Exploratory Synthesis of New Transition Metal Complexes with Polychalcogenide Ligands Using Conventional Solution Reactions and Hydro(solvo)thermal Techniques PDF Download
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Author: Songping Huang
Publisher:
ISBN:
Category : Chalcogenides
Languages : en
Pages : 532
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Book Description
Author: Songping Huang
Publisher:
ISBN:
Category : Chalcogenides
Languages : en
Pages : 532
Get Book Here
Book Description
Author: Songping Huang
Publisher:
ISBN:
Category : Chalcogenides
Languages : en
Pages : 356
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Book Description
Author:
Publisher:
ISBN:
Category : Dissertations, Academic
Languages : en
Pages : 738
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Author:
Publisher:
ISBN:
Category : Dissertation abstracts
Languages : en
Pages : 796
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Author: Adam Ruddy
Publisher:
ISBN:
Category :
Languages : en
Pages :
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Author: Peter J. Harrington
Publisher: Wiley-Interscience
ISBN:
Category : Science
Languages : en
Pages : 520
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Book Description
Examines the use of transition metal complexes as reagents for the synthesis of complex organic molecules. Presented here are total syntheses whose efficiency depends upon the unique reactivity patterns of organometallic complexes. For each total synthesis, the biological activity of the molecule is presented, followed by discussion of the principles of the organometallic processes involved.
Author: Gregory A. Marinelli
Publisher:
ISBN:
Category :
Languages : en
Pages : 124
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Author: Felix Marc Brunner
Publisher:
ISBN:
Category :
Languages : en
Pages : 143
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Book Description
As the incorporation of more renewable electricity into the power-grid leads to surplus generation, methods to utilize electricity to drive chemical reactions are becoming more relevant. Immobilizaton of molecular electrocatalysts combines the mechanistic understanding of molecular catalysts with the advantages of heterogeneous catalysts. Electrocatalysts of the type Ni(P2N2)2 are well-understood molecular catalysts that can achieve enzyme-like activity for hydrogen evolution and oxidation in solution. This extraordinary performance is attributed to their unique structure with proton shuttles in the second coordination sphere. Previously this amine substituent was used for surface attachment to immobilize this catalyst onto electrodes. However, the mobility of this substituent is crucial to the activity of the catalyst. We evaluated possible synthetic pathways to incorporate surface attachable functionality on the phosphine substituent of these ligands. Due to the high reactivity of the phosphines involved in the synthesis, incorporation of surface attachable groups through established synthetic protocols was found to be not feasible. A synthesis based on post-synthetic modification of P[superscript ArBr]2N[superscript Ph]2 was identified as the best way to incorporate attachable surface groups. This strategy was subsequently utilized to synthesize complexes of the type Ni(P2N2)2 with unprecedented, highly functionalized, surface attachable phosphine substituents. Phosphonate modified ligands and their corresponding nickel complexes were isolated and characterized. Subsequent deprotection of the phosphonic ester derivatives provided the first Ni(P2N2)2 catalyst that can be covalently attached via pendent phosphonate groups to an electrode without the involvement of hte important pendent amine groups. Mesoporous TiO2 electrodes were surface modified by attachment of the new phosphonate functionalized complexes, and these provided electrocatalytic materials that proved to be competent and stable for sustained hydrogen evolution in aqueous solution at mild pH and low over potential. We directly compared the new ligand to a previously reported complex that utilized the amine moiety for surface attachment. Using HER as the benchmark reaction, the P-attached catalyst showed a marginally (9-14%) higher turnover frequency than its N-attached counterpart. Finally, we report the synthesis of three new iridium piano-stool complexes that are immobilized on gold surfaces through thiol groups. We characterized these molecules using surface-sensitive IR spectroscopy. Further studies with these molecules are geared towards promoting the non-faradaic electrochemical tuning of catalysts using interfacial electric fields.
Author:
Publisher:
ISBN:
Category :
Languages : en
Pages :
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Author: B.I. Kharisov
Publisher: Elsevier
ISBN: 0128110627
Category : Science
Languages : en
Pages : 470
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Book Description
Direct Synthesis of Metal Complexes provides in-depth coverage of the direct synthesis of coordination and organometallic compounds. The work is primarily organized by methods, but also covers highly relevant complexes, such as metal-polymer coordination compounds. This updated reference discusses recent developments in cryosynthesis, electrosynthesis, and tribosynthesis (popular as it doesn’t require organic solvents), with special attention paid to ‘greener’ methodologies and approaches. Additionally, the book describes physical methods of zero-valent metal interaction with organic matter, including sputtering, ultrasonic treatment and synthesis in ionic liquids. The book presents completely new content as a follow-up to the 1999 Elsevier Science publication Direct Synthesis of Coordination and Organometallic Compounds that was edited by Dr. Garnovskii and Dr. Kharisov. Covers current methods and techniques of metal interactions with organic media leading to metal chelates, adducts, di- and polymetallic complexes, metal-containing macrocycles, supported coordination compounds (i.e., metal complexes on carbon nanotubes), and more Describes reactivities of distinct forms of elemental metals (powders, sheets, nanoparticles (including a host of less-common metal nanostructures) with organic phase (liquid, solid and gaseous) and water Includes experimental procedures, with examples of direct synthesis, at the end of each chapter
