Naphtho[b]-fused BODIPYs: one pot Suzuki–Miyaura–Knoevenagel synthesis and photophysical properties,Chemical Communications

当前位置： X-MOL 学术 › Chem. Commun. › 论文详情

Our official English website, www.x-mol.net, welcomes your feedback! (Note: you will need to create a separate account there.)

Naphtho[b]-fused BODIPYs: one pot Suzuki–Miyaura–Knoevenagel synthesis and photophysical properties
Chemical Communications ( IF 4.3 ) Pub Date : 2017-05-25 00:00:00 , DOI: 10.1039/c7cc02918g
Zhikuan Zhou _{1,

2,

3,

4,

5} , Jianping Zhou _{1,

2,

3,

4} , Lizhi Gai _{4,

5,

6,

7,

8} , Aihua Yuan _{1,

2,

3,

4} , Zhen Shen _{4,

5,

6,

7,

8}

Affiliation

Naphtho[b]-fused BODIPYs have been facilely synthesized via Suzuki–Miyaura–Knoevenagel reaction between mono-iodo-BODIPY or 2,6-diiodo-BODIPY with (2-formylphenyl)boronic acid. This one-pot reaction represents a very straightforward approach for tuning the absorption and emission of BODIPYs in the red visible/NIR range.

中文翻译：

萘并[ b ]融合的BODIPYs：一锅铃木-宫浦-Knoevenagel的合成和光物理性质

萘并[ b ]稠合的BODIPYs是通过单碘-BODIPY或2,6-二碘-BODIPY与（2-甲酰基苯基）硼酸之间的Suzuki-Miyaura-Knoevenagel反应轻松合成的。这种一锅法反应代表了一种非常简单的方法，可用于在红色可见光/ NIR范围内调节BODIPY的吸收和发射。

更新日期：2017-06-17

点击分享查看原文

点击收藏

阅读更多本刊新发论文本刊介绍/投稿指南