{"title":"Synthesis and properties of bifunctional oligoethers. I. Chiral oligomers from propylene oxide","authors":"C. L. Jun, A. Leborgne, N. Spassky","doi":"10.1002/polc.5070740106","DOIUrl":null,"url":null,"abstract":"<p>Racemic or chiral bifunctional oligoethers of the type H—(O—CH(CH<sub>3</sub>)—CH<sub>2</sub>—)<sub><i>n</i></sub>—Cl, <i>n</i> = 4-10, have been prepared by reacting racemic or optically active propylene oxide with teiraphenyl porphyrin (TPPH<sub>2</sub>)—AlEt<sub>2</sub>Cl initiator sysfem. The synthesized products were characterized by IR, elemental analysis, VPO, GPC, and <sup>1</sup>H and <sup>13</sup>CNMR techniques. The oligomers purified by fractional distillation exhibit narrow <i>MW</i> distributions (<i>M̄<sub>w</sub>/M̄<sub>n</sub></i> ≈ 1.03). Chiroptical properties of the oligomers and their derivatives were examined and compared with those of high molecular weight polyfpropylene oxide). Different possibilities of applicadons of these oligomers are presently under study.</p>","PeriodicalId":16867,"journal":{"name":"Journal of Polymer Science: Polymer Symposia","volume":"74 1","pages":"31-44"},"PeriodicalIF":0.0000,"publicationDate":"1986-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1002/polc.5070740106","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Polymer Science: Polymer Symposia","FirstCategoryId":"1085","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/polc.5070740106","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Racemic or chiral bifunctional oligoethers of the type H—(O—CH(CH3)—CH2—)n—Cl, n = 4-10, have been prepared by reacting racemic or optically active propylene oxide with teiraphenyl porphyrin (TPPH2)—AlEt2Cl initiator sysfem. The synthesized products were characterized by IR, elemental analysis, VPO, GPC, and 1H and 13CNMR techniques. The oligomers purified by fractional distillation exhibit narrow MW distributions (M̄w/M̄n ≈ 1.03). Chiroptical properties of the oligomers and their derivatives were examined and compared with those of high molecular weight polyfpropylene oxide). Different possibilities of applicadons of these oligomers are presently under study.