TY - JOUR
T1 - Supramolecularly imprinted polymeric solid phase microextraction coatings for synergetic recognition nitrophenols and bisphenol A
AU - Liu, Yuanchen
AU - Liu, Yujian
AU - Liu, Zhimin
AU - Du, Fuyou
AU - Qin, Guiping
AU - Li, Gongke
AU - Hu, Xianzhi
AU - Xu, Zhigang
AU - CAI, Zongwei
N1 - Funding Information:
This work was supported by grants from the National Natural Science Foundation of China ( 21565018 ) and Guangxi Key Laboratory of Electrochemical and Magneto-chemical Functional Materials (No. EMFM20182204 ). The corresponding author thanks all his co-workers who have contributed to this research in the past and Kunming University of Science and Technology for technical support. Here, the corresponding author thanks the Professor Wenwen Qu of Kunming University of Science and Technology for her help and support.
PY - 2019/4/15
Y1 - 2019/4/15
N2 - We herein firstly presented supramolecularly imprinted polymeric (SMIP) solid phase microextraction (SPME) coatings which showed synergetic recognition for nitrophenols and bisphenol A. A series of β-cyclodextrins (β-CD) with different substituents were successfully designed and synthesized. It was employed as supramolecular functional monomers for SMIPs. The orderly assembling structures settled down under the molecular imprinting process. The four of SMIPs solid phase microextraction coatings showed good selectivity for the template and could be used to extract 4-NP in real water samples. Furthermore, the inclusion effects of derived β-CDs with the 4-NP were investigated by measuring the UV–vis spectra and the theoretical calculations. The strongest intermolecular force is come from the supramolecular complex of 4-NP and β-CD-4 which shows the strongest UV–vis spectra absorption value. Meanwhile, the difference of the theoretical calculations value coming from the system of derived β-CDs and 4-NP is the largest, revealing the strongest electronic interactions between derived β-CD-4 and 4-NP. Therefore, these polymers possess inclusion interactions from β-cyclodextrin cavities and hydrogen-bonding interactions from molecular imprinting. Multiple adsorptions triggered off a synergetic recognition for target analytes. The SMIPs also performed highly selective recognition in complex real water sample with sensitive detection limits.
AB - We herein firstly presented supramolecularly imprinted polymeric (SMIP) solid phase microextraction (SPME) coatings which showed synergetic recognition for nitrophenols and bisphenol A. A series of β-cyclodextrins (β-CD) with different substituents were successfully designed and synthesized. It was employed as supramolecular functional monomers for SMIPs. The orderly assembling structures settled down under the molecular imprinting process. The four of SMIPs solid phase microextraction coatings showed good selectivity for the template and could be used to extract 4-NP in real water samples. Furthermore, the inclusion effects of derived β-CDs with the 4-NP were investigated by measuring the UV–vis spectra and the theoretical calculations. The strongest intermolecular force is come from the supramolecular complex of 4-NP and β-CD-4 which shows the strongest UV–vis spectra absorption value. Meanwhile, the difference of the theoretical calculations value coming from the system of derived β-CDs and 4-NP is the largest, revealing the strongest electronic interactions between derived β-CD-4 and 4-NP. Therefore, these polymers possess inclusion interactions from β-cyclodextrin cavities and hydrogen-bonding interactions from molecular imprinting. Multiple adsorptions triggered off a synergetic recognition for target analytes. The SMIPs also performed highly selective recognition in complex real water sample with sensitive detection limits.
KW - Imprinted polymer
KW - Molecular imprinting
KW - Multiple interactions
KW - Supramolecularly
KW - Synergetic recognition
KW - β-Cyclodextrin
UR - http://www.scopus.com/inward/record.url?scp=85060346582&partnerID=8YFLogxK
U2 - 10.1016/j.jhazmat.2019.01.039
DO - 10.1016/j.jhazmat.2019.01.039
M3 - Journal article
C2 - 30685724
AN - SCOPUS:85060346582
SN - 0304-3894
VL - 368
SP - 358
EP - 364
JO - Journal of Hazardous Materials
JF - Journal of Hazardous Materials
ER -