Marc-André Légaré

Metal-free catalytic C-H bond activation and borylation of heteroarenes

A metal-free catalyst born of frustration Boron (a Lewis acid) and nitrogen or phosphorus fragments (both Lewis bases) tend to pair up. Keeping them separated on opposite ends of the same molecule creates a “frustrated” Lewis pair. Such molecules can manifest powerful reactivity, such as scission of the hydrogen-hydrogen bond in H2. Légaré et al. now extend this reactivity to the cleavage of carbon-hydrogen bonds in heteroaromatic compounds such as furans and pyrroles (see the Perspective by Bose and Marder). Their frustrated Lewis pair complex catalyzed borylation of these compounds. The selectivity pattern of the reaction complemented that seen with the metal catalysts conventionally used. Science, this issue p. 513; see also p. 473 Boron and nitrogen centers cooperatively catalyze a reaction that has previously relied on transition metal catalysts. [Also see Perspective by Bose and Marder] Transition metal complexes are efficient catalysts for the C-H bond functionalization of heteroarenes to generate useful products for the pharmaceutical and agricultural industries. However, the costly need to remove potentially toxic trace metals from the end products has prompted great interest in developing metal-free catalysts that can mimic metallic systems. We demonstrated that the borane (1-TMP-2-BH2-C6H4)2 (TMP, 2,2,6,6-tetramethylpiperidine) can activate the C-H bonds of heteroarenes and catalyze the borylation of furans, pyrroles, and electron-rich thiophenes. The selectivities complement those observed with most transition metal catalysts reported for this transformation.

Reducing CO2 to methanol using frustrated Lewis pairs : on the mechanism of phosphine-borane mediated hydroboration of CO2

The full mechanism of the hydroboration of CO2 by the highly active ambiphilic organocatalyst 1-Bcat-2-PPh2-C6H4 (Bcat = catecholboryl) was determined using computational and experimental methods. The intramolecular Lewis pair was shown to be involved in every step of the stepwise reduction. In contrast to traditional frustrated Lewis pair systems, the lack of steric hindrance around the Lewis basic fragment allows activation of the reducing agent while moderate Lewis acidity/basicity at the active centers promotes catalysis by releasing the reduction products. Simultaneous activation of both the reducing agent and carbon dioxide is the key to efficient catalysis in every reduction step.

Transition‐Metal‐Free Catalytic Reduction of Carbon Dioxide

Metal-free systems, including frustrated Lewis pairs (FLPs) have been shown to bind CO2. By reducing the Lewis acidity and basicity of the ambiphilic system, it is possible to generate active catalysts for the deoxygenative hydroboration of carbon dioxide to methanol derivatives with conversion rates comparable to those of transition-metal-based catalysts.

Main-Group Metallomimetics: Transition Metal-like Photolytic CO Substitution at Boron

The carbon monoxide adduct of an unhindered and highly reactive CAAC-bound arylborylene, [(CAAC)B(CO)Ar] (CAAC = cyclic (alkyl) (amino)carbene), has been prepared using a transfer reaction from the linear iron borylene complex [(PMe3) (CO)3Fe=BAr]. [(CAAC)B(CO)Ar] is a source of the dicoordinate [(CAAC)ArB:] borylene that can be liberated by selective photolytic CO extrusion and that, although highly reactive, is sufficiently long-lived to react intermolecularly. Through trapping of the borylene generated in this manner, we present, among others, the first metal-free borylene(I) species containing a nitrogen-based donor, as well as a new boron-containing radical.

Nitrogen fixation and reduction at boron

Boron learns to give back to nitrogen Although diatomic nitrogen is famously inert, a variety of transition metals can bind to it through a process termed backbonding. As the nitrogen weakly shares its own electrons, some electrons from the metal reach back out to it. Nonmetals would not seem to have the capacity for this type of bonding, but now Légaré et al. show that conventionally electron-deficient boron can be coaxed into it (see the Perspective by Broere and Holland). The authors treated boron-based precursors with potassium under a nitrogen atmosphere to produce several compounds with sandwiched dinitrogen between two boron centers in reduced motifs reminiscent of metal complexes. Science, this issue p. 896; see also p. 871 A boron compound reduced by potassium can bind N2 in a motif reminiscent of transition metal complexes. Currently, the only compounds known to support fixation and functionalization of dinitrogen (N2) under nonmatrix conditions are based on metals. Here we present the observation of N2 binding and reduction by a nonmetal, specifically a dicoordinate borylene. Depending on the reaction conditions under which potassium graphite is introduced as a reductant, N2 binding to two borylene units results in either neutral (B2N2) or dianionic ([B2N2]2–) products that can be interconverted by respective exposure to further reductant or to air. The 15N isotopologues of the neutral and dianionic molecules were prepared with 15N-labeled dinitrogen, allowing observation of the nitrogen nuclei by 15N nuclear magnetic resonance spectroscopy. Protonation of the dianionic compound with distilled water furnishes a diradical product with a central hydrazido B2N2H2 unit. All three products were characterized spectroscopically and crystallographically.

Synthesis and Reduction of Sterically Encumbered Mesoionic Carbene‐Stabilized Aryldihaloboranes

Sterically hindered, in situ generated 1,3,4-substituted 1,2,3-triazol-5-ylidene mesoionic carbenes (MICs) were employed to stabilize a number of aryl- and heteroaryldihaloboranes, as well as the first MIC-supported diborane. Reduction of borane adducts of the 1-(2,6-diisopropylphenyl)-3-methyl-4-tert-butyl-1,2,3-triazol-5-ylidene ligand with KC8 in non-coordinating solvents led to intramolecular C-H- and, C-C-activation at an isopropyl residue of the supporting ligand. DFT calculations showed that each of these activation reactions proceeds via a different isomer of a borylene intermediate.

Synthesis of Carboxylate Cp*Zr(IV) Species: Toward the Formation of Novel Metallocavitands

With the intent of generating metallocavitands isostructural to species [(CpZr)3(μ(3)-O)(μ(2)-OH)3(κO,O,μ(2)-O2C(R))3](+), the reaction of Cp*2ZrCl2 and Cp*ZrCl3 with phenylcarboxylic acids was carried out. Depending on the reaction conditions, five new complexes were obtained, which consisted of Cp*2ZrCl(κ(2)-OOCPh) (1), (Cp*ZrCl(κ(2)-OOCPh))2(μ-κ(2)-OOCPh)2 (2), [(Cp*Zr(κ(2)-OOCPh))2(μ-κ(2)-OOCPh)2(μ(2)-OH)2]·Et2O (3·Et2O), [[Cp*ZrCl2](μ-Cl)(μ-OH)(μ-O2CC6H5)[Cp*Zr]]2(μ-O2CC6H5)2 (4), and [Cp*ZrCl4][(Cp*Zr)3(κ2-OOC(C6H4Br)3(μ3-O)(μ2-Cl)2(μ2-OH)] [5](+)[Cp*ZrCl4](-). The structural characterization of the five complexes was carried out. Species 3·Et2O exhibits host-guest properties where the diethyl ether molecule is included in a cavity formed by two carboxylate moieties. The secondary interactions between the cavity and the diethyl ether molecule affect the structural parameters of the complex, as demonstrated be the comparison of the density functional theory models for 3 and 3·Et2O. Species 5 was shown to be isostructural to the [(CpZr)3(μ(3)-O)(μ(2)-OH)3(κO,O,μ(2)-O2C(R))3](+) metallocavitands.

The First Boron-Tellurium Double Bond: Direct Insertion of Heavy Chalcogens into a Mn=B Double Bond

The base-stabilized borylene [Cp(OC)2 Mn=BtBu(IMe)] readily reacts with elemental chalcogens in an insertion reaction that yields borachalcone complexes [Cp(OC)2 Mn-E=BtBu(IMe)] (E=S, Se, Te). The tellurium example features the first double bond between boron and tellurium, making Te the heaviest main-group element to make multiple bonds with boron. This unprecedented interaction has been fully investigated both experimentally and computationally.

Theoretical Calculations for Highly Selective Direct Heteroarylation Polymerization: New Nitrile-Substituted Dithienyl-Diketopyrrolopyrrole-Based Polymers

Direct Heteroarylation Polymerization (DHAP) is becoming a valuable alternative to classical polymerization methods being used to synthesize π-conjugated polymers for organic electronics applications. In previous work, we showed that theoretical calculations on activation energy (Ea) of the C–H bonds were helpful to rationalize and predict the selectivity of the DHAP. For readers’ convenience, we have gathered in this work all our previous theoretical calculations on Ea and performed new ones. Those theoretical calculations cover now most of the widely utilized electron-rich and electron-poor moieties studied in organic electronics like dithienyl-diketopyrrolopyrrole (DT-DPP) derivatives. Theoretical calculations reported herein show strong modulation of the Ea of C–H bond on DT-DPP when a bromine atom or strong electron withdrawing groups (such as fluorine or nitrile) are added to the thienyl moiety. Based on those theoretical calculations, new cyanated dithienyl-diketopyrrolopyrrole (CNDT-DPP) monomers and copolymers were prepared by DHAP and their electro-optical properties were compared with their non-fluorinated and fluorinated analogues.

A Boradiselenirane and a Boraditellurirane: Isolable Heavy Analogs of Dioxiranes and Dithiiranes

The isolation of BE2 heterocycles (E = Te, Se, S) from the reaction of a manganese borylene complex with elemental chalcogens is reported. The BTe2 and BSe2 cycles-a boraditellurirane and a boradiselenirane, respectively-are the first analogs of dioxiranes based on heavy chalcogens. While the BTe2 unit is still found datively bound to manganese, the Se and S analogs were isolated in their free forms. All heterocycles have been shown to transfer a chalcogen atom, allowing for the isolation of novel borachalcones and their dimerization products.