Alginic Acid Beads Containing Fluorescent Solvatochromic Dyes Display an Emission Color Response to a Cationic Surfactant.

Lipophilic fluorescent dyes can be employed as sensors for surfactants present in concentrations above the critical micellar concentration (CMC) where the dyes are monodispersed in micelles. However, the surfactant concentration range over which these dyes are effective is narrowed because by the sigmoidal nature of their responses. To overcome this limitation, we developed a novel sensor material comprised of a labeled fluorescent solvatochromic dye covalently bonded to alginate gel, which is known to strongly adsorb cationic surfactants.

A BODIPY-Based Fluorogenic Probe for Specific Imaging of Lipid Droplets.

We developed an easily accessible boron-dipyrromethene (BODIPY)-based fluorogenic probe, which we named LD-TB. This probe emits bright fluorescence in oil; when compared with aqueous solution, a significant enhancement of fluorescence brightness is observed. Cellular experiments confirmed that the probe stains the lipid droplets (LDs) specifically in both live and fixed cells, providing background-free images.

A Straightforward Substitution Strategy to Tune BODIPY Dyes Spanning the Near-Infrared Region via Suzuki⁻Miyaura Cross-Coupling.

In this study, a series of new red and near-infrared (NIR) dyes derived from 4,4-difluoro-4-bora-3a,4a-diaza-s-indacene (BODIPY) were developed by introducing thiophene and its derivatives to the 3- and 5- positions of the dichloroBODIPY core. For the first time, cyclictriol boronates and N-methyliminodiacetic acid (MIDA) boronate were used as organoboron species to couple with 3,5-dichloroBODIPY via the one-step Suzuki⁻Miyaura cross-coupling. Six kinds of thieno-expended BODIPY dyes were synthesized in acceptable yields ranging from 31% to 79%.