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Very recently, the effect of a sulfur-centered chirality on the self-assembly of meso-sulfinylporphyrins was reported, although the level of discrimination was not high enough, see
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Very recently, the effect of a sulfur-centered chirality on the self-assembly of meso-sulfinylporphyrins was reported, although the level of discrimination was not high enough, see: Y. Matano, T. Shinokura, K. Matsumoto, H. Imahori, H. Nakano, Chem. Asian J. 2007, 2, 1417.
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84940952811
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Eds, K. M. Kadish, K. M. Smith, R. Guilard, Academic Press, San Diego
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Crystal data for 3 Ni: C79H86N 4NiO, Mr, 1166.23, triclinic, space group P1 (No. 2, a, 14.234(6, b, 14.559(5, c, 16.564(5) Å, α, 108.939(9, β, 90.923(12, γ, 95.734(12)°, V, 3226.3(19) Å3, Z, 2, ρcalcd, 1.200 g cm-3, T, 123(2) K, 25317 measured reflections, 11184 unique reflections, R, 0.0920, I>2.0σ(I, Rw, 0.2493 (all data, GOF, 1.017 (I>2.0σ(I, Crystal data for (5 Zn rac)2: C148H162Cl12N 10Zn2, Mr, 2637.06, monoclinic, space group P21/c (No. 14, a, 13.029(2, b, 25.898(5) c, 21.281(5) Å, β, 108.272(7)°, V, 6819(2) Å3, Z, 4
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S, R) 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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For a β,β-azanorbornene-fused zinc porphyrin, see Ref. [2b]. This porphyrin is not chiral because of its symmetric structure.
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For a β,β-azanorbornene-fused zinc porphyrin, see Ref. [2b]. This porphyrin is not chiral because of its symmetric structure.
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