具有较强近红外光致变色活性的螺旋烯型 β-isoindigo 硼基二吡咯烷类似物

IF 13.9 Q1 CHEMISTRY, MULTIDISCIPLINARY
Ziwei Chen, Zhigang Ni, Xing-Yu Chen, Yongqiang Xu, Chunyan Yu, SiSi Wang, Xiao-Ye Wang, Hua Lu
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引用次数: 0

摘要

由于同时实现手性和近红外吸收/发射具有挑战性,因此对近红外(NIR)光电响应的探索较少。在此,我们介绍了基于硼-二吡咯并二酮(BODIPY)的杂杂环烯型 β-isoindigo 类似物(β-IBs)的设计,它能将吸收峰转移到 800 纳米,并产生显著的科顿效应(127.8 M-1 cm-1)和吸光度不对称因子(|gabs| = 3.5 × 10-3)。在 800 纳米以外,发光不对称因子(glum)和圆偏振发光(CPL)亮度(BCPL)分别高达 1.24 × 10-3 和 1.78 M-1 cm-1。这些 β-IB 是首例在近红外区域具有最高 gabs 值且 CPL 超过 800 纳米的螺旋型化合物。理论计算证明,其强大的自旋活动是由其较大的过渡磁偶极矩引发的。这项研究不仅为合成更多种类的前所未有的螺旋型 BODIPY 类似物提供了新方法,而且还展示了卓越的近红外弦光特性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Helicene-type β-isoindigo-based boron-dipyrromethene analogs with strong near-infrared chiroptical activity

Helicene-type β-isoindigo-based boron-dipyrromethene analogs with strong near-infrared chiroptical activity

Helicene-type β-isoindigo-based boron-dipyrromethene analogs with strong near-infrared chiroptical activity

Near-infrared (NIR) chiroptical response has been less explored because it is challenging to achieve both chirality and NIR absorption/emission. Herein, we describe the design of heterohelicene-type β-isoindigo-based boron-dipyrromethene (BODIPY) analogs (β-IBs), which shift the absorption peak to 800 nm and produce significant Cotton effects (127.8 M−1 cm−1) and absorbance dissymmetry factors (|gabs| = 3.5 × 10−3). The luminescence dissymmetry factor (glum) and circularly polarized luminescence (CPL) brightness (BCPL) of up to 1.24 × 10−3 and 1.78 M−1 cm−1 were realized beyond 800 nm. These β-IBs are the first examples of helicene-type compounds with the highest gabs in the NIR region and CPL beyond 800 nm. Theoretical calculations demonstrate that the strong chiroptical activities are triggered by their large transition magnetic dipole moments. This study not only provides a new approach to the synthesis of a larger variety of unprecedented helicene-type BODIPY analogs but also demonstrates excellent NIR chiroptical properties.

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来源期刊
CiteScore
17.40
自引率
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