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Taschenbuch. Zustand: Neu. This item is printed on demand - it takes 3-4 days longer - Neuware -Diploma Thesis from the year 2003 in the subject Chemistry - Anorganic Chemistry, grade: 1,0, Technical University of Braunschweig (Institut für Anorganische und Analytische Chemie), course: TU Braunschweig und University of Alabama,…45 entries in the bibliography, language: English, abstract: From a long time ago attempts have been made to isolate carbenes. A big motivation behind the search for a stable carbene was the fact, that oxidation state II is well known for the late members of group 14, germanium, tin and lead. Therefore it should be possible to produce a compound containing a carbon in oxidation state II, which is stable enough to be detected and possibly isolated and characterized. Additionally carbenes may be useful as building blocks in organic syntheses. They form complexes with a wide variety of main group elements and transition metals in both high and low oxidiation states. Many of these complexes are highly efficient homogeneous catalysts. Carbenes are defined as compounds possessing a divalent carbon in their structure. This carbon is bound to two adjacent groups by covalent bonds. It has two nonbonding electrons which may have parallel (singlet state) or antiparallel spins (triplet state). The simplest example of a carbene is methylene.The area of carbene boron chemistry is a relatively new area of research. Like most other fields of carbene research it has been revived by the discovery of stable carbenes by Arduengo in 1991. Until then only a few neutral borane adducts with electroneutral carbon bases were known. Most carbon bases are electron deficient on the carbon and therefore electrophiles. However, a nucleophile center is needed to bind to an electron deficient acceptor like borane.The new nucleophile imidazole-2-ylides make neutral carbon borane adducts easily accessible. In 1993 Kuhn et al. found that borane adducts of these carbenes can be produced in high yields by allowing the carbene to react with BH3 Me2S complex. Other examples of boron adducts with nucleophilic carbenes are adducts with boron trifluoride and trimethoxyborate.Carbene boron adducts in which boron bears a single carbene substituent are easily accessible. Adducts with two or more carbene ligands on boron remain unknown. However, trialkylboranes with bulky substituents (e.g. trinorbornylborane, tricyclohexylborane etc.) are well documented. In view of the abundance of trialkylboranes, a compound like that appears to be a reasonable synthetic target.A number of experimental approaches have been made. On the way interesting results have been achieved besides the main goal. These include the synthesis and characterization of a new ionic imidazolium borohydride 80 pp. Englisch.
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Taschenbuch. Zustand: Neu. This item is printed on demand - it takes 3-4 days longer - Neuware -Diploma Thesis from the year 2003 in the subject Chemistry - Materials Chemistry, grade: 1, Technical University of Braunschweig, language: English, abstract: From a long time ago attempts have been made to isolate carbenes. A big mot…ivation behind the search for a stable carbene was the fact, that oxidation state II is well known for the late members of group 14, germanium, tin and lead. For lead +II is even the most stable oxidation state. Therefore it should be possible to produce a compound containing a carbon in oxidation state II, which is stable enough to be detected and possibly isolated and characterized. Additionally carbenes may be useful as building blocks in organic syntheses. They form complexes with a wide variety of main group elements and transition metals in both high and low oxidiation states. Many of these complexes are highly efficient homogeneous catalysts. Carbenes are defined as compounds possessing a divalent carbon in their structure. This carbon is bound to two adjacent groups by covalent bonds. It has two nonbonding electrons which may have parallel (singlet state) or antiparallel spins (triplet state). The preferred state depends on the relative energies of both states. If both orbitals are degenerate, the triplet state is favorable. Otherwise both electrons will occupy the orbital lower in energy with antiparallel spins. The simplest example of a carbene is methylene. The area of carbene boron chemistry is a relatively new area of research. Like most other fields of carbene research it has been revived by the discovery of stable carbenes by Arduengo in 1991. Until then only a few neutral borane adducts with electroneutral carbon bases were known. Most carbon bases are electron deficient on the carbon and therefore electrophiles. However, a nucleophile center is needed to bind to an electron deficient acceptor like borane, especially because boron is not able to provide any pi-backdonation like transition metal carbene complexes, as it lacks free electron pairs.The new nucleophile imidazole-2-ylides make neutral carbon borane adducts easily accessible. In 1993 Kuhn et al. found that borane adducts of these carbenes can be produced in high yields by allowing the carbene to react with BH3?Me2S complex. Other examples of boron adducts with nucleophilic carbenes are adducts with boron trifluoride and trimethoxyborate.Carbene boron adducts in which boron bears a single carbene substituent are easily accessible. Adducts with two or more carbene ligands on boron remain unknown. 80 pp. Englisch.
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Taschenbuch. Zustand: Neu. This item is printed on demand - Print on Demand Titel. Neuware -Diploma Thesis from the year 2003 in the subject Chemistry - Anorganic Chemistry, grade: 1,0, Technical University of Braunschweig (Institut für Anorganische und Analytische Chemie), course: TU Braunschweig und University of Alabama, 45 e…ntries in the bibliography, language: English, abstract: From a long time ago attempts have been made to isolate carbenes. A big motivation behind the search for a stable carbene was the fact, that oxidation state II is well known for the late members of group 14, germanium, tin and lead. Therefore it should be possible to produce a compound containing a carbon in oxidation state II, which is stable enough to be detected and possibly isolated and characterized. Additionally carbenes may be useful as building blocks in organic syntheses. They form complexes with a wide variety of main group elements and transition metals in both high and low oxidiation states. Many of these complexes are highly efficient homogeneous catalysts. Carbenes are defined as compounds possessing a divalent carbon in their structure. This carbon is bound to two adjacent groups by covalent bonds. It has two nonbonding electrons which may have parallel (singlet state) or antiparallel spins (triplet state). The simplest example of a carbene is methylene.The area of carbene boron chemistry is a relatively new area of research. Like most other fields of carbene research it has been revived by the discovery of stable carbenes by Arduengo in 1991. Until then only a few neutral borane adducts with electroneutral carbon bases were known. Most carbon bases are electron deficient on the carbon and therefore electrophiles. However, a nucleophile center is needed to bind to an electron deficient acceptor like borane.The new nucleophile imidazole-2-ylides make neutral carbon borane adducts easily accessible. In 1993 Kuhn et al. found that borane adducts of these carbenes can be produced in high yields by allowing the carbene to react with BH3¿Me2S complex. Other examples of boron adducts with nucleophilic carbenes are adducts with boron trifluoride and trimethoxyborate.Carbene boron adducts in which boron bears a single carbene substituent are easily accessible. Adducts with two or more carbene ligands on boron remain unknown. However, trialkylboranes with bulky substituents (e.g. trinorbornylborane, tricyclohexylborane etc.) are well documented. In view of the abundance of trialkylboranes, a compound like that appears to be a reasonable synthetic target.A number of experimental approaches have been made. On the way interesting results have been achieved besides the main goal. These include the synthesis and characterization of a new ionic imidazolium borohydrideBooks on Demand GmbH, Überseering 33, 22297 Hamburg 80 pp. Englisch.
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Taschenbuch. Zustand: Neu. nach der Bestellung gedruckt Neuware - Printed after ordering - Diploma Thesis from the year 2003 in the subject Chemistry - Anorganic Chemistry, grade: 1,0, Technical University of Braunschweig (Institut für Anorganische und Analytische Chemie), course: TU Braunschweig und University of Alabama, 45 en…tries in the bibliography, language: English, abstract: From a long time ago attempts have been made to isolate carbenes. A big motivation behind the search for a stable carbene was the fact, that oxidation state II is well known for the late members of group 14, germanium, tin and lead. Therefore it should be possible to produce a compound containing a carbon in oxidation state II, which is stable enough to be detected and possibly isolated and characterized. Additionally carbenes may be useful as building blocks in organic syntheses. They form complexes with a wide variety of main group elements and transition metals in both high and low oxidiation states. Many of these complexes are highly efficient homogeneous catalysts. Carbenes are defined as compounds possessing a divalent carbon in their structure. This carbon is bound to two adjacent groups by covalent bonds. It has two nonbonding electrons which may have parallel (singlet state) or antiparallel spins (triplet state). The simplest example of a carbene is methylene.The area of carbene boron chemistry is a relatively new area of research. Like most other fields of carbene research it has been revived by the discovery of stable carbenes by Arduengo in 1991. Until then only a few neutral borane adducts with electroneutral carbon bases were known. Most carbon bases are electron deficient on the carbon and therefore electrophiles. However, a nucleophile center is needed to bind to an electron deficient acceptor like borane.The new nucleophile imidazole-2-ylides make neutral carbon borane adducts easily accessible. In 1993 Kuhn et al. found that borane adducts of these carbenes can be produced in high yields by allowing the carbene to react with BH3 Me2S complex. Other examples of boron adducts with nucleophilic carbenes are adducts with boron trifluoride and trimethoxyborate.Carbene boron adducts in which boron bears a single carbene substituent are easily accessible. Adducts with two or more carbene ligands on boron remain unknown. However, trialkylboranes with bulky substituents (e.g. trinorbornylborane, tricyclohexylborane etc.) are well documented. In view of the abundance of trialkylboranes, a compound like that appears to be a reasonable synthetic target.A number of experimental approaches have been made. On the way interesting results have been achieved besides the main goal. These include the synthesis and characterization of a new ionic imidazolium borohydride.
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Taschenbuch. Zustand: Neu. Investigations in the field of carbene-boron chemistry | Untersuchungen zur Chemie von Carbene-Bor-Addukten | Oliver Steinhof | Taschenbuch | 80 S. | Englisch | 2011 | GRIN Publishing | EAN 9783640862634 | Verantwortliche Person für die EU: GRIN Publishing GmbH, Waltherstr. 23, 80337 München, info[at]g…rin[dot]com | Anbieter: preigu Print on Demand.
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Taschenbuch. Zustand: Neu. nach der Bestellung gedruckt Neuware - Printed after ordering - Diploma Thesis from the year 2003 in the subject Chemistry - Materials Chemistry, grade: 1, Technical University of Braunschweig, language: English, abstract: From a long time ago attempts have been made to isolate carbenes. A big motivati…on behind the search for a stable carbene was the fact, that oxidation state II is well known for the late members of group 14, germanium, tin and lead. For lead +II is even the most stable oxidation state. Therefore it should be possible to produce a compound containing a carbon in oxidation state II, which is stable enough to be detected and possibly isolated and characterized. Additionally carbenes may be useful as building blocks in organic syntheses. They form complexes with a wide variety of main group elements and transition metals in both high and low oxidiation states. Many of these complexes are highly efficient homogeneous catalysts. Carbenes are defined as compounds possessing a divalent carbon in their structure. This carbon is bound to two adjacent groups by covalent bonds. It has two nonbonding electrons which may have parallel (singlet state) or antiparallel spins (triplet state). The preferred state depends on the relative energies of both states. If both orbitals are degenerate, the triplet state is favorable. Otherwise both electrons will occupy the orbital lower in energy with antiparallel spins. The simplest example of a carbene is methylene. The area of carbene boron chemistry is a relatively new area of research. Like most other fields of carbene research it has been revived by the discovery of stable carbenes by Arduengo in 1991. Until then only a few neutral borane adducts with electroneutral carbon bases were known. Most carbon bases are electron deficient on the carbon and therefore electrophiles. However, a nucleophile center is needed to bind to an electron deficient acceptor like borane, especially because boron is not able to provide any pi-backdonation like transition metal carbene complexes, as it lacks free electron pairs.The new nucleophile imidazole-2-ylides make neutral carbon borane adducts easily accessible. In 1993 Kuhn et al. found that borane adducts of these carbenes can be produced in high yields by allowing the carbene to react with BH3?Me2S complex. Other examples of boron adducts with nucleophilic carbenes are adducts with boron trifluoride and trimethoxyborate.Carbene boron adducts in which boron bears a single carbene substituent are easily accessible. Adducts with two or more carbene ligands on boron remain unknown.
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Taschenbuch. Zustand: Neu. Investigations in the field of carbene-boron chemistry | Untersuchungen zur Chemie von Bor-Carben-Addukten | Oliver Steinhof | Taschenbuch | 80 S. | Englisch | 2012 | Examicus Verlag | EAN 9783656997818 | Verantwortliche Person für die EU: GRIN Publishing GmbH, Waltherstr. 23, 80337 München, info[at]gr…in[dot]com | Anbieter: preigu Print on Demand.
