Synthesis,characterization, and photoresponsive studies on lignin functionalized with (E)‐2‐(4‐(naphthalen‐1‐yldiazenyl)phenyl)acetic acid

A chromophoric system (E)‐2‐(4‐(naphthalen‐1‐yldiazenyl)phenyl)acetic acid incorporated onto a nature friendly biopolymeric core material, lignin (technical lignin, lignin sulphonic acid M.W. 52,400), and the photo responsive behavior of the product was investigated. The product was characterized by UV–visible, fluorescence, Fourier transform infrared, and nuclear magnetic resonance spectroscopic methods. The results of the studies show that the incorporation of the chromophoric system on to the lignin core enhanced the light absorption and light stabilization properties of the chromophoric system. The trans‐cis photoisomerization and the reverse cis‐trans thermal conversions were also assisted by the lignin core. The remarkable stability on irradiation shows that this is a novel photoresponsive system with excellent light fastening properties which would find application in coating materials, dyes, paints, inks, and many more. Copyright © 2012 John Wiley & Sons, Ltd.     

A modular phase transfer and ligand exchange protocol for quantum dots

In this paper, we describe a quantum dot (qdot) phase transfer protocol using ligand exchange and the amino acid histidine. The phase transfer from nonpolar solvents to aqueous buffers is homogeneous, and no appreciable precipitation occurs. The molecule histidine was chosen in order to first displace the organic encapsulation and second to provide a weakly chemisorbing intermediate at the qdot ionic interface. This allows the histidine to act as an intermediate shell upon which further direct ligand exchange can occur. Since this intermediate encapsulation is easily displaced by an assortment of different molecules while in aqueous buffers, we refer to this approach as modular. Characterization via FTIR and NMR revealed the extent of ligand exchange, and provides insights into the interfacial binding mechanism. The colloidal stability and photostability of the qdots was probed via UV-vis and steady state fluorescence, which revealed promising quantum yield stability of greater than 1 year. The qdots have hydrodynamic diameters of <12 nm and surface charges dependent upon ligand type and coverage. The modularity of this approach is shown by tailoring the qdot surface charge via sequential ligand exchange using mixed monolayers of carboxylic acid and poly(ethylene glycol)-terminated thiols.     

Z-scan studies and optical limiting of nanosecond laser pulses in neutral red dye

The nonlinear optical absorption, refraction and optical limiting behaviour of an organic dye, neutral red, were investigated under excitation with nanosecond laser pulses at 532 nm. The nonlinear optical responses of the material were studied both in solution and solid film, made in methanol and polyvinyl alcohol, respectively, using single-beam Z-scan technique. The open aperture Z-scans of the solution samples displayed a switch over from saturable absorption to enhanced absorption with increase in input intensity. Theoretical fit to the experimental data indicated that the dominant mechanism of nonlinear absorption is two-photon absorption. The closed aperture Z-scans of both the samples denoted positive nonlinearity, which was three orders larger in magnitude in solid film, compared with that in solution. The results of optical limiting experiments revealed that neutral red exhibited strong optical limiting of nanosecond laser pulses with a threshold lower than that of C₆₀ in toluene.     

Propagation of surface plasmon polaritons in anisotropic MIM and IMI structures

Electromagnetic wave propagation through waveguide structures consisting of anisotropic dielectric layers, assisted by surface plasmon-polaritons (SPPs) is theoretically studied. Dispersion relations corresponding to both short range and long range coupled SPP modes in metal/insulator/metal (MIM) and insulator/metal/insulator (IMI) structures, taking into consideration the anisotropy of the insulator, are derived and numerically solved. The dispersion has a prominent dependence on the anisotropy of the dielectric environment. The dependence of propagation on the misalignments of the optic axes of the insulator has also been investigated.     

Optical investigation of dynamics of phenomena of laser-based lithotripsy

Using time-resolved high-speed shadowgraphy, the dynamics of phenomena due to laser-based lithotripsy is studied. Collapsing mechanism of bubble formed therein is investigated. In order to study the mechanism, the optically implemented mathematical morphology is applied. The study of the shape of the plasma and the collapsing region of the bubble of fluid that we are studying can possibly be used for practical application for laser-based lithotripsy.     

Single-Molecule Two-Color Coincidence Detection of Unlabeled alpha-Synuclein Aggregates

Protein misfolding and aggregation into oligomeric and fibrillar structures is a common feature of many neurogenerative disorders. Single-molecule techniques have enabled characterization of these lowly abundant, highly heterogeneous protein aggregates, previously inaccessible using ensemble averaging techniques. However, they usually rely on the use of recombinantly-expressed labeled protein, or on the addition of amyloid stains that are not protein-specific. To circumvent these challenges, we have made use of a high affinity antibody labeled with orthogonal fluorophores combined with fast-flow microfluidics and single-molecule confocal microscopy to specifically detect α-synuclein, the protein associated with Parkinson's disease. We used this approach to determine the number and size of α-synuclein aggregates down to picomolar concentrations in biologically relevant samples.     

The mechanism of thermal elimination of urea and thiourea derivatives. Part 1. Rate data for pyrolysis of N-acetylurea,N-acetylthiourea,N,N -diacetylthiourea,and N-acetylthiobenzamide

Rates of thermal decomposition of N-acetylurea (1), N-acetylthiourea (2), N,N′-diacetylthiourea (3), and N-acetylthiobenzamide (4) have been measured over a 45 K range for each compound. The molecules were found to undergo unimolecular first-order elimination reactions for which log A = 11.9, 11.6, 11.8, and 13.4 s^-1, and E_a = 181.2, 135.9, 128.3, and 130.3 kJ mol^-1, respectively. The reactivities of these compounds have been compared with those of amide derivatives and with each other. Product analysis together with the kinetic data were used to outline feasible pathways for the elimination reactions of the compounds under study. © 1996 John Wiley & Sons, Inc.