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  • About
  • The Global ETD Search service is a free service for researchers to find electronic theses and dissertations. This service is provided by the Networked Digital Library of Theses and Dissertations.
    Our metadata is collected from universities around the world. If you manage a university/consortium/country archive and want to be added, details can be found on the NDLTD website.
1

Synthetic investigation of Mn(I) and Re(I) N-heterocyclic carbene complexes

Van der Westhuizen, Belinda 28 June 2011 (has links)
The study involves synthetic approaches towards the preparation of novel NHC complexes of low valent rhenium and manganese transition metals. Diverse methods of synthesis were studied. The direct approach, in which the ylidene obtained from deprotonation of 1,3-bis(2,4,6- trimethylphenyl)imidazolium chloride was added to the metal substrate, proved to be unsuccessful as isolation of the free carbene should rather be performed in an argon filled glove box under extreme inert conditions. By way of further investigation the ylidene was prepared by in situ methods and then quenched with the metal substrate. Different bases for deprotonation purposes and reaction conditions were explored. All routes employed were investigated and compared using group VII transition metal substrates Re(CO)5Br, Mn(CO)5Br, Re2(CO)10 and Mn2(CO)10. Isolation and purification of these products proved to be very challenging due to the insolubility in some organic solvents with consequent problematic spectroscopic analyses of the complexes. The tendency of the products to undergo various side reactions is observed in all reactions. Specifically, hydrolysis of the imidazolium ligand, followed by vinyl formation, yielded the mesitylformamide compound (3). The results obtained for some of the monometal substrates indicated that the target complexes were formed but could not be isolated. However, the synthesis route employing deprotonation by nBuLi as base and [Mn2(CO)10] as dimetal substrate lead to the isolation of the target dinuclear complex [Mn2(CO)9IMes] (9). Other novel complexes obtained during the course of this study include the biscarbene tetrarhenium complex [Re2(CO)9.C(OEt)C4H2OC(OEt)Re2(CO)9] (12) and various side reaction products. In many cases, metal-metal bond cleavage and carbonyl insertion was observed, as is evident in the complex IMesH[ReO4] (6) and ketene product (13). Structural and theoretical studies were performed to investigate the bond character between the carbene ligand and the metal. / Dissertation (MSc)--University of Pretoria, 2010. / Chemistry / unrestricted

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