The synthesis of novel 3-substituted pyrrole monomers possessing chiral side groups: a study of their chemical polymerisation and the assessment of their chiral discrimination properties
Source abstract
Abstract
Novel 3-substituted pyrrole monomers possessing chiral side groups were synthesised. These compounds were successfully polymerised with ferric salts and the polymer materials fabricated into sensors. The sensors were found to elicit differential changes in electrical resistance and mass, when exposed to different chiral enantiomers in the vapour phase.
Source: openaire · Quality: candidate unverified · Source record ↗
Research context
OpenAlex topics: Analytical Chemistry and Sensors · Conducting polymers and applications · Electrochemical sensors and biosensors
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
References (30)
Show source-provided references
1. Gangopadhyay · Sens. Actuators B: Chem. · 2001 · 77 · 32610.1016/S0925-4005(01)00719-5 ↗
2. Charlesworth · J. Phys. Chem. · 1993 · 97 · 541810.1021/j100122a038 ↗
3. Miasik · J. Chem. Soc., Faraday Trans. 1 · 1986 · 82 · 111710.1039/f19868201117 ↗
4. Josowicz · Anal. Chem. · 1986 · 58 · 51410.1021/ac00294a003 ↗
5. Gustafsson · Synth. Metals · 1987 · 21 · 20310.1016/0379-6779(87)90087-7 ↗
6. Josowicz · Anal. Chem. · 1987 · 59 · 25310.1021/ac00129a008 ↗
7. Hanawa · J. Chem. Soc., Faraday Trans. 1 · 1988 · 84 · 158710.1039/f19888401587 ↗
8. Y. Kunugi, K. Nigorikawa, Y. Harima, K. Yamashita, J. Chem. Soc., Chem. Commun. (1994) 873.10.1039/c39940000873 ↗
9. Bross · Adv. Mater. · 1991 · 3 · 19810.1002/adma.19910030406 ↗
10. Salmon · Electrochim. Acta · 1989 · 34 · 11710.1016/0013-4686(89)87075-6 ↗
11. Delabouglise · Synth. Metals · 1990 · 39 · 11710.1016/0379-6779(90)90205-Y ↗
12. Ibrahim · J. Electroanal. Chem. · 1995 · 387 · 13910.1016/0022-0728(95)03957-I ↗
13. K.S. Ryder, D.G. Morris, J.M. Cooper, J. Chem. Soc., Chem. Commun. (1995) 1471.10.1039/c39950001471 ↗
14. Ho-Hoang · Synth. Commun. · 1996 · 26 · 128910.1080/00397919608003488 ↗
15. Pleus · Synth. Commun. · 1997 · 27 · 291710.1080/00397919708004998 ↗
16. Pleus · Synth. Metals · 1998 · 95 · 23310.1016/S0379-6779(98)00063-0 ↗
17. T. Le Gall, M.S. Passos, S.K. Ibrahim, S. Morlat-Therias, C. Sudbrake, S.A. Fairhurst, M.A. Queiros, C.J. Pickett, J. Chem. Soc., Perkin Trans. 1 (1999) 1657.10.1039/a902324k ↗
18. A.S. Ribeiro, A. Kanazawa, D.M.A.F. Navarro, J.-C. Moutet, M. Navarro, Tetrahedron: Asymmetry 10 (1999) 3735.10.1016/S0957-4166(99)00332-8 ↗
19. Demir · J. Chem. Soc., Perkin Trans. · 2001 · 1 · 116210.1039/b008317h ↗
20. Shinohara · Polym. Commun. · 2001 · 42 · 35110.1016/S0032-3861(00)00391-8 ↗
21. Sanner · Anal. Chem. · 1998 · 70 · 144010.1021/ac970757h ↗
22. Ryan · Enantiomer · 2001 · 6 · 159
23. Papadopoulos · Tetrahedron Lett. · 1968 · 14 · 172110.1016/S0040-4039(01)99036-7 ↗
24. McKillop · Synthesis · 1979 · 410 · 48110.1055/s-1979-28728 ↗
25. Kakushima · Synth. Commun. · 1983 · 48 · 3214
26. Gustaffson · Synth. Metals · 1989 · 31 · 16310.1016/0379-6779(89)90812-6 ↗
27. Garner · Org. Synth. · 1991 · 70 · 18
28. Neises · Angew. Chem. Int. Ed. Engl. · 1978 · 17 · 52210.1002/anie.197805221 ↗
29. Hawkins · J. Mater. Chem. · 2000 · 10 · 205710.1039/b001912g ↗
30. de Lacy Costello · Synth. Metals · 2000 · 114 · 18110.1016/S0379-6779(00)00250-2 ↗