Mean-Field Effects on the Phosphorescence of Dinuclear Re(I) Complex Polymorphs

A computational study rationalizes the different phosphorescence colors of two highly emitting crystal polymorphs of a dinuclear Re(I) complex, [Re2(μ-Cl)2(CO)6(μ-4,5-(Me3Si)2pyridazine)]. The electrostatic interactions between the charge distributions on neighboring molecules inside the crystal are responsible for the different stabilization of the emitting triplet state because of the different molecular packing. These self-consistent effects play a major role in the phosphorescence of crystals made of polar and polarizable molecular units, offering a powerful handle to tune the luminescence wavelength in the solid state through supramolecular engineering

Solution conformation and dynamics of the ion pairs originating from the reaction of B(C6F5)(3) with bisindenyl dimethyl zirconium complexes

The two ion pairs [(4,7-Me(2)indenyl)(2)ZrMe](+)[MeB(C6F5)(3)](-) (1b) and [(indenyl)(2)ZrMe](+) [MeB(C6F5)(3)](-) (2b) have been generated in situ by reaction of stoichiometric B(C6F5)(3) with the corresponding dimethyl zirconocenes. It has been shown that molecular mechanics computations, guided by experimental H-1/H-1 NOE correlations, can provide information on the conformers present in solution. The dynamics of the ion pairs has also been investigated, showing the occurrence of both the processes previously characterized for this class of compounds, namely the B(C6F5)(3) migration between the two methyl groups and dissociation-recombination of the whole [MeB(C6F5)(3)](-) anion, the latter process being much faster than the first one (about three order of magnitude). Moreover, it has been shown that in certain conditions intermolecular processes can occur, which mimic the above-mentioned dissociative exchanges. In particular, the presence of species containing loosely bound [MeB(C6F5)(3)](-) anion fastens the exchange of this anion, while the presence of free B(C6F5)(3) accelerates its exchange between the two methyl sites

Dinuclear Re(I) Complexes as New Electrocatalytic Systems for CO2 Reduction

A family of dinuclear tricarbonyl rhenium (I) complexes containing bridging 1,2-diazine ligand and halide anions as ancillary ligands and able to catalyze CO2 reduction is presented. Electrochemical studies show that the highest catalytic efficiency is obtained for the complex containing the 4,5-bipenthyl-pyridazine and iodide as ancillary halogen ligands. This complex gives rise to TOF=15 s−1 that clearly outperforms the values reported for the benchmark mononuclear Re(CO)3Cl(bpy) (11.1 s−1). The role of the substituents on the pyridazine ligand and the nature of the bridging halide ligands on the catalytic activity have been deeply investigated through a systematic study on the structure-properties relationship to understand the improved catalytic efficiencies of this class of complexes

New lanthanide metalloligands and their use for the assembly of Ln-Ag bimetallic coordination frameworks : stepwise modular synthesis, structural characterization, and optical properties

Stepwise self-assembly processes using new lanthanide metalloligands (Ln-MLs) and silver salts have been successfully applied to isolate 4f-4d heterometallic coordination networks of four different structural types. In particular, the new lanthanide tetrakis-chelate complexes NEt4[Ln(L1)4] [HL1 = 1,3-bis(4\u2032-cyanophenyl)-1,3-propanedione; Ln = Eu (1a), La (1b), Nd (1c), Tb (1d)] and NEt4[Ln(L2)4] (HL2 = 1,3-bis(4\u2032-pyridyl)-1,3-propanedione; Ln = Eu (1e), Nd (1f)] have been synthetized, characterized and reacted with different silver salts. The use of NEt4[Ln(L1)4] allowed then to isolate and characterize i) neutral one-dimensional ladder-like species of formula [Ln(L1)4Ag] [Ln = Eu (2a), La(2b), Nd(2c), Tb(2d)] and ii) their supramolecular isomers [Ln(L1)4Ag] [Ln = Eu (3a), La (3b), Nd (3c), Tb (3d)] showing a very unstable 2D network structure, iii) the cationic 2D species [Ln(L1)4Ag2]X [Ln = Eu, X = PF6\u203e, CF3SO3\u203e, ClO4\u203e (4a\u20134c); Ln = Tb, Nd, La X = PF6\u203e (4d\u20134f)] and, only for lanthanum, iv) a fourth 2D species of formula [La(L1)4(H2O)Ag] (5) and sql topology. Of the eight nitrile groups on the MLs potentially coordinating, only a partial number is used for networking with Ag(I), that is, only two in families 2 and 3, and four in family 4 and in network 5. Finally, the four structural types are rationalized in terms of a new \u201cpincer-like\u201d Secondary Building Unit (SBU) consisting of a silver cation coordinating two central carbon atoms (\uf067 carbon) of two different diketonate ligands on the same ML. Therefore, it is shown that compounds 5, 4 and 2\u20133 contain, respectively, none, one or two of such pincer-like SBUs. The luminescence properties of the Ln-MLs and some of their polymeric species have been also investigated in solution and in the solid state

Dinuclear rhenium pyridazine complexes containing bridging chalcogenide anions : synthesis, characterization and computational study

The synthesis of a series of neutral dinuclear rhenium complexes of the general formula [Re2(m-ER)2(CO)6- (m-pydz)] (pydz = pyridazine; E = S, Se or Te; R = methyl or phenyl; the TeMe is not included) has been carried out via new, either one-pot or two-step, procedures. The one-pot synthesis consists of the oxidative addition of RE\u2013ER across the Re\u2013Re bond of [Re2(CO)10], in the presence of 1 equivalent of pyridazine, and affords the corresponding dinuclear complexes in high yields (ca. 85%). Furthermore, a general two-step procedure has been carried out, which involves the synthesis of heterocubane-like [Re4(m3-ER)4(CO)12] molecules and their reaction with pyridazine, quantitatively affording the corresponding dinuclear species through a symmetric [2+2] fragmentation pathway. The molecular structure of the complexes has been elucidated by single crystal XRD analysis, and TD-DFT calculations predicted the existence of conformers differing in the orientation of the chalcogen substituents with respect to the pyridazine ligand. The relative stabilities and the activation barriers for the interconversion have been calculated, observing a regular trend that has been rationalized depending on the hybridization of the chalcogen atom. Variable temperature NMR studies experimentally confirmed the theoretical prediction, showing, in solution, two conformers with different relative amounts and different interconversion rates between them, depending on the chalcogen nature. From the electrochemical point of view the S, Se and Te complexes display a bi-electronic reversible oxidation peak, differently from the two mono-electronic irreversible oxidation peaks previously observed for the O derivatives. Moreover, a progressive narrowing of the HOMO\u2013LUMO gap on going from O to Te, arising from the increase of the HOMO level, has been observed. This is in line with the decreasing electron-withdrawing strength of the chalcogenide bridging ligand, so that the energy gap for the telluride derivative is 1.64 eV, the smallest value in the whole family of the di-rhenium pyridazine complexes. The spectroscopic HOMO\u2013LUMO gap parallels this trend, with a significant red-shift of the metal-to-ligand charge transfer absorption, making the telluride complex highly promising as a photosensitizer in the field of solar energy conversion. In agreement with the narrow HOMO\u2013LUMO gap, no photoluminescence has been observed upon optical excitation

Competition studies on the activation of the C-H bond of diazines by the unsaturated triangular cluster anion [Re3(\u3bc-H) 4(CO)10]

The reactions of the unsaturated cluster anion [Re3(\u3bc-H) 4(CO)10]- (1) with 1,2-, 1,3- and 1,4-diazines (used as solvents) have been investigated. The reaction with 1,2-diazine at room temperature gives quantitatively the anion [Re3(\u3bc-H) 2(\u3bc-\u3b72-N2C4H 4)(CO)10]- (3), containing a diazine bridging through the two N atoms, characterised by single crystal X-ray analysis. The orthometallated isomer [Re3(\u3bc-H)3(\u3bc-\u3b7 2-N2C4H3)(CO)10] - (4) was obtained by refluxing 3 in toluene. The reaction of [NEt4]1 in molten 1,4-diazine (60\ub0C) affords the anion [Re 3(\u3bc-H)3(\u3bc-\u3b72-N2C 4H3)(CO)10]- (5), containing orthometallated pyrazine. The slow reaction of [NEt4]1 with 1,3-diazine at room temperature gives two orthometallated isomers 6, corresponding to the metallation of carbon C2 (6a) and C6 (6b), respectively (6b/6a ratio ca. 1.2). Differently from what previously found for the analogous cluster anion containing orthometallated pyridine, the metallation reaction of diazines showed little reversibility, and poor conversion of 5 and 6 to the starting anion 1 was observed after several days under 100 atm of H 2. Competition experiments, performed by dissolving [NEt 4]1 in equimolar mixtures of pyridine/pyrazine or pyridine/pyrimidine, showed that the anion with metallated pyridine was the kinetically preferred product and that at longer times it slowly converted to the derivatives with metallated diazines (5 or 6). \ua9 2003 Elsevier Science B.V. All rights reserved

Aggregation and ionization equilibria of bis(pentafluorophenyl)borinic acid driven by hydrogen-bonding with tetrahydrofuran

Bis(pentafluophenyl)borinic acid, Ar2BOH (1, Ar = C6F5), in dichloromethane solution is present as an equilibrium mixture of monomeric (1m) and trimeric (1t) forms. Previous studies showed that water affects both the position and the rate of this equilibrium. Here, the behavior of 1 in the presence of tetrahydrofuran (THF), a nucleophile able to behave as a Lewis base and H-bond acceptor only, has been studied, by monitoring with H-1 and F-19 NMR the course of titrations performed directly into NMR tubes. The addition, at 183 K, of 0.33 equiv of THF caused the instantaneous and quantitative formation of the hydrogen-bonded adduct between the trimer 1t and one molecule of THF. Homo- and heteronuclear 2D NMR correlation experiments led to a solution structure consistent with the C2-optimized geometry obtained by PM3 computations. The H-bonding of the THF molecule causes major deformations of the molecular geometry of the trimer, so that only one molecule of THF can interact with the trimer, in spite of its three OH groups. Intra- and intermolecular exchange processes involving this adduct have been investigated by 2D EXSY experiments, showing flopping of the cycle conformation, rotation of the aromatic rings around their B-C bonds, and exchange of THF among the three OH groups, in addition to the exchange between free 1t and the adduct. When the amount of added THF was higher than 0.33 equiv, an unexpected ionization process occurred, leading to the cation [Ar2B(OH2)2]+ and to deprotonated 1t, i.e., to the anion [Ar6B3O3H2]- of Cs symmetry. On increasing the temperature, progressive partial fragmentation of the trimeric species was observed. Both B-11 NMR evidence and PM3 computations indicated that, at variance with what is observed in the interaction with H2O, the interaction between THF and 1m occurs preferentially via an H-bonded adduct, Ar2BO-H...THF, rather than a Lewis acid-base complex, Ar2B(OH)(THF). This confirms the poor Lewis acidity of the boron atom of 1m

Ligand stereochemistry of metal clusters containing \u3c0-bonded ligands

The dummy atom formalism, originally proposed by Doman, Landis, and Bosnich for metallocenes, has been generalized in order to deal with any kind of \u3c0-bonding ligands and cluster faces (which can also be seen as polyhapto moieties). A modified VESCF approach has been used to derive a general force field for \u3b7(n)-coordinated \u3c0-bonding ligands whose performances are comparable with those of the best current force fields for cyclopentadienyl derivatives but can be used also for \u3bc3-\u3b72:\u3b72:\u3b72 and even complex coordination modes. This approach, which can be considered a further step in the building up of a general force field for metal (carbonyl) clusters, has been tested by rationalizing the dynamic stereochemistry in solution of two classes of triangular clusters: M3L3(CO)3 (M = Co, Rh, Ir; L = \u3b75-Cp, \u3b75-Cp*, \u3b75-Ind) and Co3(\u3b75-Cp)3(\u3bc3-\u3b72:\u3b72:\u3b72-RR'C6H4) (R = R' = H, Me, Et and R = Me, Et, (i)Pr; R' = H)

Molecular mechanics in crystalline media

A general, computationally easy method for minimizing the steric energy of a molecule, polymer, surface, or net within the field of a fixed, or periodically updated, crystal lattice has been devised. The goal has been obtained by coupling molecular mechanics (MM) to Kitaigorodsky\u2019s atom atom pairwise potential (AAPP). The primary outcomes of such MMAAPP computations are the \u201csolid state\u201d conformation of the molecule, its intramolecular steric energy and its interaction energy with the surrounding lattice. These computations are ideally suited for studying relative stabilities of different polymorphs, plastic deformations of a whole crystal lattice, and molecular motions of flexible guest molecules in host crystal lattices. The proposed approach can help in understanding solid-state dynamics, factors controlling reactivity in crystal lattices, and crystals as \u201csupramolecular entities\u201d. In addition, the capability of building \u201chypothetical\u201d crystals with sterically reasonable geometries can be exploited in the process of solving crystal structures from partial diffraction data

Complexes of tris(pentafluorophenyl)boron with nitrogen-containing compounds : Synthesis, reactivity and metallocene activation

The strong Lewis acid tris(pentafluorophenyl)boron, B(C6F5)(3), reacts with several nitrogen-containing Lewis bases (nitriles, amines, imines, pyridines, etc.) and also with non-basic substrates (such as pyrroles and indoles) producing in both cases the B-N coordination adduct. With particular substrates (some tertiary amines, the imine tBu(Me)C=NBn, N-methyl-pyrrole and -indole) the 1:1 borane/N-compound reaction produces zwitterions where a new B-C bond is generated. Some of the borane-N-compound adducts present Bronsted acidity and can be reacted with dimethyl group 4 complexes with generation of weakly associated ion pairs, which are active catalysts for the polymerization of olefins