Abstract
Chiral electrode materials possessing enantioselective recognition properties or capable of performing chiral electrosynthesis are of great potential interest. The synthesis of a chiral pyrrolic monomer (see figure) and the enantioselective properties of the modified electrode surface obtained upon its polymerization are reported. magnified image
References
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- 1H−NMR (CDCl3) δ(ppm): 2.05 (m 12H CH3CO) 2.79 (t J=7 Hz 2 H H‐8) 3.80 (m 114 H‐5) 4.22 (m 4 H H‐6 H‐7) 5.14 (m 3 H H‐2 H‐3 H‐4) 5.65 (d J =8 Hz 1H H‐1) 6.10 (t J = 2 Hz 2 H H‐ß ß) 6.64 (t J = 2 Hz 2H H‐β β).13C−NMR (CDCL3) δ(ppm): 20.52‐20.76 (CH3CO) 36.17 (C‐7) 44.56 (C‐8) 61.68 (C‐6) 67.62 (C‐4) 70.10 (C‐2) 72.64 (C‐3 and C‐5) 91.64 (C‐1) 108.39 (C‐β) 120.51 (C‐β) 169.18‐170.55 (CH3CO) (see ref. [16] for13C−NMR data of glucopyranose derivatives). Mass spectroscopy (D‐CI): calcd. 469; found 470 (m + H⊕) 487 (m + NH). UV/Vis spectroscopy (C2H5OH) λmax[nm] (log(ε/ M−1cm−1)): 229 (3.5) 290 (3.2). UV/VIS spectroscopy for the film on the ITO electrode: 350 nm (sh). [α](c =1. CHCl3) = + 10° for 1; [α](c =1 CHCl3) − +7° for 2.
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Dates
Type | When |
---|---|
Created | 20 years, 3 months ago (May 29, 2005, 3:26 a.m.) |
Deposited | 2 years ago (Sept. 1, 2023, 12:29 p.m.) |
Indexed | 2 weeks ago (Aug. 20, 2025, 8:49 a.m.) |
Issued | 33 years, 2 months ago (July 1, 1992) |
Published | 33 years, 2 months ago (July 1, 1992) |
Published Online | 20 years, 10 months ago (Oct. 29, 2004) |
Published Print | 33 years, 2 months ago (July 1, 1992) |
@article{Moutet_1992, title={Poly(glucose‐pyrrole) modified electrodes: A novel chiral electrode for enantioselective recognition}, volume={4}, ISSN={1521-4095}, url={http://dx.doi.org/10.1002/adma.19920040715}, DOI={10.1002/adma.19920040715}, number={7–8}, journal={Advanced Materials}, publisher={Wiley}, author={Moutet, Jean‐Claude and Saintl‐Aman, Eric and Tran‐Van, François and Angibeaud, Pierre and Utille, Jean‐Pierre}, year={1992}, month=jul, pages={511–513} }