Thesis (MSc)--Stellenbosch University, 2013. / ENGLISH ABSTRACT: In this thesis the synthesis of a range of model and siloxane functionalized salicylaldimine ligands and
[N-(n-propyl)-(2-pyridyl)] diimine ligands are described. The functionalized ligands were obtained by
the reaction of salicylaldehyde and 2-pyridinecarboxaldehyde with 3-aminopropyltriethyoxysilane.
All ligands were characterized by FT-IR and 1H NMR spectroscopy. The salicylaldimine ligands were
reacted with either Cu(II) or Pd(II) salts to form both the model and functionalized Cu(II) and Pd(II)
complexes. The Cu(II) complexes were characterized using FT-IR, EPR and UV-VIS spectroscopy
while the Pd(II) complexes were characterized using FT-IR, 1H NMR and 13C{1H} NMR
spectroscopy. The diimine ligands were reacted with Cu(II) salts to form functionalized pyridinyl
complexes which were characterized used FT-IR spectroscopy.
Two mesoporous silica supports, MCM-41 and SBA-15 were synthesized. The siloxane
functionalized salicylaldimine Cu(II) and Pd(II) complexes were immobilized onto these supports to
produce heterogenized catalysts. These catalysts were characterized using a range of solid-state
techniques: BET nitrogen adsorption/desorption, scanning electron microscopy (SEM), thermal
gravimetric analysis (TGA), ICP-AES, and powder X-ray diffraction (XRD) analysis. The powder
XRD and SEM analysis showed that the structural integrity of the catalyst supports was kept intact
during the immobilization process. BET analysis and ICP-AES showed that the complexes had been
attached to the silica supports.
Both the model complexes and heterogenized catalyst systems were tested in the oxidation of benzyl
alcohol to benzaldehyde. The model copper catalyst showed high activity in this reaction with
molecular oxygen used as oxidant and the (2,2,6,6-tetramethylpiperidin-1-yl)oxyl radical as
co-oxidant. The immobilized copper complexes showed low activity in the same reaction. This was
attributed to steric hindrance around the active site dye to its entrapment with the silica matrix thus
hindering the formation of a key intermediate in the oxidation cycle due to steric hindrance. The
palladium complexes were not active in the oxidation reaction when molecular oxygen was used as
oxidant, but showed slight activity when hydrogen peroxide was used. / AFRIKAANSE OPSOMMING: In hierdie tesis word die sintese van ‘n reeks model sowel as gefunksioneerde salisielaldemien ligande
en [N-(n-propiel)-(2-piridiel)] di-imien ligande beskryf. Die gefunksioneerde ligande is verkry deur
die reaksie van salisielaldehied en en 2-piridienaldehied met 3-aminopropieltriëtoksiesilaan. Al die
ligande is gekarakteriseer deur FT-IR en 1H-KMR spektroskopie. Die salisielaldimien ligande is met
óf Cu(II) óf Pd(II) soute reageer om beide die model en gefunksioneerde Cu(II) en Pd(II) komplekse
te vorm. Die Cu(II) komplekse is gekarakteriseer deur FT-IR, EPR en UV-Vis spektroskopie terwyl
die Pd(II) komplekse deur FT-IR, 1H-KMR en 13C{1H}-KMR spektroskopie gekarakteriseer is. Die
di-imien ligande is met Cu(II) soute reageer om gefunksioneerde piridinielkompekse te vorm wat deur
FT-IR spektroskopie gekarakteriseer is.
Twee mesoporeuse silika draers, MCM-41 en SBA-15 is gesintetiseer. Die siloksaan-gefunksioneerde
salisielaldemien Cu(II) en Pd(II) komplekse is op hierdie draers geimobiliseer om geheterogeniseerde
katalisatore te vorm. Hierdie katalisatore is gekarakteriseer deur van ‘n wye reeks vaste toestand
tegnieke gebruik te maak: BET stikstof adsorpsie/desorpsie, skandeer elektron mikroskopie (SEM),
termiese gravimetriese analise (TGA), ICP-AES en poeier-XRD analise. Die poeier-XRD en SEM
analisies het aangetoon dat die strukturele integriteit van die katalisator draers behoue gebly het
tydens die immobiliseringsproses. BET analise en ICP-AES het aangetoon dat die komplekse aan die
silika draers geheg is.
Beide die model komplekse en geimobiliseerde katalisators is getoets in die oksidasie van
bensielalkohol na bensaldehied. Die model Cu(II) katalisator het hoë aktiwiteit in hierdie reaksie
getoon met molekulêre suurstof as oksideermiddel en die (2,2,6,6-tetrametielpipiridien-1-iel)oksiel
radikaal as ko-oksideermiddel. Die geimobiliseerde Cu(II) komplekse het lae aktiwiteit in dieselfde
reaksie getoon. Dit is toegeskryf aan steriese hindernis rondom die aktiewe sentrum as gevolg van die
verstrikking binne die silika matrys, wat die vorming van ‘n belangrike tussentoestand in die
oksidasie-siklus verhinder. Die Pd(II) komplekse was nie aktief in die oksidasie-reaksie in die geval
waar molekulêre suurstof as oksideermiddel gebruik is nie, maar het effense aktiwiteit getoon waneer
waterstofperoksied gebruik is. / Sasol
| Identifer | oai:union.ndltd.org:netd.ac.za/oai:union.ndltd.org:sun/oai:scholar.sun.ac.za:10019.1/79979 |
| Date | 03 1900 |
| Creators | Joubert, Corli |
| Contributors | Mapolie, S. F., Stellenbosch University. Faculty of Science. Dept. of Chemistry and Polymer Science. |
| Publisher | Stellenbosch : Stellenbosch University |
| Source Sets | South African National ETD Portal |
| Language | en_ZA |
| Detected Language | English |
| Type | Thesis |
| Format | xxiii, 91 p. : ill. (some col.) |
| Rights | Stellenbosch University |
Page generated in 0.0124 seconds