Description:
<jats:title>Abstract</jats:title><jats:p>Enantiomerically and diastereomerically pure bis‐chelated imine‐alkoxytitanium complexes <jats:bold>6</jats:bold> and <jats:bold>7</jats:bold> have been synthesized and used as chiral dopants for converting nematic into cholesteric phases. The dopants were tested in mainly commercially available nematic liquid crystalline compounds or mixtures: LC1 (BASF), ZLI‐1695 and ZLI‐1840 (Merck), as well as <jats:italic>N</jats:italic>‐(4‐methoxybenzylidene)‐4′‐butylaniline (MBBA). The values of the helical twisting power (HTP) were determined by the Grandjean–Cano method. Exceptionally high helical twisting powers were obtained. Thus, the titanium complex <jats:bold>6 h</jats:bold> displayed a HTP value of 740 μm<jats:sup>−1</jats:sup> in MBBA, the highest HTP value reported. The helical twisting power has been found to depend strongly on the structure of the nematic phase and the substitution pattern of the chiral ligand in the titanium complexes <jats:bold>6</jats:bold> and <jats:bold>7</jats:bold>. Crystal structure analysis of <jats:bold>6 f</jats:bold> confirmed the <jats:italic>A</jats:italic>,<jats:italic>R</jats:italic>,<jats:italic>R</jats:italic> configuration of the metal complex. The chiral imine ligands <jats:bold>4</jats:bold> and <jats:bold>5</jats:bold> were derived from the regioisomeric amino alcohols <jats:bold>1</jats:bold> and <jats:bold>2</jats:bold>.</jats:p>