Highly efficient fluorescence resonance energy transfer in co-encapsulated BODIPY nanoparticles

Fluorescence resonance energy transfer (FRET) is a powerful tool used in a wide range of applications due to its high sensitivity and many other advantages. Co-encapsulation of a donor and an acceptor in nanoparticles is a useful strategy to bring the donor-acceptor pair in proximity for FRET. A highly efficient FRET system based on BODIPY-BODIPY (BODIPY: boron-dipyrromethene) donor-acceptor pair in nanoparticles was synthesized. Nanoparticles were formed by co-encapsulating a green emitting BODIPY derivative (FRET donor, lmax = 501 nm) and a red emitting BODIPY derivative (FRET acceptor, lmax = 601 nm) in an amphiphilic polymer using the precipitation method. Fluorescence measurements of encapsulated BODIPY in water following 501 nm excitation caused a 3.6 fold enhancement of the acceptor BODIPY emission at 601 nm indicating efficient energy transfer between the green emitting donor BODIPY and the red emitting BODIPY acceptor with a 100 nm Stokes shift. The calculated FRET efficiency was 96.5%. Encapsulated BODIPY derivatives were highly stable under our experimental conditions.

Origin of photoluminescence of water-soluble CuInS2 quantum dots prepared via a hydrothermal method

The donor–acceptor pair emission is the underlying mechanism of the PL of the hydrothermally-synthesized water-soluble CIS QDs.

The first 2,6-di(1,6-naphthyridin-2-yl)pyridine-based redox photochromic coordination polymer platform with selective vapochromism for trolamine

Design and fabrication of crystalline photoswitable materials play highly crucial roles for the promisingly multidisciplinary applications. Well optimizations of the self-consistent donor-acceptor pair and skillful utilizations of weak intercomponent interactions...

Current-induced thermal tunneling electroluminescence via multiple donor–acceptor-pair recombination

Current-induced thermal tunneling electroluminescence from a highly-compensated ZnO:Ga microrod via multiple donor–acceptor-pair radiative recombination.

A molecular model for reversible and irreversible hygroscopicity changes by thermal wood modification

Heat treatment (HT) is a well-known means to reduce the equilibrium wood moisture content (EMC) at a specified relative humidity (RH). EMC is profoundly decreased by the loss of accessible hydroxyl groups (OHacc) in the wood matrix by thermochemical reactions. However, the obtained EMC reduction after HT can be partly reversible, depending on the ability of the wood matrix polymers to fully mechanically relax during HT. We discuss the results of our earlier experimental study on the OHacc content and the associated EMC decrease at 93% RH by a relaxation inhibiting dry-HT vs. a relaxation enabling wet-HT. New experimental results, showing that OHacc does not significantly change during reversible EMC changes, are added to the discussion. This study quantitatively supports a molecular explanation of the reversible EMC, in which wood moisture is principally bound at sorption sites, composed of two functional groups, constituting a hydrogen-donor/acceptor pair, involving at least one OHacc group. The irreversible part of EMC reduction is assigned to the thermochemical removal of OHacc from the wood matrix. The reversible part is attributed to a process of wood polymer conformal rearrangements, bringing an isolated OHacc group in proximity of another free hydrogen-bonding functional group, creating a site for water sorption.