RESUMEN
A new efficient method was proposed for the synthesis of (18-crown-6)stilbene; the structure of the product was confirmed by X-ray diffraction analysis. In MeCN, this compound forms pseudodimeric complexes with N-(2-ammonioethyl)-4-styrylpyridinium and N-(3-ammoniopropyl)-4-styrylpyridinium diperchlorates via hydrogen bonding between the ammonium group and the crown ether oxygen atoms. The ammonioethyl derivative was synthesized for the first time. The stability constants and spectral characteristics of the complexes were measured by spectrophotometric and fluorescence titration. Photoirradiation of the pseudodimeric complex of (18-crown-6)stilbene with the ammoniopropyl dye resulted in the stereospecific [2 + 2] cross-photocycloaddition reaction. The replacement of the stilbene moiety in the crown compound by a styrylpyridine moiety led to a 5-fold increase in the quantum yield of the photoprocess. The most probable cause for this effect is the presence of photoinduced electron transfer in (18-crown-6)stilbene complexes. This assumption is confirmed by fluorescence lifetime spectroscopy and density functional theory calculations.
RESUMEN
The exciton peak in the excitation-emission matrix (EEM) of colloidal quantum dots implicitly contains information about inhomogeneous broadening and the photoluminescence (PL) and photoluminescence excitation (PLE) spectra of individual particles in the vicinity of the absorption onset. A numerical procedure for extracting this information has been developed and applied to the EEMs of polydisperse InP/ZnS core/shell colloidal quantum dots and their supernatant solutions obtained by partial precipitation with a non-solvent. The inhomogeneous broadenings obtained in this way have been converted by the sizing curve into particle-size distributions. These distributions have been found to be in agreement with the size-selective precipitation theory proposed recently. The homogeneous PL and PLE line shapes obtained by analyzing the EEMs were found to satisfy the Kennard-Stepanov relation, which is the first more or less direct evidence of its validity for colloidal quantum dots.