3)(+) are very similar, exhibiting no crystallographically significant variation in the structures investigated (range, 1.765(3)-1.774(6) A and 1.780(7)-1.805(5) A, respectively). The Kr-F bridge bond lengths are significantly longer, with values ranging from 2.089(6) to 2.140(3) A in the KrF(+) salts and from 2.027(5) to 2.065(4) A in the Kr(2)F(3)(+) salts. The Kr-F bond lengths of KrF(2) in [Kr(2)F(3)][SbF(6)].KrF(2) and [Kr(2)F(3)](2)[SbF(6)](2).KrF(2) range from 1.868(4) to 1.888(4) A and are similar to those observed in alpha-KrF(2) (1.894(5) A). The synthesis and Raman spectrum of the new salt, [Kr(2)F(3)][PF(6)].nKrF(2), are also reported. Electron structure calculations at the Hartree-Fock and local density-functional theory levels were used to calculate the gas-phase geometries, charges, Mayer bond orders, and Mayer valencies of KrF(+), KrF(2), Kr(2)F(3)(+), and the ion pairs, [KrF][MF(6)] (M = P, As, Sb, Bi), and to assign their experimental vibrational frequencies. 相似文献
13.
Deacon GB Evans DJ Junk PC Lork E Mews R Zemva B 《Dalton transactions (Cambridge, England : 2003)》2005,(13):2237-2238
Addition of 15-crown-5 to [GdF(AsF6)2], both dissolved in liquid SO2, and crystallisation at -30 degrees C has led to the isolation of the tetranuclear ionic complex [Gd4F7(15-crown-5)4][AsF6]5.6 SO2 which is stable up to--10 degrees C where SO2 loss leads to loss of crystallinity. 相似文献
14.
The fluoride ion donor properties of TcO2F3 and ReO2F3 toward AsF5, SbF5, and XeO2F2 have been investigated, leading to the formation of TcO2F3.PnF5 and ReO2F3.PnF5 (Pn = As, Sb) and TcO2F3.XeO2F2, which were characterized in the solid state by Raman spectroscopy and X-ray crystallography. TcO2F3.SbF5 crystallizes in the monoclinic system P2(1)/n, with a = 7.366(2) A, b = 10.441(2) A, c = 9.398(2) A, beta = 93.32(3) degrees, V = 721.6(3) A3, and Z = 4 at 24 degrees C, R1 = 0.0649, and wR2 = 0.1112. ReO2F3.SbF5 crystallizes in the monoclinic system P2(1)/c, with a = 5.479(1) A, b = 10.040(2) A, c = 12.426(2) A, beta = 99.01(3) degrees, V = 675.1(2) A3, and Z = 4 at -50 degrees C, R1 = 0.0533, and wR2 = 0.1158. TcO2F3.XeO2F2 crystallizes in the orthorhombic system Cmc2(1), with a = 7.895(2) A, b = 16.204(3) A, c = 5.198(1) A, beta = 90 degrees, V = 665.0(2) A3, and Z = 4 at 24 degrees C, R1 = 0.0402, and wR2 = 0.0822. The structures of TcO2F3.SbF5 and ReO2F3.SbF5 consist of infinite chains of alternating MO2F4 and SbF6 units in which the bridging fluorine atoms on the antimony are trans to each other. The structure of TcO2F3.XeO2F2 comprises two distinct fluorine-bridged chains, one of TcO2F3 and the other of XeO2F2 bridged by long Tc-F...Xe contacts. The oxygen atoms of the group 7 metals in the three structures are cis to each other and to two terminal fluorine atoms and trans to the bridging fluorine atoms. The 19F NMR and Raman spectra of TcO2F3.PnF5 and ReO2F3.PnF5 in SbF5 and PnF5-acidified HF solvents are consistent with dissociation of the adducts into cis-MO2F2(HF)2+ cations and PnF6- anions. The energy-minimized geometries of the free MO2F2+ cations and their HF adducts, cis-MO2F2(HF)2+, have been calculated by local density functional theory (LDFT), and the calculated vibrational frequencies have been used as an aid in the assignment of the Raman spectra of the solid MO2F3.PnF5 adducts and their PnF5-acidified HF solutions. In contrast, ReO2F3.SbF5 ionizes in SO2ClF solvent to give the novel Re2O4F5+ cation and Sb2F11- anion. The 19F NMR spectrum of the cation is consistent with two ReO2F2 units joined by a fluorine bridge in which the oxygen atoms are assumed to lie in the equatorial plane. The [ReO2F2(CH3CN)2][SbF6] salt was formed upon dissolution of ReO2F3.SbF5 in CH3CN and was characterized by 1H, 13C, and 19F NMR and Raman spectroscopies. The ReO2F2(CH3CN)2+ cation is a pseudooctahedral cis-dioxo arrangement in which the CH3CN ligands are trans to the oxygens and the fluorines are trans to each other. 相似文献
15.
16.
Gerken M Hazendonk P Iuga A Nieboer J Tramsek M Goreshnik E Zemva B Zheng S Autschbach J 《Inorganic chemistry》2007,46(15):6069-6077
The coordination compounds [Mg(XeF(2))(2)][AsF(6)](2), [Mg(XeF(2))(4)][AsF(6)](2), [Ca(XeF(2))(2.5)][AsF(6)](2), [Ba(XeF(2))(3)][AsF(6)](2), and [Ba(XeF(2))(5)][AsF(60](2) were characterized by solid-state (19)F and (129)Xe magic-angle spinning NMR spectroscopy. The (19)F and (129)Xe NMR data of [Mg(XeF(2))(2)][AsF(6)](2), [Mg(XeF(2)(4)][AsF(6)](2), and [Ca(XeF(2))(2.5)][AsF(6)](2) were correlated with the previously determined crystal structures. The isotropic (19)F chemical shifts and (1)J((129)Xe-(19)F) coupling constants were used to distinguish the terminal and bridging coordination modes of XeF(2). Chemical-shift and coupling-constant calculations for [Mg(XeF(2))(4)][AsF(6)](2) confirmed the assignment of terminal and bridging chemical-shift and coupling-constant ranges. The NMR spectroscopic data of [Ba(XeF(2))(3)][AsF(6)](2) and [Ba(XeF(2))(5)][AsF(6)](2) indicate the absence of any terminal XeF(2) ligands, which was verified for [Ba(XeF(2))(5)][AsF(6)](2) by its X-ray crystal structure. The adduct [Ba(XeF(2))(5)][AsF(6)](2) crystallizes in the space group Fmmm, with a = 11.6604(14) Angstrom, b = 13.658(2) Angstrom, c = 13.7802(17) Angstrom, V = 2194.5(5) Angstrom(3) at -73 degrees C, Z = 4, and R = 0.0350 and contains two crystallographically independent bridging XeF(2) molecules and one nonligating XeF(2) molecule. The AsF(6-) anions in [Mg(XeF(2))(4)][AsF(6)](2), [Ca(XeF(2))(2.5)][AsF(6)](2), [Ba(XeF(2))(3)][AsF(6)](2), and [Ba(XeF(2))(5)][AsF(6)](2) were shown to be fluxional with the fluorines-on-arsenic being equivalent on the NMR time scale, emulating perfectly octahedral anion symmetry. 相似文献
17.
In the OSF(4)/Me(2)NSiMe(3) system besides the long known Me(2)NS(O)F(3) only the trisubstituted derivative is isolated as (Me(2)N)(3)SO(+)Me(3)SiF(2)(-) (3). Similar to (Me(2)N)(3)S(+)Me(3)SiF(2)(-) compound 3 is an excellent fluoride ion donor. With AsF(5) and HF the corresponding hexafluoroarsenate (Me(2)N)(3)SO(+)AsF(6)(-) (4) and the hydrogen bifluoride (Me(2)N)(3)SO(+)HF(2)(-) (5) are formed in almost quantitative yield. X-ray structure determinations of 3-5 surprisingly showed two different types of structures for the cation. In 3 and 5 this cation has C(3) symmetry, while in the hexafluoroarsenate 4 a (Me(2)N)(3)S(+)-like structure with C(s)() symmetry is determined. The experimental results for (Me(2)N)(3)SO(+) and (Me(2)N)(3)S(+) are compared with theoretical calculations for these cations and their isoelectronic neutral counterparts, the phosphorus amides (Me(2)N)(3)PO and (Me(2)N)(3)P, respectively. 相似文献
18.
Lehmann JF Schrobilgen GJ Christe KO Kornath A Suontamo RJ 《Inorganic chemistry》2004,43(22):6905-6921
The single-crystal X-ray structures of [XF(6)][Sb(2)F(11)] (X = Cl, Br, I) have been determined and represent the first detailed crystallographic study of salts containing the XF(6)(+) cations. The three salts are isomorphous and crystallize in the monoclinic space group P2(1)/n with Z = 4: [ClF(6)][Sb(2)F(11)], a = 11.824(2) A, b = 8.434(2) A, c = 12.088(2) A, beta = 97.783(6) degrees , V = 1194.3(4) A(3), R(1) = 0.0488 at -130 degrees C; [BrF(6)][Sb(2)F(11)], a = 11.931(2) A, b = 8.492(2) A, c = 12.103(2) A, beta = 97.558(4) degrees , V = 1215.5(4) A(3), R(1) = 0.0707 at -130 degrees C; [IF(6)][Sb(2)F(11)], a = 11.844(1) A, b = 8.617(1) A, c = 11.979(2) A, beta = 98.915(2) degrees , V = 1207.8(3) A(3), R(1) = 0.0219 at -173 degrees C. The crystal structure of [IF(6)][Sb(2)F(11)] was also determined at -100 degrees C and was found to crystallize in the monoclinic space group P2(1)/m with Z = 4, a = 11.885(1) A, b = 8.626(1) A, c = 12.000(1) A, beta = 98.44(1), V = 1216.9(2) A(3), R(1) = 0.0635. The XF(6)(+) cations have octahedral geometries with average Cl-F, Br-F, and I-F bond lengths of 1.550(4), 1.666(11) and 1.779(6) [-173 degrees C]/1.774(8) [-100 degrees C] A, respectively. The chemical shifts of the central quadrupolar nuclei, (35,37)Cl, (79,81)Br, and (127)I, were determined for [ClF(6)][AsF(6)] (814 ppm), [BrF(6)][AsF(6)] (2080 ppm), and [IF(6)][Sb(3)F(16)] (3381 ppm) in anhydrous HF solution at 27 degrees C, and spin-inversion-recovery experiments were used to determine the T(1)-relaxation times of (35)Cl (1.32(3) s), (37)Cl (2.58(6) s), (79)Br (24.6(4) ms), (81)Br (35.4(5) ms), and (127)I (6.53(1) ms). Trends among the central halogen chemical shifts and T(1)-relaxation times of XF(6)(+), XO(4)(-), and X(-) are discussed. The isotropic (1)J-coupling constants and reduced coupling constants for the XF(6)(+) cations and isoelectronic hexafluoro species of rows 3-6 are empirically assessed in terms of the relative contributions of the Fermi-contact, spin-dipolar, and spin-orbit mechanisms. Electronic structure calculations using Hartree-Fock, MP2, and local density functional methods were used to determine the energy-minimized gas-phase geometries, atomic charges, and Mayer bond orders of the XF(6)(+) cations. The calculated vibrational frequencies are in accord with the previously published assignments and experimental vibrational frequencies of the XF(6)(+) cations. Bonding trends within the XF(6)(+) cation series have been discussed in terms of natural bond orbital (NBO) analyses, the ligand close-packed (LCP) model, and the electron localization function (ELF). 相似文献
19.
For a compound in a given oxidation state, its oxidizing strength increases from its anion to the neutral parent molecule to its cation. Similarly, an anion is more easily oxidized than its neutral parent molecule, which in turn is more easily oxidized than its cation. This concept was systematically exploited in our search for new superoxidizers. Transition metal fluoride anions were prepared in their highest known oxidation states by high temperature/high pressure fluorinations with elemental fluorine and subsequently converted to their more strongly oxidizing cations by a displacement reaction with a strong Lewis acid. The application of this principle resulted in new syntheses for ClF(6)(+)AsF(6)(-) and BrF(6)(+)AsF(6)(-) using the highly reactive and thermally unstable NiF(3)(+) cation that was prepared from the reaction of the NiF(6)(2)(-) anion with AsF(5) in anhydrous HF. Attempts to prepare the known KrF(+) and ClO(2)F(2)(+) cations and the yet unknown XeF(7)(+) cation by the same method were unsuccessful. The results from this and previous studies show that NiF(3)(+) is a stronger oxidative fluorinator than PtF(6), but whether its oxidizing strength exceeds that of KrF(+) remains unclear. Its failure to oxidize Kr to KrF(+) might have been due to unfavorable reaction conditions. Its failure to oxidize ClO(2)F to ClO(2)F(2)(+), in spite of its favorable oxidizer strength, is attributed to the high Lewis basicity of ClO(2)F which results in a rapid displacement reaction of NiF(3)(+) by ClO(2)F, thus generating the weaker oxidizer NiF(4) and the more difficult to oxidize substrate ClO(2)(+). Therefore, the general applicability of this approach appears to be limited to substrates that exhibit a weaker Lewis basicity than the neutral transition metal parent molecule. Compared to KrF(+)- or PtF(6)-based oxidations, the NiF(3)(+) system offers the advantages of commercially available starting materials and higher yields, but product purification can be more difficult and tedious than for KrF(+). 相似文献
20.
The electrochemical oxidations of (C6H6)Cr(CO)3, 1, and (C5H5)Co(CO)2, 2, when carried out in CH2Cl2/[NBu4][B(C6F5)4], allow the physical or chemical characterization of the 17-electron cations 1+ and 2+ at room temperature. The generation of 1+ on a synthetic time scale permits an electrochemical "switch" process involving facile substitution of CO by PPh3 as a route to (C6H6)Cr(CO)2PPh3. The radical 2+ undergoes a second-order reaction to give a product assigned as the metal-metal bonded dimer dication [Cp2Co2(CO)4]2+. The new anodic chemistry of these often-studied 18-electron compounds is made possible by increases in the solubility and thermal stability of the cation radicals in media containing the poorly nucleophilic anion [B(C6F5)4]-, TFAB. 相似文献