Knowledge base: Adam Mickiewicz University

Settings and your account

Back

New N-heterocyclic carbene palladium complexes – synthesis, structure, reactivity and catalytic activity

Sylwia Ostrowska

Abstract

The aim of this doctoral thesis was the synthesis of new palladium complexes bearing N-heterocyclic carbene ligands. Particular attention has been paid to the synthesis of complexes containing anionic ligands other than the chloride ligand, commonly used in the chemistry of palladium complexes. The equally important aim of the work was to study the catalytic properties of the synthesized complexes in selected reactions leading to the formation of carbon-carbon or carbon-heteroatom bonds, i.e. in Suzuki-Miyaura, Sonogashira, Heck couplings as well as in the dimerization of monosubstituted acetylenes. In scientific literature, the effect of the properties of anionic ligands on the catalytic activity of N-heterocyclic carbene complexes has not been described so far. A number of new N-heterocyclic carbene palladium complexes with various anionic ligands have been obtained. Their valuable catalytic properties have been demonstrated in a series of coupling reactions as well as dimerization and hydrogenation of acetylenes. New efficient procedures for the preparation of biaryls, 1,2-diarylacetylene, E-1,3-enynes have been proposed. Part of the results obtained within the doctoral degree work has been published in renowned scientific journals, which proves that they make a significant contribution to the development of catalytic methods of organic
Record ID
UAMe2acfa12cdad4b17b2a71ef10a0d731a
Diploma type
Doctor of Philosophy
Author
Sylwia Ostrowska Sylwia Ostrowska,, Wydział Chemii [nowa struktura organizacyjna] (SNŚ/WC)Szkoła Nauk Ścisłych [nowa struktura organizacyjna] (SNŚ)
Title in Polish
Nowe N-heterocykliczne karbenowe kompleksy palladu - synteza, struktura, reaktywnośc i aktywnosć katalityczna
Title in English
New N-heterocyclic carbene palladium complexes – synthesis, structure, reactivity and catalytic activity
Language
pol (pl) Polish
Certifying Unit
Faculty of Chemistry (SNŚ/WC/FoC)
Discipline
chemistry / (chemical sciences domain) / (physical sciences)
Scientific discipline (2.0)
6.5 chemical sciences
Status
Finished
Defense Date
22-05-2018
Title date
22-05-2018
Supervisor
URL
http://hdl.handle.net/10593/23449 Opening in a new tab
Keywords in English
NHC complexes palladium, PEPPSI catalysts, coupling reactions, organometallic chemistry
Abstract in English
The aim of this doctoral thesis was the synthesis of new palladium complexes bearing N-heterocyclic carbene ligands. Particular attention has been paid to the synthesis of complexes containing anionic ligands other than the chloride ligand, commonly used in the chemistry of palladium complexes. The equally important aim of the work was to study the catalytic properties of the synthesized complexes in selected reactions leading to the formation of carbon-carbon or carbon-heteroatom bonds, i.e. in Suzuki-Miyaura, Sonogashira, Heck couplings as well as in the dimerization of monosubstituted acetylenes. In scientific literature, the effect of the properties of anionic ligands on the catalytic activity of N-heterocyclic carbene complexes has not been described so far. A number of new N-heterocyclic carbene palladium complexes with various anionic ligands have been obtained. Their valuable catalytic properties have been demonstrated in a series of coupling reactions as well as dimerization and hydrogenation of acetylenes. New efficient procedures for the preparation of biaryls, 1,2-diarylacetylene, E-1,3-enynes have been proposed. Part of the results obtained within the doctoral degree work has been published in renowned scientific journals, which proves that they make a significant contribution to the development of catalytic methods of organic

Uniform Resource Identifier
https://researchportal.amu.edu.pl/info/phd/UAMe2acfa12cdad4b17b2a71ef10a0d731a/
URN
urn:amu-prod:UAMe2acfa12cdad4b17b2a71ef10a0d731a

Confirmation
Are you sure?
Report incorrect data on this page
clipboard