Author: James B. Myers
Publisher:
ISBN:
Category : Alkenes
Languages : en
Pages : 216
Book Description
Investigations Into the Synthesis and Reactivities of Transition Metal Alkenyl Complexes
Author: James B. Myers
Publisher:
ISBN:
Category : Alkenes
Languages : en
Pages : 216
Book Description
Publisher:
ISBN:
Category : Alkenes
Languages : en
Pages : 216
Book Description
Transition Metals in the Synthesis of Complex Organic Molecules
Author: Louis S. Hegedus
Publisher:
ISBN:
Category : Science
Languages : en
Pages : 488
Book Description
The third edition of Transition Metals in the Synthesis of Complex Organic Molecules is a comprehensive revision and significant expansion of the second edition. The clear and systematic approach to the formation, manipulation, and reactivity of organometallic complexes has been maintained. The book is divided into 10 chapters starting with general formalisms, electron counting, and basic principles of organometallic reaction mechanisms. The organic chemistry of transition metals is then presented by class of metal complex, with many examples of applications in the synthesis of complex natural products and pharmaceuticals. The book is ideal for advanced undergraduate and graduate students as well as all practicing synthetic organic chemists. It is written for organic chemists and offers an easy entry into the field of organotransition metal chemistry without requiring a background in inorganic chemistry.
Publisher:
ISBN:
Category : Science
Languages : en
Pages : 488
Book Description
The third edition of Transition Metals in the Synthesis of Complex Organic Molecules is a comprehensive revision and significant expansion of the second edition. The clear and systematic approach to the formation, manipulation, and reactivity of organometallic complexes has been maintained. The book is divided into 10 chapters starting with general formalisms, electron counting, and basic principles of organometallic reaction mechanisms. The organic chemistry of transition metals is then presented by class of metal complex, with many examples of applications in the synthesis of complex natural products and pharmaceuticals. The book is ideal for advanced undergraduate and graduate students as well as all practicing synthetic organic chemists. It is written for organic chemists and offers an easy entry into the field of organotransition metal chemistry without requiring a background in inorganic chemistry.
Transition Metal Reagents and Catalysts
Author: Jiro Tsuji
Publisher: John Wiley & Sons
ISBN: 9780471560272
Category : Science
Languages : en
Pages : 500
Book Description
Im Laufe der vergangenen 35 Jahre wurden unzahlige Synthesewege entwickelt, bei denen Ubergangsmetallkomplexe entweder als Reagenzien oder als Katalysatoren fungieren. Dieses Buch bietet besonders denjenigen Synthesechemikern interessante und moderne Einblicke, die bisher noch nicht mit den vielfaltigen Moglichkeiten der Organometallchemie mit Ubergangsmetallen vertraut sind. Zu wichtigen ubergangsmetallkatalysierten Reaktionen werden Anwendungsbeispiele diskutiert. (01/00)
Publisher: John Wiley & Sons
ISBN: 9780471560272
Category : Science
Languages : en
Pages : 500
Book Description
Im Laufe der vergangenen 35 Jahre wurden unzahlige Synthesewege entwickelt, bei denen Ubergangsmetallkomplexe entweder als Reagenzien oder als Katalysatoren fungieren. Dieses Buch bietet besonders denjenigen Synthesechemikern interessante und moderne Einblicke, die bisher noch nicht mit den vielfaltigen Moglichkeiten der Organometallchemie mit Ubergangsmetallen vertraut sind. Zu wichtigen ubergangsmetallkatalysierten Reaktionen werden Anwendungsbeispiele diskutiert. (01/00)
On Being Well-coordinated: A Half-century Of Research On Transition Metal Complexes
Author: John L Burmeister
Publisher: World Scientific
ISBN: 9814488003
Category : Science
Languages : en
Pages : 654
Book Description
This invaluable book distils the research accomplishments of Professor Fred Basolo during the five decades when he served as a world leader in the modern renaissance of inorganic chemistry. Its primary focus is on the very important area of chemistry known as coordination chemistry.Most of the elements in the periodic table are metals, and most of the chemistry of metals involves coordination chemistry. This is the case in the currently significant areas of research, including organometallic homogenous catalysis, biological reactions of metalloproteins, and even the solid state extended structures of new materials. In these systems, the metals are of primary importance because they are the sites of ligand substitution or redox reactions. In the solid materials, the coordination number of the metal and its stereochemistry are of major importance.Some fifty years of research on transition metal complexes carried out in the laboratory of Professor Basolo at Northwestern University is recorded here as selected scientific publications. The book is divided into three different major research areas, each dealing with some aspect of coordination chemistry. In each case, introductory remarks are presented which indicate what prompted the research projects and what the major accomplishments were. Although the research was of the academic, curiosity-driven type, some aspects have proven to be useful to others involved in projects that were much more applied in nature.
Publisher: World Scientific
ISBN: 9814488003
Category : Science
Languages : en
Pages : 654
Book Description
This invaluable book distils the research accomplishments of Professor Fred Basolo during the five decades when he served as a world leader in the modern renaissance of inorganic chemistry. Its primary focus is on the very important area of chemistry known as coordination chemistry.Most of the elements in the periodic table are metals, and most of the chemistry of metals involves coordination chemistry. This is the case in the currently significant areas of research, including organometallic homogenous catalysis, biological reactions of metalloproteins, and even the solid state extended structures of new materials. In these systems, the metals are of primary importance because they are the sites of ligand substitution or redox reactions. In the solid materials, the coordination number of the metal and its stereochemistry are of major importance.Some fifty years of research on transition metal complexes carried out in the laboratory of Professor Basolo at Northwestern University is recorded here as selected scientific publications. The book is divided into three different major research areas, each dealing with some aspect of coordination chemistry. In each case, introductory remarks are presented which indicate what prompted the research projects and what the major accomplishments were. Although the research was of the academic, curiosity-driven type, some aspects have proven to be useful to others involved in projects that were much more applied in nature.
Synthesis, Characterization, and Reactivity of Transition Metal Complexes Supported by Heteropolydentate Ligation
Author: Adam Ruddy
Publisher:
ISBN:
Category :
Languages : en
Pages :
Book Description
Publisher:
ISBN:
Category :
Languages : en
Pages :
Book Description
Synthesis and Reactivity of Transition Metal Complexes Bearing the Tridentate Bis(2-mercapto-p-tolyl)amine ([SNS]H 3) Ligand
Author: Kyle Evan Rosenkoetter
Publisher:
ISBN: 9780355307856
Category :
Languages : en
Pages : 196
Book Description
The work described herein focuses on the synthesis and characterization of new heterobimetallic complexes containing the redox-active W[SNS] 2 metalloligand and investigation into their electronic properties and reactivity. Most recent studies have explored the redox nature of the [SNS]H 3 scaffold through the synthesis and reactivity of a novel set of square-planar nickel complexes.Chapters 2 and 3 describe a modular synthetic approach towards generating a new series of heterobimetallic complexes with the general formula W[SNS]2M(L) ([SNS] = bis(2-mercapto- p-tolyl)amine; M = Ni, Pd, or Pt; and L = dppe, depe, dmpe, dppp, PR'2NRPR'2 (R = phenyl, benzyl; R'=phenyl), DPEphos or dppf). The complexes were prepared by a salt metathesis of Cl2MII(L) with the previously reported W[SNS]2 coordination complex under reducing conditions. X-ray diffraction analysis revealed interesting coordination geometries about the appended Group 10 metal centers moving from Pt and Pd (pseudo-square planar) to the first row Ni (pseudo-tetrahedral) analogue. These complexes demonstrate formal metal--metal bond formation across the series with a tunable first oxidation potential up to 600 mV.Chapter 4 investigates the use of W[SNS]2Ni(dppe) as a catalyst for the electrochemical reduction of protons to hydrogen. This complex was found to catalytically generate hydrogen with an overpotential of 700 mV, a TOF of 14 sec--1, and a Faradaic yield of 80 +/- 3 % using 4-cyanoanilinium tetrafluoroborate in non-aqueous solutions.Chapter 5 demonstrates the effect of exchanging the nickel center of the heterobimetallic complexes discussed in Chapters 2 and 3 with other first row transitions metal ions (i.e. cobalt and copper). Analysis into the observed metal--metal distances reveal stark differences across the series. Additionally, the copper ion containing complexes demonstrate dynamic behavior in solution.Chapter 6 investigates the synthesis and reactivity of a series of monomeric square-planar nickel complexes of the [SNS] scaffold to demonstrate the ligand as redox, proton, and hydrogen atom non-innocent.Appendix A illustrates the electrochemical responses observed for the monoanionic complexes from Chapter 6 in the presence of CO2 and CO. Appendices B and C describe the synthesis and characterization of a five-coordinate cobalt and a heterotrimetallic tungsten-nickel complex, respectively.
Publisher:
ISBN: 9780355307856
Category :
Languages : en
Pages : 196
Book Description
The work described herein focuses on the synthesis and characterization of new heterobimetallic complexes containing the redox-active W[SNS] 2 metalloligand and investigation into their electronic properties and reactivity. Most recent studies have explored the redox nature of the [SNS]H 3 scaffold through the synthesis and reactivity of a novel set of square-planar nickel complexes.Chapters 2 and 3 describe a modular synthetic approach towards generating a new series of heterobimetallic complexes with the general formula W[SNS]2M(L) ([SNS] = bis(2-mercapto- p-tolyl)amine; M = Ni, Pd, or Pt; and L = dppe, depe, dmpe, dppp, PR'2NRPR'2 (R = phenyl, benzyl; R'=phenyl), DPEphos or dppf). The complexes were prepared by a salt metathesis of Cl2MII(L) with the previously reported W[SNS]2 coordination complex under reducing conditions. X-ray diffraction analysis revealed interesting coordination geometries about the appended Group 10 metal centers moving from Pt and Pd (pseudo-square planar) to the first row Ni (pseudo-tetrahedral) analogue. These complexes demonstrate formal metal--metal bond formation across the series with a tunable first oxidation potential up to 600 mV.Chapter 4 investigates the use of W[SNS]2Ni(dppe) as a catalyst for the electrochemical reduction of protons to hydrogen. This complex was found to catalytically generate hydrogen with an overpotential of 700 mV, a TOF of 14 sec--1, and a Faradaic yield of 80 +/- 3 % using 4-cyanoanilinium tetrafluoroborate in non-aqueous solutions.Chapter 5 demonstrates the effect of exchanging the nickel center of the heterobimetallic complexes discussed in Chapters 2 and 3 with other first row transitions metal ions (i.e. cobalt and copper). Analysis into the observed metal--metal distances reveal stark differences across the series. Additionally, the copper ion containing complexes demonstrate dynamic behavior in solution.Chapter 6 investigates the synthesis and reactivity of a series of monomeric square-planar nickel complexes of the [SNS] scaffold to demonstrate the ligand as redox, proton, and hydrogen atom non-innocent.Appendix A illustrates the electrochemical responses observed for the monoanionic complexes from Chapter 6 in the presence of CO2 and CO. Appendices B and C describe the synthesis and characterization of a five-coordinate cobalt and a heterotrimetallic tungsten-nickel complex, respectively.
Pentadienyl and Isoprenyl Transition Metal Complexes
Author: Thomas Edward Waldman
Publisher:
ISBN:
Category : Transition metal complexes
Languages : en
Pages : 512
Book Description
Publisher:
ISBN:
Category : Transition metal complexes
Languages : en
Pages : 512
Book Description
Organometallic Chemistry
Author: Y. Ishii
Publisher: Elsevier
ISBN: 1483153789
Category : Science
Languages : en
Pages : 137
Book Description
Organometallic Chemistry — 8 focuses on the compositions, reactions, properties, and transformations of molecules, silicon carbon, molybdenum and tungsten compounds, palladium, and platinum. The selection first offers information on the theoretical aspects of the coordination of molecules to transition metal centers and generation and reactions of silicon-carbon double-bonded intermediates. Discussions focus on photolysis of naphthyldisilanes, alkenyldisilanes, phenylacetylene, and benzenoid aromatic derivatives of disilane. The book also considers classical and novel ylide systems in organometallic chemistry, including phosphorinanium and phospholanium ylides and organometallic compounds of double ylides. The text evaluates studies on the synthesis, mechanism, and reactivity of organo-molybdenum and tungsten compounds and enantioselective reactions through chiral metal-carbene intermediates. The manuscript also ponders on the synthesis and reactivity of carbon-bonded transition elements; neutron diffraction studies on transition metal hydride complexes; and applications of palladium in organic syntheses. The selection is an impressive reference for readers and chemists interested in organometallic chemistry.
Publisher: Elsevier
ISBN: 1483153789
Category : Science
Languages : en
Pages : 137
Book Description
Organometallic Chemistry — 8 focuses on the compositions, reactions, properties, and transformations of molecules, silicon carbon, molybdenum and tungsten compounds, palladium, and platinum. The selection first offers information on the theoretical aspects of the coordination of molecules to transition metal centers and generation and reactions of silicon-carbon double-bonded intermediates. Discussions focus on photolysis of naphthyldisilanes, alkenyldisilanes, phenylacetylene, and benzenoid aromatic derivatives of disilane. The book also considers classical and novel ylide systems in organometallic chemistry, including phosphorinanium and phospholanium ylides and organometallic compounds of double ylides. The text evaluates studies on the synthesis, mechanism, and reactivity of organo-molybdenum and tungsten compounds and enantioselective reactions through chiral metal-carbene intermediates. The manuscript also ponders on the synthesis and reactivity of carbon-bonded transition elements; neutron diffraction studies on transition metal hydride complexes; and applications of palladium in organic syntheses. The selection is an impressive reference for readers and chemists interested in organometallic chemistry.
Synthesis and Characterization of Transition Metal Complexes
Author: Milan M. Milutinović
Publisher:
ISBN:
Category :
Languages : en
Pages : 0
Book Description
Transition metals and their complexes have an important impact on chemistry and are found in many application in life in general. Ruthenium and rhodium are two members of noble metals and proved to be suitable for anticancer activity. With the aim of changing the coordination environment in ruthenium and rhodium complexes, this thesis presents a series of Ru(II) polypyridyl and Rh(III) pincer-type complexes. All new Ru(II) and Rh(III) complexes were characterized by NMR spectroscopy, ESI-MS spectrometry and UV-Vis spectrophotometry . For some of the complexes a single crystal X-ray crystallography was performed. The substitution reactions of Ru(II) and Rh(III) complexes with mononucleotides, oligonucleotides and amino acids were studied quantitatively by UV-Vis spectroscopy. Measurements of the activation enthalpies and entropies for all synthesized complexes are supporting an associative mechanism for the substitution process. NMR spectroscopy studies were performed on some Ru(II) complexes where after the hydrolyses of the metal-Cl bond the complexes are capable to interact with guanine derivatives forming monofunctional adducts via N7 atom. The interactions of Ru(II) and Rh(III) complexes with fully complementary 15-mer and 22-mer duplexes of DNA and fully complementary 13-mer duplexes of RNA were studied by UV-Vis spectroscopy. The interactions of ruthenium(II) and rhodium(III) complexes with calf thymus and herring testes DNA were examined by absorption using UV-Vis spectroscopy, fluorescence emission spectral studies by ethidium bromide displacement studies and viscosity measurements. ; eng
Publisher:
ISBN:
Category :
Languages : en
Pages : 0
Book Description
Transition metals and their complexes have an important impact on chemistry and are found in many application in life in general. Ruthenium and rhodium are two members of noble metals and proved to be suitable for anticancer activity. With the aim of changing the coordination environment in ruthenium and rhodium complexes, this thesis presents a series of Ru(II) polypyridyl and Rh(III) pincer-type complexes. All new Ru(II) and Rh(III) complexes were characterized by NMR spectroscopy, ESI-MS spectrometry and UV-Vis spectrophotometry . For some of the complexes a single crystal X-ray crystallography was performed. The substitution reactions of Ru(II) and Rh(III) complexes with mononucleotides, oligonucleotides and amino acids were studied quantitatively by UV-Vis spectroscopy. Measurements of the activation enthalpies and entropies for all synthesized complexes are supporting an associative mechanism for the substitution process. NMR spectroscopy studies were performed on some Ru(II) complexes where after the hydrolyses of the metal-Cl bond the complexes are capable to interact with guanine derivatives forming monofunctional adducts via N7 atom. The interactions of Ru(II) and Rh(III) complexes with fully complementary 15-mer and 22-mer duplexes of DNA and fully complementary 13-mer duplexes of RNA were studied by UV-Vis spectroscopy. The interactions of ruthenium(II) and rhodium(III) complexes with calf thymus and herring testes DNA were examined by absorption using UV-Vis spectroscopy, fluorescence emission spectral studies by ethidium bromide displacement studies and viscosity measurements. ; eng
Metal Mediated Template Synthesis of Ligands
Author: Otilia Costisor
Publisher: World Scientific
ISBN: 9789812794819
Category : Science
Languages : en
Pages : 316
Book Description
This book surveys the relatively new area of the synthesis of organic ligands when metal ions act as a template. In the last fifty years this field has undergone an explosive development, marked by a great amount of literature. The material in the book has been arranged according to the type of chemical reaction involved. In this frame, the basic principles of metal template reactions and the shape of the molecules are considered. Designed to satisfy the demands of students, young researchers doing their PhDs, and those working in the field of coordination chemistry, the book details the role of the metal ions and the specific properties of the formed complexes. Metal Mediated Template Synthesis of Ligands offers a comprehensive analysis with wide-ranging references and provides an extensive overview of research on metal-directed organic ligands over the past five decades. Contents: The Template Effect; Alkylation Reactions; Schiff Condensation; Mannich Condensation; Self Condensation of Nitriles; Self-Assembled Systems. Readership: Upper level undergraduates, graduate students, academics, researchers industrialists in inorganic, solid-state, supramolecular and organic chemistry.
Publisher: World Scientific
ISBN: 9789812794819
Category : Science
Languages : en
Pages : 316
Book Description
This book surveys the relatively new area of the synthesis of organic ligands when metal ions act as a template. In the last fifty years this field has undergone an explosive development, marked by a great amount of literature. The material in the book has been arranged according to the type of chemical reaction involved. In this frame, the basic principles of metal template reactions and the shape of the molecules are considered. Designed to satisfy the demands of students, young researchers doing their PhDs, and those working in the field of coordination chemistry, the book details the role of the metal ions and the specific properties of the formed complexes. Metal Mediated Template Synthesis of Ligands offers a comprehensive analysis with wide-ranging references and provides an extensive overview of research on metal-directed organic ligands over the past five decades. Contents: The Template Effect; Alkylation Reactions; Schiff Condensation; Mannich Condensation; Self Condensation of Nitriles; Self-Assembled Systems. Readership: Upper level undergraduates, graduate students, academics, researchers industrialists in inorganic, solid-state, supramolecular and organic chemistry.