Polyethylene glycol oligomer

FIGURE 9.2 MALDI time-of-flight mass spectra of a mixture of polyethylene glycol oligomers (a) before and (b) after application of the mass selection gate. (Reprinted with permission from reference I). 

Thirty polyethylene glycol oligomers have been separated on K - form cation exchange resin. ... 

Time of flight secondary ion mass spectrometry has been used to determine the molecular weight distribution of polyethylene glycol oligomers. ... 

Figure 4.25 (page 122) shows results obtained on TSK-GEL SW and TSK-GEL PW columns for low molecular weight polyethylene glycol (PEG) oligomers and high molecular weight dextrans. The TSK-GEL G2000PW column successfully resolved components of PEG 200, whereas the TSK-GEL G2000SW column did not (Fig. 4.25A). Therefore, the TSK-GEL G2000PW column would be preferable for this analysis.

The anionic method of polymerization is most useful for the synthesis of low molecular weight hydroxy-terminated oligomers and polymers that are to be further processed. For example, the treatment of hydroxy-terminated oligomers with isocyanates has been used to obtain polyester-urethanes (9,20), while triblock copolymers (PCL-PEG-PCL) are prepared by initiating the polymerization of e-caprolactone with the disodium alcoholate from polyethylene glycol (26). 

II. B polyethylene glycol, ethylene oxide, polystyrene, diisocyanates (urethanes), polyvinylchloride, chloroprene, THF, diglycolide, dilac-tide, <5-valerolactone, substituted e-caprolactones, 4-vinyl anisole, styrene, methyl methacrylate, and vinyl acetate. In addition to these species, many copolymers have been prepared from oligomers of PCL. In particular, a variety of polyester-urethanes have been synthesized from hydroxy-terminated PCL, some of which have achieved commercial status (9). Graft copolymers with acrylic acid, acrylonitrile, and styrene have been prepared using PCL as the backbone polymer (60). 

Every peak was uniform with respect to m, but each one had a distribution in block length with respect to the PEO blocks (n). To identify fractions, they were collected and subjected to mass spectrometry. The first fraction contained polyethylene glycol and block oligomers with a degree of polymerization m(PO) 1-3. The second fraction was homogeneous with respect to PO and contained m(PO) 4, while fraction 3 resulted from m(PO) = 5. 

MALDI is the method of choice for the analysis of synthetic polymers because it usually provides solely intact and singly charged [62] quasimolecular ions over an essentially unlimited mass range. [22,23] While polar polymers such as poly(methylmethacrylate) (PMMA), [83,120] polyethylene glycol (PEG), [120,121] and others [79,122,123] readily form [M+H] or [M+alkali] ions, nonpolar polymers like polystyrene (PS) [99,100,105,106] or non-functionalized polymers like polyethylene (PE) [102,103] can only be cationized by transition metal ions in their l-t oxidation state. [99,100] The formation of evenly spaced oligomer ion series can also be employed to establish an internal mass calibration of a spectrum. [122]... 

All peptide-catalyzed enone epoxidations described so far were performed using insoluble, statistically polymerized materials (neat or on solid supports). One can, on the other hand, envisage (i) generation of solubilized poly-amino acids by attachment to polyethylene glycols (PEG) and (ii) selective construction of amino acid oligomers by standard peptide synthesis-linked to a solid support, to a soluble PEG, or neat as a well-defined oligopeptide. Both approaches have been used. The former affords synthetically useful and soluble catalysts with the interesting feature that the materials can be kept in membrane reactors for continuously oper-... 

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