Franck-Condon factors and radiative lifetime of the A2Π(1/2)-X2Σ+ transition of ytterbium monofluoride, YbF

The fluorescence spectrum resulting from laser excitation of the A(2)Π(1/2)←X(2)Σ(+) (0,0) band of ytterbium monofluoride, YbF, has been recorded and analyzed to determine the Franck-Condon factors. The measured values are compared with those predicted from Rydberg-Klein-Rees (RKR) potential energy curves. From the fluorescence decay curve the radiative lifetime of the A(2)Π(1/2) state is measured to be 28 ± 2 ns, and the corresponding transition dipole moment is 4.39 ± 0.16 D. The implications for laser cooling YbF are discussed.     

Defocus image contrast in hexagonally-ordered mesoporous material

A transmission electron microscope was used to characterize a powder form of hexagonally-ordered mesoporous silica material. The structural symmetry built into this amorphous material allowed one to obtain three characteristic images, i.e. a hexagonal honey-comb structure and wide/narrow parallel lines. These images were found to originate primarily from phase contrast, which changed sensitively with defocusing. To further understand the contrast behaviour of these images, an analytical form of the defocus contrast theory was developed and applied to the simulation of the characteristic wide/narrow parallel line images. The simulation was found to be in good qualitative agreement with experiments, where changes in focus conditions and specimen thickness were predicted to alter the contrast in the resulting parallel-line type images.     

Ultrafast excitation transfer and charge stabilization in a newly assembled photosynthetic antenna-reaction center mimic composed of boron dipyrrin, zinc porphyrin and fullerene

A self-assembled supramolecular triad as a model to mimic the light-induced events of the photosynthetic antenna-reaction center, that is, ultrafast excitation transfer followed by electron transfer ultimately generating a long-lived charge-separated state, has been accomplished. Boron dipyrrin (BDP), zinc porphyrin (ZnP) and fullerene (C(60)), respectively, constitute the energy donor, electron donor and electron acceptor segments of the antenna-reaction center imitation. Unlike in the previous models, the BDP entity was placed between the electron donor, ZnP and electron acceptor, C(60) entities. For the construction, benzo-18-crown-6 functionalized BDP was synthesized and subsequently reacted with 3,4-dihydroxyphenyl functionalized ZnP through the central boron atom to form the crown-BDP-ZnP dyad. Next, an alkyl ammonium functionalized fullerene was used to self-assemble the crown ether entity of the dyad via ion-dipole interactions. The newly formed supramolecular triad was fully characterized by spectroscopic, computational and electrochemical methods. Steady-state fluorescence and excitation studies revealed the occurrence of energy transfer upon selective excitation of the BDP in the dyad. Further studies involving the pump-probe technique revealed excitation transfer from the (1)BDP* to ZnP to occur in about 7 ps, much faster than that reported for other systems in this series of triads, as a consequence of shorter distance between the entities. Upon forming the supramolecular triad by self-assembling fullerene, the (1)ZnP(*) produced by direct excitation or by energy transfer mechanism resulted in an initial electron transfer to the BDP entity. The charge recombination resulted in the population of the triplet excited state of C(60), from where additional electron transfer occurred to produce C(60)(?-):crown-BDP-ZnP(?+) ion pair as the final charge-separated species. Nanosecond transient absorption studies revealed the lifetime of the charge-separated state to be ~100 μs, the longest ever reported for this type of antenna-reaction center mimics, indicating better charge stabilization as a result of the different disposition of the entities of the supramolecular triad.     

Dilute Solution Properties of Styrene-N-Butyl Methacrylate (65:35) Copolymer: Short- and Long-Range Interaction of the Polymer Chain

Abstract

Viscosity and light-scattering data on styrene-n-butyl methacrylate (65:35) in chloroform are presented and tested by the two-parameter theoretical relations. The short-range interactions K and A and the long-range interaction parameter B have been calculated by different equations, using intrinsic viscosity and second virial coefficient data. These are then compared to the values of the homopolymer polystyrene. The conformation or the steric factor for the polymer chain has also been calculated. The excluded volume parameter Z, which is related to both the short- and long-range parameters, has been evaluated along with the expansion factor α _n . The higher value of the short-range parameters and the conformation factor compared to the parent styrene homopolymer is attributed to the effect of unlike monomer interactions causing extension of the polymer chain. An increase in the restriction of the internal rotation of side chains about the C-C bonds is also suggested. The excess interaction parameter has a negative value. The expansion factor α _n has been related to the excluded volume factor Z and the coefficient C is in close agreement with the theoretically calculated value of Yamakawa and Tanaka.     

Spectroscopic characterization of aqueous microdroplets containing inorganic salts

We have developed and studied methods to characterize the time-varying composition of liquid microdroplets, under controlled changes to environmental conditions, using Raman tweezers. This work has focussed on measurements of inorganic salts, such as nitrate and sulfate anions, which comprise a major fraction of the dissolved solutes in atmospheric aerosols. The experimental Raman intensities for the anions of inorganic salts in optically tweezed droplets were found to be in good agreement with theoretical estimates of photon scattering. The detection limit for sodium nitrate salt in a single particle was found to be ~4 pg. The mass of an inorganic salt in the droplet can be estimated from the Raman intensity of the anion bands using a calibration curve which is independent of droplet volume. The volume of the droplet, and concentration of solute, can be found directly from the spacing of morphology dependent resonances in the Raman band of water, or indirectly from the integrated-intensity of the Raman band for the solvent. The later strategy eliminates the uncertainty in the collection efficiency of Raman-scattered light related to varying particle sizes.     

Exploring Nucleobase Modifications in Oligonucleotide Analogues for Use as Environmentally Responsive Fluorophores and Beyond

Over the past two decades, it has become abundantly clear that nucleic acid biochemistry, especially with respect to RNA, is more convoluted and complex than previously appreciated. Indeed, the application and exploitation of nucleic acids beyond their predestined role as the medium for storage and transmission of genetic information to the treatment and study of diseases has been achieved. In other areas of endeavor, utilization of nucleic acids as a probe molecule requires that they possess a reporter group. The reporter group of choice is often a luminophore because fluorescence spectroscopy has emerged as an indispensable tool to probe the structural and functional properties of modified nucleic acids. The scope of this review spans research done in the Hudson lab at The University of Western Ontario and is focused on modified pyrimidine nucleobases and their applications as environmentally sensitive fluorophores, base discriminating fluorophores, and in service of antisense applications as well as tantalizing new results as G-quadruplex destabilizing agents. While this review is a focused personal account, particularly influential work of colleagues in the chemistry community will be highlighted. The intention is not to make a comprehensive review, citations to the existing excellent reviews are given, any omission of the wonderful and impactful work being done by others globally is not intentional. Thus, this review will briefly introduce the context of our work, summarize what has been accomplished and finish with the prospects of future developments.     

Photoinitiated Energy Transfer in Porous-Cage-Stabilised Silver Nanoparticles

We report a new composite material consisting of silver nanoparticles decorated with three-dimensional molecular organic cages based on light-absorbing porphyrins. The porphyrin cages serve to both stabilize the particles and allow diffusion and trapping of small molecules close to the metallic surface. Combining these two photoactive components results in a Fano-resonant interaction between the porphyrin Soret band and the nanoparticle-localised surface-plasmon resonance. Time-resolved spectroscopy revealed the silver nanoparticles transfer up to 37 % of their excited-state energy to the stabilising layer of porphyrin cages. These unusual photophysics cause a 2-fold current increase in photoelectrochemical water-splitting measurements. The composite structure provides a compelling proof of concept for advanced photosensitiser systems with intrinsic porosity for photocatalytic and sensing applications.