TY - JOUR
T1 - Salicylideneanilines-Based Covalent Organic Frameworks as Chemoselective Molecular Sieves
AU - Ning, Guo Hong
AU - Chen, Zixuan
AU - Gao, Qiang
AU - Tang, Wei
AU - Chen, Zhongxin
AU - Liu, Cuibo
AU - Tian, Bingbing
AU - Li, Xing
AU - Loh, Kian Ping
N1 - Publisher Copyright:
© 2017 American Chemical Society.
PY - 2017/7/5
Y1 - 2017/7/5
N2 - Porous materials such as covalent organic frameworks (COFs) are good candidates for molecular sieves due to the chemical diversity of their building blocks, which allows fine-tuning of their chemical and physical properties by design. Tailored synthesis of inherently functional building blocks can generate framework materials with chemoresponsivity, leading to controllable functionalities such as switchable sorption and separation. Herein, we demonstrate a chemoselective, salicylideneanilines-based COF (SA-COF), which undergoes solvent-triggered tautomeric switching. This is unique compared to solid-state salicylideneanilines' counterpart, which typically requires high energy input such as photo or thermal activation to trigger the enol-keto tautomerisim and cis-trans isomerization. Accompanying the tautomerization, the ionic properties of the COF can be tuned reversibly, thus forming the basis of size-exclusion, selective ionic binding or chemoseparation in SA-COF demonstrated in this work.
AB - Porous materials such as covalent organic frameworks (COFs) are good candidates for molecular sieves due to the chemical diversity of their building blocks, which allows fine-tuning of their chemical and physical properties by design. Tailored synthesis of inherently functional building blocks can generate framework materials with chemoresponsivity, leading to controllable functionalities such as switchable sorption and separation. Herein, we demonstrate a chemoselective, salicylideneanilines-based COF (SA-COF), which undergoes solvent-triggered tautomeric switching. This is unique compared to solid-state salicylideneanilines' counterpart, which typically requires high energy input such as photo or thermal activation to trigger the enol-keto tautomerisim and cis-trans isomerization. Accompanying the tautomerization, the ionic properties of the COF can be tuned reversibly, thus forming the basis of size-exclusion, selective ionic binding or chemoseparation in SA-COF demonstrated in this work.
UR - https://www.scopus.com/pages/publications/85021904273
U2 - 10.1021/jacs.7b02696
DO - 10.1021/jacs.7b02696
M3 - 文章
C2 - 28618776
AN - SCOPUS:85021904273
SN - 0002-7863
VL - 139
SP - 8897
EP - 8904
JO - Journal of the American Chemical Society
JF - Journal of the American Chemical Society
IS - 26
ER -