Author: Patricia Ann EldredgePublisher:
ISBN:
Category : Organometallic chemistry
Languages : en
Pages : 366
Book Description
The Synthesis, Characterization and Activation of Polynuclear Transition Metal Clusters
Author: Patricia Ann EldredgePublisher:
ISBN:
Category : Organometallic chemistry
Languages : en
Pages : 366
Book Description
The Synthesis, Characterization and Study of Transition Metal Complexes for the Oxidation and Activation of Hydrocarbons
Author: Robert Edward BlakePolynuclear Transition Metal Complexes Based on Azolyl Linkers: Synthesis, Characterization and Proterties
Author: Zhaoyang WangSynthesis and Characterization of Transition Metal Complexes with Bulky Tin Ligands for Application in Small Molecule Activation
Author: Veeranna YempallyPublisher:
ISBN:
Category :
Languages : en
Pages :
Book Description
The role of bulky tin ligands in the stabilization of transition metal complexes with electronic unsaturation has been studied to understand the mode of binding of small molecules at an unsaturated metal center. We were able to isolate electronically unsaturated Pt-Sn bimetallic complexes effective in the reversible activation of small molecules including CO, H2, C2H4, and NH3 at room temperature. We have examined the effect of the modification of ligands in Pt-Sn bimetallic complexes for the activation of small molecules and have observed that the Pt(SnBut3)2(CNBut)2 bimetallic complex reversibly activates hydrogen at room temperature both in the solid state and in solution. Similarly, we have also prepared bimetallic Pt-Sn complexes with an NHC carbine ligand which were also shown to activate hydrogen and alkenes reversibly. A bimetallic Fe-Sn cluster complex, Fe2 ([mu]-SnBut2)2(CO)8, was synthesized from the reaction of But3SnH with the Fe2(CO)9 and shown to be selective at activating the benzylic C-H bond of alkylaromatic solvent molecules. The new complexes containing tin have been characterized spectroscopically to gain an insight into the reaction mechanism involved in small molecule activation.
Reaction Pathways in Polynuclear Metal Carbonyls
Author: David John ZalewskiPublisher:
ISBN:
Category : Metal-metal bonds
Languages : en
Pages : 416
Book Description
Synthesis, Characterization, and Reactivity of Transition Metal Complexes Containing Multi-donor Ligands
Author: John C. LinehanSynthesis, Structure, and Reactivity of [mu]3-Sn Capped Trinuclear Nickel Clusters
![Synthesis, Structure, and Reactivity of [mu]3-Sn Capped Trinuclear Nickel Clusters PDF](https://books.google.com/books/content/images/frontcover/VkrgzwEACAAJ?fife=w80-h100)
Author: Nicole TorquatoPublisher:
ISBN:
Category :
Languages : en
Pages : 0
Book Description
Chapter 1. This section presents an overview of literature pertaining to low-valent/low-oxidation state tin hydrides, transition metal coordinated tin hydrides, and group 10 trinuclear metal cluster synthesis, characterization, and reactivity. Chapter 2. Treatment of the trichlorotin-capped trinuclear nickel cluster, [Ni3(dppm)3([mu]3-Cl)([mu]3-SnCl3)], 1, with 4 eq. NaHB(Et)3 yields a [mu]3-SnH capped trinuclear nickel cluster, [Ni3(dppm)3([mu]3-H)([mu]3-SnH)], 2 [dppm = bis(diphenylphosphino)methane]. Single-crystal X-ray diffraction, nuclear magnetic resonance (NMR) spectroscopy, and computational studies together support that cluster 2 is a divalent tin hydride. Complex 2 displays a wide range of reactivity including oxidative addition of bromoethane across the Sn center. Addition of 1 eq. iodoethane to complex 2 releases H2 (g) and generates an ethyltin-capped nickel cluster with a [mu]3-iodide, [Ni3(dppm)3([mu]3-I)([mu]3-Sn(CH2CH3))], 4. Notably, insertion of alkynes into the Sn-H bond of 2 can be achieved via addition of 1 eq. 1-hexyne to generate the 1-hexen-2-yl-tin-capped nickel cluster, [Ni3(dppm)3([mu]3H)([mu]3-Sn(C6H11))], 5. Addition of H2 (g) to 5 regenerates the starting material, 2, and hexane. The formally 44-electron cluster 2 also displays significant redox chemistry with two reversible one-electron oxidations (E = -1.3 V, -0.8 V vs. Fc0/+) and one-electron reduction process (E = -2.7 V vs. Fc0/+) observed by cyclic voltammetry. Chapter 3. H2 and D2 exchange by a [mu]3-SnH, [mu]3-H capped trinuclear nickel cluster, [Ni3(dppm)3([mu]3-H)([mu]3-SnH)], 1, (dppm = bis(diphenylphosphino)methane) was investigated through a variety of nuclear magnetic resonance (NMR) spectroscopy studies. Mechanistic studies reveal reversible exchange upon addition of D2/H2 between 1 and the deuteride species, [Ni3(dppm)3([mu]3-D)([mu]3-SnD)], 1D. Furthermore, these studies suggest a conformational change at the Ni-H functionality upon addition of H2. Variable temperature (VT) NMR studies of 1 demonstrate a temperature dependence of the Sn-H and the Ni-H resonances, with the Ni-H experiencing the largest perturbation in chemical shift. Further mechanistic insights were obtained with VT NMR studies performed under an atmosphere H2 and HD. Overall, these studies provide evidence of H2/D2 exchange by complex 1 and suggest a novel mechanism for hydrogen activation and exchange processes. Chapter 4. Spectroscopic and structural comparisons are made between a series of (OR)3Sn capped trinuclear nickel clusters. The synthesis of the (OEt)3Sn and (OPh)3Sn capped nickel clusters, [Ni3(dppm)3([mu]3-Cl)([mu]3-Sn(OEt)3)] (1), [Ni3(dppm)3([mu]3-Cl)([mu]3-Sn(OPh)3)] (2), was realized by the treatment of [Ni3(dppm)3([mu]3-Cl)([mu]3-SnCl3] with 6 eq. of KOEt or NaOPh, respectively. Treatment of complex 1 with 10 eq. glycerol results in the synthesis of the (C3H5O3)Sn capped trinuclear nickel cluster, [Ni3(dppm)3([mu]3-Cl)([mu]3-Sn(C3H5O3))] (3). The crystallographic studies of these clusters allow a detailed structural comparison. In addition, cyclic voltammetric data were obtained for complexes 1, 2, and 3 and their electrochemical properties are compared. Complex 1 and 3 exhibit reversible oxidation and reduction events. Complex 2 displays a reversible oxidation and a pseudo-reversible reduction. Chapter 5. The focus of this chapter is to briefly describe project ideas based on main group coordinated polynuclear clusters that future researchers may find worthwhile.
Functional Nanometer-Sized Clusters of Transition Metals
Author: Wei ChenPublisher: Royal Society of Chemistry
ISBN: 1849738246
Category : Science
Languages : en
Pages : 938
Book Description
This book highlights recent progress and challenges in size-controlled synthesis, size-dependent properties, characterization and applications of metal nanoclusters.
Author: Allan George Hee
Author: Lori Anne Watson