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The synthesis and characterization of novel rhodium alkenyl complexes and rhodacycloalkanes

The rhodium dimers [Cp*RhChh and [Cp*RhBr2h were reacted with alkenyl Grignard reagents MgBr(CH2)nCH=CH2 (n = 1 - 4, 6, 8, 9) in an attempt to form bis-alkenyl complexes that would be potential precursors to rhodium-containing metallacycloalkanes. The shorter-chain Grignard reagents (n = 1 - 3) prod...

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Main Author: Hager, Emma
Other Authors: Moss, John
Format: Thesis
Language:English
Published: Department of Chemistry 2024
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access_status_str Open Access
author Hager, Emma
author2 Moss, John
author_browse Hager, Emma
Moss, John
author_facet Moss, John
Hager, Emma
author_sort Hager, Emma
collection Thesis
description The rhodium dimers [Cp*RhChh and [Cp*RhBr2h were reacted with alkenyl Grignard reagents MgBr(CH2)nCH=CH2 (n = 1 - 4, 6, 8, 9) in an attempt to form bis-alkenyl complexes that would be potential precursors to rhodium-containing metallacycloalkanes. The shorter-chain Grignard reagents (n = 1 - 3) produced novel rhodium allylic complexes of composition Cp*RhBr(1i3-allyl-R) where R = H, CH3, CH2CH3. These were isolated as stable crystals and were fully characterized by analytical and spectroscopic methods. An X-ray crystal structure obtained for one of the complexes (R = CH2CH3) confirmed the allylic structure of the complex. The use of longer-chain reagents (n = 3, 4, 6, 8, 9) resulted in the fonnation of the novel bis-alkenyl complexes Cp*Rh({CH2}nCH=CH2)2(H2O). The bis-alkenyl complexes were obtained as yellow oils that were found to be stable in air and non-chlorinated solvents, but unstable in chlorinated solvents. They were characterized by NMR, MS and elemental analysis. Ring-closing metathesis (RCM) reactions were carried out on two of the bis-alkenyl complexes (n = 4, 6) in the presence of Grubbs' first-generation catalyst. NMR evidence indicated that the corresponding 11- and 15-membered ring rhodacycloalkenes had been formed. The rhodium phosphine precursors Cp*RhCh(PR3) (PR3 = PPh3, PMePh2, PMe2Ph) were prepared and reacted with the di-Grignard reagents MgBr-(CH2)n-MgBr (n = 7, 8, 9) to form a series of medium-sized rhodacycloalkanes that were larger than any synthesized previously. The rhodacycles were found to be quite unstable at room temperature. Thermal decomposition studies were conducted on some of the complexes and the major organic products were analyzed by GC-MS. In most cases the major products were 1- and 2-alkenes and n-alkanes. It was found that the nature of the tertiary phosphine ligand affected the types of decomposition products formed.
format Thesis
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institution University of Cape Town (South Africa)
language eng
last_indexed 2026-06-10T12:31:24.573Z
license_str Not specified — see source repository
provenance_str_mv Harvested via OAI-PMH from UCTD — University of Cape Town Open Access Repository
publishDate 2024
publishDateRange 2024
publishDateSort 2024
publisher Department of Chemistry
publisherStr Department of Chemistry
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source_str UCTD — University of Cape Town Open Access Repository
spelling oai:open.uct.ac.za:11427/39963 The synthesis and characterization of novel rhodium alkenyl complexes and rhodacycloalkanes Hager, Emma Moss, John Smith, Greg Chemistry The rhodium dimers [Cp*RhChh and [Cp*RhBr2h were reacted with alkenyl Grignard reagents MgBr(CH2)nCH=CH2 (n = 1 - 4, 6, 8, 9) in an attempt to form bis-alkenyl complexes that would be potential precursors to rhodium-containing metallacycloalkanes. The shorter-chain Grignard reagents (n = 1 - 3) produced novel rhodium allylic complexes of composition Cp*RhBr(1i3-allyl-R) where R = H, CH3, CH2CH3. These were isolated as stable crystals and were fully characterized by analytical and spectroscopic methods. An X-ray crystal structure obtained for one of the complexes (R = CH2CH3) confirmed the allylic structure of the complex. The use of longer-chain reagents (n = 3, 4, 6, 8, 9) resulted in the fonnation of the novel bis-alkenyl complexes Cp*Rh({CH2}nCH=CH2)2(H2O). The bis-alkenyl complexes were obtained as yellow oils that were found to be stable in air and non-chlorinated solvents, but unstable in chlorinated solvents. They were characterized by NMR, MS and elemental analysis. Ring-closing metathesis (RCM) reactions were carried out on two of the bis-alkenyl complexes (n = 4, 6) in the presence of Grubbs' first-generation catalyst. NMR evidence indicated that the corresponding 11- and 15-membered ring rhodacycloalkenes had been formed. The rhodium phosphine precursors Cp*RhCh(PR3) (PR3 = PPh3, PMePh2, PMe2Ph) were prepared and reacted with the di-Grignard reagents MgBr-(CH2)n-MgBr (n = 7, 8, 9) to form a series of medium-sized rhodacycloalkanes that were larger than any synthesized previously. The rhodacycles were found to be quite unstable at room temperature. Thermal decomposition studies were conducted on some of the complexes and the major organic products were analyzed by GC-MS. In most cases the major products were 1- and 2-alkenes and n-alkanes. It was found that the nature of the tertiary phosphine ligand affected the types of decomposition products formed. 2024-06-19T09:20:34Z 2024-06-19T09:20:34Z 2007 2024-06-19T09:14:59Z Thesis / Dissertation Masters MSc http://hdl.handle.net/11427/39963 eng application/pdf Department of Chemistry Faculty of Science
spellingShingle Chemistry
Hager, Emma
The synthesis and characterization of novel rhodium alkenyl complexes and rhodacycloalkanes
thesis_degree_str Master's
title The synthesis and characterization of novel rhodium alkenyl complexes and rhodacycloalkanes
title_full The synthesis and characterization of novel rhodium alkenyl complexes and rhodacycloalkanes
title_fullStr The synthesis and characterization of novel rhodium alkenyl complexes and rhodacycloalkanes
title_full_unstemmed The synthesis and characterization of novel rhodium alkenyl complexes and rhodacycloalkanes
title_short The synthesis and characterization of novel rhodium alkenyl complexes and rhodacycloalkanes
title_sort synthesis and characterization of novel rhodium alkenyl complexes and rhodacycloalkanes
topic Chemistry
url http://hdl.handle.net/11427/39963
work_keys_str_mv AT hageremma thesynthesisandcharacterizationofnovelrhodiumalkenylcomplexesandrhodacycloalkanes
AT hageremma synthesisandcharacterizationofnovelrhodiumalkenylcomplexesandrhodacycloalkanes