Environmental effects on electron spin relaxation in N@C60

We examine environmental effects of surrounding nuclear spins on the electron spin relaxation of the N@C60 molecule (which consists of a nitrogen atom at the centre of a fullerene cage). Using dilute solutions of N@C60 in regular and deuterated toluene, we observe and model the effect of translational diffusion of nuclear spins of the solvent molecules on the N@C60 electron spin relaxation times. We also study spin relaxation in frozen solutions of N@C60 in CS2, to which small quantities of a glassing agent, S2Cl2 are added. At low temperatures, spin relaxation is caused by spectral diffusion of surrounding nuclear 35Cl and 37Cl spins in the S2Cl2, but nevertheless, at 20 K, T2 times as long as 0.23 ms are observed.Comment: 7 pages, 6 figure

Sucrose Monoester Micelles Size Determined by Fluorescence Correlation Spectroscopy (FCS)

One of the several uses of sucrose detergents, as well as other micelle forming detergents, is the solubilization of different membrane proteins. Accurate knowledge of the micelle properties, including size and shape, are needed to optimize the surfactant conditions for protein purification and membrane characterization. We synthesized sucrose esters having different numbers of methylene subunits on the substituent to correlate the number of methylene groups with the size of the corresponding micelles. We used Fluorescence Correlation Spectroscopy (FCS) and two photon excitation to determine the translational D of the micelles and calculate their corresponding hydrodynamic radius, Rh. As a fluorescent probe we used LAURDAN (6-dodecanoyl-2-dimethylaminonaphthalene), a dye highly fluorescent when integrated in the micelle and non-fluorescent in aqueous media. We found a linear correlation between the size of the tail and the hydrodynamic radius of the micelle for the series of detergents measured

Polymerization-Induced Self-Assembly of Block Copolymer Nano-objects via RAFT Aqueous Dispersion Polymerization

In this Perspective, we discuss the recent development of polymerization-induced self-assembly mediated by reversible addition–fragmentation chain transfer (RAFT) aqueous dispersion polymerization. This approach has quickly become a powerful and versatile technique for the synthesis of a wide range of bespoke organic diblock copolymer nano-objects of controllable size, morphology, and surface functionality. Given its potential scalability, such environmentally-friendly formulations are expected to offer many potential applications, such as novel Pickering emulsifiers, efficient microencapsulation vehicles, and sterilizable thermo-responsive hydrogels for the cost-effective long-term storage of mammalian cells

Unique diffusion behavior observed in supercritical ethanol

We have systematically investigated the diffusion behavior of silica nanoparticles within supercritical ethanol, in terms of solvent properties by varying temperature (T) and pressure (P), to elucidate how the inhomogeneous solvent structures and density fluctuations in the solvent affect the diffusion behavior of solute particles. Results show that at a constant pressure, the diffusion coefficient (D) of the particles increases with increasing temperature, reaches the maximum (D^[max]) within the gaslike supercritical fluid (slightly below the ridge), and finally decreases abruptly at very low fluid density when temperature is increased further. Results reveal that D is appreciably larger than the theoretical prediction (Einstein-Stokes relationship) in the vicinity of the critical density (ρc) of the solvent. We interestingly observed that D becomes maximum (D^[max]) at a particular thermodynamic condition (Ti,Pi), which is expressed by the empirical formula T_[ri]=P^[0.16]_[ri] (for Tri>1, Pri>1). Here, Tri=Ti/Tc and P_[ri]=Pi/Pc; Tc and Pc are the temperature and the pressure at critical point, respectively. Results further reveal that D^[max] increases significantly with decreasing solvent density within the gaslike supercritical fluid where the changes in viscosities are negligible. These findings are unique, novel, and intriguing. We suggest that the enhancement of the diffusion coefficient in the vicinity of the critical density and the abrupt decrease in the diffusion coefficient in very low density gaslike fluid are associated with the change in the solvent-solvent and solute-solvent direct correlation function (related to the effective interaction potential) upon density change when the fluid crosses the ridge of density fluctuations and within the gaslike fluid