Author: Yixin Ren
Publisher:
ISBN:
Category : Ligands
Languages : en
Pages : 0
Book Description
The field of cluster chemistry is relatively young when compared to studies on single metal coordination complexes. The fundamental studies on the hexanuclear cluster core will provide a better understanding of the differences from single metal center. Research described in this thesis focuses on developing synthetic methodologies towards the preparation of hexanuclear clusters containing novel types of N-donor terminal ligands and subsequently studying the reactivity of these systems. Previous studies in the Szczepura group have shown that nitrile groups can be activated by the [Re6Se 8]2+ cluster to react with inorganic azides to form tetrazolate rings. The initial goal of the reaction was to substitute the nitrile with azide, however, cycloaddition was observed. This unexpected result emphasizes the need for further studies involving the synthesis and reactivity of various nitrile ligands. Two complexes containing a nitrile group coordinated to a hexarhenium cluster, [Re6Se8(PEt3)5 (p-nitrobenzonitrile)](SbF6)2∙acetone and [Re6Se8(PEt3)5(NCC(CH 3)3)](SbF6)2∙NCC(CH3) 3, were studied by X-ray diffraction. These structures are reported here. The formation of tetrazolate rings on the [Re6Se8] 2+ cluster core sparks interest that other cycloaddition reactions may be feasible. Two new hexarhenium clusters, [Re6Se8(PEt 3) 5(NC(CH3)O(CH2)2)](BPh 4)2 and [Re6Se8(PEt3)5(NC(CH 3)O(CH2)3)](BPh4)2, containing oxazoline and oxazine ligands were isolated in high yield and purity. Initial isolation of these cluster complexes by a former student in the Szczepura group resulted in impure materials due to reaction with halide counter ions. However, metathesis with the tetraphenylborate ion enabled us to improve the purity and yield of these products. The oxazoline and oxazine ligands are neutral and can be removed via irradiation with a Hg/Xe lamp. Details of the ring removal studies via irradiation, along with preliminary studies involving the potential catalytic reactivity of these hexarhenium clusters will be discussed.
Studies of Rhenium Based Clusters Containing Nitriles and Heterocyclic Ligands
Author: Yixin Ren
Publisher:
ISBN:
Category : Ligands
Languages : en
Pages : 0
Book Description
The field of cluster chemistry is relatively young when compared to studies on single metal coordination complexes. The fundamental studies on the hexanuclear cluster core will provide a better understanding of the differences from single metal center. Research described in this thesis focuses on developing synthetic methodologies towards the preparation of hexanuclear clusters containing novel types of N-donor terminal ligands and subsequently studying the reactivity of these systems. Previous studies in the Szczepura group have shown that nitrile groups can be activated by the [Re6Se 8]2+ cluster to react with inorganic azides to form tetrazolate rings. The initial goal of the reaction was to substitute the nitrile with azide, however, cycloaddition was observed. This unexpected result emphasizes the need for further studies involving the synthesis and reactivity of various nitrile ligands. Two complexes containing a nitrile group coordinated to a hexarhenium cluster, [Re6Se8(PEt3)5 (p-nitrobenzonitrile)](SbF6)2∙acetone and [Re6Se8(PEt3)5(NCC(CH 3)3)](SbF6)2∙NCC(CH3) 3, were studied by X-ray diffraction. These structures are reported here. The formation of tetrazolate rings on the [Re6Se8] 2+ cluster core sparks interest that other cycloaddition reactions may be feasible. Two new hexarhenium clusters, [Re6Se8(PEt 3) 5(NC(CH3)O(CH2)2)](BPh 4)2 and [Re6Se8(PEt3)5(NC(CH 3)O(CH2)3)](BPh4)2, containing oxazoline and oxazine ligands were isolated in high yield and purity. Initial isolation of these cluster complexes by a former student in the Szczepura group resulted in impure materials due to reaction with halide counter ions. However, metathesis with the tetraphenylborate ion enabled us to improve the purity and yield of these products. The oxazoline and oxazine ligands are neutral and can be removed via irradiation with a Hg/Xe lamp. Details of the ring removal studies via irradiation, along with preliminary studies involving the potential catalytic reactivity of these hexarhenium clusters will be discussed.
Publisher:
ISBN:
Category : Ligands
Languages : en
Pages : 0
Book Description
The field of cluster chemistry is relatively young when compared to studies on single metal coordination complexes. The fundamental studies on the hexanuclear cluster core will provide a better understanding of the differences from single metal center. Research described in this thesis focuses on developing synthetic methodologies towards the preparation of hexanuclear clusters containing novel types of N-donor terminal ligands and subsequently studying the reactivity of these systems. Previous studies in the Szczepura group have shown that nitrile groups can be activated by the [Re6Se 8]2+ cluster to react with inorganic azides to form tetrazolate rings. The initial goal of the reaction was to substitute the nitrile with azide, however, cycloaddition was observed. This unexpected result emphasizes the need for further studies involving the synthesis and reactivity of various nitrile ligands. Two complexes containing a nitrile group coordinated to a hexarhenium cluster, [Re6Se8(PEt3)5 (p-nitrobenzonitrile)](SbF6)2∙acetone and [Re6Se8(PEt3)5(NCC(CH 3)3)](SbF6)2∙NCC(CH3) 3, were studied by X-ray diffraction. These structures are reported here. The formation of tetrazolate rings on the [Re6Se8] 2+ cluster core sparks interest that other cycloaddition reactions may be feasible. Two new hexarhenium clusters, [Re6Se8(PEt 3) 5(NC(CH3)O(CH2)2)](BPh 4)2 and [Re6Se8(PEt3)5(NC(CH 3)O(CH2)3)](BPh4)2, containing oxazoline and oxazine ligands were isolated in high yield and purity. Initial isolation of these cluster complexes by a former student in the Szczepura group resulted in impure materials due to reaction with halide counter ions. However, metathesis with the tetraphenylborate ion enabled us to improve the purity and yield of these products. The oxazoline and oxazine ligands are neutral and can be removed via irradiation with a Hg/Xe lamp. Details of the ring removal studies via irradiation, along with preliminary studies involving the potential catalytic reactivity of these hexarhenium clusters will be discussed.
Synthesis, Reactivity, and Removal Studies of Rhenium Based Cluster Complexes with Heterocyclic Terminal Ligands
Author: Joan N. Tirado
Publisher:
ISBN:
Category : Heterocyclic compounds
Languages : en
Pages : 164
Book Description
Publisher:
ISBN:
Category : Heterocyclic compounds
Languages : en
Pages : 164
Book Description
Synthesis, Characterization, and Reactivity Studies of Hexanuclear Rhenium Cluster Complexes with Oxygen and Sulfur Donor Ligands
Author: Julia A. Edwards
Publisher:
ISBN:
Category : Oxygen
Languages : en
Pages : 242
Book Description
Publisher:
ISBN:
Category : Oxygen
Languages : en
Pages : 242
Book Description
Synthesis, Characterization, and Reactivity of Hexanuclear Rhenium Clusters Containing Nitrogen-donor Ligands
Author: Jessica L. Durham
Publisher:
ISBN:
Category : Ligands
Languages : en
Pages : 214
Book Description
Publisher:
ISBN:
Category : Ligands
Languages : en
Pages : 214
Book Description
Synthesis and Reactivity Studies of Rhenium Complexes with Sulfur Containing Organic Ligands
Author: Jeffery Alan Kanney
Publisher:
ISBN:
Category : Ligands (Biochemistry)
Languages : en
Pages : 406
Book Description
Publisher:
ISBN:
Category : Ligands (Biochemistry)
Languages : en
Pages : 406
Book Description
Heterogeneous Catalytic Studies with Rhenium Cluster-based Precursors
Author: Phillip Douglas Lane
Publisher:
ISBN:
Category :
Languages : en
Pages : 336
Book Description
When (Re(CO)$\sb3$OH) $\sb4$ was supported on Al$\sb2$O$\sb3$ followed by heating in H$\sb2$ no decomposition gas products, CO and CH$\sb4$, were observed below 650 K. Following the activation by infrared spectroscopy showed the formation of Re(CO)$\rm\sb3\{O$-$\rm Al\}\{HO$-Al$\}\sb2$ at 480 K. The activated sample, (Re$\sb4$) /Al$\sb2$O$\sb3$, when exposed to CO/H$\sb2$ at 298 K, produced CH$\sb4$ near 500 K with a shoulder near 600 K in the temperature programmed reaction (TPR) profile. Elevating the CO/H$\sb2$ treatment temperature to 500 K resulted in the formation of CH$\sb4$ at 560 K. The adsorption of CH$\sb3$OH or CH$\sb3$I to the sample produced CH$\sb4$ at 580 K. When (Re(CO)$\sb3$OH) $\sb4$ activated on SiO$\sb2$, only one CH$\sb4$ peak at 490 K was observed for CO/H$\sb2$ adsorption. When TiO$\sb2$ was used as a support, a spillover species was also observed from CO and H$\sb2$ exposure at 500 K. The spillover rate appeared to be slower on TiO$\sb2$ than was observed on Al$\sb2$O$\sb3$.
Publisher:
ISBN:
Category :
Languages : en
Pages : 336
Book Description
When (Re(CO)$\sb3$OH) $\sb4$ was supported on Al$\sb2$O$\sb3$ followed by heating in H$\sb2$ no decomposition gas products, CO and CH$\sb4$, were observed below 650 K. Following the activation by infrared spectroscopy showed the formation of Re(CO)$\rm\sb3\{O$-$\rm Al\}\{HO$-Al$\}\sb2$ at 480 K. The activated sample, (Re$\sb4$) /Al$\sb2$O$\sb3$, when exposed to CO/H$\sb2$ at 298 K, produced CH$\sb4$ near 500 K with a shoulder near 600 K in the temperature programmed reaction (TPR) profile. Elevating the CO/H$\sb2$ treatment temperature to 500 K resulted in the formation of CH$\sb4$ at 560 K. The adsorption of CH$\sb3$OH or CH$\sb3$I to the sample produced CH$\sb4$ at 580 K. When (Re(CO)$\sb3$OH) $\sb4$ activated on SiO$\sb2$, only one CH$\sb4$ peak at 490 K was observed for CO/H$\sb2$ adsorption. When TiO$\sb2$ was used as a support, a spillover species was also observed from CO and H$\sb2$ exposure at 500 K. The spillover rate appeared to be slower on TiO$\sb2$ than was observed on Al$\sb2$O$\sb3$.
Multiple Bonds between Metal Atoms
Author: F. Albert Cotton
Publisher: Springer Science & Business Media
ISBN: 9780387250847
Category : Science
Languages : en
Pages : 856
Book Description
Provides historical perspective as well as current data Abundantly illustrated with figures redrawn from literature data Covers all pertinent theory and physical chemistry Catalytic and chemotherapeutic applications are included
Publisher: Springer Science & Business Media
ISBN: 9780387250847
Category : Science
Languages : en
Pages : 856
Book Description
Provides historical perspective as well as current data Abundantly illustrated with figures redrawn from literature data Covers all pertinent theory and physical chemistry Catalytic and chemotherapeutic applications are included
American Doctoral Dissertations
Author:
Publisher:
ISBN:
Category : Dissertation abstracts
Languages : en
Pages : 776
Book Description
Publisher:
ISBN:
Category : Dissertation abstracts
Languages : en
Pages : 776
Book Description
Index to Theses with Abstracts Accepted for Higher Degrees by the Universities of Great Britain and Ireland and the Council for National Academic Awards
Author:
Publisher:
ISBN:
Category : Dissertations, Academic
Languages : en
Pages : 704
Book Description
Theses on any subject submitted by the academic libraries in the UK and Ireland.
Publisher:
ISBN:
Category : Dissertations, Academic
Languages : en
Pages : 704
Book Description
Theses on any subject submitted by the academic libraries in the UK and Ireland.
Applied Science & Technology Index
Author:
Publisher:
ISBN:
Category : Electronic journals
Languages : en
Pages : 2172
Book Description
Publisher:
ISBN:
Category : Electronic journals
Languages : en
Pages : 2172
Book Description