5 research outputs found

    Homochiral 1D Helical Chain Based on an Achiral Cu(II) Complex

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    Self-assembly of an achiral [Cu­(L)] complex produced a homochiral helical chain [Cu­(L)]<sub>3</sub>·2H<sub>2</sub>O (<b>1</b>) (L = 2-dimethylaminoethyl­(oxamato)). Interestingly, complex <b>1</b> obtained in our laboratory exhibits only a left-handed helical chain without any chiral source. Single-crystal X-ray analysis revealed the absolute structure and homochirality of its helical chain structure in the space group of <i>P</i>3<sub>2</sub>. Solid-state circular dichroism (CD) spectra confirmed the high enantio excess of the crystals obtained in different synthesis batches. Magnetic susceptibility measurements reveal a relatively strong intrachain antiferromagnetic interaction between Cu­(II) centers via an oxamato bridge (<i>J</i> = −74.4 cm<sup>–1</sup>)

    Homochiral 1D Helical Chain Based on an Achiral Cu(II) Complex

    No full text
    Self-assembly of an achiral [Cu­(L)] complex produced a homochiral helical chain [Cu­(L)]<sub>3</sub>·2H<sub>2</sub>O (<b>1</b>) (L = 2-dimethylaminoethyl­(oxamato)). Interestingly, complex <b>1</b> obtained in our laboratory exhibits only a left-handed helical chain without any chiral source. Single-crystal X-ray analysis revealed the absolute structure and homochirality of its helical chain structure in the space group of <i>P</i>3<sub>2</sub>. Solid-state circular dichroism (CD) spectra confirmed the high enantio excess of the crystals obtained in different synthesis batches. Magnetic susceptibility measurements reveal a relatively strong intrachain antiferromagnetic interaction between Cu­(II) centers via an oxamato bridge (<i>J</i> = −74.4 cm<sup>–1</sup>)

    Facile Synthetic Route to Highly Luminescent Sila[7]helicene

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    A facile synthetic route to dimethylsila[7]helicene by using a Lewis acid catalyzed double-cyclization reaction for construction of the twisted two phenanthrene moieties is described. Sila[7]helicene exhibited a high fluorescence quantum yield and a realatively large <i>g</i> value (dissymmetric factor) of circularly polarized luminencence (CPL) for small molecules

    Facile Synthetic Route to Highly Luminescent Sila[7]helicene

    No full text
    A facile synthetic route to dimethylsila[7]helicene by using a Lewis acid catalyzed double-cyclization reaction for construction of the twisted two phenanthrene moieties is described. Sila[7]helicene exhibited a high fluorescence quantum yield and a realatively large <i>g</i> value (dissymmetric factor) of circularly polarized luminencence (CPL) for small molecules

    Novel Means of Controlling the Solid-State Circular Dichroism Property in a Supramolecular Organic Fluorophore Comprising 4-[2-(Methylphenyl)ethynyl]benzoic Acid by Varying the Position of the Methyl Substituent

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    The solid-state circular dichroism (CD) of a 4-[2-(methylphenyl)­ethynyl]­benzoic acid/amine supramolecular organic fluorophore can be controlled by changing the position of the methyl substituent of the methylphenylethynyl unit on the achiral 4-[2-(methylphenyl)­ethynyl]­benzoic acid component molecule, instead of changing the chirality of the chiral amine component molecule
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