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.
Sensing and discrimination of cyanide and hydrogen sulfide using an 8-alkenyl-4,4-difluoro-4-bora-3a,4a-diaza-s-indacene derivative
8-(2-Phenylethenyl)BODIPY has been shown to be an appropriate chromo-fluorogenic probe for cyanide in H2O. Good selectivity and LOD values below the allowed cyanide concentration in drinking water were attained. Cyanide can be discriminated from hydrogen sulphide by an oxidation process with hydrogen peroxide.
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 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 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 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