研究生: |
Chi Van Nguye Chi Van Nguyen |
---|---|
論文名稱: |
合成金屬有機框架與衍生奈米結構材料應用於檢測與觸媒催化 Synthesis of Metal-Organic Frameworks (MOFs) and MOF-Derived Nanostructured materials for catalysis and sensing application |
指導教授: |
江偉宏
Wei-Hung Chiang |
口試委員: |
江志強
Jiang Jyh Chiang Toyoko Imae Toyoko Imae 吳紀聖 Jeffrey Chi-Sheng Wu 游文岳 Wen-Yueh Yu |
學位類別: |
博士 Doctor |
系所名稱: |
工程學院 - 化學工程系 Department of Chemical Engineering |
論文出版年: | 2019 |
畢業學年度: | 107 |
語文別: | 英文 |
論文頁數: | 164 |
中文關鍵詞: | Metal-Organic Frameworks (MOFs) 、Catalysis application 、Sensing application 、MOF-derived nanostructured materials |
外文關鍵詞: | Metal-Organic Frameworks (MOFs), Catalysis application, Sensing application, MOF-derived nanostructured materials |
相關次數: | 點閱:356 下載:0 |
分享至: |
查詢本校圖書館目錄 查詢臺灣博碩士論文知識加值系統 勘誤回報 |
1. Kitagawa, S.; Kitaura, R.; Noro, S.-i., Functional Porous Coordination Polymers. Angew. Chem. Int. Ed. 2004, 43, 2334-2375.
2. Zhou, H.-C.; Long, J. R.; Yaghi, O. M., Introduction to Metal-Organic Frameworks. Chem. Rev. 2012, 112, 673-674.
3. Fe´rey, G. r., Hybrid porous solids: past, present, future. Chem. Soc. Rev. 2008, 37, 191-214.
4. Xuan, W.; Zhu, C.; Liu, Y.; Cui, Y., Mesoporous metal–organic framework materials. Chem. Soc. Rev. 2012, 41, 1677-1695.
5. Kreno, L. E.; Leong, K.; Farha, O. K.; Allendorf, M.; Duyne, R. P. V.; Hupp, J. T., Metal-Organic Framework Materials as Chemical Sensors. Chem. Rev. 2012, 112, 1105-1125.
6. IV, J. J. P.; Perman, J. A.; Zaworotko, M. J., Design and synthesis of metal–organic frameworks using metal–organic polyhedra as supermolecular building blocksw. Chem. Soc. Rev. 2009, 38, 1400-1417.
7. Tranchemontagne, D. J.; S, J. L. M.-C.; O’Keeffe, M.; Yaghi, O. M., Secondary building units, nets and bonding in the chemistry of metal–organic frameworksw. Chem. Soc. Rev. 2009, 38, 1257-1283.
8. Lu, W.; Wei, Z.; Gu, Z.-Y.; Liu, T.-F.; Park, J.; Park, J.; Tian, J.; Zhang, M.; Zhang, Q.; III, T. G.; Boscha, M.; Zhou, H.-C., Tuning the structure and function of metal–organic frameworks via linker design. Chem. Soc. Rev. 2014, 43, 5561-5593.
9. Eddaoudi, M.; Moler, D. B.; Li, H.; Chen, B.; Reineke, T. M.; O’Keeffe, M.; Yaghi, O. M., Modular Chemistry: Secondary Building Units as a Basis for the Design of Highly Porous and Robust Metal-Organic Carboxylate Frameworks. Acc. Chem. Res. 2001, 34, 319-330.
10. Stock, N.; Biswas, S., Synthesis of Metal-Organic Frameworks (MOFs): Routes to Various MOF Topologies, Morphologies, and Composites. Chem. Rev. 2012, 112, 933-969.
11. Mueller, U.; Schubert, M.; Teich, F.; Puetter, H.; Schierle-Arndt, K.; Pastre, J., Metal–organic frameworks—prospective industrial applications. J. Mater. Chem. 2006, 16, 626-636.
12. METAL-ORGANIC FRAMEWORKS: Design and Application. John Wiley & Sons, Inc.: Canada, 2010; p 313.
13. Huang, Y.-Q.; Ding, B.; Song, H.-B.; Zhao, B.; Ren, P.; Cheng, P.; Wang, H.-G.; Liao, D.-Z.; Yan, S.-P., A novel 3D porous metal–organic framework based on trinuclear cadmium clusters as a promising luminescent material exhibiting tunable emissions between UV and visible wavelengths. Chem. Commun. 2006, 4906-4908.
14. Wang, C.-C.; Li, J.-R.; Lv, X.-L.; Zhangc, Y.-Q.; Guo, G., Photocatalytic organic pollutants degradation in metal–organic frameworks. Energy Environ. Sci. 2014, 7, 2831-2867.
15. Allendorf, M. D.; Bauer, C. A.; Bhakta, R. K.; Houka, R. J. T., Luminescent metal–organic frameworks. Chem. Soc. Rev. 2009, 38, 1330-1352.
16. Ahmed, I.; Jhung, S. H., Composites of metal–organic frameworks: Preparation and application in adsorption. Mater. Today 2014, 17, 136-146.
17. Wang, B.; Xie, L.-H.; Wang, X.; Liu, X.-M.; Li, J.; Li, J.-R., Applications of metal–organic frameworks for green energy and environment: New advances in adsorptive gas separation, storage and removal. Green Ener. Environ. 2018, 3, 191-228.
18. Konstas, K.; Osl, T.; Yang, Y.; Batten, M.; Burke, N.; Hill, A. J.; Hill, M. R., Methane storage in metal organic frameworks. J. Mater. Chem. 2012, 22, 16698-16708.
19. Wong-Foy, A. G.; Matzger, A. J.; Yaghi, O. M., Exceptional H2 Saturation Uptake in Microporous Metal-Organic Frameworks. J. Am. Chem. Soc. 2006, 128, 3494-3495.
20. Chen, B.; Ockwig, N. W.; Millward, A. R.; Contreras, D. S.; Yaghi, O. M., High H2 Adsorption in a Microporous Metal–Organic Framework with Open Metal Sites. Angew. Chem. Int. Ed. 2005, 44, 4745-4749.
21. Wen, J.; Fang, Y.; Zeng, G., Progress and prospect of adsorptive removal of heavy metal ions from aqueous solution using metaleorganic frameworks: A review of studies from the last decade. Chemosphere 2018, 201, 627-643.
22. Jiang, J.; Yaghi, O. M., Brønsted Acidity in Metal−Organic Frameworks. Chem. Rev. 2015, 115, 6966-6997.
23. Dhakshinamoorthy, A.; Asiric, A. M.; Garcia, H., Metal–organic frameworks catalyzed C–C and C–heteroatom coupling reactions. Chem. Soc. Rev. 2015, 44, 1922-1947.
24. Dhakshinamoorthy, A.; Garcia, H., Catalysis by metal nanoparticles embedded on metal–organic frameworks. Chem. Soc. Rev. 2012, 41, 5262-5284.
25. Luo, H.-B.; Ren, Q.; Wang, P.; Zhang, J.; Wang, L.; Ren, X.-M., High Proton Conductivity Achieved by Encapsulation of Imidazole Molecules into Proton-Conducting MOF-808. ACS Appl. Mater. Interfaces 2019, 11, 9164-9171.
26. Li, X.; Liu, Y.; Wang, J.; Gascon, J.; Li, J.; Bruggen, B. V. d., Metal–organic frameworks based membranes for liquid separation. Chem. Soc. Rev. 2017, 46, 7124-7144.
27. Zacher, D.; Shekhah, O.; ll, C. W.; Fischer, R. A., Thin films of metal–organic frameworksw. Chem. Soc. Rev. 2009, 38, 1418-1429.
28. Wang, L.; Zheng, M.; Xie, Z., Nanoscale metal–organic frameworks for drug delivery: a conventional platform with new promise. J. Mater. Chem. B 2018, 6, 707-717.
29. Truong, T.; Nguyen, C. V.; Truong, N. T.; Phan, N. T. S., Ligand-free N-arylation of heterocycles using metal–organic framework [Cu(INA)2] as an efficient heterogeneous catalyst. RSC Adv. 2015, 5, 107547-107556.
30. Khazalpour, S.; Safarifard, V.; Morsali, A.; Nematollahi, D., Electrochemical synthesis of pillared layer mixed ligand metal–organic framework: DMOF-1–Zn. RSC Adv. 2015, 5, 36547-36551.
31. Jhung, S. H.; Lee, J.-H.; Chang, J.-S., Microwave Synthesis of a Nanoporous Hybrid Material, Chromium Trimesate. Bull. Korean Chem. Soc. 2005, 26, 880-881.
32. Khan, N. A.; Jhung, S. H., Facile Syntheses of Metal-organic Framework Cu3(BTC)2(H2O)3 under Ultrasound. Bull. Korean Chem. Soc. 2009, 30, 2921-2926.
33. Pichon, A.; Lazuen-Garay, A.; James, S. L., Solvent-free synthesis of a microporous metal–organic framework. CrystEngComm 2006, 8, 211-214.
34. Torad, N. L.; Hu, M.; Kamachi, Y.; Takai, K.; Imura, M.; Naitoa, M.; Yamauchi, Y., Facile synthesis of nanoporous carbons with controlled particle sizes by direct carbonization of monodispersed ZIF-8 crystals. Chem. Commun. 2013, 49, 2521-2523.
35. Shieh, F.-K.; Wang, S.-C.; Yen, C.-I.; Wu, C.-C.; Dutta, S.; Chou, L.-Y.; Morabito, J. V.; Hu, P.; Hsu, M.-H.; Kevin C.-W. Wu; Tsung, C.-K., Imparting Functionality to Biocatalysts via Embedding Enzymes into Nanoporous Materials by a de Novo Approach: Size-Selective Sheltering of Catalase in Metal–Organic Framework Microcrystals. J. Am. Chem. Soc. 2015, 137, 4276-4279.
36. Banerjee, R.; Phan, A.; Wang, B.; Knobler, C.; Furukawa, H.; O’Keeffe, M.; Yaghi, O. M., High-Throughput Synthesis of Zeolitic Imidazolate Frameworks and Application to CO2 Capture. Science 2008, 319, 939-943.
37. Surble´, S.; Millange, F.; Serre, C.; Fe´reya, G. r.; Walton, R. I., An EXAFS study of the formation of a nanoporous metal–organic framework: evidence for the retention of secondary building units during synthesis. Chem. Commun. 2006, 1518-1520.
38. Ahnfeldt, T.; Moellmer, J.; Guillerm, V.; Staudt, R.; Serre, C.; Stock, N., High-Throughput and Time-Resolved Energy-Dispersive X-Ray Diffraction (EDXRD) Study of the Formation of CAU-1-(OH)2: Microwave and Conventional Heating. Chem. Eur. J. 2011, 17, 6462-6468.
39. Furukawa, H.; Ko, N.; Go, Y. B.; Aratani, N.; Choi, S. B.; Choi, E.; Yazaydin, A. Ö.; Snurr, R. Q.; O’Keeffe, M.; Kim, J.; Yaghi, O. M., Ultrahigh Porosity in Metal-Organic Frameworks. Science 2010, 329, 424-428.
40. Eddaoudi, M.; Kim, J.; Rosi, N.; Vodak, D.; Wachter, J.; OÕKeeffe, M.; Yaghi1, O. M., Systematic Design of Pore Size and Functionality in Isoreticular MOFs and Their Application in Methane Storage. Science 2002, 295, 469-472.
41. Chae, H. K.; Siberio-Pe´rez, D. Y.; Jaheon Kim1, Y. G.; Eddaoudi, M.; Matzger, A. J.; O’Keeffe, M.; Yaghi, O. M., A route to high surface area, porosity and inclusion of large molecules in crystals. Nature 2004, 427, 523-527.
42. Nguyen, L. T. L.; Nguyen, C. V.; Dang, G. H.; Le, K. K. A.; Phan, N. T. S., Towards applications of metal–organic frameworks in catalysis: Friedel–Crafts acylation reaction over IRMOF-8 as an efficient heterogeneous catalyst. J. Mol. Catal. A: Chemical 2011, 349, 28-35.
43. Rowsell, J. L. C.; Millward, A. R.; Park, K. S.; Yaghi, O. M., Hydrogen Sorption in Functionalized Metal-Organic Frameworks. J. Am. Chem. Soc. 2004, 126, 5666-5667.
44. Nelson, A. P.; Farha, O. K.; Mulfort, K. L.; Hupp, J. T., Supercritical Processing as a Route to High Internal Surface Areas and Permanent Microporosity in Metal-Organic Framework Materials. J. Am. Chem. Soc. 2009, 131, 458-460.
45. Férey, G.; Serre, C.; Mellot-Draznieks, C.; FranckMillange; Surble´, S.; Dutour, J.; Margiolaki, I., A Hybrid Solid with Giant Pores Prepared by a Combination of Targeted Chemistry, Simulation, and Powder Diffraction. Angew. Chem. Int. Ed. 2004, 43, 9296-6301.
46. Furukawa, H.; Gándara, F.; Zhang, Y.-B.; Jiang, J.; Queen, W. L.; Hudson, M. R.; Yaghi, O. M., Water Adsorption in Porous Metal−Organic Frameworks and Related Materials. J. Am. Chem. Soc. 2014, 136, 4369-4381.
47. Chui, S. S.-Y.; Lo, S. M.-F.; Charmant, J. P. H.; Orpen, A. G.; Williams, I. D., A Chemically Functionalizable Nanoporous Material [Cu3(TMA)2(H2O)3]n. Science 1999, 283, 1148-1150.
48. Deng, H.; Doonan, C. J.; Furukawa, H.; Ferreira, R. B.; Towne, J.; Knobler, C. B.; Wang, B.; Yaghi, O. M., Multiple Functional Groups of Varying Ratios in Metal-Organic Frameworks. Science 2010, 327, 846-850.
49. Zhang, Y.-B.; Furukawa, H.; Ko, N.; Nie, W.; Park, H. J.; Okajima, S.; Cordova, K. E.; Deng, H.; Kim, J.; Yaghi, O. M., Introduction of Functionality, Selection of Topology, and Enhancement of Gas Adsorption in Multivariate Metal-Organic Framework-177. J. Am. Chem. Soc. 2015, 137, 2641-2650.
50. Deria, P.; Mondloch, J. E.; Karagiaridi, O.; Bury, W.; Hupp, J. T.; Farha, O. K., Beyond post-synthesis modification: evolution of metal–organic frameworks via building block replacement. Chem. Soc. Rev. 2014, 43, 5896-5912.
51. Evans, J. D.; Sumby, C. J.; Doonan, C. J., Post-synthetic metalation of metal–organic frameworks. Chem. Soc. Rev. 2014, 43, 5933-5951.
52. DeCoste, J. B.; Peterson, G. W.; Jasuja, H.; Glover, T. G.; Huang, Y.-g.; Walton, K. S., Stability and degradation mechanisms of metal–organic frameworks containing the Zr6O4(OH)4 secondary building unit. J. Mater. Chem. A 2013, 1, 5642-5650.
53. Tran, U. P. N.; Le, K. K. A.; Phan, N. T. S., Expanding Applications of Metal-Organic Frameworks: Zeolite Imidazolate Framework ZIF-8 as an Efficient Heterogeneous Catalyst for the Knoevenagel Reaction. ACS. Catal. 2011, 1, 120-127.
54. Yuan, S.; Feng, L.; Wang, K.; Pang, J.; Bosch, M.; Lollar, C.; Sun, Y.; Qin, J.; Yang, X.; Zhang, P.; Wang, Q.; Zou, L.; Zhang, Y.; Zhang, L.; Fang, Y.; Li, J.; Zhou, H.-C., Stable Metal–Organic Frameworks: Design, Synthesis, and Applications. Adv. Mater. 2018, 30, 1704303.
55. Millward, A. R.; Yaghi, O. M., Metal-Organic Frameworks with Exceptionally High Capacity for Storage of Carbon Dioxide at Room Temperature. J. Am. Chem. Soc. 2005, 127, 17998-17999.
56. Cavenati, S.; Grande, C. A.; Rodrigues, A. r. E., Adsorption Equilibrium of Methane, Carbon Dioxide, and Nitrogen on Zeolite 13X at High Pressures. J. Chem. Eng. Data 2004, 49, 1095-1101.
57. Himeno, S.; Komatsu, T.; Fujita, S., High-Pressure Adsorption Equilibria of Methane and Carbon Dioxide on Several Activated Carbons. J. Chem. Eng. Data 2005, 50, 369-376.
58. Trickett, C. A.; Helal, A.; Al‑Maythalony, B. A.; Yamani, Z. H.; Cordova, K. E.; Yaghi, O. M., The chemistry of metal–organic frameworks for CO2 capture, regeneration and conversion. Nat. Rev. Mater. 2017, 2, 17045.
59. He, Y.; Zhou, W.; Qian, G.; Chen, B., Methane storage in metal–organic frameworks. Chem. Soc. Rev. 2014, 43, 5657-5678.
60. Phan, N. T. S.; Le, K. K. A.; Phan, T. D., MOF-5 as an efficient heterogeneous catalyst for Friedel–Crafts alkylation reactions. Appl. Catal. A: General 2010, 382, 246-253.
61. Nguyen, L. T. L.; Le, K. K. A.; Truong, H. X.; Phan, N. T. S., Metal–organic frameworks for catalysis: the Knoevenagel reaction using zeolite imidazolate framework ZIF-9 as an efficient heterogeneous catalyst. Catal. Sci. Technol. 2012, 2, 521-528.
62. Phan, N. T. S.; Nguyen, T. T.; Ho, P.; Nguyen, K. D., Copper-Catalyzed Synthesis of a-Aryl Ketones by Metal–Organic Framework MOF-199 as an EfficientHeterogeneous Catalyst. ChemCatChem 2013, 5, 1822-1831.
63. Truong, T.; Nguyen, C. K.; Tran, T. V.; Nguyen, T. T.; Phan, N. T. S., Nickel-catalyzed oxidative coupling of alkynes and arylboronic acids using the metal–organic framework Ni2(BDC)2(DABCO) as an efficient heterogeneous catalyst. Catal. Sci. Technol. 2014, 4, 1276-1285.
64. Phan, N. T. S.; Nguyen, T. T.; Nguyen, C. V.; Nguyen, T. T., Ullmann-type coupling reaction using metal-organic framework MOF-199 as an efficient recyclable solid catalyst. Appl. Catal. A: General 2013, 457, 69-77.
65. Silva, C. G.; Corma, A.; García, H., Metal–organic frameworks as semiconductors. J. Mater. Chem. 2010, 20, 3141-3156.
66. Hu, Z.; Deibert, B. J.; Li, J., Luminescent metal–organic frameworks for chemical sensing and explosive detection. Chem. Soc. Rev. 2014, 43, 5815-5840.
67. Cui, Y.; Yue, Y.; Qian, G.; Chen, B., Luminescent Functional Metal-Organic Frameworks. Chem. Rev. 2012, 112, 1126-1162.
68. Xiao, Y.; Cui, Y.; Zheng, Q.; Xiang, S.; Qian, G.; Chen, B., A microporous luminescent metal–organic framework for highly selective and sensitive sensing of Cu2+ in aqueous solution. Chem. Commun. 2010, 46, 5503-5505.
69. Chen, B.; Wang, L.; Zapata, F.; Qian, G.; Lobkovsky, E. B., A Luminescent Microporous Metal-Organic Framework for the Recognition and Sensing of Anions. J. Am. Chem. Soc. 2008, 130, 6718-6719.
70. Takashima, Y.; Martínez, V. M.; Furukawa, S.; Mio Kondo4, S. S.; Uehara, H.; Nakahama, M.; Sugimoto, K.; Kitagawa, S., Molecular decoding using luminescence from an entangled porous framework. Nat. Comm. 2011, 2, 168.
71. Dang, S.; Zhu, Q.-L.; Xu, Q., Nanomaterials derived from metal–organic frameworks. Nat. Rev. Mater. 2018, 3, 17075.
72. Yang, L.; Zeng, X.; Wang, W.; Cao, D., Recent Progress in MOF-Derived, Heteroatom-Doped Porous Carbons as Highly Efficient Electrocatalysts for Oxygen Reduction Reaction in Fuel Cells. Adv. Funct. Mater. 2018, 1704537.
73. Yap, M. H.; Fow, K. L.; Chen, G. Z., Synthesis and applications of MOF-derived porous nanostructures. Green Ener. Environ. 2017, 2, 218-245.
74. Pachfule, P.; Shinde, D.; Majumder, M.; Xu, Q., Fabrication of carbon nanorods and graphene nanoribbons from a metal–organic framework. Nat. Chem. 2016, 8, 718-724.
75. Guo, W.; Sun, W.; Wang, Y., Multilayer CuO@NiO Hollow Spheres: Microwave-Assisted MetalOrganic-Framework Derivation and Highly Reversible Structure-Matched Stepwise Lithium Storage. ACS Nano 2015, 9, 11462-11471.
76. Tang, J.; Salunkhe, R. R.; Liu, J.; Torad, N. L.; Imura, M.; Furukawa, S.; Yamauchi, Y., Thermal Conversion of Core−Shell Metal−Organic Frameworks: A New Method for Selectively Functionalized Nanoporous Hybrid Carbon. J. Am. Chem. Soc. 2015, 137, 1572-1580.
77. Ji, S.; Chen, Y.; Fu, Q.; Chen, Y.; Dong, J.; Chen, W.; Li, Z.; Wang, Y.; Gu, L.; He, W.; Chen, C.; Peng, Q.; Huang, Y.; Duan, X.; Wang, D.; Draxl, C.; Li, Y., Confined Pyrolysis within Metal−Organic Frameworks To Form Uniform Ru3 Clusters for Efficient Oxidation of Alcohols. J. Am. Chem. Soc. 2017, 139, 9795-9798.
78. Liu, B.; Shioyama, H.; Akita, T.; Xu, Q., Metal-Organic Framework as a Template for Porous Carbon Synthesis. J. Am. Chem. Soc. 2008, 130, 5390-5391.
79. Nguyen, C. V.; Liao, Y.-T.; Kang, T.-C.; Chen, J. E.; Yoshikawa, T.; Nakasaka, Y.; Masudab, T.; Kevin C.-W. Wu, A metal-free, high nitrogen-doped nanoporous graphitic carbon catalyst for an effective aerobic HMF-to-FDCA conversion. Green Chem. 2016, 18, 5957-5961.
80. Wang, Y.; Tao, L.; Xiao, Z.; Chen, R.; Jiang, Z.; Wang, S., 3D Carbon Electrocatalysts In Situ Constructed by Defect-Rich Nanosheets and Polyhedrons from NaCl-Sealed Zeolitic Imidazolate Frameworks. Adv. Funct. Mater. 2018, 28, 1705356.
81. Radhakrishnan, L.; Reboul, J.; Furukawa, S.; Srinivasu, P.; Kitagawa, S.; Yamauchi, Y., Preparation of Microporous Carbon Fibers through Carbonization of Al-Based Porous Coordination Polymer (Al-PCP) with Furfuryl Alcohol. Chem. Mater. 2011, 23, 1225-1231.
82. Liu, B.; Zhang, X.; Shioyama, H.; Mukai, T.; Sakai, T.; Xu, Q., Converting cobalt oxide subunits in cobalt metal-organic framework into agglomerated Co3O4 nanoparticles as an electrode material for lithium ion battery. J. Powder Sour. 2010, 195, 857-861.
83. Proietti, E.; Jaouen, F.; Lefèvre, M.; Larouche, N.; Tian, J.; Herranz, J.; Dodelet, J.-P., Iron-based cathode catalyst with enhanced power density in polymer electrolyte membrane fuel cells. Nat. Comm. 2011, 2, 416.
84. Zhang, L.; Shi, L.; Huang, L.; Zhang, J.; Gao, R.; Zhang, D., Rational Design of High-Performance DeNOx Catalysts Based on MnxCo3-xO4 Nanocages Derived from Metal−Organic Frameworks. ACS. Catal. 2014, 4, 1753-1763.
85. Wang, X.; Chen, W.; Zhang, L.; Yao, T.; Liu, W.; Lin, Y.; Ju, H.; Dong, J.; Zheng, L.; Yan, W.; Zheng, X.; Li, Z.; Wang, X.; Yang, J.; He, D.; Wang, Y.; Deng, Z.; Wu, Y.; Li, Y., Uncoordinated Amine Groups of Metal−Organic Frameworks to Anchor Single Ru Sites as Chemoselective Catalysts toward the Hydrogenation of Quinoline. J. Am. Chem. Soc. 2017, 139, 9419-9422.
86. Jagadeesh, R. V.; Murugesan, K.; Alshammari, A. S.; Neumann, H.; Pohl, M.-M.; Radnik, J.; Beller, M., MOF-derived cobalt nanoparticles catalyze a general synthesis of amines. Science 2017, 358, 326-332.
87. Xu, X.; Cao, R.; Jeong, S.; Cho, J., Spindle-like Mesoporous α‑Fe2O3 Anode Material Prepared from MOF Template for High-Rate Lithium Batteries. Nano Lett. 2012, 12, 4988-4991.
88. Zhang, L.; Wu, H. B.; Madhavi, S.; Hng, H. H.; Lou, X. W. D., Formation of Fe2O3 Microboxes with Hierarchical Shell Structures from Metal−Organic Frameworks and Their Lithium Storage Properties. J. Am. Chem. Soc. 2012, 134, 17388-17391.
89. Su, P.; Xiao, H.; Zhao, J.; Yao, Y.; Shao, Z.; Li, C.; Yang, Q., Nitrogen-doped carbon nanotubes derived from Zn–Fe-ZIF nanospheres and their application as efficient oxygen reduction electrocatalysts with in situ generated iron species. Chem. Sci. 2013, 4, 2941-2946.
90. Wu, H. B.; Wei, S.; Zhang, L.; Xu, R.; Hng, H. H.; Lou, X. W. D., Embedding Sulfur in MOF-Derived Microporous Carbon Polyhedrons for Lithium–Sulfur Batteries. Chem. Eur. J. 2013, 19, 10804-10808.
91. Banerjee, A.; Gokhale, R.; Bhatnagar, S.; Jog, J.; Bhardwaj, M.; Lefez, B.; Hannoyerc, B.; Ogale, S., MOF derived porous carbon–Fe3O4 nanocomposite as a high performance, recyclable environmental superadsorbent. J. Mater. Chem. 2012, 22, 19694-19699.
92. Gadipelli, S.; Guo, Z. X., Tuning of ZIF-Derived Carbon with High Activity, Nitrogen Functionality, and Yield – A Case for Superior CO2 Capture. ChemSusChem 2015, 8, 2123-2132.
93. Hou, Y.; Huang, T.; Wen, Z.; Mao, S.; Cui, S.; Chen, J., Metal−Organic Framework-Derived Nitrogen-Doped Core-Shell-Structured Porous Fe/Fe 3 C@C Nanoboxes Supported on Graphene Sheets for Effi cient Oxygen Reduction Reactions. Adv. Energy Mater. 2014, 4, 1400337.
94. Ma, T. Y.; Dai, S.; Jaroniec, M.; Qiao, S. Z., Metal−Organic Framework Derived Hybrid Co3O4-Carbon Porous Nanowire Arrays as Reversible Oxygen Evolution Electrodes. J. Am. Chem. Soc. 2014, 136, 13925-13931.
95. Xia, B. Y.; Yan, Y.; Li, N.; Wu, H. B.; Lou, X. W.; Wang, X., A metal–organic framework-derived bifunctional oxygen electrocatalyst. Nature Energy 2016, 1, 15006.
96. Zhang, J.; Fang, J.; Han, J.; Yan, T.; Shi, L.; Zhang, D., N, P, S co-doped hollow carbon polyhedra derived from MOF-based core–shell nanocomposites for capacitive deionization. J. Mater. Chem. A 2018, 6, 15245-15252.
97. Wang, X.; Huang, F.; Rong, F.; He, P.; Que, R.; Jiang, S. P., Unique MOF-derived hierarchical MnO2 nanotubes@NiCo-LDH/CoS2 nanocage materials as high performance supercapacitors. J. Mater. Chem. A 2019, 7, 12018-12028.
98. Zhong, B.; Zhang, L.; Yu, J.; Fan, K., Ultrafine iron-cobalt nanoparticles embedded in nitrogen-doped porous carbon matrix for oxygen reduction reaction and zinc-air batteries. J. Colloid Interface Sci. 2019, 546, 113-120.
99. Xiaa, J.; Heb, G.; Zhang, L.; Sun, X.; Wang, X., Hydrogenation of nitrophenols catalyzed by carbon black-supported nickel nanoparticles under mild conditions. Appl. Catal. B: Environmental 2016, 180, 408-415.
100. Sahiner, N.; Sema Yildiz; Al-Lohedana, H., The resourcefulness of p(4-VP) cryogels as template for in situ nanoparticle preparation of various metals and their use in H2 production, nitrocompound reduction and dyedegradation. Appl. Catal. B: Environmental 2015, 166, 145-154.
101. Mitchell, S. C.; R. H. Waring, In Ullmanns Encyclopedia of Industrial Chemistry. Wiley-VCH, Weinheim, Germany: 2000.
102. Yang, F.; Chi, C.; Wang, C.; Wang, Y.; Li, Y., High graphite N content in nitrogen-doped graphene as an efficient metal-free catalyst for reduction of nitroarenes in water. Green Chem. 2016, 18, 4254-4262.
103. Cai, S.; Duan, H.; Rong, H.; Wang, D.; Li, L.; He, W.; Li, Y., Highly Active and Selective Catalysis of Bimetallic Rh3Ni1 Nanoparticles in the Hydrogenation of Nitroarenes. ACS Catal. 2013, 3, 608-612.
104. Saha, A.; Ranu, B., Highly Chemoselective Reduction of Aromatic Nitro Compounds by Copper Nanoparticles/ Ammonium Format. J. Org. Chem. 2008, 73, 6867-6870.
105. Junge, K.; Wendt, B.; Shaikh, N.; Beller, M., Iron-catalyzed selective reduction of nitroarenes to anilines using organosilanes. Chem. Commun. 2010, 46, 1769-1771.
106. Wienh€ofer, G.; Sorribes, I.; Boddien, A.; Westerhaus, F.; Junge, K.; Junge, H.; Llusar, R.; Beller, M., General and Selective Iron-Catalyzed Transfer Hydrogenation of Nitroarenes without Base. J. Am. Chem. Soc. 2011, 133, 12875-12879.
107. Blaser, H.-U.; Steiner, H.; Studer, M., Selective Catalytic Hydrogenation of Functionalized Nitroarenes: An Update. ChemCatChem 2009, 1, 210-221.
108. Kundu, S.; Lau, S.; Liang, H., Shape-Controlled Catalysis by Cetyltrimethylammonium Bromide Terminated Gold Nanospheres, Nanorods, and Nanoprisms. J. Phys. Chem. C 2009, 113, 5250-5156.
109. Sarmah, P. P.; Dutta, D. K., Chemoselective reduction of a nitro group through transfer hydrogenation catalysed by Ru0 -nanoparticles stabilized on modified Montmorillonite clay. Green Chem. 2012, 14, 1086-1093.
110. Wang, X.; Sun, G.; Routh, P.; Kim, D.-H.; Huang, W.; Chen, P., Heteroatom-doped graphene materials: syntheses, properties and applications. Chem. Soc. Rev. 2014, 43, 7067-7098.
111. Pumera, M., Graphene-based nanomaterials and their electrochemistry. Chem. Soc. Rev. 2010, 39, 4146-4157.
112. Dong, X.-C.; Xu, H.; Wang, X.-W.; Huang, Y.-X.; Chan-Park, M. B.; Zhang, H.; Wang, L.-H.; Huang, W.; Chen, P., 3D GrapheneCobalt Oxide Electrode for High-Performance Supercapacitor and Enzymeless Glucose Detection. ACS Nano 2012, 6, 3206-3213.
113. Yong, Y.-C.; Dong, X.-C.; Chan-Park, M. B.; Song, H.; Chen, P., Macroporous and Monolithic Anode Based on Polyaniline Hybridized Three-Dimensional Graphene for High-Performance Microbial Fuel Cells. ACS Nano 2012, 6, 2394-2400.
114. Jeon, I.-Y.; Zhang, S.; Zhang, L.; Choi, H.-J.; Seo, J.-M.; Xia, Z.; Dai, L.; Baek, J.-B., Edge-Selectively Sulfurized Graphene Nanoplatelets as Effi cient Metal-Free Electrocatalysts for Oxygen Reduction Reaction: The Electron Spin Effect. Adv. Mater. 2013, 25, 6238-6145.
115. Rani, P.; Jindal, V. K., Designing band gap of graphene by B and N dopant atoms. RSC Adv. 2013, 3, 802-811.
116. Li, J.-C.; Hou, P.-X.; Liu, C., Heteroatom-Doped Carbon Nanotube and Graphene-Based Electrocatalysts for Oxygen Reduction Reaction. Small 2017, 13, 1702002.
117. Wang, S.; Iyyamperumal, E.; Roy, A.; Xue, Y.; Yu, D.; Dai, L., Vertically Aligned BCN Nanotubes as Efficient Metal-Free Electrocatalysts for the Oxygen Reduction Reaction: A Synergetic Effect by Co-Doping with Boron and Nitrogen. Angew. Chem. Int. Ed. 2011, 50, 11756-11760.
118. Zheng, Y.; Jiao, Y.; Ge, L.; Jaroniec, M.; Qiao, S. Z., Two-Step Boron and Nitrogen Doping in Graphene for Enhanced Synergistic Catalysis. Angew. Chem. Int. Ed. 2013, 52, 3100-3116.
119. Umrao, S.; Gupta, T. K.; Kumar, S.; Singh, V. K.; Sultania, M. K.; Jung, J. H.; Oh, I.-K.; Srivastava, A., Microwave-Assisted Synthesis of Boron and Nitrogen co-doped Reduced Graphene Oxide for the Protection of Electromagnetic Radiation in Ku-Band. ACS Appl. Mater. Interfaces 2015, 7, 19831-19842.
120. Choi, C. H.; Chung, M. W.; Kwon, H. C.; Park, S. H.; Woo, S. I., B, N- and P, N-doped graphene as highly active catalysts for oxygen reduction reactions in acidic media†. J. mater. Chem. A 2013, 1, 3694-3699.
121. Wu, Z.-S.; Winter, A.; Chen, L.; Sun, Y.; Turchanin, A.; Feng, X.; Müllen, K., Three-Dimensional Nitrogen and Boron Co-doped Graphene for High-Performance All-Solid-State Supercapacitors. Adv. Mater. 2012, 24, 5130-5135.
122. Qie, L.; Lin, Y.; Connell, J. W.; Xu, J.; Dai, L., Highly Rechargeable Lithium-CO2 Batteries with a Boron and Nitrogen-Codoped Holey-Graphene Cathode. Angew. Chem. Int. Ed. 2017, 56, 6970-6974.
123. Wei, J.; Hu, Y.; Liang, Y.; Kong, B.; Zhang, J.; Song, J.; Bao, Q.; Simon, G. P.; Jiang, S. P.; Wang, H., Nitrogen-Doped Nanoporous Carbon/Graphene Nano-Sandwiches: Synthesis and Application for EfficientOxygen Reduction. Adv. Funct. Mater. 2015, 25, 5768-5777.
124. Hutter, J.; Iannuzzi, M.; Schiffmann, F.; VandeVondele, J., cp2k: atomistic simulations of condensed matter systems. WIREs Comput. Mol. 2014, 4, 15-25.
125. Csonka, G. I.; Perdew, J. P.; Ruzsinszky, A.; Philipsen, P. H. T.; Lebègue, S.; Paier, J.; Vydrov, O. A.; Ángyán, J. G., Assessing the performance of recent density functionals for bulk solids. Phys. Rev. B 2009, 79, 155107.
126. Grimme, S.; Antony, J.; Ehrlich, S.; Krieg, H., A consistent and accurate ab initio parametrization of density functional dispersion correction (DFT-D) for the 94 elements H-Pu. J. Chem. Phys. 2010, 132, 154104.
127. VandeVondele, J.; Hutter, J., Gaussian basis sets for accurate calculations on molecular systems in gas and condensed phases. J. Chem. Phys. 2007, 127, 114105.
128. Antropov, V. P.; Katsnelson, M. I.; Harmon, B. N., Spin dynamics in magnets: Equation of motion and finite temperature effect. Phys. Rev. B 1996, 54, 1703-171.
129. Hartwigsen, C.; Goedecker, S.; Hutter, J., Relativistic separable dual-space Gaussian pseudopotentials from H to Rn. Phys. Rev. B 1998, 58, 3641-3662.
130. Sidik, R. A.; Anderson, A. B.; Subramanian, N. P.; Kumaraguru, S. P.; Popov, B. N., O2 Reduction on Graphite and Nitrogen-Doped Graphite: Experiment and Theory. J. Phys. Chem. B 2006, 110, 1787-1793.
131. Zheng, F.; Yang, Y.; Chen, Q., High lithium anodic performance of highly nitrogen-doped porous carbon prepared from a metal-organic framework. Nat. Comm. 2014, 5, 6261.
132. Tong, Y.; Chen, P.; Zhou, T.; Xu, K.; Chu, W.; Wu, C.; Xie, Y., A Bifunctional Hybrid Electrocatalyst for Oxygen Reduction and Evolution: Cobalt Oxide Nanoparticles Strongly Coupled to B,N-Decorated Graphene. Angew. Chem. Int. Ed. 2017, 56, 7121-7125.
133. Baik, S.; Lee, J. W., Effect of boron–nitrogen bonding on oxygen reduction reaction activity of BN Co-doped activated porous carbons. RSC Adv. 2015, 5, 24661-24669.
134. Chiang, W.-H.; Chen, G.-L.; Hsieh, C.-Y.; Lo, S.-C., Controllable boron doping of carbon nanotubes with tunable dopant functionalities: an effective strategy toward carbon materials with enhanced electrical properties. RSC Adv. 2015, 5, 97579-97588.
135. Perrone, A.; Caricato, A. P.; Luches, A.; Dinescu, M.; Ghica, C.; Sandu, V.; Andrei, A., Boron carbonitride films deposited by pulsed laser ablation. Appl. Surf. Sci. 1998, 133, 239-242.
136. Mannan, M. A.; Nagano, M.; Shigezumi, K.; Kida, T.; Hirao, N.; Baba, Y., Characterization of Boron Carbonitride (BCN) Thin Films Deposited by Radiofrequency and Microwave Plasma Enhanced Chemical Vapor Deposition. Am. J. Appl. Sci. 2007, 5, 736-741.
137. Srinivas, G.; Zhu, Y.; Piner, R.; Skipper, N.; Ellerby, M.; Ruoff, R., Synthesis of graphene-like nanosheets and their hydrogen adsorption capacity. Carbon 2010, 48, 630-635.
138. Hassan, F. M.; Chabot, V.; Li, J.; Kim, B. K.; Ricardez-Sandoval, L.; Yu, A., Pyrrolic-structure enriched nitrogen doped graphene for highly efficient next generation supercapacitors. J. Mater. Chem. A 2013, 1, 2904-2912.
139. Kudin, K. N.; Ozbas, B.; Schniepp, H. C.; Prud’homme, R. K.; Aksay, I. A.; Car, R., Raman Spectra of Graphite Oxide and Functionalized Graphene Sheets. Nano Lett. 2008, 8, 36-41.
140. Chen, Z.; Ren, W.; Gao, L.; Liu, B.; Pei, S.; Cheng, H.-M., Three-dimensional flexible and conductive interconnected graphene networks grown by chemical vapour deposition. Nat. Mater. 2011, 10, 424-428.
141. Kong, X.-k.; Sun, Z.-y.; Chen, M.; Chen, C.-l.; Chen, Q.-w., Metal-free catalytic reduction of 4-nitrophenol to 4-aminophenol by N-doped graphene. Energy Environ. Sci. 2013, 6, 3260-3266.
142. Mei, Y.; Lu, Y.; Polzer, F.; Ballauff, M., Catalytic Activity of Palladium Nanoparticles Encapsulated in Spherical Polyelectrolyte Brushes and Core-Shell Microgels. Chem. Mater. 2007, 19, 1062-1069.
143. Divband, B.; Khatamian, M.; Eslamian, G. R. K.; Darbandi, M., Synthesis of Ag/ZnO nanostructures by different methods and investigation of their photocatalytic efficiency for 4-nitrophenol degradation. Appl. Surf. Sci. 2013, 284, 80-86.
144. Adelroth, P.; Sigurdson, H.; Hallen, S.; Brzezinski, P., Kinetic coupling between electron and proton transfer in cytochrome c oxidase: Simultaneous measurements of conductance and absorbance changes. Proc. Natl. Acad. Sci. USA 1996, 93, 12292-12297.
145. Nitzan, A., A Relationship between Electron-Transfer Rates and Molecular Conduction. J. Phys. Chem. A 2001, 105, 2677-2679.
146. Antolini, E., Carbon supports for low-temperature fuel cell catalysts. Appl. Catal. B: Environmental 2009, 88, 1-24.
147. Gounder, R., Hydrophobic microporous and mesoporous oxides as Brønsted and Lewis acid catalysts for biomass conversion in liquid water. Catal. Sci. Technol. 2014, 4, 2877-2886.
148. Climent, M. J.; Corma, A.; Iborra, S., Conversion of biomass platform molecules into fuel additives and liquid hydrocarbon fuels. Green Chem. 2014, 16, 516-547.
149. Mariscal, R.; Maireles-Torres, P.; Ojeda, M.; Sa´daba, I.; Granados, M. L. p., Furfural: a renewable and versatile platform molecule for the synthesis of chemicals and fuels. Energy Environ. Sci. 2016, 9, 1144-1189.
150. Gallezot, P., Conversion of biomass to selected chemical products. Chem. Soc. Rev. 2012, 41, 1538-1558.
151. Matsagar, B. M.; Hossain, S. A.; Islam, T.; Alamri, H. R.; Alothman, Z. A.; Yamauchi, Y.; Dhepe, P. L.; Wu, K. C.-W., Direct Production of Furfural in One-pot Fashion from Raw Biomass Using Brønsted Acidic Ionic Liquids. Sci. Rep. 2017, 7, 13508.
152. Liao, Y.-T.; Matsagar, B. M.; Kevin, C.-W. Wu, Metal−Organic Framework (MOF)-Derived Effective Solid Catalysts for Valorization of Lignocellulosic Biomass. ACS Sustainable Chem. Eng. 2018, 6, 13628-13643.
153. Sang, B.; Li, J.; Tian, X.; Yuan, F.; Zhu, Y., Selective aerobic oxidation of the 5-hydroxymethylfurfural to 2,5-furandicarboxylic acid over gold nanoparticles supported on graphitized carbon: Study on reaction pathways. Mol. Catal. 2019, 470, 67-74.
154. Matsagar, B. M.; Munshi, M. K.; Kelkar, A. A.; Dhepe, P. L., Conversion of concentrated sugar solutions into 5-hydroxymethyl furfural and furfural using Brönsted acidic ionic liquids. Catal. Sci. Technol. 2015, 5, 5086-5090.
155. Ortiz-Cervantes, C.; Flores-Alamo, M.; García, J. J., Hydrogenation of Biomass-Derived Levulinic Acid into γ‑Valerolactone Catalyzed by Palladium Complexes. ACS Catal. 2015, 5, 1424-1431.
156. Zhu, S.; Xue, Y.; Guo, J.; Cen, Y.; Wang, J.; Fan, W., Integrated Conversion of Hemicellulose and Furfural into γ‑Valerolactone over Au/ZrO2 Catalyst Combined with ZSM‑5. ACS Catal. 2016, 6, 2035-2042.
157. Bui, L.; Luo, H.; Gunther, W. R.; Romn-Leshkov, Y., Domino Reaction Catalyzed by Zeolites with Brønsted and Lewis Acid Sites for the Production of g-Valerolactone from Furfural. Angew. Chem. Int. Ed. 2013, 52, 8022-8025.
158. Deng, L.; Li, J.; Lai, D.-M.; Fu, Y.; Guo, Q.-X., Catalytic Conversion of Biomass-Derived Carbohydrates into g-Valerolactone without Using an External H2 Supply. Angew. Chem. Int. Ed. 2009, 48, 6529-6532.
159. Wright, W. R. H.; Palkovits, R., Development of Heterogeneous Catalysts for the Conversion of Levulinic Acid to g-Valerolactone. ChemSusChem 2012, 5, 1657-1667.
160. (PNNL), P. N. N. L.; (NREL, N. R. E. L. Top Value Added Chemicals From Biomass; U.S. Department of Energy, 2004; p 52.
161. Muranaka, Y.; Suzuki, T.; Sawanishi, H.; Hasegawa, I.; Mae, K., Effective Production of Levulinic Acid from Biomass through Pretreatment Using Phosphoric Acid, Hydrochloric Acid, or Ionic Liquid. Ind. Eng. Chem. Res. 2014, 53, 11611-11621.
162. Zhang, Z., Synthesis of g-Valerolactone from Carbohydrates and its Applications. ChemSusChem 2016, 9, 156-171.
163. Song, S.; Yao, S.; Cao, J.; Di, L.; Wu, G.; Guan, N.; Li, L., Heterostructured Ni/NiO composite as a robust catalyst for thehydrogenation of levulinic acid to -valerolactone. Appl. Catal. B: Environmental 2017, 217, 115-124.
164. Elif I. Gurbuz, Jean Marcel R. Gallo, David Martin Alonso, Stephanie G. Wettstein, Wee Y. Lim, and James A. Dumesic, Angew. Chem. Int. Ed. 2013, 52, 1270 -1274.
165. Rodenas, Y.; Mariscal, R.; Fierro, J. L. G.; Alonso, D. M.; Dumesic, J. A.; Granados, M. L., Improving the production of maleic acid from biomass: TS-1 catalysed aqueous phase oxidation of furfural in the presence of γ-valerolactone. Green Chem. 2018, 20, 2845-2856.
166. Fábos, V. r.; Mika, L. s. T.; Horváth, I. n. T., Selective Conversion of Levulinic and Formic Acids to γ‑Valerolactone with the Shvo Catalyst. Organometallics 2014, 33, 181-187.
167. Delhomme, C.; Schaper, L.-A.; Zhang-Preße, M.; Raudaschl-Sieber, G.; Weuster-Botz, D.; Kühn, F. E., Catalytic hydrogenation of levulinic acid in aqueous phase. J. Organometallic Chem. 2013, 724, 297-299.
168. Hengst, K.; Schubert, M.; Carvalho, H. W. P.; Lu, C.; Kleist, W.; Grunwaldt, J.-D., Synthesis of -valerolactone by hydrogenation of levulinic acid over supported nickel catalysts. Appl. Catal. A: General 2015, 502, 18-26.
169. Tan, J.; Cui, J.; Deng, T.; Cui, X.; Ding, G.; Zhu, Y.; Li, Y., Water-Promoted Hydrogenation of Levulinic Acid to g-Valerolactone on Supported Ruthenium Catalyst. ChemCatChem 2015, 7, 508-512.
170. Xiao, C.; Goh, T.-W.; Qi, Z.; Goes, S.; Brashler, K.; Perez, C.; Huang, W., Conversion of Levulinic Acid to γ‑Valerolactone over Few-Layer Graphene-Supported Ruthenium Catalysts. ACS Catal. 2016, 6, 593-599.
171. Chalid, M., A.A. Broekhuis, and H.J. Heeres, Experimental and kinetic modeling studies on the biphasic hydrogenation of levulinic acid to γ-valerolactone using a homogeneous water-soluble Ru–(TPPTS) catalyst. J. Mol. Catal. A: Chemical, 2011. 341. 14-21
172. Sudhakar, M.; Kumar, V. V.; Naresh, G.; Kantam, M. L.; Bhargava, S. K.; Venugopal, A., Vapor phase hydrogenation of aqueous levulinic acid over hydroxyapatite supported metal (M= Pd, Pt, Ru, Cu, Ni) catalysts. Appl. Catal. B: Environmental 2016, 180, 113-120.
173. Al-Shaal, M. G.; Calin, M.; Delidovich, I.; Palkovits, R., Microwave-assisted reduction of levulinic acid with alcohols producing γ-valerolactone in the presence of a Ru/C catalyst. Catal. Commun. 2016, 75, 65-68.
174. Al-Shaal, M. G.; Wright, W. R. H.; Palkovits, R., Exploring the ruthenium catalysed synthesis of γ-valerolactone in alcohols and utilisation of mild solvent-free reaction conditions. Green Chem. 2012, 14, 1260-1263.
175. Ftouni, J.; Muñoz-Murillo, A.; Goryachev, A.; Hofmann, J. P.; Hensen, E. J. M.; Lu, L.; Kiely, C. J.; Bruijnincx, P. C. A.; Weckhuysen, B. M., ZrO2 Is Preferred over TiO2 as Support for the Ru-Catalyzed Hydrogenation of Levulinic Acid to γ‑Valerolactone. ACS Catal. 2016, 6, 5462-5472.
176. Tan, J.; Cui, J.; Ding, G.; Deng, T.; Zhu, Y.; Li, Y.-w., Efficient aqueous hydrogenation of levulinic acid to γ-valerolactone over a highly active and stable ruthenium catalyst. Catal. Sci. Technol. 2016, 6, 1469-1475.
177. Tan, J.; Cui, J.; Cui, X.; Deng, T.; Li, X.; Zhu, Y.; Li, Y., Graphene-Modified Ru Nanocatalyst for Low-Temperature Hydrogenation of Carbonyl Groups. ACS Catal. 2015, 5, 7379-7384.
178. Sun, J.-K.; Xu, Q., Functional materials derived from open framework templates/precursors: synthesis and applications. Energy Environ. Sci. 2014, 7, 2071-2100.
179. Cao, W.; Luo, W.; Ge, H.; Su, Y.; Wang, A.; Zhanga, T., UiO-66 derived Ru/ZrO2@C as a highly stable catalyst for hydrogenation of levulinic acid to γ-valerolactone. Green Chem. 2017, 19, 2201-2211.
180. Kuwahara, Y.; Kango, H.; Yamashita, H., Catalytic Transfer Hydrogenation of Biomass-Derived Levulinic Acid and Its Esters to γ‑Valerolactone over Sulfonic Acid-Functionalized UiO-66. ACS Sustainable Chem. Eng. 2017, 5, 1141-1152.
181. Fang, X.; Shang, Q.; Wang, Y.; Jiao, L.; Yao, T.; Li, Y.; Zhang, Q.; Luo, Y.; Jiang, H.-L., Single Pt Atoms Confined into a Metal–Organic Framework for Efficient Photocatalysis. Adv. Mater. 2018, 30, 1705112.
182. Sánchez-Sánchez, M.; Getachew, N.; Díaz, K.; Díaz-García, M.; Chebude, Y.; Díaz, I., Synthesis of metal–organic frameworks in water at room temperature: salts as linker sources. Green Chem. 2015, 17, 1500-1509.
183. Yan, H.; Yang, Y.; Tong, D.; Xiang, X.; Hu, C., Catalytic conversion of glucose to 5-hydroxymethylfurfural over SO42/ZrO2 and SO42/ZrO2–Al2O3 solid acid catalysts. Catal. Commun. 2009, 10, 1558-1568.
184. Upare, P. P.; Lee, J.-M.; Hwang, D. W.; Halligudi, S. B.; Hwang, Y. K.; Chang, J.-S., Selective hydrogenation of levulinic acid to g-valerolactone over carbon-supported noble metal catalysts. J. Ind. Eng. Chem. 2011, 11, 287-292.
185. Yan, Z.-p.; Lin, L.; Liu, S., Synthesis of γ-Valerolactone by Hydrogenation of Biomass-derived Levulinic Acid over Ru/C Catalyst. Energy & Fuels 2009, 23, 3853-3858.
186. Hynesa, M. J.; Jonson, B., Lead, glass and the environment. Chem. Soc. Rev. 1997, 26, 133-145.
187. AR, F.; DR, S., Current needs for increased accuracy and precision in measurements of low levels of lead in blood. Environ. Res. 1992, 2, 125-133.
188. Kavallieratos, K.; Rosenberg, J. M.; Chen, W.-Z.; Ren, T., Fluorescent Sensing and Selective Pb(II) Extraction by a Dansylamide Ion-Exchanger. J. Am. Chem. Soc. 2005, 127, 6514-6515.
189. Kim, H. N.; Ren, W. X.; Kim, J. S.; Yoon, J., Fluorescent and colorimetric sensors for detection of lead, cadmium, and mercury ions. Chem. Soc. Rev. 2012, 41, 3210-3244.
190. Bannon, D. I.; Murashchik, C.; Zapf, C. R.; Farfel, M. R.; J. Julian Chisoim, J., Graphite Furnace Atomic Absorption Spectroscopic Measurement of Blood Lead in Matrix-Matched Standards. Clin. Chem. 1994, 40, 1730-1734.
191. Carter, K. P.; Young, A. M.; Palmer, A. E., Fluorescent Sensors for Measuring Metal Ions in Living Systems. Chem. Rev. 2014, 114, 4564-4601.
192. Wang, X.; Guo, X., Ultrasensitive Pb2+ detection based on fluorescence resonance energy transfer (FRET) between quantum dots and gold nanoparticles. Analyst 2009, 134, 1348-1354.
193. Zhou, Y.; Chen, H.-H.; Yan, B., An Eu3+ post-functionalized nanosized metal–organic framework for cation exchange-based Fe3+-sensing in an aqueous environment. J. Mater. Chem. A 2014, 2, 13691-13697.
194. Marbella, L.; Serli-Mitasev, B.; Basu, P., Development of a Fluorescent Pb2+ Sensor. Angew. Chem. Int. Ed. 2009, 48, 3996-3998.
195. Wang, Y.; Hu, J.; Zhuang, Q.; Ni, Y., Label-Free Fluorescence Sensing of Lead(II) Ions and Sulfide Ions Based on Luminescent Molybdenum Disulfide Nanosheets. ACS Sustainable Chem. Eng. 2016, 4, 2535-2541.
196. Cui, L.; Wu, J.; Li, J.; Ju, H., Electrochemical Sensor for Lead Cation Sensitized with a DNA Functionalized Porphyrinic Metal−Organic Framework. Anal. Chem. 2015, 87, 10635-10641.
197. Li, C.-L.; Liu, K.-T.; Lin, Y.-W.; Chang, H.-T., Fluorescence Detection of Lead(II) Ions Through Their Induced Catalytic Activity of DNAzymes. Anal. Chem. 2011, 83, 225-230.
198. Kwon, J. Y.; Jang, Y. J.; Lee, Y. J.; Kim, K. M.; Seo, M. S.; Nam, W.; Yoon, J., A Highly Selective Fluorescent Chemosensor for Pb2+. J. Am. Chem. Soc. 2005, 127, 10107-10111.
199. Brown, C. M.; Carta, V.; Wolf, M. O., Thermochromic Solid-State Emission of Dipyridyl Sulfoxide Cu(I) Complexes. Chem. Mater. 2018, 30, 5786-5795.
200. Stavila, V.; Talin, A. A.; Allendorf, M. D., MOF-based electronic and optoelectronic devices. Chem. Soc. Rev. 2014, 43, 5994-6010.
201. Wałe˛sa-Chorab, M.; Patroniak, V.; Kubicki, M.; Ka˛dziołka, G.; Przepiórski, J.; Michalkiewicz, B., Synthesis, structure, and photocatalytic properties of new dinuclear helical complex of silver(I) ions. J. Catal. 2012, 291, 1-8.
202. Cavka, J. H.; Jakobsen, S.; Olsbye, U.; Guillou, N.; Lamberti, C.; Bordig, S.; Lillerud, K. P., A New Zirconium Inorganic Building Brick Forming Metal Organic Frameworks with Exceptional Stability. J. Am. Chem. Soc. 2008, 130, 13850-13851.
203. He, C.; Liu, D.; Lin, W., Nanomedicine Applications of Hybrid Nanomaterials Built from Metal-Ligand Coordination Bonds: Nanoscale Metal-Organic Frameworks and Nanoscale Coordination Polymers. Chem. Rev. 2015, 115, 11079-11108.
204. Huang, R.-W.; Wei, Y.-S.; Dong, X.-Y.; Wu, X.-H.; Du, C.-X.; Zang, S.-Q.; Mak, T. C. W., Hypersensitive dual-function luminescence switching of a silver-chalcogenolate cluster-based metal–organic framework. Nat. Chem. 2017, 9, 689-697.
205. Hua, Y.; Xu, B.; Liu, P.; Chen, H.; Tian, H.; Cheng, M.; Kloo, L.; Sun, L., High conductivity Ag-based metal organic complexes as dopant-free hole-transport materials for perovskite solar cells with high fill factors. Chem. Sci. 2016, 7, 2633-2638.
206. Chang, H.-N.; Liu, L.-W.; Hao, Z. C.; Cui, G.-H., A 3D Ag(I) metal-organic framework for sensing luminescence and photocatalytic activities. J. Mol. Struct. 2018, 1155, 496-502.
207. Drake, P. L.; Hazelwood, K. J., Exposure-Related Health Effects of Silver and Silver Compounds: A Review. Ann. occup. Hyg. 2005, 49, 575-585.
208. Wang, C.-c.; Jing, H.-p.; Wang, P., Three silver-based complexes constructed from organic carboxylic acid and 4,4'-bipyridine-like ligands: Syntheses, structures and photocatalytic properties. J. Mol. Struct. 2014, 1074, 92-99.
209. Huang, T.-H.; Yan, J.; Yang, H.; Qiang, L.; Du, H.-M., Synthesis, structure, characterization and fluorescent properties of Agþ complexes with extended p/p interactions. J. Mol. Struct. 2015, 1101, 66-72.
210. Li, H.; Han, Y.; Shao, Z.; Li, N.; Huang, C.; Hou, H., Water-stable Eu-MOF fluorescent sensors for trivalent metal ions and nitrobenzene. Dalton Trans. 2017, 46, 12201-12208.
211. III, S. W. T.; Joly, G. D.; Swager, T. M., Chemical Sensors Based on Amplifying Fluorescent Conjugated Polymers. Chem. Rev. 2007, 107, 1339-1386.
212. Brouwer, A. M., Standards for photoluminescence quantum yield measurements in solution (IUPAC Technical Report). Pure Appl. Chem. 2011, 83, 2213-2228.
213. Hou, J.-X.; Gao, J.-P.; Liu, J.; Jing, X.; Li, L.-J.; Du, J.-L., Highly selective and sensitive detection of Pb2+ and UO2 2+ ions based on a carboxyl-functionalized Zn(II)-MOF platform. Dyes and Pigments 2019, 160, 159-164.
214. Han, Y.; Li, J.-R.; Xie, Y.; Guo, G., Substitution reactions in metal–organic frameworks and metal–organic polyhedra. Chem. Soc. Rev. 2014, 43, 5952-5981.
215. Wang, M.-S.; Guo, S.-P.; Li, Y.; Cai, L.-Z.; Zou, J.-P.; Xu, G.; Zhou, W.-W.; Zheng, F.-K.; Guo, G.-C., A Direct White-Light-Emitting Metal-Organic Framework with Tunable Yellow-to-White Photoluminescence by Variation of Excitation Light. J. Am. Chem. Soc. 2009, 131, 13572-13573.
216. Lin, S.; Cui, Y.-Z.; Qiu, Q.-M.; Han, H.-L.; Li, Z.-F.; Liu, M.; Xin, X.-L.; Jin, Q.-H., Synthesis, characterization, luminescent properties of silver (I) complexes based on organic P-donor ligands and mercaptan ligands. Polyhedron 2017, 134, 319-329.
217. Yang, Y. Y.; Zhou, L.-X.; Zheng, Y. Q.; Zhu, H.-L.; Li, W.-Y., Hydrothermal synthesis, photoluminescence and photocatalytic properties of two silver(I) complexes. J. Solid State Chem. 2017, 253, 211-218.
218. Cui, Y.-Z.; Yuan, Y.; Li, Z.-F.; Liu, M.; Jin, Q.-H.; Jiang, N.; Cui, L.-N.; Gao, S., From ring, chain to network: Synthesis, characterization, luminescent properties of silver(I) complexes constructed by diphosphine ligands and various N-donor ligands. Polyhedron 2016, 112, 118-129.
219. Zhang, S.; Wang, Z.; Zhang, H.; Cao, Y.; Sun, Y.; Yiping Chen; Huang, C.; Yu, X., Self-assembly of two fluorescent supramolecular frameworks constructed from unsymmetrical benzene tricarboxylate and bipyridine. Inorganica Chimica Acta 2007, 360, 2704-2710.
220. Wu, Y.-J.; Hu, D.-C.; Yao, X.-Q.; Yang, Y.-X.; Liu, J.-C., Two new complexes constructed by semirigid carboxylic acid ligand: Synthesis, crystal structures, absorption of organic dye and photoluminescence properties. Inorganica Chimica Acta 2016, 453, 488-493.
221. Fei, H.; U, L. P.; Rogow, D. L.; Bresler, M. R.; Abdollahian, Y. A.; Oliver, S. R. J., Synthesis, Characterization, and Catalytic Application of a Cationic Metal-Organic Framework: Ag2(4,40-bipy)2(O3SCH2CH2SO3). Chem. Mater. 2010, 22, 2027-2032.
222. Wua, Y.; Wua, X.; Fang, S.; Yang, S.; Li, W.; Wang, H.; Yu, X., A novel hexanuclear silver(I) complex with photoluminescence properties. Polyhedron 2017, 122, 155-160.
223. Lu, X.; Ye, J.; Zhang, D.; Xie, R.; Bogale, R. F.; Suna, Y.; Zhao, L.; Zhao, Q.; Ning, G., Silver carboxylate metal–organic frameworks with highly antibacterial activity and biocompatibility. J. Inorg. Biochem. 2014, 138, 114-121.
224. Ding, Y.; Zhu, H.; Zhang, X.; Zhu, J.-J.; Burd, C., Rhodamine B derivative-functionalized upconversion nanoparticles for FRET-based Fe3+-sensing. Chem. Commun. 2013, 49, 7797-7799.
225. Wang, M.; Wang, J.; Xue, W.; Wu, A., A benzimidazole-based ratiometric fluorescent sensor for Cr3+ and Fe3+ in aqueous solution. Dyes and Pigments 2013, 97, 475-480.
226. Dang, S.; Ma, E.; Sun, Z.-M.; Zhang, H., A layer-structured Eu-MOF as a highly selective fluorescent probe for Fe3+ detection through a cation-exchange approach. J. Mater. Chem. 2012, 22, 16920-16926.
227. Hao, Z.; Song, X.; Zhu, M.; Meng, X.; Zhao, S.; Su, S.; Yang, W.; Song, S.; Zhang, H., One-dimensional channel-structured Eu-MOF for sensing small organic molecules and Cu2+ ion. J. Mater. Chem. A 2013, 1, 11043-11050.
228. Tang, Q.; Liu, S.; Liu, Y.; Miao, J.; Li, S.; Zhang, L.; Shi, Z.; Zheng, Z., Cation Sensing by a Luminescent Metal−Organic Framework with Multiple Lewis Basic Sites. Inorg. Chem. 2013, 52, 2799-2801.
229. Nguyen, C. V.; Chiang, W.-H.; Kevin. C.-W. Wu, Water- and Thermal-Stable Silver-based Photoluminescent Metal-Organic Coordination Polymer for Highly Selective Lead Ion Sensing. Bull. Chem. Soc. Jan. 2019.
230. Zhou, X.-H.; Li, L.; Li, H.-H.; Li, A.; Yang, T.; Huang, W., A flexible Eu(III)-based metal–organic framework: turn-off luminescent sensor for the detection of Fe(III) and picric acid. Dalton Trans. 2013, 42, 12403-12409.
231. He, G.; Peng, H.; Liu, T.; Yang, M.; Zhang, Y.; Fang, Y., A novel picric acid film sensor via combination of the surface enrichment effect of chitosan films and the aggregation-induced emission effect of siloles. J. Mater. Chem. 2009, 19, 7347-7353.
232. Yang, C.-X.; Ren, H.-B.; Yan, X.-P., Fluorescent Metal−Organic Framework MIL-53(Al) for Highly Selective and Sensitive Detection of Fe3+ in Aqueous Solution. Anal. Chem. 2013, 85, 7441-7446.
233. Qu, K.; Wang, J.; Ren, J.; Qu, X., Carbon Dots Prepared by Hydrothermal Treatment of Dopamine as an Effective Fluorescent Sensing Platform for the Label-Free Detection of Iron Achtungtrenung(III) Ions and Dopamine. Chem. Eur. J. 2013, 19, 7243-7249.
234. Wen, G.-X.; Han, M.-L.; Wu, X.-Q.; Wu, Y.-P.; Dong, W.-W.; Zhao, J.; Li, D.-S.; Ma, L.-F., A multi-responsive luminescent sensor based on a super-stable sandwich-type terbium(III)–organic framework. Dalton Trans. 2016, 45, 15492-15499.