Effects of Auxiliary Ligands of Pd(II) Dimers on Induction of Chiral Nematic Phases: Chirality Inversion and Photo-responsive Structural Change
Effects of Auxiliary Ligands of Pd(II) Dimers on Induction of Chiral Nematic Phases: Chirality Inversion and Photo-responsive Structural Change
复制标题
Pd(II) 二聚体辅助配体对手性向列相诱导的影响:手性反转和光响应结构变化
DOI:
10.1039/c4dt02812k
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发表时间:
2015
期刊:
影响因子:
--
通讯作者:
Akihiko Yamagishi and Hisako Sato*
中科院分区:
文献类型:
--
作者:
Kenji Tamura;Jun Yoshida;Takafumi Kitazawa;Masahiro Taniguchi;Akihiko Yamagishi and Hisako Sato*
Dinuclear square planar palladium(II) complexes, [{Pd(II)La}2(baet)] (La− = β-diketonato and baet2− = 1,2-diacetyl-1,2-bis(3-methylbutanoyl)ethanato), were prepared and used as chiral dopants to induce chiral nematic phases. The following β-diketones were used as LaH: pentane-2,4-dione (acacH), dibenzoylmethane (dbmH), di-4-nonyloxybenzoylmethane (C9-dbmH) and 3-[4′-(4′′-(octyloxy)phenylazo)phenyl]-2,4-dione (C8-azoacacH). When the enantiomers were doped in a nematic liquid crystal, they induced a chiral nematic phase with a helical twisting power (HTP) of 5–50 μm−1. In particular, the sample doped with [{Pd(II)(C8-azoacac)}2(baet)] exhibited a reversible change of the circular dichroism spectrum under alternate irradiation at 350 nm and 460 nm. It implied that the HTP changed reversibly in response to the cis–trans isomerization of the coordinated C8-azoacac ligand.