Multimodal study of secondary interactions in Cp*Ir complexes of imidazolylphosphines bearing an NH group.

Hydrogen bonding phenomena are explored using a combination of X-ray diffraction, NMR and IR spectroscopy, and DFT calculations. Three imidazolylphosphines R(2)PImH (ImH = imidazol-2-yl, R = t-butyl, i-propyl, phenyl, 1a-1c) and control phosphine (i-Pr)(2)PhP (1d) lacking an imidazole were used to make a series of complexes of the form Cp*Ir(L(1))(L(2))(phosphine). In addition, in order to suppress intermolecular interactions with either imidazole nitrogen, 1e, a di(isopropyl)imidazolyl analogue of 1b was made along with its doubly (15)N-labeled isotopomer to explore bonding interactions at each imidazole nitrogen. A modest enhancement of transfer hydrogenation rate was seen when an imidazolylphosphine ligand 1b was used. Dichloro complexes (L(1) = L(2) = Cl, 2a-2c,2e) showed intramolecular hydrogen bonding as revealed by four X-ray structures and various NMR and IR data. Significantly, hydride chloride complexes [L(1) = H, L(2) = Cl, 3a-3c and 3e-((15)N)(2)] showed stronger hydrogen bonding to chloride than hydride, though the solid-state structure of 3b evinced intramolecular Ir-H...H-N bonding reinforced by intermolecular N...H-N bonding between unhindered imidazoles. These results are compared to literature examples, which show variations in preferred hydrogen bonding to hydride, halide, CO, and NO ligands. Surprising differences were seen between the dichloro complex 2b with isopropyl groups on phosphorus, which appeared to exist as a mixture of two conformers, and related complex 2a with tert-butyl groups on phosphorus, which exists in chlorinated solvents as a mixture of conformer 2a-endo and chelate 5a-Cl, the product of ionization of one chloride ligand. This difference became apparent only through a series of experiments, especially (15)N chemical shift data from 2D (1)H-(15)N correlation. The results highlight the difficulty of characterizing hemilabile, bifunctional complexes and the importance of innocent ligand substituents in determining structure and dynamics.

Anhydrides of real and hypothetical [hydroxy(R-O)iodo]benzenes.

The anhydrides of [hydroxy(methanesulfonato-O)]iodobenzene (HMIB) and [hydroxy(toluenesulfonato-O)]iodobenzene (HTIB) were prepared by drying acetonitrile solutions of the compounds. The anhydrides of the hypothetical compounds [hydroxy(chloroacetato)-O]iodobenzene and [hydroxy(iodoacetato)-O]iodobenzene were obtained from aqueous solutions. Crystallographic structures were obtained for the anhydrides, except that of HTIB. The electron-domain geometries of the I atoms vis-a-vis secondary I...O bonds were explored. The presence of delocalized bonding in groupings of O and I atoms was suggested. A linear relationship between the C-I-O angles and the I-O bond orders was observed.

Structure activity relationships of 5-, 6-, and 7-methyl-substituted azepan-3-one cathepsin K inhibitors.

The syntheses, in vitro characterizations, and rat and monkey in vivo pharmacokinetic profiles of a series of 5-, 6-, and 7-methyl-substituted azepanone-based cathepsin K inhibitors are described. Depending on the particular regiochemical substitution and stereochemical configuration, methyl-substituted azepanones were identified that had widely varied cathepsin K inhibitory potency as well as pharmacokinetic properties compared to the 4S-parent azepanone analogue, 1 (human cathepsin K, K(i,app) = 0.16 nM, rat oral bioavailability = 42%, rat in vivo clearance = 49.2 mL/min/kg). Of particular note, the 4S-7-cis-methylazepanone analogue, 10, had a K(i,app) = 0.041 nM vs human cathepsin K and 89% oral bioavailability and an in vivo clearance rate of 19.5 mL/min/kg in the rat. Hypotheses that rationalize some of the observed characteristics of these closely related analogues have been made using X-ray crystallography and conformational analysis. These examples demonstrate the potential for modulation of pharmacological properties of cathepsin inhibitors by substituting the azepanone core. The high potency for inhibition of cathepsin K coupled with the favorable rat and monkey pharmacokinetic characteristics of compound 10, also known as SB-462795 or relacatib, has made it the subject of considerable in vivo evaluation for safety and efficacy as an inhibitor of excessive bone resorption in rat, monkey, and human studies, which will be reported elsewhere.

Syntheses of Cationic, Six-Coordinate Cadmium(II) Complexes Containing Tris(pyrazolyl)methane Ligands. Influence of Charge on Cadmium-113 NMR Chemical Shifts.

Treating a thf (thf = tetrahydrofuran) suspension of Cd(acac)(2) (acac = acetylacetonate) with 2 equiv of HBF(4).Et(2)O results in the immediate formation of [Cd(2)(thf)(5)](BF(4))(4) (1). Crystallization of this complex from thf/CH(2)Cl(2) yields [Cd(thf)(4)](BF(4))(2) (2), a complex characterized in the solid state by X-ray crystallography. Crystal data: monoclinic, P2(1)/n, a = 7.784(2) Å, b = 10.408(2) Å, c = 14.632(7) Å, beta = 94.64(3) degrees, V = 1181.5(6) Å(3), Z = 2, R = 0.0484. The geometry about the cadmium is octahedral with a square planar arrangement of the thf ligands and a fluorine from each (BF(4))(-) occupying the remaining two octahedral sites. Reactions of [Cd(2)(thf)(5)](BF(4))(4) with either HC(3,5-Me(2)pz)(3) or HC(3-Phpz)(3) yield the dicationic, homoleptic compounds {[HC(3,5-Me(2)pz)(3)](2)Cd}(BF(4))(2) (3) and {[HC(3-Phpz)(3)](2)Cd}(BF(4))(2) (4) (pz = 1-pyrazolyl). The solid state structure of 3 has been determined by X-ray crystallography. Crystal data: rhombohedral, R&thremacr;, a = 12.236(8) Å, c = 22.69(3) Å, V = 2924(4) Å(3), Z = 3, R = 0.0548. The cadmium is bonded to the six nitrogen donor atoms in a trigonally distorted octahedral arrangement. Four monocationic, mixed ligand tris(pyrazolyl)methane-tris(pyrazolyl)borate complexes {[HC(3,5-Me(2)pz)(3)][HB(3,5-Me(2)pz)(3)]Cd}(BF(4)) (5), {[HC(3,5-Me(2)pz)(3)][HB(3-Phpz)(3)]Cd}(BF(4)) (6), {[HC(3-Phpz)(3)][HB(3,5-Me(2)pz)(3)]Cd}(BF(4)) (7), and {[HC(3-Phpz)(3)][HB(3-Phpz)(3)]Cd}(BF(4)) (8) are prepared by appropriate conproportionation reactions of 3or 4 with equimolar amounts of the appropriate homoleptic neutral tris(pyrazolyl)borate complexes [HB(3,5-Me(2)pz)(3)](2)Cd or [HB(3-Phpz)(3)](2)Cd. Solution (113)Cd NMR studies on complexes 3-8 demonstrate that the chemical shifts of the new cationic, tris(pyrazolyl)methane complexes are very similar to the neutral tris(pyrazolyl)borate complexes that contain similar substitution of the pyrazolyl rings.

Synthesis and Ligand Substitution Reactions of a Mesitylphosphido-Bridged Platinum(II) Dimer.

The stable primary phosphine complexes trans-M(PH(2)Mes)(2)Cl(2) (1, M = Pd; 2, M = Pt; Mes = 2,4,6-(t-Bu)(3)C(6)H(2)) were prepared from Pd(PhCN)(2)Cl(2) and K(2)PtCl(4), respectively. Reaction of Pt(COD)Cl(2) (COD = 1,5-cyclooctadiene) with less bulky arylphosphines gives the unstable cis-Pt(PH(2)Ar)(2)Cl(2) (3, Ar = Is = 2,4,6-(i-Pr)(3)C(6)H(2); 4, Ar = Mes = 2,4,6-Me(3)C(6)H(2)). Spontaneous dehydrochlorination of 4 or direct reaction of K(2)PtCl(4) with 2 equiv of PH(2)Mes gives the insoluble primary phosphido-bridged dimer [Pt(PH(2)Mes)(&mgr;-PHMes)Cl](2) (5), which was characterized spectroscopically, including solid-state (31)P NMR studies. The reversible reaction of 5 with PH(2)Mes gives [Pt(PH(2)Mes)(2)(&mgr;-PHMes)](2)[Cl](2) (6), while PEt(3) yields [Pt(PEt(3))(2)(&mgr;-PHMes)](2)[Cl](2) (7), which on recrystallization forms [Pt(PEt(3))(&mgr;-PHMes)Cl](2) (8). Complex 5 and PPh(3) afford [Pt(PPh(3))(&mgr;-PHMes)Cl](2) (9). Addition of 1,2-bis(diphenylphosphino)ethane (dppe) to 5 gives the dicationic [Pt(dppe)(&mgr;-PHMes)](2)[Cl](2) (10-Cl), which was also obtained as the tetrafluoroborate salt 10-BF(4)() by deprotonation of [Pt(dppe)(PH(2)Mes)Cl][BF(4)] (11) with Et(3)N or by reaction of [Pt(dppe)(&mgr;-OH)](2)[BF(4)](2) with 2 equiv of PH(2)Mes. Complexes 8, 9, and 10-Cl.2CH(2)Cl(2).2H(2)O were characterized crystallographically.

Regioselective Substitution Reactions of Sulfur(VI)-Nitrogen-Phosphorus Rings: Reactions of the Halogenated Cyclic Thionylphosphazenes [NSOX(NPCl(2))(2)] (X = Cl or F) with Oxygen-Based Nucleophiles.

The reactions of the cyclic thionylphosphazenes [NSOX(NPCl(2))(2)] (1, X = Cl; 2, X = F) with three oxygen-based nucleophiles of increasing basicity, sodium phenoxide (NaOPh), sodium trifluoroethoxide (NaOCH(2)CF(3)), and sodium butoxide (NaOBu) have been studied. The reaction of 1 and 2 with 4 equiv of NaOPh at 25 degrees C yielded the regioselectively tetrasubstituted species [NSOX{NP(OPh)(2)}(2)] (5d, X = Cl; 6d, X = F). Further reaction of 5d with an additional 2 equiv of NaOPh over several days or at elevated temperatures gave the fully substituted compound [NSO(OPh){NP(OPh)(2)}(2)] (5e), whereas 6d did not react further. The reaction of 1 and 2 with 5 equiv of NaOCH(2)CF(3) yielded in both cases [NSO(OCH(2)CF(3)){NP(OCH(2)CF(3))(2)}(2)] (7e), and similarly reaction with 5 equiv of NaOBu yielded [NSO(OBu){NP(OBu)(2)}(2)] (9e). In all cases, the reactions were monitored by (31)P NMR and (where applicable) (19)F NMR and were found to involve complete substitution at phosphorus via a predominantly vicinal pathway, followed by substitution at sulfur. Substitutional control of the reactions of NaOPh, NaOBu, with 1 and 2 was found to conform to the following general order of reactivity, PCl(2) > PCl(OR) > SOX (X = Cl, F). Although the reaction with NaOCH(2)CF(3) followed the same order of reactivity, a significant enhancement of reaction rate was detected with each equivalent of trifluoroethoxide added. Reaction of 7e with excess NaOCH(2)CF(3) led to elimination of (CF(3)CH(2))(2)O and the formation of the salts Na[NSO(OCH(2)CF(3))NP(OCH(2)CF(3))(2)NP(OCH(2)CF(3))O] (11) and Na[NS(O)O{NP(OCH(2)CF(3))(2)}(2)] (12). Crystals of 6d are triclinic, space group P&onemacr;, with a = 9.789(3) Å, b = 11.393(4) Å, c = 12.079(5) Å, alpha = 107.40(3) degrees, beta = 91.23(3) degrees, gamma = 93.18(3), V = 1283.6(8) Å(3), and Z = 2. Crystals of 5e are monoclinic, space group C2/c, with a = 32.457(3) Å, b = 10.747(1) Å, c = 18.294(2) Å, beta = 110.37(1) degrees, V = 5982.4(9) Å(3), and Z = 8.

Metal Complexes of Mesitylphosphine: Synthesis, Structure, and Spectroscopy.

A series of primary phosphine homoleptic complexes [ML(4)](n)()(+)X(n)() (1, M = Ni, n = 0; 2, M = Pd, n = 2, X = BF(4); 3, M = Cu, n = 1, X = PF(6); 4, M = Ag, n = 1, X = BF(4); L = PH(2)Mes, Mes = 2,4,6-Me(3)C(6)H(2)] was prepared from mesitylphosphine and Ni(COD)(2), [Pd(NCMe)(4)][BF(4)](2), [Cu(NCMe)(4)]PF(6), and AgBF(4), respectively. Reactions of 1-4 with MeC(CH(2)PPh(2))(3) (triphos) or [P(CH(2)CH(2)PPh(2))(3)] (tetraphos) afforded the derivatives [M(L')L](n)()(+)X(n)() (L' = triphos; 6, M = Ni, n = 0; 7, M = Cu, n = 1, X = PF(6); 8, M = Ag, n = 1, X = BF(4); L' = tetraphos; 9, M = Pd, n = 2, X = BF(4)). Addition of NOBF(4) to 1 yielded the nitrosyl compound [NiL(3)(NO)]BF(4), 5. The solution structure and dynamics of 1-9 were studied by (31)P NMR spectroscopy (including the first reported analyses of a 12-spin system for 1-2). Complexes 1, 3, 6, and 7.solvent were characterized crystallographically. The structural and spectroscopic studies suggest that the coordination properties of L are dominated by its relatively small cone angle and that the basicity of L is comparable to that of more commonly used tertiary phosphines.

Adducts of Titanium Tetrachloride with Alkylselenium Compounds: Molecular Precursors to Titanium Diselenide Films.

Treatment of titanium tetrachloride (2 equiv) with dimethyl diselenide or diethyl diselenide (1 equiv) in hexane at 0 degrees C, followed by crystallization at -20 degrees C, afforded (TiCl(4))(2)(Se(2)(CH(3))(2)) (78%) and (TiCl(4))(2)(Se(2)(CH(2)CH(3))(2)) (63%), respectively, as red and orange crystalline solids. (TiCl(4))(2)(Se(2)(CH(2)CH(3))(2)) is stable in solution and in the solid state at 23 degrees C, but (TiCl(4))(2)(Se(2)(CH(3))(2)) decomposes to TiCl(4)(Se(CH(3))(2))(2), gray selenium, and other products upon standing in hexane solution, in the solid state, or upon sublimation at 250 degrees C. Treatment of titanium tetrachloride with 2 equiv of dimethyl selenide or diethyl selenide in hexane at ambient temperature afforded a spectroscopically pure brick red solid of TiCl(4)(Se(CH(3))(2))(2) (96%) or TiCl(4)(Se(CH(2)CH(3))(2))(2) (96%), respectively. X-ray crystal structures of (TiCl(4))(2)(Se(2)(CH(2)CH(3))(2)), TiCl(4)(Se(CH(3))(2))(2), and TiCl(4)(Se(CH(2)CH(3))(2))(2) were determined to establish solid state nuclearities. (TiCl(4))(2)(Se(2)(CH(2)CH(3))(2)) crystallizes in the hexagonal space group P3(1)21 with a = 12.106(1) Å, c = 10.786(1) Å, V = 1368.8(4) Å(3), and Z = 3. TiCl(4)(Se(CH(3))(2))(2) crystallizes in the monoclinic space group P2(1)/n with a = 8.175(1) Å, b = 13.051(1) Å, c = 16.871(3) Å, beta = 102.675(8) degrees, V = 1756.3(2) Å(3), and Z = 4. TiCl(4)(Se(CH(2)CH(3))(2))(2) crystallizes in the monoclinic space group P2(1)/n with a = 6.404(4) Å, b = 16.376(7) Å, c = 13.058(8) Å, beta = 101.45(4) degrees, V = 1342(1) Å(3), and Z = 4. TiCl(4)(Se(CH(3))(2))(2) and TiCl(4)(Se(CH(2)CH(3))(2))(2) were evaluated as precursors to titanium diselenide films. TiCl(4)(Se(CH(3))(2))(2) was not a good precursor, but TiCl(4)(Se(CH(2)CH(3))(2))(2) afforded rose-bronze colored titanium diselenide films at substrate temperatures of 500-600 degrees C. The films were characterized by X-ray powder diffraction, scanning electron microscopy, and X-ray photoelectron spectroscopy. Surprisingly, titanium diselenide films prepared from TiCl(4)(Se(CH(2)CH(3))(2))(2) are moisture sensitive and are apparently hydrolyzed by ambient moisture to titanium dioxide and hydrogen selenide. The relevance of the coordination chemistry to the development of precursors to titanium diselenide films is discussed.

Molecular Structures of the Heavier Alkali Metal Salts of Supermesitylphosphane: A Systematic Investigation.

The molecular structures of the rubidium and cesium derivatives of supermesitylphosphane [i.e., (2,4,6-(t)Bu(3)C(6)H(2))PH(2) = (t)Bu(3)MesPH(2)] as well as several base adducts of these are reported. Sodium hydride, potassium hydride, rubidium metal, and cesium metal react with (t)Bu(3)MesPH(2) in tetrahydrofuran solution at room temperature to produce MPRH salts 1-4 [M = Na (1), K (2), Rb (3), Cs (4); R = (t)Bu(3)Mes] in good yields. X-ray-quality crystals of 2 and 3 were obtained by slow evaporation of solutions of the corresponding MP(H)(t)Bu(3)Mes species dissolved in toluene/thf. Complex 4 was crystallized from hot toluene. On the other hand, slow evaporation of a toluene/tetrahydrofuran solution of CsP(H)(t)Bu(3)Mes (4) produces crystals of the composition {[CsP(H)(t)Bu(3)Mes](2)(&mgr;-THF)(0.9).toluene}(x)() (5). Crystallization of 4 in the presence of pyridine yields crystals of {[CsP(H)(t)Bu(3)Mes](2)(&mgr;-pyridine)}(x)() (6). Also, crystallization of complexes 3 and 4 from toluene/N-methylimidazole (N-MeIm) gives the isomorphous complexes {[RbP(H)(t)Bu(3)Mes](2)(&mgr;-N-MeIm)}(x)() (7) and {[CsP(H)(t)Bu(3)Mes](2)(&mgr;-N-MeIm)}(x)() (8), respectively. However, crystallization of 4 from toluene in the presence of bidentate or polydentate bases such as dimethoxyethane or pentamethyldiethylenetriamine does not result in incorporation of these bases into the lattice. Instead, the toluene solvate {[CsP(H)(t)Bu(3)Mes](2)(eta(3)-toluene)(0.5)}(x)() (9) is obtained. On the other hand, crystallization of 4 from toluene/ethylenediamine gives the base adduct {[CsP(H)(t)Bu(3)Mes](2)(&mgr;-ethylenediamine)}(x)() (10). Complex 3 crystallizes in the triclinic space group P&onemacr;. Crystal data for 3 at 218 K: a = 6.71320(10) Å, b = 10.5022(2) Å, c = 14.9733(3) Å, alpha = 91.3524(13) degrees, beta = 102.5584(13) degrees, gamma = 107.7966(14) degrees; Z = 1; R(1) = 6.55%. Complex 4 crystallizes in the triclinic space group P&onemacr;. Crystal data for 4 at 223 K: a = 7.0730(14) Å; b = 10.395(2) Å; c = 14.933(2) Å; alpha = 81.97(1) degrees; beta = 76.35(2) degrees; gamma = 71.824(14) degrees; Z = 1; R(1) = 4.56%. Complex 5 crystallizes in the monoclinic space group P2(1)/c. Crystal data for 5 at 243 K: a = 15.039(2) Å; b = 16.152(3) Å; c = 20.967(5) Å; beta = 91.53(2) degrees; Z = 4; R(1) = 4.83%. Complex 6 crystallizes in the orthorhombic space group Pbcn. Crystal data for 6 at 298 K: a = 14.686(2) Å; b = 21.295(5) Å; c = 28.767(5) Å; Z = 8; R(1) = 5.61%. Complex 7 crystallizes in the orthorhombic space group Pbcn. Crystal data for 7 at 218 K: a = 14.5533(2) Å; b = 21.4258(5) Å; c = 28.5990(5) Å; Z = 8; R(1) = 4.61%. Complex 8 crystallizes in the orthorhombic space group Pbcn. Crystal data for 8 at 219 K: a = 14.6162(2) Å; b = 21.3992(3) Å; c = 28.7037(2) Å; Z = 8; R(1) = 3.57%. Complex 9 crystallizes in the triclinic space group P&onemacr;. Crystal data for 9 at 293 K: a = 11.147(4) Å; b = 14.615(4) Å; c = 14.806(5) Å; alpha = 70.57(3) degrees; beta = 71.85(3) degrees; gamma = 72.93(2) degrees; Z = 2; R(1) = 5.13%. Complex 10 crystallizes in the triclinic space group P&onemacr;. Crystal data for 10 at 173 K: a = 10.5690(4) Å; b = 15.0376(5) Å; c = 15.3643(5) Å; alpha = 111.8630(10) degrees; beta = 100.4120(10) degrees; gamma = 97.4820(2) degrees; Z = 2; R(1) = 4.87%. A common feature of the molecular structures of complexes 2-10 is an infinitely extended polymeric ladder framework in the solid state. Both solution and solid-state NMR data are presented.

Approaches to Alkaline Earth Metal-Organic Chemical Vapor Deposition Precursors. Synthesis and Characterization of Barium Fluoro-beta-ketoiminate Complexes Having Appended Polyether "Lariats"

The synthesis and characterization of a family of beta-ketoimines derived from 1,1,1,5,5,5-hexafluoro-2,4-pentanedione (hfa) and the corresponding volatile barium beta-ketoiminate-polyether complexes having the general formula Ba[CF(3)COCHC(NR)CF(3)](2) where R = (CH(2)CH(2)O)(2)CH(3), (CH(2)CH(2)O)(2)CH(2)CH(3), and (CH(2)CH(2)O)(3)CH(2)CH(3) is reported. These complexes can be transported in the vapor phase at 160 degrees C/0.05 Torr without decomposition. The beta-ketoiminate ligands are synthesized by condensation of the appropriate amine-terminated poly(ethylene oxide)s with the trimethylsilyl enol ether derivative of hfa and converted to barium beta-ketoiminate-polyether complexes by reaction with BaH(2). The poly(ethylene oxide) amines are in turn synthesized by triphenylphosphine-mediated reduction of the corresponding poly(ethylene oxide) azides (synthesized via the tosylates) to afford the amines in good yields and analytical purity. The amines, beta-ketoimines, and barium complexes were characterized by elemental analysis, (1)H, (19)F, and (13)C NMR spectroscopy, mass spectroscopy, and thermogravimetric analysis. The eight- and ten-coordinate Ba(2+) complexes having the formula Ba[CF(3)COCHC(NR)CF(3)](2) where R = (CH(2)CH(2)O)(2)CH(2)CH(3) [C(22)H(28)N(2)F(12)O(6)Ba; space group = monoclinic, P2(1); a = 12.1175(2) Å, b = 14.9238(2) Å, c = 16.9767(3) Å, alpha = gamma = 90 degrees, beta = 90.0840(10) degrees, Z = 4] and R = (CH(2)CH(2)O)(3)CH(2)CH(3) [C(26)H(36)N(2)F(12)O(8)Ba; space group = triclinic, P&onemacr; (#2); a = 10.971(2) Å, b = 12.134(2) Å, c = 15.280(4) Å, alpha = 89.94(2) degrees, beta = 110.00(2) degrees, gamma = 116.75(2) degrees, Z = 2] were characterized by single-crystal X-ray diffraction. Both analyses reveal monomeric structures with the beta-ketoiminate ligands coordinated to the Ba(2+) center through all available oxygen and nitrogen atoms. These complexes are substantially more volatile than Ba(2,2,6,6,-tetramethyl-3,5-heptanedionate)(2) but less so than the most volatile Ba(1,1,1,5,5,5-hexafluoro-2,4-pentanedionate)(2).polyether complexes.

Tris[(alkylthio)methyl]silanes: Syntheses and Structures of Chromium, Molybdenum, and Tungsten Complexes with a Tripodal Thioether Ligand.

The first member of a new family of tripodal thioether ligands, the methyltris[(alkylthio)methyl]silanes MeSi(CH(2)SR)(3) (R = Me), has been synthesized and characterized. Reactivity studies lead to the isolation of the complete series of group 6 metal carbonyl derivatives {eta(3)-MeSi(CH(2)SMe)(3)}M(CO)(3) (M = Cr, Mo, W), whose structures have been determined by single-crystal X-ray diffraction. The three complexes are isomorphous and display distorted octahedral structures with face-capping tridentate thioether ligands. {eta(3)-MeSi(CH(2)SMe)(3)}Cr(CO)(3) is monoclinic, P2(1)/c, a = 8.1658(2) Å, b = 15.0563(2) Å, c = 26.5791(3) Å, beta = 90.3653(6) degrees, V = 3267.74(8) Å(3), Z = 8. {eta(3)-MeSi(CH(2)SMe)(3)}Mo(CO)(3) is monoclinic, P2(1)/c, a = 8.34630(6) Å, b = 15.2747(2) Å, c = 27.1865(4) Å, beta = 90.8987(9) degrees, V = 3465.44(10) Å(3), Z = 8. {eta(3)-MeSi(CH(2)SMe)(3)}W(CO)(3) is monoclinic, P2(1)/c, a = 8.1582(2) Å, b = 14.9903(2) Å, c = 26.7268(4) Å, beta = 90.6568(8) degrees, V = 3268.30(9) Å(3), Z = 8.

One-Dimensional Copper(I) Coordination Polymers Based on a Tridentate Thioether Ligand.

The one-dimensional copper(I) coordination polymers Cu(3){MeSi(CH(2)SMe)(3)}(2)X(3) (X = Cl, Br) and [{MeSi(CH(2)SMe)(3)}Cu(NCMe)]Y (Y = OSO(2)CF(3), BF(4), PF(6)) were readily obtained in very good to excellent yields (80-95%) by reacting CuX or [Cu(NCMe)(4)]Y, respectively, with the tridentate thioether ligand MeSi(CH(2)SMe)(3) in acetonitrile. The new complexes were characterized by a combination of analytical and spectroscopic techniques, including electrospray ionization mass spectrometry and, for the bromo and hexafluorophosphate derivatives, single-crystal X-ray diffraction. Both complexes exhibit one-dimensional chain structures with approximately tetrahedral copper centers and bridging unidentate/bidentate thioether ligands.

Metallo 2,3-Disulfidothienoquinoxaline, 2,3-Disulfidothienopyridine, and 2-Sulfido-3-oxidothienoquinoxaline Complexes: Synthesis and Characterization.

The 2,3-disulfidothienoquinoxaline complexes of Cp(2)Mo and dppePd and the 2,3-disulfidothienopyridine complexes of Cp(2)Mo were obtained as products from the S(8) oxidation of the corresponding metallo-1,2-enedithiolate complexes. The analogous 2-sulfido-3-oxidothienoquinoxaline complexes of Cp(2)Ti, Cp(2)Mo, dppPd, and dppePt were prepared from 1-(quinoxalin-2-yl)-2-bromoethanone and the corresponding polysulfido complex. Both Cp(2)Mo{S(2)C(10)H(4)N(2)S} and Cp(2)Mo{SOC(10)H(4)N(2)S} have been characterized crystallographically. These complexes contain an extended planar ring where the metal is bound to substituents at the 2- and 3-positions of the thiophene ring. The oxidation products of the Cp(2)Mo derivatives all have EPR g values near 1.98 and (97/95)Mo hyperfine of

Synthesis, Structure, and Molecular Orbital Studies of Yttrium, Erbium, and Lutetium Complexes Bearing eta(2)-Pyrazolato Ligands: Development of a New Class of Precursors for Doping Semiconductors.

Treatment of yttrium metal with bis(pentafluorophenyl)mercury (1.5 equiv), 3,5-di-tert-butylpyrazole (3 equiv), and pyridine (2 equiv) in toluene at ambient temperature for 120 h afforded tris(3,5-di-tert-butylpyrazolato)bis(pyridine)yttrium(III) (33%). In an analogous procedure, the reaction of erbium metal with 3,5-dialkylpyrazole (alkyl = methyl or tert-butyl), bis(pentafluorophenyl)mercury, and a neutral nitrogen donor (4-tert-butylpyridine, pyridine, n-butylimidazole, or 3,5-di-tert-butylpyrazole) yielded tris(3,5-di-tert-butylpyrazolato)bis(4-tert-butylpyridine)erbium(III) (63%), tris(3,5-di-tert-butylpyrazolato)bis(pyridine)erbium(III) (88%), tris(3,5-di-tert-butylpyrazolato)bis(n-butylimidazole)erbium(III) (48%), tris(3,5-dimethylpyrazolato)bis(4-tert-butylpyridine)erbium(III) (50%), and tris(3,5-di-tert-butylpyrazolato)(3,5-di-tert-butylpyrazole)erbium(III) (59%), respectively. Treatment of tris(cyclopentadienyl)lutetium(III) or tris(cyclopentadienyl)erbium(III) with 3,5-di-tert-butylpyrazole (3 equiv) and 4-tert-butylpyridine (2 equiv) in toluene at ambient temperature for 24 h afforded tris(3,5-di-tert-butylpyrazolato)bis(4-tert-butylpyridine)lutetium(III) (83%) and tris(3,5-di-tert-butylpyrazolato)bis(4-tert-butylpyridine)erbium(III) (41%), respectively. The X-ray crystal structures of all new complexes were determined. The X-ray structure analyses revealed seven- and eight-coordinate lanthanide complexes with all-nitrogen coordination spheres and eta(2)-pyrazolato ligands. Molecular orbital calculations were carried out on dichloro(pyrazolato)diammineyttrium(III). The calculations demonstrate that eta(2)-bonding of the pyrazolato ligand is favored over the eta(1)-bonding mode and give insight into the bonding between yttrium and the pyrazolato ligands. Complexes bearing 3,5-di-tert-butylpyrazolato ligands can be obtained in a high state of purity and sublime without decomposition (150 degrees C, 0.1 mmHg). Application of these complexes as source compounds for chemical vapor deposition processes is discussed.

Structural Diversity in the Solid-State Structures of the Rubidium and Cesium Salts of 2,6-Dimesitylphenylphosphane.

A coordination environment reminiscent of a paddle-wheel is exhibited by aryl groups about one of the two cesium ions in CsP(H)Dmp (Dmp=2,6-dimesitylphenyl; structure depicted on the right), which has now been synthesized and is found to exhibit Cs+ {Cs2 [P(H)Dmp]3 }- contact ion pairs in the solid state. In contrast, the analogous rubidium compound displays a Rb4 P4 cube as the central structural motif.

The Weak-Link Approach to the Synthesis of Inorganic Macrocycles.

Homobimetallic macrocycles are prepared from flexible ligands in high yield by means of a new and general synthetic strategy called the "weak-link approach" [Eq. (a)]. Small aromatic molecules can be aligned inside the cage based on their interactions with the two Rh centers of the macrocycle.

Reversible Ligand Pairing and Sorting Processes Leading to Heteroligated Palladium(II) Complexes with Hemilabile Ligands.

Halide-induced ligand pairing and sorting processes have been observed in the context of Pd(II) complexes with hemilabile P,S and P,O ligands. Mixing of the ligands Ph2PCH2CH2SMe (7) and Ph2PCH2CH2SPh (8) with a Pd(II) precursor in CH2Cl2 results in a mixture of [(7)2ClPd]Cl, [(8)2Cl2Pd], and [(7)(8)ClPd]Cl complexes at 20 °C. This equilibrium can be driven toward the heteroligated structure [(7)(8)ClPd]Cl by (1) cooling the mixture or (2) precipitation with hexanes, leading to the exclusive formation of semiopen heteroligated complex cis-[κ 2-(7)-κ 1-(8)ClPd]Cl (9a), as confirmed by a single-crystal X-ray diffraction study and solid state CPMAS 31P{1H} NMR spectroscopy. Dissolution of 9a in CH2Cl2 leads to the original mixture of complexes, which illustrates the reversible nature of this ligand pairing and sorting process. Similar processes occur when a combination of P,S and P,O ligands is used. The semiopen heteroligated complexes can be chemically manipulated in a reversible fashion to form closed complexes, allowing for control of the relative position and flexibility between neighboring substituents in these "tweezer"-like structures. Control experiments suggest these ligand sorting and pairing processes occur via a halide-induced ligand rearrangement (HILR) reaction.