Abstract

AbstractThe cationic nature of heptamethine cyanines gives them the capacity to form aggregates with salts by electrostatic interactions. In this work, NaCl promoted J‐aggregate formation of aza‐coating heptamethine cyanines is explored. NaCl can induce theN‐benzyloxycarbonylCy‐CO2Bzto assemble into a J‐aggregate having an absorption at 890 nm. Its excellent fluorescence response to NaCl implies that it has great potential for use as a probe for tracing salt stress in plants. Moreover, NaCl also promotes formation of J‐aggregates from the N‐ethyloxycarbonylCy‐CO2Et. The aggregate shows an intense absorption at 910 nm compared to the monomer which absorbs at 766 nm. Its J‐aggregated form can serve as a photothermal agent. And the photothermal conversion efficiency is increased from 29.37 % to 57.59 %. This effort leads to the development of two applications of new cyanine J‐aggregates including one for tracing salt stress of plants and the other for promoting photothermal therapy of tumors.

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