Article ID Journal Published Year Pages File Type
175689 Dyes and Pigments 2015 5 Pages PDF
Abstract

•The naphthalene-fused BODIPY exhibits significant bathochromic shifts.•The BODIPY dye exhibits an enlarged Stokes shift of 56 nm in CHCl3.•The BODIPY dye can be used to image living cells.

A new fluorescent dye of 4,4-Difluoro-4-bora-3a,4a-diaza-s-indacene (BODIPY) was prepared by fusing naphthalene unit to the zig–zag edge of BODIPY core by oxidization with iron (III) chloride. The naphthalene-fused BODIPY exhibits significant bathochromic shifts in both absorption and fluorescence spectrum compared with the non-fused BODIPY. In addition, the dye emits strong saturated-red fluorescence with a quantum yield of 55% and an enlarged Stokes of 56 nm in CHCl3 due to the formation of dimers and the desymmetrization of the molecule, which can be used to image living cells by fluorescence microscopy. Cell imaging experiments demonstrated its potential application as a probe in bioorganisms due to its excellent imaging effect and large Stokes shift.

Graphical abstractFigure optionsDownload full-size imageDownload as PowerPoint slide

Related Topics
Physical Sciences and Engineering Chemical Engineering Chemical Engineering (General)
Authors
, , , , , ,