BODIPY–BODIPY dyad: assessing the potential as a viscometer for molecular and ionic liquids† †Electronic supplementary information (ESI) available: Details on the synthesis and purification of BODIPY dyes and ILs, sample preparations and physical properties of ILs as well as spectral data. See DOI: 10.1039/c4ra09757b Click here for additional data file.

An unprecedented amplification of near-infrared emission in a Bodipy derived π-system by stress or gelation† †Electronic supplementary information (ESI) available: Experimental details, synthesis procedures and characterization data of the compounds, and additional figures. CCDC 1523313. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/c7sc01696d Click here for additional data file. Click here for additional data file.

A dual-response BODIPY-based fluorescent probe for the discrimination of glutathione from cystein and homocystein† †Electronic supplementary information (ESI) available: Synthesis, spectroscopic properties, NMR and mass spectra. See DOI: 10.1039/c5sc00216h Click here for additional data file.

1. Time dependent spectral changes of BODIPY-S in the presence of thiols. ......S2 2. MS of BODIPY-S with GSH, Cys and Hcy..............................................S3 3. Photophysical spectra of BODIPY 4 and BODIPY-S +Cys..........................S4 4. Time dependent Spectral changes of S-S-BODIPY in the presence of thiols. ...S5 5. NMR and MS of the product of S-S-BODIPY with thiols..........

BODIPY-BODIPY dyad: assessing the potential as a viscometer for molecular and ionic liquids.

A symmetrical BODIPY-BODIPY dyad with a diyne linker was prepared in two steps; the lifetime decay of this rotor appeared to correlate with the viscosity of the media, thus making this dyad a suitable small molecule viscometer for molecular solvents. The potential of using the rotor to probe the viscosity of ionic liquids was also investigated.

Triazolophostins: a library of novel and potent agonists of IP3 receptors† †Electronic supplementary information (ESI) available: Synthetic procedures and spectral data for all new compounds, crystal data for disaccharide 4 and details of the docking study. CCDC 1022279. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/c5ob00440c Click here for additional data file. Click here for additional data file.

Total synthesis of malagashanine: a chloroquine potentiating indole alkaloid with unusual stereochemistry† †Electronic supplementary information (ESI) available: Experimental details and spectral data are provided. CCDC 1489617. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/c6sc03578g Click here for additional data file. Click here for additional data file.