Molecular recognition of alkali‐ions by crown‐ether‐functionalized poly(alkylthiophenes)
Source abstract
Abstract
New crown‐ether‐functionalized alkyl(oligothiophene)s (see Figure) have been synthesized and electropolymerized to alkali metal ion sensitive poly(alkylthiophene)s. It is shown for the first time that the redox chemistry of a conducting polymer is strongly influenced by the specific host‐guest interaction, although the crown ether units are not π‐conjugated to the conducting backbone but separated by an insulating oxa‐alkyl chain. magnified image
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Research context
OpenAlex topics: Conducting polymers and applications · Analytical Chemistry and Sensors · Electrochemical Analysis and Applications
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References (42)
Show source-provided references
1. 10.1002/adma.1989001040410.1002/adma.19890010404 ↗
2. 10.1080/0026894850807619610.1080/00268948508076196 ↗
3. 10.1149/1.211424910.1149/1.2114249 ↗
4. 10.1016/0013-4686(89)87075-610.1016/0013-4686(89)87075-6 ↗
5. Lemaire M. · J. Chim. Phys. · 1989 · 86 · 19310.1051/jcp/1989860193 ↗
6. (b)M.Lemaire D.Delabouglise R.Garreau A.Guy J.Roncali J. Chem. Soc. Chem. Commun.1988 658–66110.1039/c39880000658 ↗
7. (c)D.Kotkar V.Joshi K.Ghosh J. Chem. Soc. Chem. Commun.1988 917–918.10.1039/c39880000917 ↗
8. 10.1002/adma.1992004071510.1002/adma.19920040715 ↗
9. 10.1016/0022-0728(93)80112-U10.1016/0022-0728(93)80112-U ↗
10. 10.1002/adma.1991003040610.1002/adma.19910030406 ↗
11. Vögtle F. · 1981
12. 1982
13. 1984
14. (a)J. P.Collin J. P.Sauvage J. Chem. Soc. Chem. Commun. 1987 1075–1076.10.1039/C39870001075 ↗
15. 10.1016/0022-0728(89)80205-010.1016/0022-0728(89)80205-0 ↗
16. 10.1016/0013-4686(91)85173-510.1016/0013-4686(91)85173-5 ↗
17. 10.1016/0022-0728(90)87100-X10.1016/0022-0728(90)87100-X ↗
18. 10.1016/0013-4686(91)80019-510.1016/0013-4686(91)80019-5 ↗
19. 10.1016/0022-0728(90)85147-W10.1016/0022-0728(90)85147-W ↗
20. 10.1021/cr00012a00910.1021/cr00012a009 ↗
21. 10.1055/s-1984-3073710.1055/s-1984-30737 ↗
22. 10.1016/S0040-4039(00)91417-510.1016/S0040-4039(00)91417-5 ↗
23. Barco A. · Synthesis · 1976 · 124 · 125
24. 10.1002/anie.19900419110.1002/anie.199004191 ↗
25. P.Bäuerle F.Würthner F.Effenberger Synthesis in press.
26. P.Bäuerle K.‐U.Gaudl S.Scheib F.Würthner S.Heid Chem. Ber. in press.
27. 10.1016/S0022-0728(81)80450-010.1016/S0022-0728(81)80450-0 ↗
28. P.Bäuerle F.Pfau H.Schlupp F.Würthner K.‐U.Gaudl M. BalpardaCaro P.Fischer J. Chem. Soc. Perkin Trans. 21993 489–494.
29. J.Roncali R.Garreau D.Delabouglise F.Garnier M.Lemaire J. Chem. Soc. Chem. Commun.1989 679–681.10.1039/c39890000679 ↗
30. 10.1016/0379-6779(90)90060-X10.1016/0379-6779(90)90060-X ↗
31. K.‐U.Gaudl Ph.D. Thesis University of Stuttgart1992.
32. 10.1002/adma.1991003100810.1002/adma.19910031008 ↗
33. 10.1039/cs989180040910.1039/cs9891800409 ↗
34. 10.1002/adma.1992004090810.1002/adma.19920040908 ↗
35. (b)T. K.Hansen T.Joergnsen J.Becher J. Chem. Soc. Chem. Commun.1992 1550–1552.10.1039/C39920001550 ↗
36. Weber E. · 1981 · 1
37. 10.1021/cr00068a00310.1021/cr00068a003 ↗
38. 10.1021/cr00008a00310.1021/cr00008a003 ↗
39. 10.1139/v91-10510.1139/v91-105 ↗
40. 10.1063/1.46255010.1063/1.462550 ↗
41. 10.1021/j100175a10210.1021/j100175a102 ↗
42. Salbeck J. · DECHEMA‐Monogr. · 1987 · 112 · 177