Fluorescence Excitation and Dispersed Fluorescence Spectra of the 1-Hydronaphthyl Radical (1-CH) in Solid -Hydrogen.

Matrix isolation spectroscopy with -hydrogen (-H) has previously been employed to record IR absorption spectra of hydrogenated and protonated polycyclic aromatic hydrocarbons (PAHs), prospective carriers of unidentified infrared and diffuse interstellar bands. Despite the promising prospects of -H as matrix host, especially the rather weak interaction with the guest molecules and the resulting small matrix shifts, -H matrix isolation spectroscopy has rarely been applied to study electronic transitions of guest molecules. Here, we present the dispersed fluorescence and fluorescence excitation spectrum of the 1-hydronaphthyl radical (1-CH) isolated in solid -H.

IR-VUV spectroscopy of pyridine dimers, trimers and pyridine-ammonia complexes in a supersonic jet.

The infrared spectra of the C-H stretching vibrations of (pyridine)m, m = 1-3, and the N-H stretching vibrations of (pyridine)m-(NH3)n, m = 1, 2; n = 1-4, complexes were investigated by infrared (IR)-vacuum ultraviolet (VUV) spectroscopy under jet-cooled conditions. The ionization potential (IP0) of the pyridine monomer was determined to be 74 546 cm-1 (9.242 eV), while its complexes showed only smooth curves of the ionization thresholds at ∼9 eV, indicating large structural changes in the ionic form.

Strong Hydrogen Bonding with Inorganic Pendant Polyhedral Oligomeric Silsesquioxane Nanoparticles Provides High Glass Transition Temperature Poly(methyl methacrylate) Copolymers.

We report a series of poly(methyl methacrylate) (PMMA) copolymers containing small amounts of methacrylamide (MAAM) and pendant polyhedral oligomeric silsesquioxane (POSS) methyl acrylate (MAPOSS) segments. The hydrogen bonding interactions of the MAAM monomer units and the inorganic POSS nanoparticle units improved the thermal and mechanical properties of the PMMA copolymers. For example, PMMA copolymerization with 5 wt% PMAAM and 5 wt% PMAPOSS monomers could enhance the glass transition temperature to 142°C, with higher modulus, higher water contact angle, and reasonably high transparency.

Ternary polybenzoxazine/POSS/SWCNT hybrid nanocomposites stabilized through supramolecular interactions.

In this study we linked zero-dimensional polyhedral oligomeric silsesquioxane (POSS) with one-dimensional single-walled carbon nanotubes (SWCNTs) as dual-dimensional nanohybrid complexes within polybenzoxazine matrices, stabilized through noncovalent supramolecular interactions. First, we synthesized a new bifunctionalized benzoxazine (Py-Bz-T), presenting thymine (T) and pyrene (Py) units, that displayed excellent thermal properties after thermal curing, because its T moieties increased the physical cross-linking density. Second, we prepared Py-Bz-T/OBA-POSS [octuply adenine (A)-functionalized POSS] nanocomposites and investigated, using nuclear magnetic resonance and Fourier transform infrared spectroscopies, the multiple hydrogen bonding AT interactions between Py-Bz-T and OBA-POSS.

Symmetry forbidden vibronic spectra and internal conversion in benzene.

The spectra of symmetry-forbidden transitions and internal conversion were investigated in the present work. Temperature dependence was taken into account for the spectra simulation. The vibronic coupling, essential in the two processes, was calculated based on the Herzberg-Teller theory within the Born-Oppenheimer approximation.