sigma-Bond Metathesis Reactions Involving Palladium(II) Hydride and Methyl Complexes: A Theoretical Assessment.

Inorg Chem

Laboratoire de Chimie Quantique, UPR 139 du CNRS, Université Louis Pasteur, 4 rue Blaise Pascal, F-67000 Strasbourg, France, and Debye Institute, Department of Metal-Mediated Synthesis, Utrecht University, Padualaan 8, 3584CH Utrecht, The Netherlands.

Published: July 1997

sigma-Bond metathesis reactions of water and methanol with palladium hydride and methyl complexes to yield hydrogen and methane, respectively, have been studied using ab-initio molecular orbital methods at the second-order Møller-Plesset (MP2) perturbation level. The calculations show that such reactions are feasible and that they can in some instances be competitive with an oxidative addition/reductive elimination sequence. A key factor is the presence of an additional lone pair not engaged in the initial bonding of the metal atom with the reacting water or alcohol. Another important controlling factor is the respective charges of the reacting entities. The importance of the choice and of the disposition of the ancillary ligands in the coordination sphere is emphasized.

Download full-text PDF

Source
http://dx.doi.org/10.1021/ic960807lDOI Listing

Publication Analysis

Top Keywords

sigma-bond metathesis
8
metathesis reactions
8
hydride methyl
8
methyl complexes
8
reactions involving
4
involving palladiumii
4
palladiumii hydride
4
complexes theoretical
4
theoretical assessment
4
assessment sigma-bond
4

Similar Publications

Addition and Oxidation Reactivity of a Pentacoordinate Nickelacyclobutane.

Chemistry

December 2024

Organic Chemistry and Catalysis, Faculty of Science, Utrecht University, Institute for Sustainable and Circular Chemistry, Universitetisweg 99, 3584 CG, Utrecht, The, Netherlands.

Nickelacyclobutanes are reactive intermediates in catalytic cycles including cyclopropanation and insertion reactions. The stoichiometric study of these intermediates has shown that their reactivity is highly influenced by the coordination environment of the nickel center. A pentacoordinated nickelacyclobutane embedded in a diphosphine pincer ligand has been shown to selectively undergo various reactions with exogenous ligands, including [2+2] cycloreversion and carbene transfer to an isocyanide.

View Article and Find Full Text PDF

Unveiling the molecular mechanism of Mn and Zn-catalyzed Ullmann-type C-O cross-coupling reactions.

Phys Chem Chem Phys

December 2024

Department of Chemistry, CMS College Kottayam (Autonomous) Mahatma Gandhi University, Kottayam, Kerala, 686001, India.

A detailed theoretical study delving into the molecular mechanisms of the Ullmann-type -arylation reactions catalyzed by manganese and zinc metal ions has been investigated with the aid of the density functional theory (DFT) method. In contrast to the redox-active mechanisms proposed for classical Ullmann-type condensation reaction, a redox-neutral mechanism involving σ-bond metathesis emerged as the most appealing pathway for the investigated high-valent Mn(II) and Zn(II)-catalyzed -arylation reactions. The mechanism remains invariant with respect to the nature of the central metal, ligand, base, This unusuality in the mechanism has been dissected by considering three cases: ligand-free and ligand-assisted Mn(II)-catalyzed -arylation reaction and ligand-assisted Zn(II)-catalyzed -arylation reactions.

View Article and Find Full Text PDF

First-principles analyses were performed for understanding the mechanistic details of Fe-catalysed asymmetric hydrogenation of alkenes in the presence of silane that has recently been experimentally realized. The catalytic hydrogenation is expected to proceed through initial hydride transfer from Fe-H to the CC bond of alkene, followed by σ-bond metathesis of hydrosilane to afford a chiral alkane product and an iron silyl species, which then reacts with H to regenerate the iron hydride species another σ-bond metathesis. The mechanistic details and the origin of the regioselectivity and stereoselectivity of these reactions are understood on the basis of detailed potential energy surface analysis, charge transfer and noncovalent interactions involved therein, strain energy and isodesmic studies in the solvated stage.

View Article and Find Full Text PDF

Half-Sandwich Cerium and Lanthanum Dialkyl Complexes: Synthesis, Structure, and Reactivity Studies.

Inorg Chem

November 2024

Key Laboratory of Applied Chemistry of Chongqing Municipality, College of Chemistry and Chemical Engineering, Southwest University, Chongqing 400715, China.

Cerium and lanthanum dialkyl complexes [η-1,2,4-(MeC)CH]Ln(CHCH--NMe) (Ln = Ce and La ), supported by a tri-butylcyclopentadienyl ligand, have been successfully synthesized. Studies demonstrate that these complexes possess diverse reactivity toward various small molecules. For example, the reaction of complexes and with diphenyl dichalcogenides PhEEPh (E = S, Se) results in the formation of lanthanide thiolates [(η-1,2,4-(MeC)CH)Ln(SPh)(μ-SPh)] (Ln = Ce and La ) and selenolates [(η-1,2,4-(MeC)CH)Ln(SePh)(μ-SePh)] (Ln = Ce and La ), concomitantly releasing PhE(CHCH--NMe).

View Article and Find Full Text PDF

We report the development of an earth-abundant metal catalyst for methane C-H borylation. The post-synthetic metalation of bipyridine-functionalized zirconium metal-organic framework (MOF) with NiBr, followed by treatment with NaEtBH affords MOF-supported monomeric bipyridyl-nickel(II) dihydride species via active site isolation. The heterogeneous and recyclable nickel catalyst selectively borylates methane at 200 °C using pinacolborane (HBpin) to afford CHBpin in 61 % yield with a turnover number (TON) up to 1388.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!