https://www.selleckchem.com/products/d-galactose.html Interestingly, upon mixing with the platinum(II) probes, polyelectrolytes with bottlebrush architectures have been found to exhibit larger spectroscopic changes than linear polyelectrolytes with the same chemical composition. Combined with the reported theoretical studies on counterion condensation of polyelectrolytes, the platinum(II) complexes are found to function as spectroscopic probes for sensing the charge densities of the polyelectrolytes with different lengths and diverse architectures. Moreover, platinum(II) probes pre-organized in nanostructured aggregates have been found to intercalate into double-stranded DNA, which are naturally occurring biological polyelectrolytes with helical architectures and intercalation sites, to give significant enhancement of spectroscopic changes when compared to the intercalation of monomeric platinum(II) probes into double-stranded DNA.The selective interplay between dimensional morphology transition and signal transfer is an important feature for both nanomaterials and biosystems. While most of those reported examples considered either dimensional transition or signal transfer, the integrated interplay or selectivity for these two aspects in single self-assembled system has been rarely studied. Here, we report that a positively charged chiral π-building block could self-assemble into multidimensional nanostructures, which showed tunable circularly polarized luminescence (CPL). Impressively, when these CPL-active multidimensional structures interacted with two achiral dyes (positively charged ThT and negatively charged CNA), 3D nanocubes and 0D nanospheres showed neither chirality transfer nor energy transfer, while 2D nanoplates could successfully trigger a selective chirality or energy transfer depending on the charge type of acceptor dyes, which then emitted an enhanced CPL signal. This work demonstrated rational design of charged π-building block for the construction