A magnetic fluorescence molecularly imprinted polymer sensor with selectivity for dibutyl phthalate via Mn doped ZnS quantum dots

Molecularly imprinted polymers with Mn-doped ZnS quantum dots were prepared using dibutyl phthalate as the template molecule, 3-aminopropyltriethoxysilane as the functional monomer and the tetraethoxysilane as the cross-linker.

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RETRACTED: Simple and sensitive molecularly imprinted polymer-MPA capped Mn-doped ZnS quantum dots-based phosphorescence probe for cyanotoxins determination in algae metabolites

Chemical Physics Letters ◽

10.1016/j.cplett.2019.136750 ◽

2019 ◽

Vol 735 ◽

pp. 136750

Author(s):

Cheng Li ◽

Yun Wang ◽

Juan Han ◽

Liang Ni

Keyword(s):

Quantum Dots ◽

Molecularly Imprinted Polymer ◽

Imprinted Polymer ◽

Molecularly Imprinted ◽

Phosphorescence Probe ◽

Mn Doped

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Recent developments in molecularly imprinted polymer nanofibers and their applications

Analytical Methods ◽

10.1039/c5ay01609f ◽

2015 ◽

Vol 7 (18) ◽

pp. 7406-7415 ◽

Cited By ~ 16

Author(s):

Shabi Abbas Zaidi

Keyword(s):

Molecularly Imprinted Polymer ◽

Molecularly Imprinted Polymers ◽

Imprinted Polymer ◽

Polymer Nanofibers ◽

Molecularly Imprinted ◽

Imprinted Polymers ◽

Recent Developments ◽

Analyte Detection

Molecularly imprinted polymers (MIPs) have been potential and versatile candidates for analyte detection.

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Simple and Sensitive Molecularly Imprinted Polymer – Mn-Doped ZnS Quantum Dots Based Fluorescence Probe for Cocaine and Metabolites Determination in Urine

Analytical Chemistry ◽

10.1021/acs.analchem.5b04250 ◽

2016 ◽

Vol 88 (5) ◽

pp. 2734-2741 ◽

Cited By ~ 42

Author(s):

María Pilar Chantada-Vázquez ◽

Juan Sánchez-González ◽

Elena Peña-Vázquez ◽

María Jesús Tabernero ◽

Ana María Bermejo ◽

...

Keyword(s):

Quantum Dots ◽

Molecularly Imprinted Polymer ◽

Fluorescence Probe ◽

Imprinted Polymer ◽

Molecularly Imprinted ◽

Mn Doped

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Application of ratiometric fluorescence sensor-based microwave-assisted synthesized CdTe quantum dots and mesoporous structured epitope-imprinted polymers for highly efficient determination of tyrosine phosphopeptide

Analytical Methods ◽

10.1039/c9ay00276f ◽

2020 ◽

Vol 12 (1) ◽

pp. 63-72 ◽

Cited By ~ 5

Author(s):

Nasibeh Saeedzadeh Amiri ◽

Mohammad-Reza Milani Hosseini

Keyword(s):

Quantum Dots ◽

Molecularly Imprinted Polymer ◽

Ratiometric Fluorescence ◽

Imprinted Polymer ◽

Molecularly Imprinted ◽

Imprinted Polymers ◽

Microwave Assisted ◽

Silica Materials ◽

Fluorescence Methods

Molecularly imprinted polymer coated quantum dot sensor modified with ratiometric fluorescence methods and mesoporous structured epitope imprinted silica materials (QDs@SiO2@EMSiO2) have been fabricated for detection of tyrosine phosphopeptide.

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Reusable molecularly imprinted polymeric nanospheres for diclofenac removal from water samples

Journal of Chemical Research ◽

10.1177/1747519820925998 ◽

2020 ◽

pp. 174751982092599

Author(s):

Noha Amaly ◽

Georges Istamboulie ◽

Ahmed Y El-Moghazy ◽

Thierry Noguer

Keyword(s):

Molecularly Imprinted Polymer ◽

Molecularly Imprinted Polymers ◽

Water Samples ◽

Imprinted Polymer ◽

Molecularly Imprinted ◽

Imprinted Polymers ◽

Residue Removal ◽

Pharmaceutical Pollutants ◽

Polymer Nanospheres ◽

Average Size

The preparation of efficient molecularly imprinted polymers materials (MIPs) for pharmaceutical residue removal is still a challenging task. Herein, we design uniformly molecularly imprinted polymer nanospheres via a precipitation polymerization method using methacrylic acid (MAA) as functional monomer and N,N-methylenebis(acrylamide) (MBAA) as a crosslinker for removal of diclofenac (DFC) as a model for pharmaceutical pollutants. Nanospheres with average size 200 nm were prepared with MAA:MBAA at a ratio of 1:7 and acetonitrile/toluene (1:1) as a porogenic solvent. The successful synthesis is evidenced by Fourier transform infrared spectroscopy, scanning electron microscopy, and with a particle size analyzer. The rebinding experiments confirmed that the more introduction of the carboxyl groups from MAA could remarkably improve the imprinting effect with a significantly increased imprinting factor and specific rebinding capacity reached 450 mg/g after 15 min. Furthermore, the adsorption capacity of the molecularly imprinted polymers is maintained above 85% after seven regeneration cycles, indicating that the molecularly imprinted polymers can be used multiple times. Moreover, the developed molecularly imprinted polymers show promising DFC removal efficiency from real water samples, which suggests that the prepared molecularly imprinted polymer nanospheres are promising in DFC separation.

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Molecularly Imprinted Polymer and Computational Study of (E)-4-(2- cyano-3-(dimethylamino)acryloyl)benzoic Acid from Poly(ethylene terephthalate) Plastic Waste

Current Analytical Chemistry ◽

10.2174/1573411015666190131123843 ◽

2020 ◽

Vol 16 (2) ◽

pp. 119-137 ◽

Cited By ~ 1

Author(s):

Asmaa M. Fahim ◽

Bartłomiej Wasiniak ◽

Jerzy P. Łukaszewicz

Keyword(s):

Benzoic Acid ◽

Molecularly Imprinted Polymer ◽

Molecularly Imprinted Polymers ◽

Ethylene Terephthalate ◽

Computational Study ◽

Imprinted Polymer ◽

Molecularly Imprinted ◽

Imprinted Polymers ◽

Poly Ethylene Terephthalate ◽

Poly Ethylene

Background: Molecularly imprinted polymers (MIPs) are utilized in the separation of a pure compound from complex matrices. A stable template-monomer complex generates MIPs with the highest affinity and selectivity for the template. In this investigation, degradation of Poly(ethylene terephthalate) PET afforded the (E)-4-(2-cyano-3-(dimethylamino) acryloyl) benzoic acid (4) (TAM) which used TAM as template which interacts with Methacrylic Acid (MAA) monomer, in the presence of CH3CN as progen. The TAM-MMA complex interactions are dependent on stable hydrogen bonding interaction between the carboxylic acid group of TAM and the hydroxyl group of MMA with minimal interference of porogen CH3CN. The DFT/B3LYP/6-31+G model chemistry was used to optimize their structures and frequency calculations. The binding energies between TAM with different monomers showed the most stable molar ratio of 1:4 which was confirmed through experimental analysis. Methods: The present work describes the synthesis of (E)-4-(2-cyano-3-(dimethylamino) acryloyl) benzoic acid (4) (TAM) from PET waste and formation of molecularly imprinted polymer from TAM with the methacrylic acid monomer. The optimization of molecular imprinted was stimulated via DFT/B3LYP/6-31G (d). The imprinted polymer film was characterized via thermal analysis, pore size, FT-IR and scanning electron microscopy. Results: The most stable molecularly imprinted polymers (MIPs) showed binding energy of TAM(MMA4)=-2063.456 KJ/mol with a small value of mesopores (10-100 Å). Also, the sorption capability of TAM-MIPs showed 6.57 mg/g using STP-MIP-9VC. Moreover, the average pore size ranged between 0.2-1 nm with the BET surface about 300 m2/g. Conclusion: The proposed TAM exhibited a high degree of selectivity for MMA in comparison with other different monomers through hydrogen bond interaction, which was thermally stable, good reproducibility and excellent regeneration capacity and elucidated in the computational study and analytical analysis.

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Synthesis and Evaluation of a Molecularly Imprinted Polymer Selective to 2,4,6-Trichlorophenol

Australian Journal of Chemistry ◽

10.1071/ch04004 ◽

2004 ◽

Vol 57 (8) ◽

pp. 759 ◽

Cited By ~ 34

Author(s):

Lachlan Schwarz ◽

Clovia I. Holdsworth ◽

Adam McCluskey ◽

Michael C. Bowyer

Keyword(s):

Molecularly Imprinted Polymer ◽

Molecularly Imprinted Polymers ◽

Competitive Binding ◽

Imprinted Polymer ◽

Binding Studies ◽

Molecularly Imprinted ◽

Imprinted Polymers ◽

Target Molecule ◽

High Preference ◽

Structural Analogues

Molecularly imprinted polymers (MIPs) selective for the phenolic contaminant 2,4,6-trichlorophenol (2,4,6-TCP) were prepared and evaluated in three porogens of differing character (hexane, acetonitrile, dichloromethane). Rebinding of 2,4,6-TCP was found to be most effective in dichloromethane (imprinting factor: 13.2). Competitive binding studies performed against a range of close structural analogues showed a high preference for the target molecule, although partial recognition towards 2,4-dichlorophenol was also observed. Specificity was found to be dependent upon the presence of ring chlorine on the target, which suggested that these atoms participate in secondary binding interactions that are essential for successful recognition in the polymer cavity.

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