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Journal articles on the topic 'Multi-functional Metal Organic Frameworks'

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Author: Grafiati

Published: 7 September 2023

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1

Li, Baiyan, Matthew Chrzanowski, Yiming Zhang, and Shengqian Ma. "Applications of metal-organic frameworks featuring multi-functional sites." Coordination Chemistry Reviews 307 (January 2016): 106–29. http://dx.doi.org/10.1016/j.ccr.2015.05.005.

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2

Vilela, Sérgio M. F., Duarte Ananias, Ana C. Gomes, Anabela A. Valente, Luís D. Carlos, José A. S. Cavaleiro, João Rocha, João P. C. Tomé, and Filipe A. Almeida Paz. "Multi-functional metal–organic frameworks assembled from a tripodal organic linker." Journal of Materials Chemistry 22, no. 35 (2012): 18354. http://dx.doi.org/10.1039/c2jm32501b.

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3

Wriedt, Mario, Darpandeep Aulakh, Wen An, Juby Varghese, Xuan Zhang, Kim R. Dunbar, and Marius Ciobanu. "Functional zwitterionic metal–organic frameworks with multi stimulus-responsive properties." Acta Crystallographica Section A Foundations and Advances 74, a1 (July 20, 2018): a203. http://dx.doi.org/10.1107/s0108767318097969.

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4

Cui, Yuanjing, Jun Zhang, Huajun He, and Guodong Qian. "Photonic functional metal–organic frameworks." Chemical Society Reviews 47, no. 15 (2018): 5740–85. http://dx.doi.org/10.1039/c7cs00879a.

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5

Cui, Yuanjing, Yanfeng Yue, Guodong Qian, and Banglin Chen. "Luminescent Functional Metal–Organic Frameworks." Chemical Reviews 112, no. 2 (June 21, 2011): 1126–62. http://dx.doi.org/10.1021/cr200101d.

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6

Zhao, Dian, Yuanjing Cui, Yu Yang, and Guodong Qian. "Sensing-functional luminescent metal–organic frameworks." CrystEngComm 18, no. 21 (2016): 3746–59. http://dx.doi.org/10.1039/c6ce00545d.

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7

Maji, Tapas Kumar. "Stimuli-responsive functional metal–organic frameworks." Acta Crystallographica Section A Foundations and Advances 73, a2 (December 1, 2017): C302. http://dx.doi.org/10.1107/s2053273317092713.

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8

Liu, Wenxian, Jijiang Huang, Qiu Yang, Shiji Wang, Xiaoming Sun, Weina Zhang, Junfeng Liu, and Fengwei Huo. "Multi-shelled Hollow Metal-Organic Frameworks." Angewandte Chemie 129, no. 20 (March 23, 2017): 5604–8. http://dx.doi.org/10.1002/ange.201701604.

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9

Liu, Wenxian, Jijiang Huang, Qiu Yang, Shiji Wang, Xiaoming Sun, Weina Zhang, Junfeng Liu, and Fengwei Huo. "Multi-shelled Hollow Metal-Organic Frameworks." Angewandte Chemie International Edition 56, no. 20 (March 23, 2017): 5512–16. http://dx.doi.org/10.1002/anie.201701604.

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10

Rabiee, Navid, Mohammad Rabiee, Soheil Sojdeh, Yousef Fatahi, Rassoul Dinarvand, Moein Safarkhani, Sepideh Ahmadi, et al. "Porphyrin Molecules Decorated on Metal-Organic Frameworks for Multi-Functional Biomedical Applications." Biomolecules 11, no. 11 (November 17, 2021): 1714. http://dx.doi.org/10.3390/biom11111714.

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Metal–organic frameworks (MOFs) have been widely used as porous nanomaterials for different applications ranging from industrial to biomedicals. An unpredictable one-pot method is introduced to synthesize NH2-MIL-53 assisted by high-gravity in a greener media for the first time. Then, porphyrins were deployed to adorn the surface of MOF to increase the sensitivity of the prepared nanocomposite to the genetic materials and in-situ cellular protein structures. The hydrogen bond formation between genetic domains and the porphyrin’ nitrogen as well as the surface hydroxyl groups is equally probable and could be considered a milestone in chemical physics and physical chemistry for biomedical applications. In this context, the role of incorporating different forms of porphyrins, their relationship with the final surface morphology, and their drug/gene loading efficiency were investigated to provide a predictable pattern in regard to the previous works. The conceptual phenomenon was optimized to increase the interactions between the biomolecules and the substrate by reaching the limit of detection to 10 pM for the Anti-cas9 protein, 20 pM for the single-stranded DNA (ssDNA), below 10 pM for the single guide RNA (sgRNA) and also around 10 nM for recombinant SARS-CoV-2 spike antigen. Also, the MTT assay showed acceptable relative cell viability of more than 85% in most cases, even by increasing the dose of the prepared nanostructures.

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11

Sanda, Suresh, Soumava Biswas, Srinivasulu Parshamoni, and Sanjit Konar. "Unraveling the multi-functional behavior in a series of Metal Organic Frameworks." Journal of Solid State Chemistry 229 (September 2015): 103–11. http://dx.doi.org/10.1016/j.jssc.2015.05.012.

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12

Jiao, Long, Joanne Yen Ru Seow, William Scott Skinner, Zhiyong U. Wang, and Hai-Long Jiang. "Metal–organic frameworks: Structures and functional applications." Materials Today 27 (July 2019): 43–68. http://dx.doi.org/10.1016/j.mattod.2018.10.038.

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13

Almeida Paz, Filipe A., Jacek Klinowski, Sérgio M. F. Vilela, João P. C. Tomé, José A. S. Cavaleiro, and João Rocha. "Ligand design for functional metal–organic frameworks." Chem. Soc. Rev. 41, no. 3 (2012): 1088–110. http://dx.doi.org/10.1039/c1cs15055c.

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14

Mendes, Ricardo F., and Filipe A. Almeida Paz. "Transforming metal–organic frameworks into functional materials." Inorganic Chemistry Frontiers 2, no. 6 (2015): 495–509. http://dx.doi.org/10.1039/c4qi00222a.

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15

Xu, Chunping, Ruiqi Fang, Rafael Luque, Liyu Chen, and Yingwei Li. "Functional metal–organic frameworks for catalytic applications." Coordination Chemistry Reviews 388 (June 2019): 268–92. http://dx.doi.org/10.1016/j.ccr.2019.03.005.

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16

Das, Madhab C., Shengchang Xiang, Zhangjing Zhang, and Banglin Chen. "Functional Mixed Metal-Organic Frameworks with Metalloligands." Angewandte Chemie International Edition 50, no. 45 (September 16, 2011): 10510–20. http://dx.doi.org/10.1002/anie.201101534.

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17

Sakamoto, Ryota, Naoya Fukui, Hiroaki Maeda, Ryojun Toyoda, Shinya Takaishi, Tappei Tanabe, Joe Komeda, Pilar Amo-Ochoa, Félix Zamora, and Hiroshi Nishihara. "Layered metal-organic frameworks and metal-organic nanosheets as functional materials." Coordination Chemistry Reviews 472 (December 2022): 214787. http://dx.doi.org/10.1016/j.ccr.2022.214787.

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18

Liu, Bo, Min Tu, Denise Zacher, and Roland A. Fischer. "Multi Variant Surface Mounted Metal-Organic Frameworks." Advanced Functional Materials 23, no. 30 (March 1, 2013): 3790–98. http://dx.doi.org/10.1002/adfm.201202996.

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19

Medishetty, Raghavender, Lydia Nemec, Venkatram Nalla, Sebastian Henke, Marek Samoć, Karsten Reuter, and Roland A. Fischer. "Multi-Photon Absorption in Metal-Organic Frameworks." Angewandte Chemie International Edition 56, no. 46 (October 24, 2017): 14743–48. http://dx.doi.org/10.1002/anie.201706492.

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20

Cheng, Xuanxuan, Zhongyi Jiang, Xiaopo Cheng, Song Guo, Lei Tang, Hao Yang, Hong Wu, et al. "Bimetallic metal-organic frameworks nanocages as multi-functional fillers for water-selective membranes." Journal of Membrane Science 545 (January 2018): 19–28. http://dx.doi.org/10.1016/j.memsci.2017.09.056.

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21

Ma, Dingxuan, Baiyan Li, and Zhan Shi. "Multi-functional sites catalysts based on post-synthetic modification of metal-organic frameworks." Chinese Chemical Letters 29, no. 6 (June 2018): 827–30. http://dx.doi.org/10.1016/j.cclet.2017.09.028.

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22

Chen, Xiao-Ming. "Crystal Engineering and Applications of Functional Metal-Organic Frameworks." Acta Crystallographica Section A Foundations and Advances 70, a1 (August 5, 2014): C16. http://dx.doi.org/10.1107/s2053273314099835.

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As a new kind of molecular materials composed of metal ions (or clusters) and organic bridging ligands that are interconnected by coordination bonds, porous metal-organic frameworks (MOFs) have many useful characteristics, such as high crystallinity, high porosity, structural diversity, designable frameworks, framework flexibility, as well as unique and modifiable organic pore surface. Therefore, they exhibit very promising potential applications in molecular adsorption/separation, catalysis, and sensors, etc. For example, they can be used for selective adsorption and separation of different gas molecules, such as CO2 and N2, capture of CO2 [2], sensing of small organic molecules and gas molecules, such as O2 and CO2, as well as catalysts and devices for solid-phase microextraction. In this presentation, the design and synthesis, unique pore surface, interesting functionalities will be presented by selected examples, in particular those of metal-azolate frameworks (MAFs) and a few devices useful for practical applications, from our group [1-3]. This work was supported by MoST (973 project) and NSFC.

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23

Tong, Xiao-Lan, Hai-Lu Lin, Jian-Hua Xin, Fen Liu, Min Li, and Xia-Ping Zhu. "Recent Advances as Materials of Functional Metal-Organic Frameworks." Journal of Nanomaterials 2013 (2013): 1–11. http://dx.doi.org/10.1155/2013/616501.

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Metal-organic frameworks (MOFs), also known as hybrid inorganic-organic materials, represent an emerging class of materials that have attracted the imagination of solid-state chemists because MOFs combine unprecedented levels of porosity with a range of other functional properties that occur through the metal moiety and/or the organic ligand. The purpose of this critical review is to give a representative and comprehensive overview of the arising developments in the field of functional metal-organic frameworks, including luminescence, magnetism, and porosity through presenting examples. This review will be of interest to researchers and synthetic chemists attempting to design multifunctional MOFs.

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24

Kong, Xueqian, Hexiang Deng, Fangyong Yan, Jihan Kim, Joseph A. Swisher, Berend Smit, Omar M. Yaghi, and Jeffrey A. Reimer. "Mapping of Functional Groups in Metal-Organic Frameworks." Science 341, no. 6148 (July 25, 2013): 882–85. http://dx.doi.org/10.1126/science.1238339.

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We determined the heterogeneous mesoscale spatial apportionment of functional groups in a series of multivariate metal-organic frameworks (MTV-MOF-5) containing BDC (1,4-benzenedicarboxylate) linkers with different functional groups—B (BDC-NH2), E (BDC-NO2), F [(BDC-(CH3)2], H [BDC-(OC3H5)2], and I [BDC-(OC7H7)2]—using solid-state nuclear magnetic resonance measurements combined with molecular simulations. Our analysis reveals that these methods discern between random (EF), alternating (EI and EHI), and various cluster (BF) forms of functional group apportionments. This combined synthetic, characterization, and computational approach predicts the adsorptive properties of crystalline MTV-MOF systems. This methodology, developed in the context of ordered frameworks, is a first step in resolving the more general problem of spatial disorder in other ordered materials, including mesoporous materials, functionalized polymers, and defect distributions within crystalline solids.

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25

Cui, Yuanjing, Bin Li, Huajun He, Wei Zhou, Banglin Chen, and Guodong Qian. "Metal–Organic Frameworks as Platforms for Functional Materials." Accounts of Chemical Research 49, no. 3 (February 15, 2016): 483–93. http://dx.doi.org/10.1021/acs.accounts.5b00530.

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26

Bukhari, Syed Nasir Abbas, Naveed Ahmed, Muhammad Wahab Amjad, Muhammad Ajaz Hussain, Mervat A. Elsherif, Hasan Ejaz, and Nasser H. Alotaibi. "Covalent Organic Frameworks (COFs) as Multi-Target Multifunctional Frameworks." Polymers 15, no. 2 (January 4, 2023): 267. http://dx.doi.org/10.3390/polym15020267.

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Covalent organic frameworks (COFs), synthesized from organic monomers, are porous crystalline polymers. Monomers get attached through strong covalent bonds to form 2D and 3D structures. The adjustable pore size, high stability (chemical and thermal), and metal-free nature of COFs make their applications wider. This review article briefly elaborates the synthesis, types, and applications (catalysis, environmental Remediation, sensors) of COFs. Furthermore, the applications of COFs as biomaterials are comprehensively discussed. There are several reported COFs having good results in anti-cancer and anti-bacterial treatments. At the end, some newly reported COFs having anti-viral and wound healing properties are also discussed.

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27

Seoane, Beatriz, Sonia Castellanos, Alla Dikhtiarenko, Freek Kapteijn, and Jorge Gascon. "Multi-scale crystal engineering of metal organic frameworks." Coordination Chemistry Reviews 307 (January 2016): 147–87. http://dx.doi.org/10.1016/j.ccr.2015.06.008.

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28

Li, Qiaowei, and Binbin Tu. "Metal–organic frameworks with multi-components in order." Acta Crystallographica Section A Foundations and Advances 73, a2 (December 1, 2017): C842. http://dx.doi.org/10.1107/s2053273317087320.

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29

Liang, Jieying, and Kang Liang. "Multi‐enzyme Cascade Reactions in Metal‐organic Frameworks." Chemical Record 20, no. 10 (July 24, 2020): 1100–1116. http://dx.doi.org/10.1002/tcr.202000067.

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30

Arhangelskis, Mihails, Athanassios D. Katsenis, Andrew J. Morris, and Tomislav Friščić. "Computational evaluation of metal pentazolate frameworks: inorganic analogues of azolate metal–organic frameworks." Chemical Science 9, no. 13 (2018): 3367–75. http://dx.doi.org/10.1039/c7sc05020h.

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We report a periodic density-functional theory evaluation of putative frameworks, including a topologically novel arhangelskite (arh) structure, based on the pentazolate ion, the ultimate all-nitrogen, inorganic member of the azolate series of aromatic 5-membered ring anions.

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31

Ma, Yuan Hui, Cheng Chun Tang, and Lei Zhang. "Property and Research Process of Metal-Organic Frameworks." Advanced Materials Research 427 (January 2012): 119–22. http://dx.doi.org/10.4028/www.scientific.net/amr.427.119.

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Metal-organic frameworks (MOFs) are new functional materials, which are developing quickly last years, especially as new hydrogen storage materials. This review introduces concept, characteristics, application, classification, and synthesis and development trend of metal-organic frameworks. Some new problems and difficulties in metal-organic frameworks study and next challenges are also discussed.

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32

Andrew Lin, Kun-Yi, Hsuan-Ang Chang, and Bo-Jau Chen. "Multi-functional MOF-derived magnetic carbon sponge." Journal of Materials Chemistry A 4, no. 35 (2016): 13611–25. http://dx.doi.org/10.1039/c6ta04619c.

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33

Sun, Jian-Ke, and Jie Zhang. "Functional metal–bipyridinium frameworks: self-assembly and applications." Dalton Transactions 44, no. 44 (2015): 19041–55. http://dx.doi.org/10.1039/c5dt03195h.

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Metal–organic frameworks as newly emerged materials have experienced rapid development in the last few years. This perspective highlights recent progress of study on the self-assembly of metal–bipyridinium frameworks and their intriguing properties for various applications.

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34

Huang, Yue, and San Huang Ke. "Hydrogen Storage in Metal-Organic Frameworks." Applied Mechanics and Materials 316-317 (April 2013): 946–49. http://dx.doi.org/10.4028/www.scientific.net/amm.316-317.946.

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Understanding of the physisorption of H2 in metal-organic frameworks (MOFs) is critical to improving its performance for hydrogen storage. By using first-principles calculations employing the van der Waals density functional (vdW-DF) method which can properly describe the vdW interaction, we investigate the binding energy of H2 in MOF-5 crystal. The accuracy of this methodology is first examined and good accuracy comparable to the correlated wavefunction methods is found. Calculations for the true crystal structure show that the small fragment models used in previous calculations cannot represent well the property of the crystal. The good accuracy and the ability to deal with the true crystal structure make the vdW-DF method a good candidate for investigating hydrogen storage in MOFs.

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35

Gu, Ying, Yuan Shuai Zhu, Bao Li, and Wu Lin Chen. "Deposition of Metal Clusters into the Functionalized Metal Organic Frameworks." Advanced Materials Research 496 (March 2012): 230–34. http://dx.doi.org/10.4028/www.scientific.net/amr.496.230.

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Utilizing first-principles density functional theory calculations, we identify that weak adhesion of metal clusters (for example Cu and Au) on pristine MOF-5, IRMOF-3, IRMOF-3-OH and IRMOF-3-SH, which reveals that metal clusters may be unable to stably exist in the pore of MOFs. Furthermore, upon removing the hydrogen of NH2, SH and OH functional groups, the adsorption energy between metal cluster and functionalized MOFs improve, which ascribes to chemical adsorption. Meanwhile, these metal clusters become cationic as a result of the formation of metal-O, S or N adhesion bonds. Hence, our study may provide a candidate approach to deposit metal clusters into the pore of MOFs.

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36

Ma, Shengqian, and Le Meng. "Energy-related applications of functional porous metal–organic frameworks." Pure and Applied Chemistry 83, no. 1 (November 10, 2010): 167–88. http://dx.doi.org/10.1351/pac-con-10-09-20.

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As a new type of functional materials, porous metal–organic frameworks (MOFs) have experienced tremendous development in the past decade. Their amenability to design, together with the functionalizable nanospace inside their frameworks, has afforded them great potential for various applications. In this review, we provide a brief summary of the current status of porous MOFs in energy-related applications, mainly, energy gas storage, CO2 capture, gas separation, catalysis, and fuel cells.

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37

Bosch, Mathieu, Muwei Zhang, and Hong-Cai Zhou. "Increasing the Stability of Metal-Organic Frameworks." Advances in Chemistry 2014 (September 18, 2014): 1–8. http://dx.doi.org/10.1155/2014/182327.

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Metal-organic frameworks (MOFs) are a new category of advanced porous materials undergoing study by many researchers for their vast variety of both novel structures and potentially useful properties arising from them. Their high porosities, tunable structures, and convenient process of introducing both customizable functional groups and unsaturated metal centers have afforded excellent gas sorption and separation ability, catalytic activity, luminescent properties, and more. However, the robustness and reactivity of a given framework are largely dependent on its metal-ligand interactions, where the metal-containing clusters are often vulnerable to ligand substitution by water or other nucleophiles, meaning that the frameworks may collapse upon exposure even to moist air. Other frameworks may collapse upon thermal or vacuum treatment or simply over time. This instability limits the practical uses of many MOFs. In order to further enhance the stability of the framework, many different approaches, such as the utilization of high-valence metal ions or nitrogen-donor ligands, were recently investigated. This review details the efforts of both our research group and others to synthesize MOFs possessing drastically increased chemical and thermal stability, in addition to exemplary performance for catalysis, gas sorption, and separation.

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38

Janiak, Christoph. "Functional Organic Analogues of Zeolites Based on Metal–Organic Coordination Frameworks." Angewandte Chemie International Edition in English 36, no. 1314 (August 4, 1997): 1431–34. http://dx.doi.org/10.1002/anie.199714311.

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39

Almeida Paz, Filipe. "The Road to Functional Lanthanide-Phosphonate Metal-Organic Frameworks." Acta Crystallographica Section A Foundations and Advances 70, a1 (August 5, 2014): C1228. http://dx.doi.org/10.1107/s2053273314087713.

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The endless possible combination of metal centers and organic ligands renders the field of Metal-Organic Frameworks (MOFs) an extremely rich playground for the design of new functional materials. The symbiotic co-existence of organic and inorganic components in these compounds embody the final products with unusual properties, which may, for example, ally photoluminescence with catalysis and even thermal robustness for more advanced technological applications. Our research group has focused on the development of functional MOFs based on rare-earth cations and polyphosphonate organic ligands, many of which designed and prepared in our laboratories. This poster summarizes the synthesis, structural elucidation and photophysical and catalytic properties of the novel one- (1D) and three-dimensional (3D) materials prepared using the tripodal (benzene-1,3,5-triyltris(methylene))triphosphonic acid (H6bmt) and the bipodal 1,4-phenylenebis(methylene)diphosphonic acid (H4pmd) organic ligands: [Ln(H4bmt)(H5bmt)(H2O)2]·3H2O (system 1: 1D), [Ln2(H3bmt)2(H2O)2]·H2O (system 2: 3D), and [Ln(Hpmd)(H2O)] (system 3: 3D) (please note: Ln stands for a rare-earth cation) [1-3]. System 1 is an outstanding heterogeneous catalyst in the methanolysis of styrene oxide at nearly room temperature, even outperforming the well-known nano-sized HKUST-1 MOF material. System 2 exhibits unusual photoluminescent properties: the Tb-containing material has an absolute emission quantum yield of ca. 46%; for the Eu-containing compound this value is easily increased from ca. 15% to 54% by removing, under vacuum, all water molecules in the material, this being only possible due to its typical zeolitic behaviour. System 3 can be prepared in large quantitites as either micro- or nano-sized crystals, with the latter exhibiting a remarkable high heterogeneous catalytic activity. Fundação para a Ciência e a Tecnologia (FCT, Portugal; EXPL/CTM-NAN/0013/2013 - FCOMP-01-0124-FEDER-041282), Bruker AXS (Karlsruhe, Germany), the European Union, QREN, FEDER, COMPETE and Laboratório Associado CICECO (PEst-C/CTM/LA0011/2013) are gratefully acknowledged for funding the research and the dissemination of the results. The presenting author also wishes to thank all the collaborators involved in the referenced publications.

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40

Li, Zhi-Gang, Kai Li, Li-Yuan Dong, Tian-Meng Guo, Muhammad Azeem, Wei Li, and Xian-He Bu. "Acoustic Properties of Metal-Organic Frameworks." Research 2021 (June 1, 2021): 1–11. http://dx.doi.org/10.34133/2021/9850151.

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Metal-organic frameworks (MOFs) have attracted significant attention in the past two decades due to their diverse physical properties and associated functionalities. Although numerous advances have been made, the acoustic properties of MOFs have attracted very little attention. Here, we systematically investigate the acoustic velocities and impedances of 19 prototypical MOFs via first-principle calculations. Our results demonstrate that these MOFs exhibit a wider range of acoustic velocities, higher anisotropy, and lower acoustic impedances than their inorganic counterparts, which are ascribed to their structural diversity and anisotropy, as well as low densities. In addition, the piezoelectric properties, which are intimately related to the acoustic properties, were calculated for 3 MOFs via density functional perturbation theory, which reveals that MOFs can exhibit significant piezoelectricity due to the ionic contribution. Our work provides a comprehensive study of the fundamental acoustic properties of MOFs, which could stimulate further interest in this new exciting field.

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41

Donà, Lorenzo, Jan Gerit Brandenburg, and Bartolomeo Civalleri. "Metal–organic frameworks properties from hybrid density functional approximations." Journal of Chemical Physics 156, no. 9 (March 7, 2022): 094706. http://dx.doi.org/10.1063/5.0080359.

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The chemical versatility and modular nature of Metal–Organic Frameworks (MOFs) make them unique hybrid inorganic–organic materials for several important applications. From a computational point of view, ab initio modeling of MOFs is a challenging and demanding task, in particular, when the system reaches the size of gigantic MOFs as MIL-100 and MIL-101 (where MIL stands for Materials Institute Lavoisier) with several thousand atoms in the unit cell. Here, we show how such complex systems can be successfully tackled by a recently proposed class of composite electronic structure methods revised for solid-state calculations. These methods rely on HF/density functional theory hybrid functionals (i.e., PBEsol0 and HSEsol) combined with a double-zeta quality basis set. They are augmented with semi-classical corrections to take into account dispersive interactions (D3 scheme) and the basis set superposition error (gCP). The resulting methodologies, dubbed “sol-3c,” are cost-effective yet reach the hybrid functional accuracy. Here, sol-3c methods are effectively applied to predict the structural, vibrational, electronic, and adsorption properties of some of the most common MOFs. Calculations are feasible even on very large MOFs containing more than 2500 atoms in the unit cell as MIL-100 and MIL-101 with reasonable computing resources. We propose to use our composite methods for the routine in silico screening of MOFs targeting properties beyond plain structural features.

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42

Zou, Chao, and Chuan-De Wu. "Functional porphyrinic metal–organic frameworks: crystal engineering and applications." Dalton Transactions 41, no. 14 (2012): 3879. http://dx.doi.org/10.1039/c2dt11989g.

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43

Jiang, Hai-Long, and Qiang Xu. "Porous metal–organic frameworks as platforms for functional applications." Chemical Communications 47, no. 12 (2011): 3351. http://dx.doi.org/10.1039/c0cc05419d.

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44

Jiang, Hai-Long, Trevor A. Makal, and Hong-Cai Zhou. "Interpenetration control in metal–organic frameworks for functional applications." Coordination Chemistry Reviews 257, no. 15-16 (August 2013): 2232–49. http://dx.doi.org/10.1016/j.ccr.2013.03.017.

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45

Li, Zhongfeng, Qimeng Zhang, Xu Xiao, Yang Tian, Xin Zhang, Jun Gao, Zhuoyong Zhang, and Xiang Li. "Metal-organic frameworks: For functional surface enhancement Raman scattering." Chinese Science Bulletin 65, no. 35 (July 28, 2020): 4027–36. http://dx.doi.org/10.1360/tb-2020-0749.

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46

Almeida Paz, Filipe A., Jacek Klinowski, Sergio M. F. Vilela, Joao P. C. Tome, Jose A. S. Cavaleiro, and Joao Rocha. "ChemInform Abstract: Ligand Design for Functional Metal-Organic Frameworks." ChemInform 43, no. 17 (March 29, 2012): no. http://dx.doi.org/10.1002/chin.201217248.

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47

Mendes, Ricardo F., and Filipe A. Almeida Paz. "ChemInform Abstract: Transforming Metal-Organic Frameworks into Functional Materials." ChemInform 46, no. 28 (June 25, 2015): no. http://dx.doi.org/10.1002/chin.201528272.

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48

Das, Madhab C., Shengchang Xiang, Zhangjing Zhang, and Banglin Chen. "ChemInform Abstract: Functional Mixed Metal-Organic Frameworks with Metalloligands." ChemInform 43, no. 7 (January 23, 2012): no. http://dx.doi.org/10.1002/chin.201207211.

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49

Denny, Michael S., Mark Kalaj, Kyle C. Bentz, and Seth M. Cohen. "Multicomponent metal–organic framework membranes for advanced functional composites." Chemical Science 9, no. 47 (2018): 8842–49. http://dx.doi.org/10.1039/c8sc02356e.

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Abstract:

Several strategies are presented for combining different metal–organic frameworks (MOFs) into composite mixed-matrix membranes. Some membranes are shown to be component for multistep organic catalytic transformations.

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50

Rojas, Sara, Paul S. Wheatley, Elsa Quartapelle-Procopio, Barbara Gil, Bartosz Marszalek, Russell E. Morris, and Elisa Barea. "Metal–organic frameworks as potential multi-carriers of drugs." CrystEngComm 15, no. 45 (2013): 9364. http://dx.doi.org/10.1039/c3ce41289j.

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