587 research outputs found
A General Rhodium Catalyst for the Deuteration of Boranes and Hydrides of the Group 14 Elements
Pinacolborane, catecholborane, triethylsilane, triphenylsilane, dimethylphenylsilane, 1, 1, 1, 3, 5, 5, 5-heptamethyltrisiloxane, triethylgermane, triphenylgermane, and triphenylstannane deuterated at the heteroatom position have been catalytically prepared in 50-70% isolated yield, through H/D exchange between the D2 molecule and the respective boranes and hydrides of the group 14 elements, in the presence of the rhodium(I)-monohydride catalyst precursor RhH{Âż3-P, O, P-[xant(PiPr2)2]} (xant(PiPr2)2 = 9, 9-dimethyl-4, 5-bis(diisopropylphosphino)xanthene)
Kinetic Analysis and Sequencing of Si-H and C-H Bond Activation Reactions: Direct Silylation of Arenes Catalyzed by an Iridium-Polyhydride
The saturated trihydride IrH3{Âż3-P, O, P-[xant(PiPr2)2]} (1; xant(PiPr2)2 = 9, 9-dimethyl-4, 5-bis(diisopropylphosphino)xanthene) coordinates the Si-H bond of triethylsilane, 1, 1, 1, 3, 5, 5, 5-heptamethyltrisiloxane, and triphenylsilane to give the s-complexes IrH3(Âż2-H-SiR3){Âż2-cis-P, P-[xant(PiPr2)2]}, which evolve to the dihydride-silyl derivatives IrH2(SiR3){Âż3-P, O, P-[xant(PiPr2)2]} (SiR3 = SiEt3 (2), SiMe(OSiMe3)2 (3), SiPh3 (4)) by means of the oxidative addition of the coordinated bond and the subsequent reductive elimination of H2. Complexes 2-4 activate a C-H bond of symmetrically and asymmetrically substituted arenes to form silylated arenes and to regenerate 1. This sequence of reactions defines a cycle for the catalytic direct C-H silylation of arenes. Stoichiometric isotopic experiments and the kinetic analysis of the transformations demonstrate that the C-H bond rupture is the rate-determining step of the catalysis. As a consequence, the selectivity of the silylation of substituted arenes is generally governed by ligand-substrate steric interactions
Ammonia Borane Dehydrogenation Promoted by a Pincer-Square-Planar Rhodium(I) Monohydride: A Stepwise Hydrogen Transfer from the Substrate to the Catalyst
The pincer d8-monohydride complex RhH{xant(PiPr2)2} (xant(PiPr2)2 = 9, 9-dimethyl-4, 5-bis(diisopropylphosphino)xanthene) promotes the release of 1 equiv of hydrogen from H3BNH3 and H3BNHMe2 with TOF50% values of 3150 and 1725 hâ1, to afford [BH2NH2]n and [BH2NMe2]2 and the tandem ammonia borane dehydrogenationâcyclohexene hydrogenation. DFT calculations on the ammonia borane dehydrogenation suggest that the process takes place by means of cis-Âż2-PP-species, through four stages including: (i) Shimoi-type coordination of ammonia borane, (ii) homolytic addition of the coordinated HâB bond to afford a five-coordinate dihydride-boryl-rhodium(III) intermediate, (iii) reductive intramolecular proton transfer from the NH3 group to one of the hydride ligands, and (iv) release of H2 from the resulting square-planar hydride dihydrogen rhodium(I) intermediate
Iridium-Promoted B-B Bond Activation: Preparation and X-ray Diffraction Analysis of a mer-Tris(boryl) Complex
The tris(boryl) complex Ir(Bcat)3{Âż3-P,O,P-[xant(PiPr2)2]} has been prepared. Its X-ray diffraction analysis structure reveals that the boryl groups are disposed in a mer rearrangement despite of the very strong trans influence of the boryl ligands. An energy decomposition analysis method coupled to natural orbitals for chemical valence suggests that the p-backdonation from the metal to the pz atomic orbital of the boron atom decreases about 43% in the Ir-B bonds disposed mutually trans with regard to the other one
Amide-Directed Formation of Five-Coordinate Osmium Alkylidenes from Alkynes
The amide-directed synthesis of five-coordinate osmium alkylidene derivatives from alkynes is reported. These types of complexes, which have been elusive until now because of the tendency of osmium to give hydride alkylidyne species, are prepared by reaction of the dihydride OsH2Cl2(PiPr3)2 (1) with terminal alkynes containing a distal amide group. Complex 1 reacts with N-phenylhex-5-ynamide and N-phenylhepta-6-ynamide to give OsCl2{=C(CH3)(CH2)nNH(CO)Ph}(PiPr3)2 (n = 3 (2), 4 (3)). The relative position of carbonyl and NH groups in the organic substrates has no influence on the reaction. Thus, treatment of 1 with N-(pent-4-yn-1-yl)benzamide leads to OsCl2{=C(CH3)(CH2)3NHC(O)Ph}(PiPr3)2 (4). The new compounds are intermediate species in the cleavage of the C-C triple bond of the alkynes. Under mild conditions, they undergo the rupture of the Ca-CH3 bond of the alkylidene, which comes from the alkyne triple bond, to afford six-coordinate hydride-alkylidyne derivatives. In dichloromethane, complex 2 gives a 10:7 mixture of OsHCl2{=C(CH2)3C(O)NHPh}(PiPr3)2 (5) and OsHCl2{=CCH(CH3)(CH2)2C(O)NHPh}(PiPr3)2 (6). The first complex contains a linear separation between the alkylidyne Ca atom and the amide group, whereas the spacer is branched in the second complex. In contrast to the case for 2, complex 4 selectively affords OsHCl2{=C(CH2)3NHC(O)Ph}(PiPr3)2 (7). In spite of their instability, these compounds give the alkylidene-allene metathesis, being a useful entry to five-coordinate vinylidene complexes, including the dicarbon-disubstituted OsCl2(=C=CMe2)(PiPr3)2 (8) and the monosubstituted OsCl2(=C=CHCy)(PiPr3)2 (9)
Osmium- And Iridium-Promoted C-H Bond Activation of 2, 2'-Bipyridines and Related Heterocycles: Kinetic and Thermodynamic Preferences
The d2-hexahydride complex OsH6(PiPr3)2 (1) promotes the activation of C-H bonds of 2, 2'-bipyridines and related heterocycles. The study of the same reactions with the deuteride counterpart OsD6(PiPr3)2 (1-d) reveals that the activation of the C-H bonds situated in the sterically less hindered positions is kinetically preferred. However, the isolated products are the result of the thermodynamic control of the reactions. Thus, reactions of 1 with 2, 2'-bipyridine, 6-phenyl-2, 2'-bipyridine, and 6-methyl-2, 2'-bipyridine give the "rollover cyclometalation" products OsH3{Âż2-C, N-[C5(R)H2N-py]}(PiPr3)2 (R = H (2), Ph (3), Me (4)), whereas 3, 5-dimethyl-6-phenyl-2, 2'-bipyridine affords OsH2{Âż3-C, N, C-[C5H3N-(Me)2py-C5H4]}(PiPr3)2 (5), containing a dianionic C, N, C-pincer ligand. The behavior of substrates pyridyl-benzimidazolium and -imidazolium is similar. Reaction of 1 with 3-methyl-1-(6-phenylpyridin-2-yl)-1H-benzimidazolium tetrafluoroborate leads to OsH3{Âż2-C, C-[MeBzim-C5(Ph)H2N]}(PiPr3)2 (6), bearing an anionic Cpy, CNHC-chelate. On the other hand, 3-methyl-1-(6-phenylpyridin-2-yl)-1H-imidazolium tetrafluoroborate yields [OsH2{Âż3-C, N, C-(MeIm-py-C6H4)}(PiPr3)2]BF4 (7), containing a monoanionic C, N, C-pincer with a NHC-unit coordinated in an abnormal fashion. The reactivity pattern of these substrates is also observed with the d4-iridium-pentahydride IrH5(PiPr3)2 (8), which has generated IrH2{Âż2-C, N-[C5(R)H2N-py]}(PiPr3)2 (R = H, (9), Ph (10)) and IrH{Âż3-C, N, C-[C5H3N-(Me2)py-C5H4]}(PiPr3)2 (11). The osmium(IV)-carbon bonds display a higher degree of covalency than the iridium(III)-carbon bonds. In contrast to 2, the metalated carbon atom of 9 undergoes the addition of a proton of methanol to give [IrH2{Âż2-N, N-(bipy)}(PiPr3)2]BF4 (12)
An Acyl-NHC Osmium Cooperative System: Coordination of Small Molecules and Heterolytic BâH and OâH Bond Activation
The hexahydride complex OsH6(PiPr3)2 (1) activates the CâOMe bond of 1-(2-methoxy-2-oxoethyl)-3-methylimidazolium chloride (2), in addition to promoting the direct metalation of the imidazolium group, to afford a five-coordinate OsCl(acyl-NHC)(PiPr3)2 (3) compound. The latter coordinates carbon monoxide, oxygen, and molecular hydrogen to give the corresponding carbonyl (4), dioxygen (5), and dihydrogen (6) derivatives. Complex 3 also promotes the heterolytic bond activation of pinacolborane (HBpin), using the acyl oxygen atom as a pendant Lewis base. The hydride ligand and the Bpin substituent of the Fischer-type carbene of the resulting complex 7 activate the OâH bond of alcohols and water. As a consequence, complex 3 is a metal ligand cooperating catalyst for the generation of molecular hydrogen, by means of both the alcoholysis and hydrolysis of pinacolborane, via the intermediates 7 and 6.Financial support from the MINECO of Spain (Projects CTQ2014-52799-P and CTQ2014-51912-REDC), the DiputacioÌn General de AragoÌn (E-35), and the European Social Fund (FSE) and FEDER. M.P.G. thanks the Spanish MINECO for her FPI fellowship. T.B. thanks the Spanish MINECO for funding through the Juan de la Cierva program
Synthesis, structure, and photophysical properties of platinum(II) (N, C, N) pincer complexes derived from purine nucleobases
The synthesis of a series of Pt{Îș3-N,C,NâČ-[L]}X (X = Cl, RCâĄC) pincer complexes derived from purine and purine nucleosides is reported. In these complexes, the 6-phenylpurine skeleton provides the N,C-cyclometalated fragment, whereas an amine, imine, or pyridine substituent of the phenyl ring supplies the additional NâČ-coordination point to the pincer complex. The purine N,C-fragment has two coordination positions with the metal (N1 and N7), but the formation of the platinum complexes is totally regioselective. Coordination through the N7 position leads to the thermodynamically favored [6.5]-Pt{Îș3-N7,C,NâČ-[L]}X complexes. However, the coordination through the N1 position is preferred by the amino derivatives, leading to the isomeric kinetic [5.5]-Pt{Îș3-N1,C,NâČ-[L]}X complexes. Extension of the reported methodology to complexes having both pincer and acetylide ligands derived from nucleosides allows the preparation of novel heteroleptic bis-nucleoside compounds that could be regarded as organometallic models of Pt-induced interstrand cross-link. Complexes having amine or pyridine arms are green phosphorescence emitters upon photoexcitation at low concentrations in CH2Cl2 solution and in poly(methyl methacrylate) (PMMA) films. They undergo self-quenching at high concentrations due to molecular aggregation. The presence of intermolecular ÏâÏ stacking and weak Pt···Pt interactions was also observed in the solid state by X-ray diffraction analysis
Ligand design and preparation, photophysical properties, and device performance of an encapsulated-type pseudo-tris(heteroleptic) iridium(iii) emitter
The organic molecule 2-(1-phenyl-1-(pyridin-2-yl)ethyl)-6-(3-(1-phenyl-1-(pyridin-2-yl)ethyl)phenyl)pyridine (H3L) has been designed, prepared, and employed to synthesize the encapsulated-type pseudo-tris(heteroleptic) iridium(III) derivative Ir(Îș6-fac-C,CâČ,Câł-fac-N,NâČ,Nâł-L). Its formation takes place as a result of the coordination of the heterocycles to the iridium center and the ortho-CH bond activation of the phenyl groups. Dimer [Ir(ÎŒ-Cl)(η4-COD)]2 is suitable for the preparation of this compound of class [Ir(9h)] (9h = 9-electron donor hexadentate ligand), but Ir(acac)3 is a more appropriate starting material. Reactions were carried out in 1-phenylethanol. In contrast to the latter, 2-ethoxyethanol promotes the metal carbonylation, inhibiting the full coordination of H3L. Complex Ir(Îș6-fac-C,CâČ,Câł-fac-N,NâČ,Nâł-L) is a phosphorescent emitter upon photoexcitation, which has been employed to fabricate four yellow emitting devices with 1931 CIE (x:y) ⌠(0.52:0.48) and a maximum wavelength at 576 nm. These devices display luminous efficacies, external quantum efficiencies, and power efficacies at 600 cd mâ2, which lie in the ranges 21.4â31.3 cd Aâ1, 7.8â11.3%, and 10.2â14.1 lm W1â, respectively, depending on the device configuration
Preparation and degradation of rhodium and iridium diolefin catalysts for the acceptorless and base-free dehydrogenation of secondary alcohols
Rhodium and iridium diolefin catalysts for the acceptorless and base-free dehydrogenation of secondary alcohols have been prepared, and their degradation has been investigated, during the study of the reactivity of the dimers [M(”-Cl)(I4-C8H12)]2 (M = Rh (1), Ir (2)) and [M(”-OH)(I4-C8H12)]2 (M = Rh (3), Ir (4)) with 1, 3-bis(6'-methyl-2'-pyridylimino)isoindoline (HBMePHI). Complex 1 reacts with HBMePHI, in dichloromethane, to afford equilibrium mixtures of 1, the mononuclear derivative RhCl(I4-C8H12){¿1-Npy-(HBMePHI)} (5), and the binuclear species [RhCl(I4-C8H12)]2{”-Npy, Npy-(HBMePHI)} (6). Under the same conditions, complex 2 affords the iridium counterparts IrCl(I4-C8H12){¿1-Npy-(HBMePHI)} (7) and [IrCl(I4-C8H12)]2{”-Npy, Npy-(HBMePHI)} (8). In contrast to chloride, one of the hydroxide groups of 3 and 4 promotes the deprotonation of HBMePHI to give [M(I4-C8H12)]2(”-OH){”-Npy, Niso-(BMePHI)} (M = Rh (9), Ir (10)), which are efficient precatalysts for the acceptorless and base-free dehydrogenation of secondary alcohols. In the presence of KOtBu, the [BMePHI]- ligand undergoes three different degradations: Alcoholysis of an exocyclic isoindoline-N double bond, alcoholysis of a pyridyl-N bond, and opening of the five-membered ring of the isoindoline core.
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