A new class of supramolecular assemblies derived from a powerful Lewis acid in the form of dirhodium(II) tetra(trifluoroacetate) and various planar polycyclic aromatic hydrocarbons (PAHs) as donors has been prepared using a solventless technique. As a result, a number of novel adducts [Rh2(O2CCF3)4]x(L)y with various stoichiometries, x:y = 1:2, 1:1, 3:2, and 3:1, have been isolated in crystalline form. The following PAHs have been employed: acenaphthylene C12H8 (L1); acenaphthene C12H10 (L2); anthracene (L3) and phenanthrene (L4), C14H10; pyrene (L5) and fluoranthene (L6), C16H10; a series of isomers of the C18H12 composition: 1,2-benzanthracene (L7), triphenylene (L8), and chrysene (L9). Single-crystal X-ray diffraction studies have revealed a variety of structural motifs ranging from discrete molecules to extended 1D chains and 2D networks. In the bis-adducts, [Rh2(O2CCF3)4](L)2, an aromatic ligand is axially coordinated to the rhodium atoms through two long inequivalent Rh-C linkages at each end of the dirhodium complex. In the 1D complexes ([Rh2(O2CCF3)4](L))infinity aromatic ligands serve as bidentate links between two dirhodium units, while in 2D structures PAHs act as polydentate linkers, each coordinated to several rhodium atoms. Each linkage of a PAH consisted of an off-centered eta(2) coordination toward a single rhodium center. Simple Hückel calculations performed on the PAHs were used to calculate pi-electron densities for the C-C bonds, and these densities were compared to the experimental results.
The ambidentate character of dimethyl sulfoxide, already known for dirhodium carboxylates, has been remarkably manifested in new ways. Three novel complexes of dirhodium(II) tetra(trifluoroacetate) with the DMSO ligand, namely, [Rh2(O2CCF3)4]m(DMSO)n with m:n = 7:8 (1), 1:1 (2), and 3:2 (3), have been obtained by deposition from the vapor phase, and their crystal structures have been determined by X-ray crystallography. The crystallographic parameters are as follows: for 1, monoclinic space group P2(1)/c with a = 28.261(2) A, b = 16.059(4) A, c = 17.636(2) A, beta = 92.40(4) degrees, and Z = 2; for 2, triclinic space group P1 with a = 8.915(2) A, b = 10.592(2) A, c = 11.916(2) A, alpha = 84.85(1) degrees, beta = 88.86(1) degrees, and gamma = 65.187(8) degrees, and Z = 2; and for 3, triclinic space group P1 with a = 8.876(2) A, b = 9.017(2) A, c = 19.841(3) A, alpha = 101.91(2) degrees, beta = 97.144(8) degrees, gamma = 100.206(9) degrees, and Z = 1. In the oligomeric molecule of 1, six DMSO ligands bridge seven dirhodium tetra(trifluoroacetate) units in a bidentate fashion via S and O atoms, and two additional DMSO molecules terminate the chain. In the structure of the monoadduct Rh2(O2CCF3)4(DMSO) (2), the dirhodium blocks are bridged through the O atoms of DMSO ligands, forming a one-dimensional polymeric chain. Compound 3 also has an infinite chain structure with the molecules of dimethyl sulfoxide acting in a bidentate mu-DMSO-S,O mode. Every second DMSO molecule is missing in 3, so that two of every three Rh2(O2CCF3)4 units are associated through the O atoms of carboxylate groups to give the overall composition [Rh2(O2CCF3)4]3(DMSO)2.
The monoadduct of dirhodium tetra(trifluoroacetate) with THF has been obtained by deposition from the vapor phase. The compound Rh(2)(O(2)CCF(3))(4)(THF) crystallizes in two isomeric forms, 1 and 2, whose structures have been determined by X-ray crystallography. The crystallographic parameters are as follows: for 1, triclinic space group P&onemacr; with a = 9.557(2) Å, b = 10.126(2) Å, c = 11.840(4) Å, alpha = 95.97(2) degrees, beta = 90.40(2) degrees, gamma = 115.58(1) degrees, and Z = 2; for 2, triclinic space group P&onemacr; with a = 8.6347(3) Å, b = 9.678(1) Å, c = 13.773(4) Å, alpha = 73.182(5) degrees, beta = 74.622(5) degrees, gamma = 89.76(1) degrees, and Z = 2. Compound 1 is unique as the only extended structure where dirhodium carboxylate molecules are bridged by a single exogenous atom. The oxygen atom of the THF ligand coordinates to the axial positions of two Rh(2) units so that a one-dimensional zigzag chain is formed. The bridging is slightly asymmetric with Rh-O(THF) distances of 2.363(6) and 2.407(6) Å, and the Rh-O(THF)-Rh angle is 111.8(3) degrees. The crystal structure of 2 is not polymeric. Pairs of Rh(2)(O(2)CCF(3))(4)(THF) units are associated through O atoms of carboxylate groups to produce a dimer of dimers. The lengths of the terminal Rh-O(THF) and axial bridging Rh.O(Ac) interactions are 2.214(7) and 2.406(6) Å, respectively.
The quadruply bonded dimolybdenum complexes with alkyl-substituted pyridines of the formula Mo(2)Cl(4)(R-py)(4) (R-py = 4-pic (4-methylpyridine) (1), 3,5-lut (3,5-dimethylpyridine) (2), and 4-Bu(t)-py (4-tert-butylpyridine) (3)) have been prepared. Nine different compounds, in which there are 11 independent molecules, have been obtained in crystalline form, and their crystal structures have been investigated by X-ray diffraction. Three types of geometric isomers which differ by the angle of internal rotation about the Mo-Mo axis have been recognized in these structures. The eclipsed structures 1-3a display pyridine ligands opposite to each other across the metal-metal bond and have a virtual symmetry D(2)(h)(). The noncentrosymmetric D(2)(d)() structures 1-3b have each pyridine ligand opposite to a Cl atom. The molecules 3c-f have a partially staggered D(2) geometry with N-Mo-Mo-N torsion angles ranging from 10.4 degrees to 25.2 degrees. As a result of this work it is now clear that Mo(2)Cl(4)(R-py)(4) compounds do not show a preference for D(2)(h)() conformation rather than D(2)(d)() conformation. In fact, they seem unusually unrestricted in their rotational conformation, and packing forces appear to have a major influence on the conformation adopted. Further clarification of this question will require spectroscopic study of solutions.
The interaction between octachlorodirhenium anions and diethylphosphine has been shown to strongly depend on reaction conditions, mainly the nature of the solvent and the amount of phosphine. As a result, novel dirhenium products with oxidation states ranging from Re(II) to Re(IV) have been obtained. The reaction of [Re(2)Cl(8)](2)(-) with an excess of PEt(2)H in dichloromethane or acetonitrile led to the first example of a face-sharing complex of rhenium(IV) with three phosphido-bridges, namely [Bu(n)(4)N][Re(2)(&mgr;-PEt(2))(3)Cl(6)] (1). The unusual edge-sharing Re(2)(&mgr;-PEt(2))(2)Cl(4)(PEt(2)H)(4) (2) complex of rhenium(III) with C(i)() core symmetry, containing both terminal phosphines and phosphido-bridges, has been obtained by carrying out the reaction with an excess of PEt(2)H in a benzene (or propanol) - HCl mixture at room temperature. A new example of the 1,2,7,8-type of dirhenium(II) complex, Re(2)Cl(4)(PEt(2)H)(4) (3), having diethylphosphine ligands located cis on each Re atom, has been isolated from the reaction of [Re(2)Cl(8)](2)(-) with PEt(2)H in an ethanol-HCl medium. The solid-state structures of complexes 1-3 have been investigated by X-ray crystallography. Complexes 1 and 2 both crystallized in two forms: [Bu(n)(4)N][Re(2)(&mgr;-PEt(2))(3)Cl(6)] 1a, P2(1)/n with a = 10.482(1) Å, b = 16.512(2) Å, c = 23.986(2) Å, beta = 93.637(8) degrees, and Z = 4; [Bu(n)(4)N][Re(2)(&mgr;-PEt(2))(3)Cl(6)].1.5 C(7)H(8) 1b, C2/c with a = 38.746(9) Å, b = 10.322(2) Å, c = 27.277(3) Å, beta = 110.35(1) degrees, and Z = 8; Re(2)(&mgr;-PEt(2))(2)Cl(4)(PEt(2)H)(4) 2a, P2(1)/n with a = 11.081(3) Å, b = 11.029(3) Å, c = 15.627(2) Å, beta = 90.05(1) degrees, and Z = 2; 2b, P2(1)/c with a = 16.094(3) Å, b = 15.193(3) Å, c = 15.548(3) Å, beta = 100.98(3) degrees, and Z = 4. X-ray data for complex Re(2)Cl(4)(PEt(2)H)(4) 3 are as follows: P2(1)/n with a = 10.445(2) Å, b = 10.113(3) Å, c = 13.473(2) Å, beta = 102.17(2) degrees, and Z = 2. Three bridging &mgr;-PEt(2) groups in the face-sharing complex 1 span a short metal-metal distance of 2.4060(6) Å, averaged over 1a and 1b, with a small Re-PEt(2)-Re angle of 61.34(7) degrees. The rhenium-rhenium bond length in the edge-sharing complex 2 is 2.7545(7) Å, averaged over 2a and 2b, while the bridging Re-PEt(2)-Re angle is 72.16(6) degrees, and the P-Re-P angle for the terminal phosphine ligands is 87.11(7) degrees. The Re-Re bond distance in 3, 2.2533(8) Å, is typical for triply bonded dirhenium complexes, and the P-Re-P angle for the cis phosphine groups is 93.12(6) degrees.
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