Deborah A. Longbottom

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Organization: University of Cambridge , England
Department: Department of Chemistry
Title: Professor(PhD)

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Co-reporter:Annhelen Lu, Thomas P. Smart, Thomas H. Epps III, Deborah A. Longbottom, and Rachel K. O’Reilly
Macromolecules 2011 Volume 44(Issue 18) pp:7233-7241
Publication Date(Web):September 6, 2011
DOI:10.1021/ma201256m
We have prepared a range of well-defined copolymers of styrene and l-proline functionalized styrene (5–11 kDa) using reversible addition–fragmentation chain transfer (RAFT) polymerization techniques and explored their use in supported catalysis. Upon deprotection of the l-proline functionalities, the solution self-assembly of these copolymers was investigated in mixed solvent systems. The resulting assemblies were characterized by dynamic light scattering, transmission electron microscopy (on graphene oxide substrates, along with cryo-TEM and tomography), and scanning electron microscopy. The application of these functional assemblies as supported catalysts for the aldol condensation reaction was explored using cyclohexanone and 4-nitrobenzaldehyde. The rate and selectivity of solution catalysis in our self-assembled system were comparable to those of l-proline, and a significant advantage of our system was that the polymer support could be utilized at lower catalyst loadings with comparable activity and also could be recycled a number of times while maintaining activity and selectivity.
Co-reporter:Amanda C. Evans, Annhelen Lu, Courtney Ondeck, Deborah A. Longbottom and Rachel K. O’Reilly
Macromolecules 2010 Volume 43(Issue 15) pp:6374-6380
Publication Date(Web):July 9, 2010
DOI:10.1021/ma1008447
Two families of organocatalytically active polystyrene-based copolymers with tunable incorporations of 4-hydroxyproline have been synthesized using two different controlled radical polymerization technologies: nitroxide-mediated polymerization (NMP) and reversible addition−fragmentation chain transfer (RAFT) polymerization. Both of these methodologies allow ready access to a number of polymeric species with controllable molecular weights, narrow molecular weight distributions (ca. 1.2), and reliable functionality incorporations (between 3 and 26%). The organocatalytic activity and selectivity of the NMP-derived family of copolymers with variable incorporations of l-proline have been investigated using the aldol reaction, which provided high conversion to products (>95%) with very good diastereo- and enantioselectivities. We propose that these materials have potential as highly efficient recoverable organocatalyst supports whose solubility and loading can be readily tailored to the desired application.
Co-reporter:Ama C. Evans;Jared Skey;Megan Wright;Wenjun Qu;Courtney Ondeck;Rachel K. O'Reilly
Journal of Polymer Science Part A: Polymer Chemistry 2009 Volume 47( Issue 24) pp:6814-6826
Publication Date(Web):
DOI:10.1002/pola.23721

Abstract

We report the application of reversible addition-fragmentation chain transfer polymerization using a novel chain transfer agent toward the synthesis of a variety of copolymers containing proline-derived monomeric units. This methodology enables ready access to a number of polymeric species with narrow molecular weight distributions, reliable functional unit incorporations, and high conversions. The methodology is also a facile approach to novel copolymeric species incorporating amino acids, which possess unique material properties and the potential for further organocatalytic application. © 2009 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2009

2H-1,2-Oxazine, 6-butyl-3,6-dihydro-2-phenyl-, (6R)-
2H-1,2-Oxazine, 3,6-dihydro-6-(1-methylethyl)-2-phenyl-, (6R)-
4-Hexen-3-ol, 2-methyl-6-(phenylamino)-, (3R,4Z)-
2,6-Dodecadien-4-ol, 1-(phenylamino)-, (2Z,4R,6E)-
2H-1,2-Oxazine, 6-(1,1-dimethylethyl)-3,6-dihydro-2-phenyl-, (6S)-
Stannane, (1E)-1,3-butadienyltributyl-
2,4-Pentadienoic acid, 5-(triphenylgermyl)-, (2Z,4E)-
2-Hexenedioic acid, 6-methyl ester, (2Z)-
1-Propene, 1-iodo-3,3-dimethoxy-, (1E)-