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The synthesis of novel, unsymmetrically substituted, chiral naphthalene and perylene diimides: Photophysical, electrochemical, chiroptical and intramolecular charge transfer properties

机译:新型,不对称取代的手性萘和per二酰亚胺的合成:光物理,电化学,手性和分子内电荷转移性质

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摘要

A novel naphthalene monoimide and two unsymmetric chiral diimides (naphthalene and perylene) were synthesized; for comparison purposes, the perylene monoimide with the same substituent in the naphthalene monoimide was prepared. The naphthalene monoimide exhibited intramolecular charge transfer complexa-tion in polar solvents. Excimer-like emissions were obtained in non-polar, polar protic and aprotic solvents in the cases of both the naphthalene monoimide and diimide. The specific optical rotation values of unsym-metrical chiral naphthalene and perylene diimides were -221.6 and -24, respectively at 20 °C. The Chiral naphthalene diimide showed prominent, negative Cotton effects centred at 362 and 382 nm in CH3CN.
机译:合成了新型的萘单酰亚胺和两个不对称的手性二酰亚胺(萘和per);为了比较,制备了在萘单酰亚胺中具有相同取代基的per单酰亚胺。萘单酰亚胺在极性溶剂中表现出分子内电荷转移络合物。对于萘一酰亚胺和二酰亚胺,在非极性,极性质子和非质子溶剂中获得了准分子样发射。非对称手性萘和per二酰亚胺的比旋光度值在20°C时分别为-221.6和-24。在CH3CN中,手性萘二酰亚胺显示出明显的负棉花效应,集中在362和382 nm。

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