Thieno-pyrrole-fused BODIPY intermediate as a platform to multifunctional NIR agents.
Ontology highlight
ABSTRACT: We report the synthesis, photophysical and electrochemical properties, and in vivo fluorescence imaging of a series of new thieno-pyrrole-fused near-infrared (NIR) BODIPY agents by using a versatile intermediate as a building block. The versatile thieno-pyrrole-fused BODIPY intermediate was rationally designed to bear bromo-substituents and absorb in the mid-red region (635 nm) to act as an organic electrophile for the development of NIR multifunctional agents. The use of subsequent palladium-catalyzed and nucleophilic substitution reactions afforded highly conjugated NIR BODIPYs. The novel BODIPYs exhibit long-wavelength absorptions in the NIR region (650-840 nm). The agents produce sharp fluorescence bands, and most of them display respectable quantum yields of fluorescence (0.05-0.87) u
SUBMITTER: Awuah SG
PROVIDER: S-EPMC7323977 | biostudies-literature | 2013 Dec
REPOSITORIES: biostudies-literature
ACCESS DATA