The preparation and characterization (elemental analysis, (1)H NMR, and cyclic voltammetry) of the new compounds MM(TiPB)(4), where MM = MoW and W(2) and TiPB = 2,4,6-triisopropylbenzoate, are reported. Together with Mo(2)(TiPB)(4), previously reported by Cotton et al. (Inorg. Chem. 2002, 41, 1639), the new compounds have been studied by electronic absorption, steady-state emission, and transient absorption spectroscopy (femtosecond and nanosecond). The compounds show strong absorptions in the visible region of the spectrum that are assigned to MMdelta to arylcarboxylate pi* transitions, (1)MLCT. Each compound also shows luminescence from two excited states, assigned as the (1)MLCT and (3)MMdeltadelta* states. The energy of the emission from the (1)MLCT state follows the energy ordering MM = Mo(2) > MoW > W(2), but the emission from the (3)MMdeltadelta* state follows the inverse order: MM = W(2) > MoW > Mo(2). Evidence is presented to support the view that the lower energy emission in each case arises from the (3)MMdeltadelta* state. Lifetimes of the (1)MLCT states in these systems are approximately 0.4-6 ps, whereas phosphorescence is dependent on the MM center: Mo(2) approximately 40 micros, MoW approximately 30 micros, and W(2) approximately 1 micros.
The reactions between [Mo(2)L(2)(CH(3)CN)(6)][BF(4)](2) compounds and [Bu(n)(4)N](2)[O(2)CCO(2)] in CH(3)CN are shown to proceed under kinetic control to the formation of a mixture of molecular triangles and squares. The molecular triangles [L(2)Mo(2)(O(2)CCO(2))](3) I (L = DPhF, PhNCHNPh) and II (L = DAniF, p-MeO-C(6)H(4)NCHNC(6)H(4)-p-OMe) are the major products, and when 0.75 equivalents of [Bu(n)(4)N](2)[O(2)CCO(2)] is employed, they are formed to the exclusion of the square. The molecular structure of II is reported based on a single crystal X-ray determination. The molecular triangles do not enter into an equilibrium with their molecular square counterparts in CH(2)Cl(2), in contrast to their perfluoroterephthalate bridged counterparts. The compounds I and II are orange and have a strong electronic transition at lambda(max) approximately 460 nm assignable to metal-to-ligand charge transfer ((1)MLCT) involving the oxalate bridge. Electronic structure calculations employing density functional theory on model compounds [(HCO(2))(2)Mo(2)(O(2)CCO(2))](3) and [(HNCHNH)(2)Mo(2)(O(2)CCO(2))](3) have been carried out and indicate the frontier occupied molecular orbitals are Mo(2) delta combinations e(4)a(2), and the lowest unoccupied are bridge pi* for the formamidinates and delta* for formates as ancillary ligands. Compounds I and II show quasi-reversible oxidation waves in their cyclic voltammograms and oxidation of II in 2-methyl-THF by reaction with AgPF(6) (1 equivalent) leads to a metal centered EPR signal, g approximately 1.95. The electronic absorption spectrum shows a low-energy broad band centered at 6418 cm(-1), which is assigned to an intervalence charge transfer (IVCT) band of a class III mixed valence ion.
Quadruply bonded dinuclear metal complexes of molybdenum and tungsten have the MM configuration σ(2)π(4)δ(2) and a considerable degree of attention has been devoted to studies of the δ → δ(*) transition. For compounds of the type M(2)(O(2)CR)(4), the CO(2) π(*) orbitals introduce a M(2) δ to ligand π(*) transition, a (1)MLCT absorption which may be lower in energy than the δ → δ(*) and is more intense, thus obscuring the observation of the latter. When the R group is a conjugated organic system such as an aryl group, the (1)MLCT shifts to even lower energy and emission is seen from this S(1) state in addition to phosphorescence from the T(1) state which may be either (3)MLCT or (3)MMδδ(*). The latter typically occurs around 1100 nm with a lifetime that ranges from ~1 μs (M = W) to 100 μs (M = Mo). The S(1)(1)MLCT states have lifetimes of ~1-20 ps, allowing for fs and ns studies of the charge distribution/localization with time in both the S(1) and T(1) states, which is quite rare for transition metal coordination complexes. Of particular interest and focus have been complexes of the type trans-M(2)L(2)L'(2) where L and L' are carboxylate or amidinate groups for which only one set of ligands allows for expansive Lπ-M(2)δ-Lπ conjugation and has a low energy (1)MLCT. Compounds of this type have excited states that may be considered as mixed valence (MV) ions [L-M(2)(+)-L(-)] ↔ [L(-)-M(2)(+)-L] where the hole resides on the M(2) unit and the electron is either localized on one ligand, a class I or II MV ion, or is fully delocalized over both ligands, a class III ion in the Robin and Day scheme. Examples of these systems will be described along with the newly prepared complexes trans-M(2)(T(i)PB)(2)(O(2)CC≡C-9-anthracene)(2), M = Mo, W, that have the IR-active reporter groups CO(2) and C≡C.
The reaction between M(2)(TiPB)(4) (M = Mo, W) where TiPB = 2,4,6-triisopropylbenzoate and 6-carboethoxy-2-azulenecarboxylic acid (2 equiv.) in toluene leads to the formation of complexes M(2)(TiPB)(2)(6-carboethoxy-2-azulenecarboxylate)(2). Compound (M = Mo) is blue and compound (M = W) is green. Both are air sensitive, hydrocarbon soluble species that gave the corresponding molecular ions in their mass spectra (MALDI-TOF). They show metal based oxidations and ligand based reductions. Electronic structure calculations (DFT and time dependent DFT) indicate that the two azulene carboxylate pi systems are coupled by their interactions with the M(2)delta orbitals. Their intense colors arise from M(2)delta to azulene pi* electronic transitions. While compound exhibits weak emission at approximately 900 nm, no emission has been detected for . Both and have been studied by fs and ns transient absorption spectroscopy. The X-ray analysis of the molecular structure of in the solid state confirmed the paddlewheel nature of its W(2)(O(2)C)(4) core and the trans orientation of the ligands.
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