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Recent Advances In Glylons Science, Cornelia Rosu Jan 2010

Recent Advances In Glylons Science, Cornelia Rosu

LSU Master's Theses

A variety of sugar- based polyamides called glylons were synthesized by using different pathways. The sugar- units were derived from D- glucaric acid and D-galactaric acid. Glylons D-glucaric- based with pendant free hydroxyl groups showed a low solubility in organic solvents, due to hydroxyl preference to form strong intra- and intermolecular H- bonding. To minimize these interactions an acetalation reaction was performed. Monoacetalated D-glucaric-based po-lymers exhibited a better solubility in a broader range of solvents but the residual hydroxyl groups favored aggregation. Completely blocked bis-acetalated galactaric-based glylons are so-luble in a broad range of solvents including toluene/methanol mixtures. Deprotection reaction …


Synthesis Of Aza-Bridged Tetraphosphine Ligands For A Dirhodium Hydroformylation Catalyst, Scott Michael Boudreaux Jan 2010

Synthesis Of Aza-Bridged Tetraphosphine Ligands For A Dirhodium Hydroformylation Catalyst, Scott Michael Boudreaux

LSU Master's Theses

A novel tetraphosphine ligand rac-et,ph-P4 (et,ph-P4 = PEt2CH2CH2(Ph)PCH2P(Ph)CH2CH2PEt2) is used for the formation of a highly active and regioselective hydroformylation catalyst. The active catalytic species, Rh2H2(ƒÝ-CO)2(et,ph-P4)]2+, is formed in situ under H2/CO pressure. This is one of the most impressive examples of homobimetallic cooperativity in homogeneous catalysis. The fragmentation of this catalyst by CO has been investigated and confirmed by in situ NMR spectroscopic studies. A new tetraphosphine ligand rac-et,ph-P4-Ph (et,ph-P4-Ph = PEt2(o-C6H4)P(Ph)CH2(Ph)P(o-C6H4)PEt2) has been synthesized to combat this fragmentation problem. However, the inability to successfully separate the meso and racemic isomers of the ligand has led to more alteration …