Physical properties of poly(ethylene glycol) (PEG)-based resins for combinatorial solid phase organic chemistry: A comparison of PEG-cross-linked and PEG-grafted resins

被引:87
作者
Grotli, M
Gotfredsen, CH
Rademann, J
Buchardt, J
Clark, AJ
Duus, JO
Meldal, M
机构
[1] Carlsberg Lab, Dept Chem, SPOCC Ctr, DK-2500 Valby, Denmark
[2] Carlsberg Lab, Dept Physiol, DK-2500 Valby, Denmark
来源
JOURNAL OF COMBINATORIAL CHEMISTRY | 2000年 / 2卷 / 02期
关键词
D O I
10.1021/cc990048c
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Three series of poly(ethylene glycol) (PEG)-based polymers were synthesized and characterized with respect to their physical properties. Polyoxyethylene-polyoxypropylene (POEPOP), polyoxyethylene-polyoxetane (SPOCC), and polyoxyethylene-polystyrene (POEPS-3) were synthesized respectively by anion polymerization, cation polymerization, and radical polymerization. Both bulk and suspension modes were used to synthesize the polymers from derivatized PEG monomers (PEG 400, PEG 900, and PEG 1500). The three supports were compared with two commercially available PEG-grafted supports (TentaGel S OH, ArgoGel-OH) and two polystyrene supports (aminomethylated polystyrene [PS-NH2] and macroporous aminomethylated polystyrene [PLAMS]) with respect to their swelling properties, loading, NMR spectral quality, as well as solvent and reagent accessibility. Loadings of 0.3-0.7 mmol/g were obtained for the PEG-based resins. Swelling of the PEG-based resins was determined to be higher than that of the PEG-grafted resins and polystyrene supports. The PEG-based resins gave better resolved high-resolution NMR spectra than the PEG-grafted resins when examined by magic angle spinning nanoprobe (MAS) NMR spectroscopy. Moreover, fluorescence quenching of polymer bound 2-amino-benzoate by protonation with p-toluenesulfonic acid showed moderate to fast diffusion through the polymer depending on the solvent and the polymer matrix.
引用
收藏
页码:108 / 119
页数:12
相关论文
共 38 条
[31]   SPOCC: A resin for solid-phase organic chemistry and enzymatic reactions on solid phase [J].
Rademann, J ;
Grotli, M ;
Meldal, M ;
Bock, K .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1999, 121 (23) :5459-5466
[32]  
Rapp W, 1989, PEPTIDES 1988, P199
[33]   POEPOP and POEPS: Inert polyethylene glycol crosslinked polymeric supports for solid synthesis [J].
Renil, M ;
Meldal, M .
TETRAHEDRON LETTERS, 1996, 37 (34) :6185-6188
[34]   An NMR method to identify nondestructively chemical compounds bound to a single solid-phase-synthesis bead for combinatorial chemistry applications [J].
Sarkar, SK ;
Garigipati, RS ;
Adams, JL ;
Keifer, PA .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1996, 118 (09) :2305-2306
[35]   COMBINATORIAL SYNTHESIS - THE DESIGN OF COMPOUND LIBRARIES AND THEIR APPLICATION TO DRUG DISCOVERY [J].
TERRETT, NK ;
GARDNER, M ;
GORDON, DW ;
KOBYLECKI, RJ ;
STEELE, J .
TETRAHEDRON, 1995, 51 (30) :8135-8173
[36]   Synthesis and applications of small molecule libraries [J].
Thompson, LA ;
Ellman, JA .
CHEMICAL REVIEWS, 1996, 96 (01) :555-600
[37]  
VAGNER J, 1994, INNOVATION PERSPECTI, P347
[38]   Solvent and reagent accessibility within oligo(ethylene glycol) ether [PEG] cross-linked polystyrene beads [J].
Wilson, ME ;
Paech, K ;
Zhou, WJ ;
Kurth, MJ .
JOURNAL OF ORGANIC CHEMISTRY, 1998, 63 (15) :5094-5099