A convenient
method to prepare luminescently thermotropic liquid
crystalline (TLC) with chiral centers is established by combining
cationic Gemini surfactants, C
n
H2n+1(CH3)2N+(CH2)2N+(CH3)2C
n
H2n+1·Br2 (n–2–n·2Br, n = 10, 12, 14, and 16, respectively) and guanosine 5′-monophosphate
disodium salt (GMP). Under thermally annealing, the complexes of surfactant-GMP
(n-GMP) self-assemble into TLCs with circularly polarized
luminescence (CPL) performance, except for 10-GMP. The phase structure
and CPL handedness in TLCs can be regulated by changing the alkyl
chain length of n–2–n·2Br. Columnar tetragonal (Colt) mesophase of 12-GMP
exhibits right-handed CPL (R-CPL) emission, while
chiral smectic C (SmC*) phases containing 14- or 16-GMP display left-handed
CPL (L-CPL) emission. The introduction of K+ or Sr2+ triggers n-GMP to be G-quadruplexes
with identical chirality and luminescence, and further regulates the
phase structure and CPL property. TLCs can be transformed to be columnar
rectangular (Colr) or Colt phases with R-CPL emission. We find that the mesogenic units feature
the same chiral moiety can realize R- and L-CPL emitting, and prepare the tunable CPL-active LCs through
natural biomolecules. These results deepen our understanding of chiral
luminescence mesogens and G-quadruplex structures, providing the new
insight for the fabrication of nondoped LC materials with CPL performance.