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We use the tacticity nomenclature of organic polymer chemistry because, in the usual nomenclature of coordination polymers, the term heterochiral does not distinguish between the R,S,R,S and R,R,S,S sequences. For a stereoregular organometallic polymer, see: J. Rasburn, D. A. Foucher, W. F. Reynolds, I. Manners, G. J. Vancso, Chem. Commun. 1998, 843-844
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We use the tacticity nomenclature of organic polymer chemistry because, in the usual nomenclature of coordination polymers, the term heterochiral does not distinguish between the R,S,R,S and R,R,S,S sequences. For a stereoregular organometallic polymer, see: J. Rasburn, D. A. Foucher, W. F. Reynolds, I. Manners, G. J. Vancso, Chem. Commun. 1998, 843-844.
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2: C58H40Au2F6N 2O4P2, Mr, 1398.82, orthorhombic, space group C2221, Z, 8, a, 11.8033(3, b, 28.8564(4, c, 38.3325(9) Å, V, 13056.1(5) Å3, μ(MoKα, 0.71073 Å, T, 150(2) K, 21457 reflections collected, 11503 unique, R 1(I>2σI, 0.0425, wR2, 0.1246. 4: C61.50H51Au2Cl3F6N 2O6P2, Mr, 1590.27, orthorhombic, space group Pbca, a, 14.6995(2, b, 25.8284(3, c, 32.3400(4) Å, V, 12278.4(3) Å3, μ(MoKα, 0.71073 Å, T, 150(2) K, 40220 reflections collected, 10836 unique, R1I>2σI, 0.0476, wR
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- anions and 2.35 dichloroethane molecules per asymmetric unit of 5. CCDC-641696-641698 contain the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via www.ccdc.cam.ac.uk/data_request/cif.
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31P NMR resonances are too broad to allow resolution of peaks for specific triads S,S,S, S,R,S, S,S,R.
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31P NMR resonances are too broad to allow resolution of peaks for specific triads S,S,S, S,R,S, S,S,R.
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