ABSTRACT
A bisindole-bridged-porphyrin tweezer (1), a pair of zinc porphyrins (PZn's) connected to bisindole bridge (BB) via the Cu(I)-mediated alkyne-azide click chemistry, exhibited unique switching in forward and backward photoinduced energy transfer by specific guest bindings. The addition of Cu(2+) caused a change in electronic absorption and fluorescence quenching of 1. MALDI-TOF-MS and FT-IR analyses indicated the formation of stable coordination complex between 1 and Cu(2+) (1-Cu(II)). Without Cu(2+) coordination, the excitation energy flows from BB to PZn's with significantly high energy transfer efficiency. In contrast, the direction of energy flow in 1 was completely reversed by the coordination of Cu(2+). The difference in fluorescence quantum yield between 1 and 1-Cu(II) indicates that more than 95% of excitation energy of PZn flows into Cu(II)-coordinated BB. The energy transfer efficiency was further controlled by bidentate ligand coordination onto 1-Cu(II). When pyrophosphate ion was added to 1-Cu(II), the recovery of fluorescence emission from PZn was observed. The quantum mechanical calculations indicated that the Cu(II)-coordinated BB has square planar geometry, which can be distorted to form octahedral geometry due to the coordination of bidentate ligands.
ABSTRACT
A zinc porphyrin-based receptor containing four triazole groups at the ortho-position of each phenyl group (1) was utilized as a useful probe for the determination of contaminants in acetonitrile (MeCN). Through the simple observation of the absorption spectrum of 1 in MeCN, the cyanide contamination concentration could be directly determined.
ABSTRACT
A new type of fluorescent probe (1) with two triazole groups that are conjugated with a carbazole moiety was synthesized by a Cu(I)-catalyzed alkyne-azide click reaction for the selective and sensitive detection of cyanide via fluorescence enhancement by ligand exchange and metal ion removal.
