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024 | 7 | _ | |2 DOI |a 10.1021/ic300042q |
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084 | _ | _ | |2 WoS |a Chemistry, Inorganic & Nuclear |
100 | 1 | _ | |0 P:(DE-HGF)0 |a Fielden, J. |b 0 |
245 | _ | _ | |a Chiral Hexanuclear Ferric Wheels |
260 | _ | _ | |a Washington, DC |b American Chemical Society |c 2012 |
300 | _ | _ | |a 2734 - 2736 |
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440 | _ | 0 | |0 14061 |a Inorganic Chemistry |v 51 |x 0020-1669 |y 5 |
500 | _ | _ | |3 POF3_Assignment on 2016-02-29 |
500 | _ | _ | |a We thank Joost de Groot (Forschungszentrum Julich) and Louise Natrajan (University of Manchester) for help with X-ray diffraction and paramagnetic NMR. Work at the Ames Laboratory was supported by the Department of Energy, Basic Energy Sciences, under Contract DE-AC02-07CH11358. |
520 | _ | _ | |a The homochiral iron(III) wheels [Fe(6){(S)-pedea}(6)Cl(6)] and [Fe(6){(R)-pedea)}(6)Cl(6)] [(R)- and (S)-2; pedea = phenylethylaminodiethoxide] exhibit high optical activities and antiferromagnetic exchange. These homochiral products react with each other, producing the centrosymmetric, crystallographically characterized [Fe(6){(S)-pedea}(3){(R)-pedea}(3)Cl(6)] diastereomer [(RSRSRS)-2]. (1)H NMR and UV-vis studies indicate that exchange processes are slow in both homo- and heterochiral systems but that, upon combination, the reaction between (R)- and (S)-2 occurs quickly. |
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650 | _ | 2 | |2 MeSH |a Circular Dichroism |
650 | _ | 2 | |2 MeSH |a Crystallography, X-Ray |
650 | _ | 2 | |2 MeSH |a Ferric Compounds: chemistry |
650 | _ | 2 | |2 MeSH |a Magnetic Resonance Spectroscopy |
650 | _ | 2 | |2 MeSH |a Models, Molecular |
650 | _ | 2 | |2 MeSH |a Stereoisomerism |
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700 | 1 | _ | |0 P:(DE-Juel1)VDB12080 |a Kögerler, P. |b 3 |u FZJ |
773 | _ | _ | |0 PERI:(DE-600)1484438-2 |a 10.1021/ic300042q |g Vol. 51, p. 2734 - 2736 |p 2734 - 2736 |q 51<2734 - 2736 |t Inorganic chemistry |v 51 |x 0020-1669 |y 2012 |
856 | 7 | _ | |u http://dx.doi.org/10.1021/ic300042q |
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