Reported here is an efficient recognition of K+ by 15-crown-5 functionalized gold nanoparticles in aqueous matrix containing physiologically important cations, such as Li+, Cs+, NH4+, Mg2+, Ca2+, and excess amount of Na+. Upon exposure to K+, the colloidal solution changes from red to blue, in response to surface plasmon absorption of dispersed and aggregated nanoparticles. The concentration ranges of K+ detected in this study are 0.099-0.48 mM and 7.6 microM-0.14 mM, when concentrations of colloidal gold are 54.9 and 7.1 nM, respectively. Recognition of K+ and formation of the aggregates are proposed via a sandwich complex of 2:1 between 15-crown-5 moiety and K+. Also discussed is the possibility of a preorganized structure of 15-crown-5 at the water-organic interface for the efficient complexation with K+.

Colorimetry, one of the central themes in contemporary chemistry, generally relies on spectrometers to quantify specimens of interest. Developed herein is a rapid screening scheme to determine whether the amount of an analyte falls into a diagnostic concentration range by the naked eye. This is particularly important for applications under circumstances where instruments are not readily available. The aforementioned goal is demonstrated by utilizing copper-thiol chemistry as a model system in which polymerization occurs within a certain range of copper-to-cysteine mole ratios; hence, the targeted range of copper concentration is tunable by adjusting the amount of cysteine. Within and outside the range, the solutions appear cloudy and homogeneous, respectively. The reaction mechanism is proposed and scrutinized. The detection scheme is applied successfully on samples of human serum (15.7-23.6 μM) and pond water (<3.0 ppm or 47 μM) with a handy laser pointer.