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- W2003203695 abstract "Abstract Metal complexing behavior of enantiomerically pure α,ω‐diiminoalkanes possessing the two terminal binaphthyl units ( L 1 and L 2) was studied. The ligands L 1 and L 2 were prepared by the reaction of optically pure 2′‐butoxy‐3‐formyl‐2‐hydroxy‐1,1′‐binaphthyl with propane and pentane diamines. Reactions of L 1 and L 2 with equimolar amount of Cu(OAc) 2 afforded quantitatively multinuclear complexes 1 . The structure of 1 was confirmed by MALDI–TOF MS spectroscopy, X‐ray single‐crystal‐structure analysis, and UV/vis and CD spectroscopic analyses. The reaction of L 1 having a 1,3‐propanediyl spacer resulted in the formation of a self‐assembled product, which was assigned as enantiopure trinuclear circular helicate 1a , while the ligand having a 1,5‐pentanediyl spacer L 2 gave a different self‐assembled product, dinuclear side‐by‐side complex 1b . The circular dichroism (CD) spectrum of 1a in solution showed intense Cotton effects in both the π–π* transition of the naphthalene units and the LMCT region of the N , O ‐chelate moieties. The CD spectrum of 1b was completely different from that of 1a ; in particular the Cotton effects in the LMCT region were very weak, contrary to those of 1a . These results suggest that 1a retains some chirality induced on the N , O ‐chelating moieties even in solution, while the induced chirality on the N , O ‐chelating moieties in 1b is not very significant, being consistent with the consequences of the X‐ray single‐crystal‐structure studies. Chirality, 2006. © 2006 Wiley‐Liss, Inc." @default.
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- W2003203695 date "2006-01-01" @default.
- W2003203695 modified "2023-09-27" @default.
- W2003203695 title "Self-assembly of multinuclear complexes with enantiomerically pure chiral binaphthoxy imine ligands: Effect of the alkyl spacer connecting two binaphthyl units on the metal binding" @default.
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- W2003203695 doi "https://doi.org/10.1002/chir.20308" @default.
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