Effects of auxiliary ligands of Pd(II) dimers on induction of chiral nematic phases: chirality inversion and the photo-responsive structural change

Tamura, K; Yoshida, J; Taniguchi, M; Kitazawa, T; Yamagishi, A; Sato, H

HERO ID

2902256

Reference Type

Journal Article

Year

2015

Language

English

PMID

25594884

HERO ID 2902256
In Press No
Year 2015
Title Effects of auxiliary ligands of Pd(II) dimers on induction of chiral nematic phases: chirality inversion and the photo-responsive structural change
Authors Tamura, K; Yoshida, J; Taniguchi, M; Kitazawa, T; Yamagishi, A; Sato, H
Journal Dalton Transactions (Online)
Volume 44
Issue 7
Page Numbers 3209-3215
Abstract Dinuclear square planar palladium(ii) complexes, [{Pd(ii)La}2(baet)] (La(-) = β-diketonato and baet(2-) = 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.
Doi 10.1039/c4dt02812k
Pmid 25594884
Is Certified Translation No
Dupe Override No
Is Public Yes
Language Text English