Real-time optical and electronic sensing with a β-amino enone linked, triazine-containing 2D covalent organic framework

被引:127
作者
Kulkarni, Ranjit [1 ,2 ]
Noda, Yu [1 ,2 ]
Barange, Deepak Kumar [2 ]
Kochergin, Yaroslav S. [1 ,2 ,3 ]
Lyu, Pengbo [4 ]
Balcarova, Barbora [2 ]
Nachtigall, Petr [4 ]
Bojdys, Michael J. [1 ,2 ]
机构
[1] Humboldt Univ, Dept Chem, Brook Taylor Str 2, D-12489 Berlin, Germany
[2] CAS, Inst Organ Chem & Biochem, Flemingovo Nam 2, Prague 16610, Czech Republic
[3] Charles Univ Prague, Dept Organ Chem, Hlavova 8, Prague 12840, Czech Republic
[4] Charles Univ Prague, Dept Phys & Macromol Chem, Hlavova 8, Prague 12840, Czech Republic
基金
欧洲研究理事会;
关键词
ADSORPTION; POLYMER;
D O I
10.1038/s41467-019-11264-z
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Fully-aromatic, two-dimensional covalent organic frameworks (2D COFs) are hailed as candidates for electronic and optical devices, yet to-date few applications emerged that make genuine use of their rational, predictive design principles and permanent pore structure. Here, we present a 2D COF made up of chemoresistant beta-amino enone bridges and Lewis-basic triazine moieties that exhibits a dramatic real-time response in the visible spectrum and an increase in bulk conductivity by two orders of magnitude to a chemical trigger - corrosive HCl vapours. The optical and electronic response is fully reversible using a chemical switch (NH3 vapours) or physical triggers (temperature or vacuum). These findings demonstrate a useful application of fully-aromatic 2D COFs as real-time responsive chemosensors and switches.
引用
收藏
页数:8
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