Divergent reactivity of 2-vinylpyridine and 1-vinylpyrazole in rhodium-phosphine systems: C-H activation and dinuclear chemistry

The Rh-I-Rh-III mixed valence dinuclear complex Rh-2-Cl-2(mu-H)(mu-eta(2),kappa(2)-C, N-NC5H4-2-(Z)CH=CH)( PPhMe2)(3) has been prepared by reaction of [Rh(mu-Cl)(eta(2)-coe)(2)](2) with 2-vinylpyridine in the presence of dimethylphenylphosphine as a result of C-H activation of the terminal olefinic proton. The X- ray structure presents anagostic Rh center dot center dot center dot HC and pi-pi interactions between aromatic rings. In contrast, 1-vinylpyrazole does not undergo a C-H activation process, resulting in the formation of dinuclear species supported by 1 vinylpyrazole bridges. Anagostic Rh center dot center dot center dot HC interactions and CH center dot center dot center dot Cl hydrogen bonds are responsible for the 3D packing of the complex. El complejo dinuclear de valencia mixta RhI-RhIII Rh2-Cl2(µ-H)(µ-¿2,¿2-C,N-NC5H4-2-(Z)CH=CH)(PPhMe2)3 ha sido preparado por reacción de [Rh(µ-Cl)(¿2-coe)2]2 con 2-vinilpiridina en presencia de dimetilfenilfosfina, como resultado de la activación C-H del protón terminal de la olefina. La estructura de rayos-X presenta enlaces anagósticos Rh···HC, así como interacciones p-p entre anillos aromáticos. Por otro lado, la reacción con 1-vinilpirazol no da lugar a una activación C-H sino que se observa la formación de una especie dinuclear soportada por ligandos 1-vinilpirazol puente. Diferentes interacciones anagósticas Rh···HC y de enlace de hidrógeno CH···Cl son responsables del empaquetamiento tridimensional del complejo

Preparation of Butadienylpyridines by Iridium-NHC-Catalyzed Alkyne Hydroalkenylation and Quinolizine Rearrangement

Iridium(I) N-heterocyclic carbene complexes of formula Ir(¿2O, O’-BHetA)(IPr)(¿2-coe) [BHetA=bis-heteroatomic acidato, acetylacetonate or acetate; IPr=1, 3-bis(2, 6-diisopropylphenyl)imidazolin-2-carbene; coe=cyclooctene] have been prepared by treating Ir(¿2O, O’-BHetA)(¿2-coe)2 complexes with IPr. These complexes react with 2-vinylpyridine to afford the hydrido-iridium(III)-alkenyl cyclometalated derivatives IrH(¿2O, O’-BHetA)(¿2N, C-C7H6N)(IPr) through the iridium(I) intermediate Ir(¿2O, O’-BHetA)(IPr)(¿2-C7H7N). The cyclometalated IrH(¿2O, O’-acac)(¿2N, C–C7H6N)(IPr) complex efficiently catalyzes the hydroalkenylation of aromatic and aliphatic terminal alkynes and enynes with 2-vinylpyridine to afford 2-(4R-butadienyl)pyridines with Z, E configuration as the major reaction products (yield up to 89 %). In addition, unprecedented (Z)-2-butadienyl-5R-pyridine derivatives have been obtained as minor reaction products (yield up to 21 %) from the elusive 1Z, 3gem-butadienyl hydroalkenylation products. These compounds undergo a thermal 6p-electrocyclization to afford bicyclic 4H-quinolizine derivatives that, under catalytic reaction conditions, tautomerize to 6H-quinolizine to afford the (Z)-2-(butadienyl)-5R-pyridine by a retro-electrocyclization reaction. © 2021 The Authors. Chemistry - A European Journal published by Wiley-VCH Gmb

Iridium(i) complexes bearing hemilabile coumarin-functionalised N-heterocyclic carbene ligands with application as alkyne hydrosilylation catalysts

A set of iridium(i) complexes of formula IrCl(¿C, ¿2-IRCouR')(cod) or IrCl(¿C, ¿2-BzIRCouR')(cod) (cod = 1, 5-cyclooctadiene; Cou = coumarin; I = imidazolin-2-carbene; BzI = benzimidazolin-2-carbene) have beeen prepared from the corresponding azolium salt and [Ir(µ-OMe)(cod)]2 in THF at room temperature. The crystalline structures of 4b and 5b show a distorted trigonal bipyramidal configuration in the solid state with a coordinated coumarin moiety. In contrast, an equilibrium between this pentacoordinated structure and the related square planar isomer is observed in solution as a consequence of the hemilability of the pyrone ring. Characterization of both species by NMR was achieved at the low and high temperature limits, respectively. In addition, the thermodynamic parameters of the equilibrium, ¿HR and ¿SR, were obtained by VT 1H NMR spectroscopy and fall in the range 22-33 kJ mol-1 and 72-113 J mol-1 K-1, respectively. Carbonylation of IrCl(¿C, ¿2-BzITolCou7, 8-Me2)(cod) resulted in the formation of a bis-CO derivative showing no hemilabile behaviour. The newly synthesised complexes efficiently catalyze the hydrosilylation of alkynes at room temperature with a preference for the ß-(Z) vinylsilane isomer. © The Royal Society of Chemistry

Variation on the p-acceptor ligand within a Rhi-N-Heterocyclic carbene framework: divergent catalytic outcomes for phenylacetylene-methanol transformations

A series of neutral and cationic rhodium complexes bearing IPr {IPr=1, 3-bis-(2, 6-diisopropylphenyl)imidazolin-2-carbene} and p-acceptor ligands are reported. Cationic species [Rh(¿4-cod)(IPr)(NCCH3)]+ and [Rh(CO)(IPr)(L)2]+ (L=pyridine, CH3CN) were obtained by chlorido abstraction in suitable complexes, whereas the cod-CO derivative [Rh(¿4-cod)(IPr)(CO)]+ was formed by the carbonylation of [Rh(¿4-cod)(IPr)(NCCH3)]+. Alternatively, neutral derivatives of type RhCl(IPr)(L)2 {L=tBuNC or P(OMe)3} can be accessed from [Rh(µ-Cl)(¿2-coe)(IPr)]2. In addition, the mononuclear species Rh(CN)(¿4-cod)(IPr) was prepared by cyanide-chlorido anion exchange, which after carbonylation afforded the unusual trinuclear compound [Rh{1¿C, 2¿N-(CN)}(CO)(IPr)]3. Divergent catalytic outcomes in the phenylacetylene-methanol transformations have been observed. Thus, enol ethers, arisen from hydroalkoxylation of the alkyne, were obtained with neutral Rh-CO catalyst precursors whereas dienol ethers were formed with cationic catalysts. Variable amounts of alkyne dimerization, cyclotrimerization or polymerization products were obtained in the absence of a strong p-acceptor ligand on the catalyst. © 2021 The Authors. European Journal of Inorganic Chemistry published by Wiley-VCH Gmb

Bis(hydrosulfido)-bridged dinuclear rhodium(I) complexes as a platform for the synthesis of trinuclear sulfido aggregates with the core [MRh2(μ3-S2)] (M = Rh, Ir, Pd, Pt, Ru)

The reaction of [Rh(μ-SH)(CO)(PPh3)]2 or [Rh(μ-SH){P(OPh)3}2]2 with [Cp*MCl2]2 (M = Rh, Ir) in the presence of NEt3 afforded the Rh3 and IrRh2 sulfido-bridged compounds [Cp*M(μ3-S)2Rh2(CO)2(PPh3)2] (M = Rh, 1; Ir, 2) and [Cp*Rh(μ3-S)2Rh2{P(OPh)3}4] (3). The reaction with [MCl2(cod)] (M = Pd, Pt), cis-[PtCl2(PPh3)2] or [(η6-C6H6)RuCl2]2 under the same experimental conditions gave [(cod)M(μ3-S)2Rh2{P(OPh)3}4] (M = Pd, 6; Pt, 7), [(cod)M(μ3-S)2Rh2(CO)2(PPh3)2] (M = Pd, 8; Pt, 9), [(PPh3)2Pt(μ3-S)2Rh2(CO)2(PPh3)2] (10) and [(η6-C6H6)Ru(μ3-S)2Rh2(CO)2(PPh3)2] (12), with PdRh2, PtRh2 and RuRh2 trimetallic cores. The aggregates derived from [Rh(μ-SH)(CO)(PPh3)]2 were isolated as a mixture of trans and cis isomers in which the trans isomer predominates. The reaction of [Rh(μ-SH){P(OPh)3}2]2 with 2 equiv. of n-BuLi at 253 K followed by addition of [Cp*IrCl2]2 gave [Cp*Ir(μ3-S)2Rh2{P(OPh)3}4] (4) and [Cp*2ClIr2(μ3-S)2Rh{P(OPh)3}2] (5) in a 3:2 ratio. The RuRh2 compound [(η6-C6H6)Ru(μ3-S)2Rh2{P(OPh)3}4] (11) was prepared similarly from [Rh(μ-SH){P(OPh)3}2]2 and [(η6-C6H6)RuCl2]2 using n-BuLi as a deprotonating agent. The molecular structures of compounds 3, 6, 7, 9 and 11 have been determined by X-ray analysis. The trinuclear complexes exhibit an asymmetric triangular metal core with two triply bridging sulfido ligands resulting in a distorted trigonal-bipyramidal M3(μ3-S)2 heterometallic metal–sulfur core.Financial support from the Ministerio de Ciencia e Innovación (MICINN/FEDER) of Spain (Project CTQ2010-15221), the Diputación General de Aragón (E07), and CONSOLIDER INGENIO-2010, Projects MULTICAT (CSD2009-00050) and Factoría de Cristalización (CSD2006-0015) is gratefully acknowledged.Peer Reviewe

Synthesis of a square-planar rhodium alkylidene N-heterocyclic carbene complex and its reactivity toward alkenes

The first rhodium alkylidene square-planar complex stabilized by an N-heterocyclic carbene ligand, RhCl(-CHPh)(IPr)PPh3 (2; IPr = 1,3-bis(2,6-diisopropylphenyl)imidazol-2-carbene), has been prepared by reaction of RhCl(IPr)(PPh3)2 (1) with phenyldiazomethane and its dynamic behavior in solution studied. Treatment of 2 with alkenes results in the formation of the ¿2-olefin complexes RhCl(¿2-CH2-CHR)(IPr)PPh3 (3, R = H; 4, R = Ph; 5, R = OEt) and new olefins arising from the coupling of the alkylidene with the alkenes, likely via a metallacyclobutane intermediate

Microwave-synthesized freestanding iron-carbon nanotubes on polyester composites of woven Kevlar fibre and silver nanoparticle-decorated graphene

We synthesized Ag nanoparticle-decorated multilayered graphene nanosheets (Ag-graphene) from graphite nanoplatelets and silver nitrate through 90-100 s of microwave exposure, without the use of any mineral acids or harsh reducing agents. Fe nanoparticle-decorated carbon nanotubes (Fe-CNTs) were grown on polypyrrole (PPy) deposited on woven Kevlar fibre (WKF), using ferrocene as a catalyst, under microwave irradiation. Fe-CNTs grown on WKF and Ag-graphene dispersed in polyester resin (PES) were combined to fabricate Ag-graphene/Fe-CNT/PPy-coated WKF/PES composites by vacuum-assisted resin transfer moulding. The combined effect of Fe-CNTs and Ag-graphene in the resulting composites resulted in a remarkable enhancement of tensile properties (a 192.56% increase in strength and 100.64% increase in modulus) as well as impact resistance (a 116.33% increase). The electrical conductivity significantly increased for Ag-graphene/Fe-CNT/PPy-coated WKF/PES composites. The effectiveness of electromagnetic interference shielding, which relies strongly on the Ag-graphene content in the composites, was 25 times higher in Ag-graphene/Fe-CNT/PPy-coated WKF/PES than in neat WKF/PES composites. The current work offers a novel route for fabricating highly promising, cost effective WKF/PES composites through microwave-assisted synthesis of Fe-CNTs and Ag-graphene.ope

Activation and Deactivation of a Robust Immobilized Cp*Ir-Transfer Hydrogenation Catalyst: A Multielement in Situ X-ray Absorption Spectroscopy Study

A highly robust immobilized [Cp*IrCl2]2 precatalyst on Wang resin for transfer hydrogenation, which can be recycled up to 30 times, was studied using a novel combination of X-ray absorption spectroscopy (XAS) at Ir L3-edge, Cl K-edge, and K K-edge. These culminate in in situ XAS experiments that link structural changes of the Ir complex with its catalytic activity and its deactivation. Mercury poisoning and “hot filtration” experiments ruled out leached Ir as the active catalyst. Spectroscopic evidence indicates the exchange of one chloride ligand with an alkoxide to generate the active precatalyst. The exchange of the second chloride ligand, however, leads to a potassium alkoxide–iridate species as the deactivated form of this immobilized catalyst. These findings could be widely applicable to the many homogeneous transfer hydrogenation catalysts with Cp*IrCl substructure