Abstract
We herein report the construction of a novel azo-linked conjugated microporous polymers (Ag@AzoTPE-CMP), which possesses permanent porous structure and Ag+ loading up of 7.62% in the skeleton as effective sorption sites. Ag@AzoTPE-CMP shows considerable adsorption capacity of iodine of 202 wt% in iodine vapor at 350 K. In addition, Ag@AzoTPE-CMP can effectively remove heavy ions from ethanol-water solution.
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Introduction
Conjugated microporous polymers (CMPs) are a unique class of porous organic polymers (POPs), which show a permanent three-dimensional pore structure and extended π-conjugated skeleton. Taking advantage of the large surface areas, microporosity, the large pore volume as well as high thermal and chemical stability, these porous materials are of great important applications in various fields such as gas storage1,2,3, light emitters4,5,6, light-harvesting antennae7,8,9, heterogeneous catalyst10,11,12,13,14, super-capacitive energy storage15,16,17,18, and fluorescent sensors19,20, etc. In all of these applications, the porosity of the CMPs is an essential as a class of functional porous medium. Cooper et al. have done a lot of works in this point, they utilize the designable flexibility of the conjugated networks of CMPs, making it possible to finely tune the porosity of CMPs by varying the strut length and geometry of monomers21,22,23. Recently, researchers have found that CMPs can be used as effective absorbents for safe and long-term capture and storage of iodine, not only because of their high surface areas, but also owing to containing high affinity binding sites for iodine adsorption24,25,26,27,28. In order to enhance the iodine capture ability of CMPs, several strategies have been employed, for example, increasing the surface areas, bearing ionic bond, phenyl ring, and triple-bond, containing enriched π-electron, and introducing heteroatom groups such as N-rich and S-rich groups into the polymers24,25,26,27,28. These novel materials have exhibited a high iodine uptake capacity, such as PAF-24-25 (SBET = 82–262 m2 g−1, 260–276 wt.%)24, HCMP-3 (SBET = 82 m2 g−1, 276 wt.%)25, AzoPPN (SBET = 400 m2 g−1, 290 wt.%)26, SCMP-II (SBET = 120 m2 g−1, 345 wt.%)27, and SCMP-2 (SBET = 855 m2 g−1, 222 wt.%)28.
In the field of iodine adsorption, CMPs has made some impressive progress, but it remains to be developed. It is well-known that the properties of materials were crucially determined by the characters of building units. Azo compounds are one of the most widely used ligands in coordination chemistry29, and have been widely used in optics30 and drug delivery systems31. The obtained azo-porous networks possess outstanding properties: (1) azo-linked porous polymers based on -N=N- bonds are promising iodine adsorbents due to their electron rich pore surface; (2) the surface of CMPs with a lot of polar groups can significantly enhance their iodine binding energy, resulting in enhancement in iodine uptake. In addition, diazo-coupling polymerization of aryl amines with phenols exhibits cost-effective advantages such as cheap catalyst, mild reaction conditions, and high yield used in the polymerization, which are essential for scale-up preparation of porous materials with potential application.
Taking into account the advantages above, herein, a novel azo-linked CMP network was synthesized based on diazo-coupling reaction of 4-(1,2,2-tris(4-aminophenyl) vinyl) aniline (TAVA) and 1,3,5-trihydroxybenzen (TDB), which possessed plenty of polar -OH groups on the surface of the skeleton (AzoTPE-CMP) (Fig. 1). It is well-known that MOFs loaded with metal silver ions have been proven to be an efficient method for developing new iodine adsorption materials32. However, the poor stability of MOFs materials limits their practical applications. In this work, the integration of azo and phenolic -OH gave the ability of the CMP to chelate with metal silver ions, yielding Ag-doped CMP network with Ag+ loading up of 7.62% (Ag@AzoTPE-CMP). Served as absorbents, the Ag+-coordinated CMP exhibits high-speed iodine capture both in vapor and solution, and excellent detection of heavy metal ion. Besides that, the resultant metal silver coordinated CMP showed good stability and recyclability.
Synthesis and Characterization
AzoTPE-CMP network was synthesized by diazo-coupling reaction of 4-(1,2,2-tris(4-aminophenyl) vinyl) aniline (TAVA) and 1,3,5-trihydroxybenzen (TDB). The general synthetic route towards AzoTPE-CMP polymer is shown in Fig, 1. The insoluble polymers were filtered and washed with water, tetrahydrofuran, chloroform and methanol, respectively, in order to remove the inorganic salts, organic monomers, residual catalyst, and oligomers.
The AzoTPE-CMP was extensively characterized using the solid-state cross-polarization magic angle spinning (CP/MAS) 13C NMR, powder X-ray diffraction (PXRD), FT-IR spectroscopy, elemental analysis, scanning electron microscopy (SEM), and thermogravimetric analysis (TGA) (for details, see supporting information). Firstly, the structural integrity of polymers was verified by using CP-MAS 13C NMR (Fig. S1). The broad chemical shifts appeared in the region between 120 and 170 ppm is associated with the aromatic carbon atoms of the framework. The peaks located at 108 ppm, which was attributed to the vinyl carbons of TAVA, also verified the successful synthesis of CMP. The broad featureless PXRD patterns of CMPs indicate that the two polymers have amorphous characters (Fig. S2). The structural integrity of CMPs was further verified using FT-IR analysis (Fig. S3). For AzoTPE-CMP, the bands around 1650 and 1400 cm−1 were attributed to the stretching of C=C and N=N bonds, and the broad peaks around 3430 cm−1 were assigned to the Ar-OH groups, confirmed the successful coupling reaction between the monomers. For Ag@AzoTPE-CMP, a new peak appeared at 1368 cm−1, possibly assigning to the C-O vibration of Ar-OAg, which indicated Ag+ was coordinated with phenolic -OH (Fig. S3). The scanning electron microscopy (SEM) analysis was performed in order to investigate the bulk scale morphology of the CMPs (Fig. 2a,b). From SEM images, we can see that the polymers are composed of irregular spherical solids from nanometers to microns. The two azo-linked CMPs were composed of agglomerated plate-shaped particles with a particle size more than 1 micron. Further analysis of the CMPs by TGA showed that the AzoTPE-CMP network was thermally stable up to 380 °C under N2 atmosphere presumably due to well-spaced charged groups within three-dimensional network. The slight weight loss below 200 °C was mostly associated with the trapped moisture and solvent molecules in the pores (Fig. S4). Compare to AzoTPE-CMP, Ag@AzoTPE-CMP displayed much higher stability, and its value was as high as 500 °C. Through high-resolution transmission electron microscopy (HR-TEM), we can see that Ag particles have been included successfully for Ag@AzoTPE-CMP compared with non-Ag AzoTPE-CMP (Fig. S5). Notably, AzoTPE-CMP and Ag@AzoTPE-CMP polymers showed strong and broad absorption in the UV/Vis adsorption range from 200 to 450 nm (Fig. S6a). Compare to AgNO3/AzoTPE-CMP complex, the Ag@AzoTPE-CMP exhibited a broad absorbance band, also suggesting the coordination between Ag+ and phenolic -OH (Fig. S6a). Then, we investigated the luminescence properties of the two CMPs. The AzoTPE-CMP was non-emissive, and the Ag@AzoTPE-CMP showed the emission band at 402 nm (Fig. S6b).
In addition, X-ray photoelectron spectroscopy (XPS) was performed to explore whether and how the silver coordinated with the porous polymer. Both survey scan and narrow scan (N1s) were performed. C1s (~282.50 ev), O1s (~530.53 ev) and N1s (~400.01 ev) peaks were observed in the XPS spectra of the two samples (Fig. S7). The new peaks at 700–800 eV and 300–400 eV in the O1s XPS spectrum of Ag@AzoTPE-CMP may be assigned to -O-Ag, implying that Ag+ might coordinate with the phenolic -OH, and AgNO3 was not simply physically adsorbed. Moreover, the BE of N1s changed little, implying that -N=N- might not involve coordination with metal ions. Based on the above analysis, it can be deduced that AgNO3 should be chelated with Ar-OH to form Ar-O-Ag moieties during the metallization process.
In order to characterize the porosity parameters of azo-linked CMPs, the nitrogen sorption isotherms were measured at 77 K. As shown in Fig. 2c, AzoTPE-CMP displays a combination of type-I and IV sorption profiles, according to the IUPAC classification. At low relative pressure, a sharp nitrogen gas uptake reflects the microporous nature of the AzoTPE-CMP network. And the nitrogen sorption in the high-pressure region (P/P0 > 0.9) increases with increasing pressure, suggesting a large external surface owing to the loose packing of small particles. The apparent Brunauer-Emmett-Teller (BET) surface areas for the polymers were calculated over the relative pressure range P/P0 = 0.015–0.1, which was found to give a positive value of C in the BET equation. AzoTPE-CMP exhibited the BET surface area of 366 m2 g−1. The total pore volume calculated with nitrogen gas adsorbed at P/P0 = 0.99 was 1.072 cm3 g−1, and the pore size mainly centered at 1.7 nm, as obtained by the nonlocal density functional theory (NLDFT) (Fig. 2d). Compare to AzoTPE-CMP, Ag@AzoTPE-CMP showed the lower BET surface area and the total pore volume were 47 m2 g−1 and 0.110 cm3 g−1, respectively. In addition, the pore size mainly centered at 0.5 nm. These results indicated that the metal silver ions have been loaded into the pores of the CMP skeleton.
Discussion
Iodine capture
The considerable porous characters, nitrogen- and silver-rich nature of AzoTPE-CMP prompted us to assessing their performances for iodine capture. The I2 capture process was conducted at 350 K and ambient pressure, which are typical fuel reprocessing conditions. Due to the sample’s color was deep-black, an apparent color change was not observed with time progressed. Figure 3a shows the weight of the CMPs at various time intervals during the iodine uptake. The iodine capture uptake increased significantly with extended contact time. The results suggested that the mass of iodine uptake increased significantly in the initial 10 h and reached a platform thereafter, implying the system basically is saturated after 36 h. The saturated I2 loading of AzoTPE-CMP and Ag@AzoTPE-CMP were measured to be 108 and 202 wt.%, respectively. The thermogravimetric analysis (TGA) of the I2-loaded CMP samples reveal a significant weight loss from 90 to 300 °C (Fig. 3b), the calculated iodine mass loss were 122 and 194 wt.% for AzoTPE-CMP and Ag@AzoTPE-CMP, respectively, which are close to the saturated adsorption value. The I2 uptake for Ag@AzoTPE-CMP is 1.87-times than that of AzoTPE-CMP, which may be attributed to the coordination interaction of silver ions with iodine molecules. X-ray photoelectron spectroscopy (XPS) of the Ag@AzoTPE-CMP indicated that the coexistence of elemental iodine and triiodide ions, which suggests a hybrid of physisorption and chemisorption (Fig. S8). However, the XPS of AzoTPE-CMP implied that the adsorption of iodine was mainly physisorption. Therefore, Ag@AzoTPE-CMP displayed a higher adsorption iodine value than that of AzoTPE-CMP. Furthermore, the two samples can be efficiently recycled and reused for five cycles without significant loss of iodine uptake (Fig. S9). At the same time, the addition of loading I2 of azo-linked CMP in fresh ethanol could be easily remove the encapsulated iodine from the network. The color of the ethanol solution deepened from colorless to dark brown, which clearly indicates that I2 guests are released from the azo-linked networks (Fig. S10).
In addition, the capability of trapping iodine of the two CMP polymers was also tested in solution at ambient conditions. The two samples (30 mg) were immersed in cyclohexane solution of I2 in a small sealed flask at room temperature. The purple color of the iodine solution gradually changed from dark purple to light purple and finally to paler (Fig. S11). The UV/vis spectroscopy was used to characterize the adsorption kinetic of iodine (Fig. S12). The UV/Vis absorption intensity of the samples was decreased with the prolonged action time. The adsorption kinetics of iodine at 25 °C were presented, as illustrated in Fig. S13. Two stages of adsorption kinetics of the iodine were observed: the adsorption capacity for iodine increased quickly during the first 8 h, and after that a slowly increased iodine uptake until equilibrium. The adsorption performances of the two CMPs can be best fitted by Langmuir pseudo-first-order kinetic models (Fig. S14), which show the correlation coefficient R2 values of 0.9232 and 0.9336 for AzoTPE-CMP and Ag@AzoTPE-CMP, respectively. Finally, the two polymers exhibited the removal efficiencies of up to 99.9% in the iodine solutions with a concentration of 4 mg mL−1, which far exceeded that of functionalized MIL-53-NH2 (60%)33, metalloporphyrin-based NiP-CMP (56%)34. Moreover, the adsorption isotherm is a significant factor in determining the saturated adsorption capacity (Fig. S15). The adsorption plot of equilibrium concentration versus adsorption capacity showed that the two adsorption stages. Firstly, the equilibrium absorption increased linearly with the increase of iodine concentration. Compared with the Freundlich equation, the fitting of Langmuir equation is more in line with the experimental curve, the calculation results suggested that a monolayer adsorption behavior for iodine on the surface of the two samples. The adsorption reached the maximum uptake without relation to the increasing iodine concentration. From the kinetic studies, AzoTPE-CMP and Ag@AzoTPE-CMP represent a high iodine uptake of 1991 and 2598 mg g−1, respectively.
Detection of heavy metal
In recent years, with the rapid development of various industries in the world, the amount of industrial wastewater emissions also showed a sharp upward trend, which makes the water pollution become more and more serious, and the task of wastewater management needs to be carried out urgently. Heavy metal wastewater is considered to be one of the most serious industrial wastes endangering the environment and human health. In this work, the Ag@AzoTPE-CMP was found to be capable of efficiently detecting heavy metal ions (such as Cu2+, Hg2+, Cr3+, Ni2+) (Figs 4a and S16). When the Ag@AzoTPE-CMP was treated in the ethanol-water solutions of corresponding metal salts with different concentrations, which can quenched the fluorescence of the Ag@AzoTPE-CMP. Cu2+, Cr3+, Hg2+, Ni2+ can quench the degree of fluorescence up to 99%, 97%, 96%, and 93%, respectively. Remarkably, as the concentration of Cu2+ decreased to 10−6 and 10−7 M, over 52% of the fluorescence was quenched. Even when the Cu2+ concentration was decreased to 10−9 M, the degree of fluorescence quenching was as high as 35% (Fig. 4b). The Ag@AzoTPE-CMP with such a high sensitivity for reporting Cu2+ outperform other Cu2+ chemo-sensors thus far reported35,36,37,38. Then, we further investigated the scope of ion species that can be sensed (Fig. 4a). Compared to Cu2+ ions, the Ag@AzoTPE-CMP exhibited low sensitivity and torpid response to other metal ions, such as Zn2+, Na+, Ba2+, and Ca2+, etc. These results clearly demonstrate that the Ag@AzoTPE-CMP are responsive to transition metal ions, such as Cu2+, Hg2+, Cr3+, Ni2+ (Fig. 4a). Besides the high sensitive of Ag@AzoTPE-CMP toward Cu2+, the anti-interference ability of the sensor is vitally important. Therefore, the emission spectra of Ag@AzoTPE-CMP dispersed in ethanol-water solutions containing three equal concentrations (10−2 M) of each metal ion (1: Zn2+, Ba2+ and Na+, Fig. 4c; 2: Al3+, Mn2+ and Ca2+, Fig. S17a; 3: La3+, Mg2+, Co2+, Fig. S17b) and subsequent addition of Cu2+ (10−3 M) have been monitored. It is apparent that the effective fluorescence quenching could occur upon adding 10−3 M Cu2+ into the parallel tests (Figs 4c and S17). These results indicate that Ag@AzoTPE-CMP possess outstanding anti-interference ability, sensitivity in the detection of Cu2+ even in the complicated system.
Conclusions
In summary, two azo-linked conjugated microporous polymers have been successfully developed using a facile diazo-coupling reaction. Due to the metal silver effect, the Ag+ loading CMP showed the I2 uptake is 1.87-times than that of AzoTPE-CMP. In addition, Ag@AzoTPE-CMP displays outstanding performance for the detection of heavy ions such as Cu2+, Hg2+, Cr3+, Ni2+. Particularly, compared to other metal cations, Ag@AzoTPE-CMP shows more effective in the detection of Cu2+. These results clearly demonstrated that there is a wealth of opportunity for producing novel absorbent materials with enhanced iodine capture capacity, remove of heavy ions, and expanded the scope of applications.
Synthesis of AzoTPE-CMP
Taking the preparation of AzoTPE-CMP as an example, the diazo-coupling reaction was carried out in two steps. Firstly, 4-(1, 2, 2-tris(4-aminophenyl)vinyl)benzenamine (1.5 mmol) was loaded in a 250 mL flask charged with 100 ml of deionized water, and 0.7 mL of concentrated hydrochloric acid. After stirred for 15 min at 0–5 °C, the mixture was added with 30 mL of aqueous solution of sodium nitrite (3.1 mmol) and stirred for 25 min to make amino groups be completely converted to diazonium salts. Subsequently, the mixture was neutralized with dilute solution of Na2CO3, and then mixed with 30 mL of aqueous solution of m-trihydroxybenzene (2 mmol) and Na2CO3 (3 mmol) at 0–5 °C. After 12 h solid sample was separated from the reaction solution by filtration, and washed by the solvents in the order: water, methanol, and THF, respectively. Followed by freeze drying, polymer sample was obtained in a high (78% yield)39.
Synthesis of Ag@AzoTPE-CMP
Preparation of Ag nanoparticles in AzoTPE-CMP. A piece of AzoTPE-CMP (50 mg) was placed in 20 mL of aqueous solution 1 M NaOH to exchange the protons of -OH groups with Na+. After 3 h the Na+ exchanged AzoTPE-CMP was collected through filtration and washed with H2O. The wet Na+@AzoTPE-CMP was placed in 20 mL of H2O resulting in pH = 10. In that system, 100 mg of AgNO3 were added and allowed to react overnight. The collected monolithic piece was washed extensively with H2O, soaked in ethanol to exchange the H2O, and dried again with supercritical CO2. The final grey-white powder product was collected Ag@AzoTPE-CMP (200 mg)40.
References
Dawson, R., Adams, D. J. & Cooper, A. I. Chemical tuning of CO2 sorption in robust nanoporous organic polymers. Chem. Sci. 2(6), 1173–1177 (2011).
Patel, H. A. et al. High capacity carbon dioxide adsorption by inexpensive covalent organic polymers. J. Mater. Chem. 22, 8431–8437 (2012).
Wang, X. Y., Zhao, Y., Wei, L. L., Zhang, C. & Jiang, J. X. Nitrogen-rich conjugated microporous polymers: impact of building blocks on porosity and gas adsorption. J. Mater. Chem. A 3(42), 21185–21193 (2015).
Xu, Y. H., Chen, L., Guo, Z. Q., Nagai, A. & Jiang, D. L. Light-emitting Conjugated polymers with microporous network architecture: interweaving scaffold promotes electronic conjugation, facilitates exciton migration, and improves luminescence. J. Am. Chem. Soc. 133(44), 17622–17625 (2011).
Wei, Y. B. et al. Solid-state emissive cyanostilbene based conjugated microporous polymers via cost-effective Knoevenagel polycondensation. Polym. Chem. 7(24), 3983–3988 (2016).
Xu, Y. H., Nagai, A. & Jiang, D. L. Core-shell conjugated microporous polymers: a new strategy for exploring color-tunable and controllable light emissions. Chem. Commun. 49(16), 1591–1593 (2013).
Rao, K. V., Haldar, R., Maji, T. K. & George, S. J. Dynamic, conjugated microporous polymers: visible light harvesting via guest-responsive reversible swelling. J. Phys. Chem. Chem. Phys. 18(1), 156–163 (2016).
Yang, L. N. et al. Construction of light-harvesting system for enhanced catalytic performance of Pd nanoframes toward Suzuki coupling reaction. J. Mater. Chem. A 5(21), 10150–10153 (2017).
Chen, L., Honsho, Y., Seki, S. & Jiang, D. L. Light-harvesting conjugated microporous polymers: rapid and highly efficient flow of light energy with a porous polyphenylene framework as antenna. J. Am. Chem. Soc. 132(19), 6742–6748 (2010).
Xiong, J. et al. Formation of cyclic carbonates from CO2 and epoxides catalysed by a cobalt coordinated conjugated microporous polymer. Chem Cat Chem. 9, 2584–2587 (2017).
Cao, Q., Yin, Q., Chen, Q., Dong, Z. B. & Han, B. H. Fluorinated porous conjugated polyporphyrins through direct C−H arylation polycondensation: preparation, porosity, and use as heterogeneous catalysts for baeyer-villiger oxidation. J. Chem. – Eur. 23(41), 9831–9837 (2017).
Bhosale, M. E., Illathvalappil, R., Kurungot, S. & Krishnamoorthy, K. Conjugated porous polymers as precursors for electrocatalysts and storage electrode materials. Chem. Commun. 52(2), 316–318 (2016).
Schwab, M. G. et al. Photocatalytic hydrogen evolution through fully conjugated poly(azomethine) networks. Chem. Commun. 46(47), 8932–8934 (2010).
Zhang, K., Kopetzki, D., Seeberger, P. H., Antonietti, M. & Vilela, F. Surface area control and photocatalytic activity of conjugated microporous poly(benzothiadiazole) networks. Angew. Chem. Int. Ed. 52(5), 1432–1436 (2013).
Kou, Y., Xu, Y. H., Guo, Z. Q. & Jiang, D. L. Supercapacitive energy storage and electric power supply using an aza-fused π-conjugated microporous framework. Angew. Chem. Int. Ed. 50(37), 8753–8757 (2011).
Zhuang, X. D. et al. Two-dimensional sandwich-type, graphene-based conjugated microporous polymers. Angew. Chem. Int. Ed. 52(37), 9668–9672 (2013).
Patra, B. C., Khilari, S., Satyanarayana, L., Pradhan, D. & Bhaumik, A. A new benzimidazole based covalent organic polymer having high energy storage capacity. Chem. Commun. 52(48), 7592–7595 (2016).
Lee, J. S. M. et al. Porosity-engineered carbons for super-capacitive energy storage using conjugated microporous polymer precursors. J. Mater. Chem. A 4(20), 7665–7673 (2016).
Chen, Q. et al. Tetraphenylethylene-based fluorescent porous organic polymers: preparation, gas sorption properties and photoluminescence properties. J. Mater. Chem. 21, 13554–13560 (2011).
Rao, K. V., Mohapatra, S., Maji, T. K. & George, S. J. Guest-responsive reversible swelling and enhanced fluorescence in a super-absorbent, dynamic microporous polymer. J. Chem. – Eur. 18(15), 4505–4509 (2012).
Dawson, R., Cooper, A. I. & Adams, D. J. Nanoporous organic polymer networks. Prog. Polym. Sci. 37(4), 530–563 (2012).
Jiang, J. X., Trewin, A., Adams, D. J. & Cooper, A. I. Band gap engineering in fluorescent conjugated microporous polymers. Chem. Sci. 2(9), 1777–1781 (2011).
Jiang, J. X. et al. Metal-organic conjugated microporous polymers. Angew. Chem. Int. Ed. 50(5), 1072–1075 (2011).
Yan, Z. J., Yuan, Y., Tian, Y. Y., Zhang, D. M. & Zhu, G. S. Highly efficient enrichment of volatile iodine by charged porous aromatic frameworks with three sorption sites. Angew. Chem. Int. Ed. 54(43), 12733–12737 (2015).
Liao, Y. Z., Weber, J., Mills, B. M., Ren, Z. H. & Faul, C. F. J. Highly efficient and reversible iodine capture in hexaphenylbenzene-based conjugated microporous polymers. Macromolecule 49(17), 6322–6333 (2016).
Li, H., Ding, X. S. & Han, B. H. Porous azo-bridged porphyrin–phthalocyanine network with high iodine capture capability. J. Chem. – Eur. 22(33), 11863–11868 (2016).
Ren, F. et al. Novel thiophene-bearing conjugated microporous polymer honeycomb-like porous spheres with ultrahigh iodine uptake. Chem. Commun. 52(63), 9797–9800 (2016).
Qian, X. et al. Capture and reversible storage of volatile iodine by novel conjugated microporous polymers containing thiophene units. ACS Appl. Mater. Interfaces 8(32), 21063–21069 (2016).
Balch, A. L. & Petridis, D. Coordination of palladium by azo and related functional groups. Inorg. Chem. 8(11), 2247–2252 (1969).
Browne, W. R. & Feringa, B. L. Making molecular machines work. Nat. Nanotechnol. 1, 25–35 (2006).
Beharry, A. A. & Woolley, G. A. Azobenzene photoswitches for biomolecules. Chem. Soc. Rev. 40(8), 4422–4437 (2011).
Li, B. et al. Functionalized metal organic frameworks for effective capture of radioactive organic iodides. Faraday Discuss. 201, 47–61 (2017).
Falaise, C. et al. Capture of iodine in highly stable metal–organic frameworks: a systematic study. Chem. Commun. 49(87), 10320–10322 (2013).
Sigen, A. et al. Highly efficient and reversible iodine capture using a metalloporphyrin-based conjugated microporous polymer. Chem. Commun. 50(62), 8495–8498 (2014).
Meng, X. et al. A multifunctional proton-conducting and sensing pillar-layer framework based on [24-MC-6] heterometallic crown clusters. Chem. Commun. 49(76), 8483–8485 (2013).
Liu, B., Wu, W. P., Hou, L. & Wang, Y. Y. Four uncommon nanocage-based Ln-MOFs: highly selective luminescent sensing for Cu2+ ions and selective CO2 capture. Chem. Commun. 50(63), 8731–8734 (2014).
Hao, Z. M. et al. One-dimensional channel-structured Eu-MOF for sensing small organic molecules and Cu2+ ion. J. Mater. Chem. A 1(36), 11043–11050 (2013).
Li, Z. P., Zhang, Y. W., Xia, H., Mu, Y. & Liu, X. M. A robust and luminescent covalent organic framework as a highly sensitive and selective sensor for the detection of Cu2+ ions. Chem. Commun. 52(39), 6613–6616 (2016).
Ji, G. P. et al. Hierarchically mesoporous o-hydroxyazobenzene polymers: synthesis and their applications in CO2 capture and conversion. Angew. Chem. Int. Ed. 55, 9685–9689 (2016).
Katsoulidis, A. P., He, J. Q. & Kanatzidis, M. G. Functional monolithic polymeric organic framework aerogel as reducing and hosting media for ag nanoparticles and application in capturing of iodine vapors. Chem. Mater. 24, 1937–1943 (2012).
Acknowledgements
The financial support of the National Natural Science Foundation of China (Grants no. 21501065), Science and Technology Program of Jilin Province (Grants no. 20160101319JC, 20180520159JH), and Changbai Mountain Scholars Program (Grants no. 2013073) is acknowledged.
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Y. Xu conceived the project, designed experiments and provided funding. M. Liu, C. Yao and C. Liu performed and analyzed experiments. Y. Xu. and M. Liu. wrote the manuscript.
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Liu, M., Yao, C., Liu, C. et al. Ag+ doped into azo-linked conjugated microporous polymer for volatile iodine capture and detection of heavy metal ions. Sci Rep 8, 14072 (2018). https://doi.org/10.1038/s41598-018-32383-5
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DOI: https://doi.org/10.1038/s41598-018-32383-5
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