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We report the first real-time imaging of individualized boron nitride nanotubes (BNNTs) via stabilization with a rhodamine surfactant and fluorescence microscopy. We study the rotational and translational diffusion and find them to agree with predictions based on a confined, high-aspect-ratio rigid rod undergoing Brownian motion. We find that the behavior of BNNTs parallels that of individualized carbon nanotubes (CNTs), indicating that BNNTs could also be used as model rigid rods to study soft matter systems, while avoiding the experimental disadvantages of CNTs due to their strong light absorption. The use and further development of our technique and findings will accelerate the application of BNNTs from material engineering to biological studies.

Boron dipyrromethene (BODIPY) molecular rotors have shown sensitivity toward viscosity, polarity, and temperature. Here, we report a 1,3,5,7-tetramethyl-8-phenyl-BODIPY modified with a polyethylene glycol (PEG) chain, for temperature sensing and live cell imaging. This new PEG-BODIPY dye presents an increase in nonradiative decay as temperature increases, which directly influences its lifetime. This change in lifetime is dependent on changes in both temperature and viscosity at low viscosity values, but is only dependent on temperature at high viscosity values. The dependence of fluorescence lifetime with temperature allows for temperature monitoring in vitro and in cells, with sub degree resolution. When in contact with cells, the PEG-BODIPY spontaneously penetrates and stains the cell but not the nucleus. Furthermore, no significant cell toxicity was found even at 100 μM concentration. Using fluorescence lifetime imaging microscopy (FLIM), we were able to observe the changes in the lifetime of PEG-BODIPY within the cell at different temperatures. The use of FLIM and molecular probes such as PEG-BODIPY can provide important information about cellular temperature and heat dissipation upon medically relevant stimuli, such as radiofrequency ablation and photodynamic therapy.

Spin-lattice relaxation times, T(1), have been measured from 200-340 K for the protons in H(2) and HD molecules dissolved in toluene-d(8) and incarcerated in C(60). It is found that HD relaxes more slowly than H(2) in both environments and at all temperatures, as expected from the smaller values of the spin-rotation and dipole-dipole coupling in HD compared to H(2). More detailed analysis using models developed to describe relaxation in both condensed media and the gas phase indicates that transitions among the rotational states of H(2) occur at a rate similar to those of HD in both toluene-d(8) solution and in C(60), in contrast to the situation in gas phase collisions between hydrogen and He or Ar, where the lifetimes of rotational states of HD are markedly shorter than those for H(2). Measurements of the relative (1)H chemical shifts of H(2) and HD, the coupling constant J(HD), and the widths of the HD peaks at various temperatures revealed only small effects with insufficient accuracy to warrant more detailed interpretation.