Organometallics p. 1067 - 1079 (1989)
Update date:2022-07-30
Topics:
Meyer, Edouard Marc
Gambarotta, Sandro
Floriani, Carlo
Chiesi-Villa, Angiola
Guastini, Carlo
The synthesis of homoleptic aryl derivatives of group 11 metals has been performed by reacting the monochlorides [CuCl], [AgCl], and [AuCOCl] with MesMgBr (Mes ≡ 2,4,6-Me3C6H2). The resulting products [Cu5Mes5] (1), [Ag4Mes4] (2), and [Au5Mes5]·2THF (3) have been isolated as crystalline thermally stable compounds. They have, in the solid state, cyclic structures whose molecular geometries are discussed within. MW determination by cryoscopy in benzene and 1H NMR spectra in both C6D6 and C6D12 showed that the three oligomeric structures were in equilibrium with the respective dimeric form of the molecule. In each case the dimeric form was the prevailing species in solution. The solution equilibrium was very rapidly established for the silver and gold complexes and was relatively slower for the copper complex. In the case of the copper complex the rate of equilibrium was solvent dependent, being much faster in toluene (t1/2 for Cu5Mes5 being ca. 0.66 h) than in cyclohexane (t1/2 being ca. 56 h). The addition of electron-rich arenes to cyclohexane solutions of 1 greatly enhanced the rate of conversion of the pentamer to dimer. Addition of ligands to the solution containing the dimers allowed us to isolate complexes of different molecular complexity. The addition of THT (tetrahydrothiophene) to a THF solution of 1 resulted in the formation of the complex [Cu4Mes4THT2] (5). The results of the reactions of 1-3 with phosphines are reported and appear to be strongly dependent on the nature of the metal. PPh3 and dppe (Ph2PCH2CH2PPh2) stabilize the copper(I) dimer in solution, and subsequently they promote a ligand rearrangement with the formation of the corresponding cuprate. dppm (Ph2PCH2PPh2) reacts with 1 and 2 with the protolysis and elimination of the mesityl group to form [Cu3(Ph2PCHPPh2)3]·2C 7H8 (8) and [Ag3(Ph2PCHPPh2)3]·2C 7H8 (9), respectively. Complex 2 reacts with dppe in the same way as 1 or 3 depending on the nature of the solvent. Full characterization of the complexes was prevented by their thermal and photochemical instability. The reaction of phosphines PPh3, dppm, and dppe did not affect the [AuMes] functionality; in all three cases formation of the [P-Au-Mes] dicovalent gold(I) complexes [AuMesPPh3] (10), [Au2Mes2(μ-dppm)] (11), and [Au2Mes2(μ-dppe)] (12) was observed. The structures of six compounds have been determined. Crystallographic details for complexes 1, 2, 3, 5, 9, and 12 are as follows: Complex 1: space group P21/n (monoclinic), a = 16.094 (4) A?, b = 16.022 (4) A?, c = 19.259 (5) A?, β = 97.49 (3)°, V = 4924 (2) A?3, Z = 4, Dcalcd = 1.232 g cm-3. The final R factor was 0.10 for 1629 observed reflections. Complex 2: space group R3 (rhombohedral), a = b = c = 18.395 (3) A?, α = β = γ = 116.28 (2)°, V = 3038 (4) A?3, Z = 3, Dcalcd = 1.489 g cm-3. The final R factor was 0.062 (Rw = 0.064) for 1966 observed reflections. Complex 3: space group Pnma (orthorhombic), a = 21.864 (10) A?, b = 27.188 (11) A?, c = 8.951 (5) A?, V = 5321 (4) A?3, Z = 4, Dcalcd = 2.153 g cm-3. The final R factor was 0.052 (Rw = 0.050) for 2023 observed reflections. Complex 5: space group P1 (triclinic), a = 12.907 (3) A?, b = 20.624 (6) A?, c = 8.708 (2) A?, α = 102.14 (3)°, β = 107.38 (3)°, γ = 89.64 (3)°, V = 2159 (1) A?3, Z = 2, Dcalcd = 1.396 g cm-3. The final R factor was 0.057 (Rw = 0.062) for 3117 observed reflections. Complex 9: space group P21/n (monoclinic), a = 14.004 (2) A?, b = 23.632 (4) A?, c = 24.572 (4) A?, β = 101.66 (1)°, V = 7964 (2) A?3, Z = 4, Dcalcd = 1.384 g cm-3. The final R factor was 0.061 for 5695 observed reflections. Complex 12: space group P1 (triclinic), a = 11.700 (2) A?, b = 12.475 (2) A?, c = 7.647 (1) A?, α = 101.52 (1)°, β = 95.81 (1)°, γ = 109.55 (1)°, V = 1013.4 (3) A?3, Z = 1, Dcalcd = 1.650 g cm-3. The final R factor was 0.036 for 3659 observed reflections.
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