0000000000307238
AUTHOR
Katherine Chulvi
BODIPY dyes functionalized with 2-(2-dimethylaminophenyl)ethanol moieties as selective OFF–ON fluorescent chemodosimeters for the nerve agent mimics DCNP and DFP
[EN] Two OFF-ON fluorescent chemodosimeters based on a BODIPY core for the detection of nerve agent mimics have been synthesized. Their reactivity towards diethylcyanophosphonate (DCNP) and diisopropylfluorophosphate (DFP) has been tested in organic and aqueous phase. These chemodosimeters selectively detect the nerve agent mimics with good LODs. The chemodosimeters hold their sensing properties on solid supports, allowing the preparation of a hand held sensing kit. The sensing in solid-liquid phase has been demonstrated. The X-ray structure of compound 2 has been resolved.
Structure and Conformational Studies of Aza-Crown 8-Amino-BODIPY Derivatives: Influence of Steric Hindrance on Their Photophysical Properties
Herein, we report the synthesis, X-ray crystal structure and photophysical studies of six new 8-amino-BODIPY derivatives containing crown or azo-crown ether moieties. The influence of steric hindrance, caused by the crown ether, on the planarity of the BODIPY core and its relationship with the fluorescent properties has been established. 1H NMR spectroscopic studies were undertaken to clarify the changes in fluorescence observed in the presence of ZnII.
Halogen-containing BODIPY derivatives for photodynamic therapy
Abstract Two iodinated (1 and 2) and two brominated (3 and 4) BODIPY-based photosensitizers are prepared and characterized using slightly modified synthetic procedures previously described. 1–4 present intense absorption bands in the 510–540 nm interval and very weak emissions due to the presence of halogen atoms in their structure. Irradiation of aqueous solutions of 1–4 with visible light (wavelength > 475 nm) induce the generation of singlet oxygen with quantum yields of ca. 0.62–0.66 for the photosensitizers containing iodine atoms (1 and 2) and of ca. 0.16–0.21 for the brominated counterparts (3 and 4). In vitro studies carried out with HeLa, SCC-13 and HaCaT cell lines and the four ph…
Crystal structure of 4-{2-[4-(dimethylamino)phenyl]diazen-1-yl}-1-methylpyridinium iodide
The molecular geometry of the ionic title compound, C14H17N4+·I−or DAZOP+·I−, is essentially featureless. Regarding the crystal structure, in addition to the obvious cation–anion Coulombic interactions, the packing is mostly directed by non-covalent interactions involving both ring systems, as well as the iodide anion. It consists of cationic molecules aligned along [101] and disposed in an antiparallel fashion while linked into π-bonded dimeric entities by a stacking contact involving symmetry-related phenyl rings, with a centroid–centroid distance of 3.468 (3) Å and a slippage of 0.951 Å. The dimers are, in addition, sustained by a number of C—H...I and I...π (I...centroid = 3.876 Å) inte…
Discrimination of nerve gases mimics and other organophosphorous derivatives in gas phase using a colorimetric probe array.
A colorimetric array for the chromogenic discrimination of organophosphorous derivatives in gas phase has been developed. The array allows us to classify the nerve agent simulants DFP, DCP and DCNP.
Concentration depending fluorescence of 8-(di-(2-picolyl)) aminoBODIPY in solution
[EN] An 8-dipicolylBODIPY derivative has been prepared and its photophysical properties evaluated under different conditions. Two different structures, hemicyanine and cyanine, are observed (depending on the solvent or the solution concentration). The hemicyanine form is not emissive whereas the cyanine form is fluorescent. This behavior is related with the planarity degree of the BODIPY core. The X-ray structure of the compound is reported and it shows that in solid state the hemicyanine form is present. The hemicyanine form seems to be stabilized by aggregation and is the main compound in concentrated solutions whereas the cyanine form is present in diluted solutions that are photochemica…
CCDC 1819378: Experimental Crystal Structure Determination
Related Article: Mónica Gorbe, Ana M. Costero, Félix Sancenón, Ramón Martínez-Máñez, Rafael Ballesteros-Cillero, Luis. E. Ochando, Katherine Chulvi, Raúl Gotor, Salvador Gil|2019|Dyes Pigm.|160|198|doi:10.1016/j.dyepig.2018.08.007
CCDC 1549738: Experimental Crystal Structure Determination
Related Article: Ana M. Costero, María L. Betancourt-Mendiola, Pablo Gaviña, Luis E. Ochando, Salvador Gil, Katherine Chulvi and Eduardo Peña-Cabrera|2017|Eur.J.Org.Chem.|2017|6283|doi:10.1002/ejoc.201701016
CCDC 966420: Experimental Crystal Structure Determination
Related Article: María de Lourdes Betancourt-Mendiola, Eduardo Peña-Cabrera, Salvador Gil, Katherine Chulvi, Luis E. Ochando, Ana M. Costero|2014|Tetrahedron|70|3735|doi:10.1016/j.tet.2014.03.095
CCDC 1549735: Experimental Crystal Structure Determination
Related Article: Ana M. Costero, María L. Betancourt-Mendiola, Pablo Gaviña, Luis E. Ochando, Salvador Gil, Katherine Chulvi and Eduardo Peña-Cabrera|2017|Eur.J.Org.Chem.|2017|6283|doi:10.1002/ejoc.201701016
CCDC 1549736: Experimental Crystal Structure Determination
Related Article: Ana M. Costero, María L. Betancourt-Mendiola, Pablo Gaviña, Luis E. Ochando, Salvador Gil, Katherine Chulvi and Eduardo Peña-Cabrera|2017|Eur.J.Org.Chem.|2017|6283|doi:10.1002/ejoc.201701016
CCDC 1549739: Experimental Crystal Structure Determination
Related Article: Ana M. Costero, María L. Betancourt-Mendiola, Pablo Gaviña, Luis E. Ochando, Salvador Gil, Katherine Chulvi and Eduardo Peña-Cabrera|2017|Eur.J.Org.Chem.|2017|6283|doi:10.1002/ejoc.201701016
CCDC 1819380: Experimental Crystal Structure Determination
Related Article: Mónica Gorbe, Ana M. Costero, Félix Sancenón, Ramón Martínez-Máñez, Rafael Ballesteros-Cillero, Luis. E. Ochando, Katherine Chulvi, Raúl Gotor, Salvador Gil|2019|Dyes Pigm.|160|198|doi:10.1016/j.dyepig.2018.08.007
CCDC 1549737: Experimental Crystal Structure Determination
Related Article: Ana M. Costero, María L. Betancourt-Mendiola, Pablo Gaviña, Luis E. Ochando, Salvador Gil, Katherine Chulvi and Eduardo Peña-Cabrera|2017|Eur.J.Org.Chem.|2017|6283|doi:10.1002/ejoc.201701016
CCDC 982038: Experimental Crystal Structure Determination
Related Article: Raúl Gotor, Pablo Gaviña, Luis E. Ochando, Katherine Chulvi, Alejandro Lorente, Ramón Martínez-Máñez, Ana M. Costero|2014|RSC Advances|4|15975|doi:10.1039/C4RA00710G
CCDC 1819379: Experimental Crystal Structure Determination
Related Article: Mónica Gorbe, Ana M. Costero, Félix Sancenón, Ramón Martínez-Máñez, Rafael Ballesteros-Cillero, Luis. E. Ochando, Katherine Chulvi, Raúl Gotor, Salvador Gil|2019|Dyes Pigm.|160|198|doi:10.1016/j.dyepig.2018.08.007
CCDC 1549734: Experimental Crystal Structure Determination
Related Article: Ana M. Costero, María L. Betancourt-Mendiola, Pablo Gaviña, Luis E. Ochando, Salvador Gil, Katherine Chulvi and Eduardo Peña-Cabrera|2017|Eur.J.Org.Chem.|2017|6283|doi:10.1002/ejoc.201701016
CCDC 1819381: Experimental Crystal Structure Determination
Related Article: Mónica Gorbe, Ana M. Costero, Félix Sancenón, Ramón Martínez-Máñez, Rafael Ballesteros-Cillero, Luis. E. Ochando, Katherine Chulvi, Raúl Gotor, Salvador Gil|2019|Dyes Pigm.|160|198|doi:10.1016/j.dyepig.2018.08.007