Conformational fluctuation in palladium(II)-methyl aldopentopyranoside complexes |
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Authors: | Thorsten Allscher |
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Affiliation: | Department of Chemistry and Biochemistry, Ludwig-Maximilians-Universität, Butenandtstraße 5-13, D-81377 Munich, Germany |
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Abstract: | Four methyl d-pentopyranosides (β-Ara, α-Lyx, β-Rib, β-Xyl), as well as Me-β-l-Ara, some of them residing in a well-defined conformation in the solution state (Ara, Xyl) and some showing pronounced chair inversion in solution (Lyx, Rib), form bidentate chelates of the general formula [Pd(chxn)(LH−2)-κO,O′] and [Pd(tmen)(LH−2)-κO,O′], chxn = (R,R)-cyclohexane-1,2-diamine, tmen = N,N,N′,N′-ethane-1,2-diamine and L = glycoside, with PdIIN2-type metal probes. The dynamic behaviour of the free glycosides is maintained in their chelates, the only case where the metal is bonded by a cis-vicinal diol function. Thus, one fluctuating chelate was detected with the lyxopyranoside in the κO2,3 binding mode, and two fluctuating chelates were found for the ribopyranoside (κO2,3 and κO3,4). No fluctuating chelate was found for the arabinopyranoside (the free arabinopyranoside being non-fluctuating as well), or for the xylopyranoside (no cis-vicinal diol function). In addition, syn-diaxial chelation (κO2,4) was observed for the ribopyranoside and the xylopyranoside. The spectroscopic results were supplemented by X-ray analyses. |
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Keywords: | Methyl aldopentosides Monosaccharide chelates Palladium Chair inversion |
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