This study demonstrates how temperature and concentration affect photophysical properties in DNA-stabilized silver nanoclusters, indicating dynamic equilibria with Ag+-carrying DNA strands.
DNA-stabilized silver nanoclusters (DNA-AgNCs) are versatile emitters whose photophysical properties are defined by the DNA template. In this study, we explore the unusual temperature- and concentration-dependent behavior of two NIR-emissive DNA-AgNCs: one stabilized by two 16-base DNA oligomers (16mer), and another embedded within a 3-base shortened version of these strands (13mer). Using a combination of optical spectroscopy and mass spectrometry, we show that Ag+-carrying DNA strands can reversibly attach to DNA-AgNCs and fine-tune their photophysical properties. For 13mer-AgNC, we demonstrate the presence of three different species, (13mer)2-[Ag20]10+, (13mer)3-[Ag27]17+, and (13mer)4-[Ag34]24+, depending on concentration and temperature. For the AgNC stabilized by two 16-base DNA strands, (16mer)2-[Ag20]10+, emission wavelength and intensity vary with temperature, although no significant concentration-dependent spectral shifts are observed. While mass-spectrometry revealed the existence of (16mer)3-[Ag27]17+, time-resolved anisotropy uncovered the formation of aggregates of (16mer)2-[Ag20]10+. These findings demonstrate the presence of dynamic equilibria between Ag+-carrying DNA strands and DNA-AgNCs.
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Cerretani et al. (2025) studied this question.
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