The structural nature of the phonon sidebands in the fluorescence and excitation spectra of pentacene guests in p‐terphenyl crystals at 4.2 K are investigated using site‐selective spectroscopy. The distinct features in the phonon sideband structure were observed to depend significantly on the guest site configuration of pentacene occupying four inequivalent sites in the triclinic p‐terphenyl lattice. The sharp peaks dominating the phonon sideband structure are assumed to arise from the pseudolocal phonons. The eigenvalues and eigenvectors of the pseudolocal phonons are calculated carrying out a modified normal mode analysis on the distinct pentacene site configurations including the contribution of all intermolecular atom‐pair interactions.

Here in this contribution, blue and red luminescent 1-dodecanethiol (DT) terminated gold nanoclusters (AuNC) were prepared by a simple two-step synthesis route where the first step involved the surfactant-free synthesis of bare AuNC in N,N′-dimethylformamide (DMF) and the second step is the termination of the as-prepared bare AuNC by 1-dodecanethiol. The blue and red luminescent DT-terminated AuNC were isolated by a solvent-induced precipitation followed by an ultra-centrifugation technique. Both the bare AuNC and the blue and red luminescent DT-terminated AuNC exhibit stable photoluminescence and good solubility in various solvents. The photo-physical, electronic, structural, and morphological properties of the bare AuNC and the blue and red luminescent DT-terminated AuNC were examined by performing UV-Vis absorption spectroscopy, stationary and time-resolved PL spectroscopy, X-ray photoelectron spectroscopy (XPS), femtosecond transient absorption spectroscopy, Fourier-transform infrared spectroscopy (FTIR-ATR), and high-resolution transmission electron microscopy (HRTEM) experiments.