Synthesis and Characterisation of Late Transition Metal Complexes Containing Novel Mixed N-heterocyclic Carbene and Thione Donors PDF Download
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Languages : en
Pages : 122
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Author:
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Languages : en
Pages : 122
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Languages : en
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The discovery of N-heterocyclic carbenes (NHC) has dramatically affected the world of catalysis. Their inherent properties that make them excellent auxiliary ligands for catalytic processes have countless laboratories worldwide probing and exploiting every notable feature they possess. However, while there is no shortage of attention in this field of research, there has been considerably less interest in NHCs with an ability chelate to metals via a mixed-donor ligand architecture. Thus, this thesis describes the synthesis and application of a ligand set comprised of bidentate mixed-donor NHC ligands. The ligands prepared all contain a mesitylimidazol-2-ylidene core unit, but incorporate different donor-functionalized tethers. These mixed-donor NHC ligands are synthesized by using a strong base, such as KN(SiMe3)2, to deprotonate the imidazolium salt precursors. This strategy was used to effectively prepare 1-mesityl-3-(2-(mesitylamino)ethyl)imidazol-2-ylidene, Mes[CNH] and 1-mesityl-3-(2-aminoethyl)imidazol-2-ylidene, Mes[CNH2]. Mes[CNH] was found to be a convenient proligand for the synthesis of various M-NHC (M = Rh, Ir, Ru, Pd, Ni, Fe, Ag, Li) compounds. These Mes[CNH]-M complexes demonstrated the hemilabile character of the Mes[CNH] ligand forming complexes that incorporated either a coordinated or uncoordinated amino tether. Mes[CNH]M(diene)Cl, Mes[CN]M(diene) and [Mes[CNH]M(diene)]BF4(M = Rh, Ir; diene = 1,5-cyclooctadiene, 2,5-norbornadiene) were synthesized and investigated for their ability to perform hydrogenation and hydrosilylation reactions with various substrates. Mes[CNH]Ru(=CHPh)(PCy3)Cl2, Mes[CNH]Ru(=CHPh)(py)Cl2 (py = pyridine) and Mes[CNH]Ru(=CHPh)(PMe3)Cl2 were also synthesized and fully characterized. The activity of the former two Ru complexes was studied for their ability to catalyze ring-closing metathesis (RCM) and ring-opening metathesis polymerization (ROMP) reactions. In addition, the phosphine dissociation rate of Mes[CNH]Ru(=CHPh)(PCy3).
Author: Anna Candace Badaj
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Category :
Languages : en
Pages :
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Author: John C. Linehan
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Category :
Languages : en
Pages : 514
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Author: Timothy Gordon Larocque
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Category :
Languages : en
Pages :
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N-heterocyclic carbenes (NHCs) have played a dominant role in organometallic chemistry for decades and revolutionized the field of homogenous catalysis. NHCs have been thoroughly studied, both experimentally and theoretically, and have shown unique reactivity towards transition metals, chalcogens, azides and pnictogens. This thesis is aimed at utilizing the unique reactivity of N-heterocyclic carbenes to develop novel, robust catalysts to mediate organic transformations. The multi-faceted work within this thesis explores the use of NHCs as ancillary ligands on early and late transition metals as potential catalysts for olefin polymerization and ring-closing metathesis, respectively. This work also includes exploring the synthesis and coordination of ancillary ligands derived from the unique reactivity of NHCs towards azides, chalcogens and pnictinidenes. The reactivity of a novel aryl-substituted acyclic imino-N-heterocyclic carbene to early transition metals, cyclooctasulfur and Grubbs-type ruthenium benzylidene complexes was explored. The reactivity of imidazol-2-imide towards Grubbs-type ruthenium benzylidene complexes and the synthesis and coordination of a novel group of ligands bearing an imidazol-2-imine scaffold were also explored. Lastly, this work will include the reactivity of IMes=PPh to Grubbs-type ruthenium benzylidene complexes.
Author: Eva Zolnhofer
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Category :
Languages : en
Pages :
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Author: Zaozao Qiu
Publisher: Springer Science & Business Media
ISBN: 3642243614
Category : Science
Languages : en
Pages : 143
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Zaozao Qiu shows in this thesis that transition metals can mediate or catalyze the cycloaddition or coupling reactions of carboryne with alkynes or alkenes to afford benzocarboranes, alkenylcarboranes or dihydrobenzocarboranes. These results represent powerful strategies to assemble useful complex molecules from very simple precursors in a single operation. Carboranes have many applications in medicine. However, their unique structures make derivatization difficult and the limited efficient synthetic methods to obtain functional carborane materials have restricted applications of carboranes within a narrow scope. This work breaks a new ground in metal-carboryne chemistry and will have a significant impact on synthetic, cluster and materials chemistry.
Author: Jameel Raddah Al-Thagfi
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Category :
Languages : en
Pages :
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Author: Brian Christopher Gruver
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Category : Dissertations, Academic
Languages : en
Pages : 148
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Author: Korbinian Riener
Publisher:
ISBN: 9783843926225
Category :
Languages : en
Pages :
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