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1

Hu, Chuanjiang, Charles E. Schulz, and W. Robert Scheidt. "All high-spin (S = 2) iron(ii) hemes are NOT alike." Dalton Transactions 44, no. 42 (2015): 18301–10. http://dx.doi.org/10.1039/c5dt02795k.

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2

Müller-Buschbaum, Klaus. "3D-[Pr(Im)3(ImH)]@ImH: Ein dreidimensionales Netzwerk mit vollständiger Stickstoffkoordination aus einer Imidazolschmelze / 3D-[Pr(Im)3(ImH)]@ImH: A Three-Dimensional Network with Complete Nitrogen Coordination Obtained from an Imidazole Melt." Zeitschrift für Naturforschung B 61, no. 7 (2006): 792–98. http://dx.doi.org/10.1515/znb-2006-0704.

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The reaction of a melt of unsubstituted imidazole with praseodymium metal yields bright green crystals of 3D-[Pr(Im)3(ImH)]@ImH. Imidazolate ligands coordinate η1 via both N atoms their 1,3 positioning within the heterocycle being responsible for the connection of praseodymium atoms. A 3-dimensional network is formed with imidazole molecules from the melt intercalated in the crystal structure. The imidazole molecules can be released and temperature dependent reversibly be exchanged with gas molecules including argon. Thus the solvent free high temperature synthesis of rare earth elements with
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3

Hao, Tong, Hui-Zi Li, Fei Wang, and Jian Zhang. "Tetrahedral Imidazolate Frameworks with Auxiliary Ligands (TIF-Ax): Synthetic Strategies and Applications." Molecules 28, no. 16 (2023): 6031. http://dx.doi.org/10.3390/molecules28166031.

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Zeolitic imidazolate frameworks (ZIFs) are an important subclass of metal–organic frameworks (MOFs). Recently, we reported a new kind of MOF, namely tetrahedral imidazolate frameworks with auxiliary ligands (TIF-Ax), by adding linear ligands (Hint) into the zinc–imidazolate system. Introducing linear ligands into the M2+-imidazolate system overcomes the limitation of imidazole derivatives. Thanks to the synergistic effect of two different types of ligands, a series of new TIF-Ax with interesting topologies and a special pore environment has been reported, and they have attracted extensive atte
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4

Wu, Qi, Zhen Yao, and Jianfeng Li. "Synthesis and characterization of (cryptand-222)potassium (2-methylimidazolato)(meso-tetraphenylporphinato)ferrate(II)–2-methylimidazole–tetrahydrofuran (1/1/2)." Acta Crystallographica Section C Structural Chemistry 73, no. 9 (2017): 688–91. http://dx.doi.org/10.1107/s2053229617009202.

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Metalloporphyrin complexes containing an additional imidazole ligand can provide information about the effect of deprotonation or hydrogen bonding on the axial histidine unit in heme proteins. The title high-spin five-coordinate imidazolate-ligated iron(II) porphyrinate, [K(C18H36N2O6)][Fe(C4H5N2)(C44H28N4)]·C4H6N2·2C4H8O, has been synthesized and investigated. The solvated salt crystallizes with one 2-methylimidazole molecule, two tetrahydrofuran solvent molecules and a potassium cation chelated inside a cryptand-222 (4,7,13,16,21,24-hexaoxa-1,10-diazabicyclo[8.8.8]hexacosane) molecule. The i
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5

Jaafar, Amani, Carlos Platas-Iglesias, and Rana A. Bilbeisi. "Thiosemicarbazone modified zeolitic imidazolate framework (TSC-ZIF) for mercury(ii) removal from water." RSC Advances 11, no. 27 (2021): 16192–99. http://dx.doi.org/10.1039/d1ra02025k.

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Zeolitic imidazolate frameworks Ald-ZIF were obtained by mixing two imidazole-based linkers with zinc(ii). Post-synthetically modified Ald-ZIFs with thiosemicarbazide group improved mercury(ii) removal efficiency from water at a capacity of 1667 mg g<sup>−1</sup>.
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6

Shi, Qi, Fei Wang, Xiaozhen Kang, et al. "A single precursor approach for ZIF synthesis: transformation of a new 1D [Zn(Im)(HIm)2(OAc)] structure to 3D Zn(Im)2 frameworks." CrystEngComm 17, no. 21 (2015): 3998–4005. http://dx.doi.org/10.1039/c5ce00211g.

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We successfully use a 1-dimensional (1D) chain structure with the formula [Zn(Im)(HIm)<sub>2</sub>(OAc)] (Im = imidazolate, HIm = imidazole, OAc = carboxylate) as a single precursor/source of a metal and ligand to directly prepare 3-dimensional (3D) [Zn(Im)<sub>2</sub>] frameworks.
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7

Sponza, Deli̇a Teresa, and Ruki̇ye Özteki̇n. "Zeolitic Imidazolate/Fe3O4 Nanocomposite for Removal of Polystyrene and 4-tert-butylphenol via Adsorption." WSEAS TRANSACTIONS ON ENVIRONMENT AND DEVELOPMENT 19 (October 17, 2023): 1071–82. http://dx.doi.org/10.37394/232015.2023.19.101.

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Simultaneous removal of microplastics and endocrine disruptors was performed with high yields using Zeolitic imidazolate/Fe3O4 nanocomposite. Polystyrene and 4-tert-butylphenol were used to indicate the microplastic and endocrine disruptors. Under optimal conditions for maximum yields, the matrix was as follows: 1.5 mg/l Zeolitic imidazolate/Fe3O4 nanocomposite, 30 min adsorption time at a Zeolitic imidazolate to Fe3O4 ratio of 1/1, and 6 mg/l individual polystyrene 4-tert-butylphenol concentrations. Under these conditions, 99% and 98% removals were detected for polystyrene and 4-tert-butylphe
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8

Szilágyi, István, László Horváth, Imre Labádi, Klara Hernadi, István Pálinkó, and Tamás Kiss. "Mimicking catalase and catecholase enzymes by copper(II)-containing complexes." Open Chemistry 4, no. 1 (2006): 118–34. http://dx.doi.org/10.1007/s11532-005-0009-6.

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AbstractAn imidazolate-bridged copper(II)-zinc(II) complex (Cu(II)-diethylenetriamino-μ-imidazolato-Zn(II)-tris(2-aminoethyl)amine perchlorate (denoted as “Cu,Zn complex”) and a simple copper(II) complex (Cu(II)-tris(2-aminoethyl) amine chloride (“Cu-tren”) were prepared and immobilised on silica gel (by hydrogen or covalent bonds) and montmorillonite (by ion exchange). The immobilised substances were characterised by FT-IR spectroscopy and their thermal characteristics were also studied. The obtained materials were tested in two probe reactions: catalytic oxidation of 3,5-di-tert-butyl catech
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9

Noh, Kyungkyou, Jaeung Sim, Jonghoon Kim, and Jaheon Kim. "Metal imidazolate sulphate frameworks as a variation of zeolitic imidazolate frameworks." Chemical Communications 58, no. 18 (2022): 2983–86. http://dx.doi.org/10.1039/d1cc07046k.

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10

Frentzel-Beyme, Louis, Marvin Kloß, Roman Pallach, et al. "Porous purple glass – a cobalt imidazolate glass with accessible porosity from a meltable cobalt imidazolate framework." Journal of Materials Chemistry A 7, no. 3 (2019): 985–90. http://dx.doi.org/10.1039/c8ta08016j.

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11

Liu, Chuanyao, and Aisheng Huang. "One-step synthesis of the superhydrophobic zeolitic imidazolate framework F-ZIF-90 for efficient removal of oil." New Journal of Chemistry 42, no. 4 (2018): 2372–75. http://dx.doi.org/10.1039/c7nj04373b.

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12

Patel, R. N., Nripendra Singh, K. K. Shukla, and U. K. Chauhan. "Novel copper(II)-dien-imidazole/imidazolate-bridged copper(II) complexes." Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy 61, no. 1-2 (2005): 287–97. http://dx.doi.org/10.1016/j.saa.2004.03.009.

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13

Ko, S. W., and H. Chung. "Photocatalytic Degradation of Tetracycline Hydrochloride using Hybrid C60 Fullerene Nanowhisker-Zeolitic Imidazolate Framework-8 Composite under Blue Light Emitting Diode Irradiation." Asian Journal of Chemistry 36, no. 12 (2024): 2755–59. https://doi.org/10.14233/ajchem.2024.31962.

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The C60 fullerene nanowhisker (FNW)-zeolitic imidazolate framework-8 (ZIF-8) composite was synthesized using C60 fullerene nanowhisker, 2-methyl imidazole, zinc nitrate hexahydrate in methanol. The characterization of C60 FNW-ZIF-8 composite was identified using X-ray diffraction (XRD), Raman spectroscopy and scanning electron microscopy (SEM). The photocatalytic activity for tetracycline hydrochloride degradation was confirmed by UV-visible spectroscopy. A kinetic study indicated that hybrid nanocomposite catalyzed the photodegradation of tetracycline hydrochloride under blue light emitting d
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14

Sunatsuki, Yukinari, Hiromi Ohta, Masaaki Kojima, et al. "Supramolecular Spin-Crossover Iron Complexes Based on Imidazole−Imidazolate Hydrogen Bonds." Inorganic Chemistry 43, no. 14 (2004): 4154–71. http://dx.doi.org/10.1021/ic0498384.

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15

Ram, N. Patel, P. Patel Ayodhya, and B. Pandeya Krishna. "Synthesis, magnetic and spectral properties of binuclear imidazolate bridged copper(II)-copper(II) and copper(II)-zinc(II) complexes." Journal of Indian Chemical Society Vol. 78, Jan 2001 (2001): 6–8. https://doi.org/10.5281/zenodo.5846016.

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Department of Chemistry, A P. S. University, Rewa-486 003, India <em>Manuscript received 1 November 1999, revised 17 April 2000. accepted 26 August 2000</em> Two new binuclear imidazolate bridged complexes, [(PAN)Cu(im)Cu(PAN)] (ClO<sub>4</sub>)<sub>2</sub>&nbsp;and&nbsp;[(PAN)Cu(im)Zn(PAN)](ClO<sub>4</sub>)<sub>2</sub> (PAN =1. (2-pyridylazo)-2-naphthol, im = imidazolate) have been prepared. Room temperature magnetic susceptibility of [(PAN)Cu(im)Cu(PAN)] (ClO<sub>4</sub>)<sub>2</sub>&nbsp;(reveals the presence of intramolecular antiferromagnetic interactions through the imidazolate bridge. X
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16

Hayashi, Hideki, Adrien P. Côté, Hiroyasu Furukawa, Michael O’Keeffe, and Omar M. Yaghi. "Zeolite A imidazolate frameworks." Nature Materials 6, no. 7 (2007): 501–6. http://dx.doi.org/10.1038/nmat1927.

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17

Zhang, Jian, Tao Wu, Cong Zhou, Shumei Chen, Pingyun Feng, and Xianhui Bu. "Zeolitic Boron Imidazolate Frameworks." Angewandte Chemie International Edition 48, no. 14 (2009): 2542–45. http://dx.doi.org/10.1002/anie.200804169.

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18

Zhang, Jian, Tao Wu, Cong Zhou, Shumei Chen, Pingyun Feng, and Xianhui Bu. "Zeolitic Boron Imidazolate Frameworks." Angewandte Chemie 121, no. 14 (2009): 2580–83. http://dx.doi.org/10.1002/ange.200804169.

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19

Singh, Shristy, and Gurmeet Kaur. "Environment friendly synthesis and characterization of manganese(II) Imidazolate framework." E3S Web of Conferences 509 (2024): 01005. http://dx.doi.org/10.1051/e3sconf/202450901005.

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This work describes the synthesis and characterization of manganese (II) imidazolate framework (MIF) using an environmentally friendly approach. The MIF, which is novel compound was synthesized for the first time using water as the solvent and imidazole as the ligand under temperate reaction conditions. The synthesized MIF was characterized by multitude of analytical techniques, considering (powder) X-ray diffraction (PXRD), Transmission electron microscopy (TEM), Energy dispersive X-ray spectrometry (EDX) and Fourier-transform infrared spectroscopy (FTIR). The characterization results disclos
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20

Lee, Wan-Chi, Heng-Ta Chien, Yang Lo, Hao-Che Chiu, Tung-ping Wang, and Dun-Yen Kang. "Synthesis of Zeolitic Imidazolate Framework Core–Shell Nanosheets Using Zinc-Imidazole Pseudopolymorphs." ACS Applied Materials & Interfaces 7, no. 33 (2015): 18353–61. http://dx.doi.org/10.1021/acsami.5b04217.

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21

Gustafsson, Mikaela, and Xiaodong Zou. "Crystal formation and size control of zeolitic imidazolate frameworks with mixed imidazolate linkers." Journal of Porous Materials 20, no. 1 (2012): 55–63. http://dx.doi.org/10.1007/s10934-012-9574-1.

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22

Luanwuthi, Santamon, Atiweena Krittayavathananon, Pattarachai Srimuk, and Montree Sawangphruk. "In situ synthesis of permselective zeolitic imidazolate framework-8/graphene oxide composites: rotating disk electrode and Langmuir adsorption isotherm." RSC Advances 5, no. 58 (2015): 46617–23. http://dx.doi.org/10.1039/c5ra05950j.

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23

Sassone, Daniele, Sergio Bocchini, Marco Fontana, et al. "Imidazole-imidazolate pair as organo-electrocatalyst for CO2 reduction on ZIF-8 material." Applied Energy 324 (October 2022): 119743. http://dx.doi.org/10.1016/j.apenergy.2022.119743.

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24

Elliott, Michael G., and Rex E. Shepherd. "Pentaammineruthenium(II/III) imidazole and imidazolate complexes of 2-carboxylatoimidazolate and 2-imidazolecarboxaldehyde." Inorganic Chemistry 26, no. 13 (1987): 2067–73. http://dx.doi.org/10.1021/ic00260a012.

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25

Zhang, Jian, Tao Wu, Pingyun Feng, and Xianhui Bu. "Hydrogen-bonded boron imidazolate frameworks." Dalton Trans. 39, no. 7 (2010): 1702–4. http://dx.doi.org/10.1039/b924633a.

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26

Junggeburth, Sebastian C., Katharina Schwinghammer, Kulpreet S. Virdi, Christina Scheu, and Bettina V. Lotsch. "Towards Mesostructured Zinc Imidazolate Frameworks." Chemistry - A European Journal 18, no. 7 (2012): 2143–52. http://dx.doi.org/10.1002/chem.201101530.

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27

Safin, Damir A., Koen Robeyns, and Yaroslav Filinchuk. "Magnesium imidazolate – a first porous zeolitic imidazolate framework with alkali and alkaline earth metals." Acta Crystallographica Section A Foundations and Advances 72, a1 (2016): s402. http://dx.doi.org/10.1107/s2053273316094134.

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28

Wang, Hao, Lauren R. Grabstanowicz, Heather M. Barkholtz, et al. "Impacts of Imidazolate Ligand on Performance of Zeolitic-Imidazolate Framework-Derived Oxygen Reduction Catalysts." ACS Energy Letters 4, no. 10 (2019): 2500–2507. http://dx.doi.org/10.1021/acsenergylett.9b01740.

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29

Hussain, M. Althaf, Yarasi Soujanya, and G. Narahari Sastry. "Computational Design of Functionalized Imidazolate Linkers of Zeolitic Imidazolate Frameworks for Enhanced CO2 Adsorption." Journal of Physical Chemistry C 119, no. 41 (2015): 23607–18. http://dx.doi.org/10.1021/acs.jpcc.5b08043.

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30

Tian, Yun-Qi, Hai-Jun Xu, Yi-Zhi Li, and Xiao-Zeng You. "[CoIICuI2(Im)4];∞: A Layered Bimetallic Imidazolate Polymer, the First Hybridized Cobalt(II) Imidazolate." Zeitschrift für anorganische und allgemeine Chemie 630, no. 10 (2004): 1371–73. http://dx.doi.org/10.1002/zaac.200400111.

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31

Zhu, Zhishun, and Xiulan Zhang. "Controlled Delivery of 2-Mercapto 1-Methyl Imidazole by Metal–Organic Framework for Efficient Inhibition of Copper Corrosion in NaCl Solution." Materials 16, no. 20 (2023): 6712. http://dx.doi.org/10.3390/ma16206712.

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In this paper, zeolitic imidazolate framework-8 was modified by N-(3-aminopropyl)-imidazole to obtain a novel MOF called AMOF. Subsequently, AMOF served as a carrier for the delivery of 2-mercapto-1-methyl imidazole (MMI) to inhibit the corrosion of Cu. Scanning electron microscopy, Fourier transform infrared spectroscopy, and X-ray diffraction were applied to characterize the morphologies and structures of AMOF and AMOF@MMI. Ultraviolet-visible spectroscopy and thermogravimetric analysis were adopted to value the capacity of the load and release of the AMOF, respectively. The mass ratio of lo
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32

H., L. NIGAM, B. PANDEYA KRISHNA, and S. VERMA V. "D.M.E. Behaviour of Copper(II)-Glycylglycine and Copper(II)-Giycylglycine-lmidazole Systems." Journal Of India Chemical Society Vol.66, Aug-Oct 1989 (1989): 541–45. https://doi.org/10.5281/zenodo.5995146.

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Department of Chemistry, A. P. S. University,&nbsp;Rewa-486 003 Polarographic behaviour of the binary system copper(II)-glygly and ternary systems copper(II)-glygly-lmH (1&nbsp;: 1: 0.5 and 1: 1&nbsp;:1) have been studied at d.m.e. The polarographic waves for various species formed have been&nbsp;identified. The imidazolate bridged binuclear copper(II) complex of glygly undergoes one-step reversible reduction suggesting simultaneous two-electron reduction or the two copper centres. If has been proposed that the bridging imidazolate ion accepts the electrons from the d.m.e. and transfers them s
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33

Elmorsy, Esraa S., Ayman Mahrous, Wael A. Amer, and Mohamad M. Ayad. "Nitrogen-Doped Carbon Dots in Zeolitic Imidazolate Framework Core-Shell Nanocrystals: Synthesis and Characterization." Solid State Phenomena 336 (August 30, 2022): 81–87. http://dx.doi.org/10.4028/p-206xsy.

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Metal-organic frameworks (MOFs) have exciting properties and promising applications in different fields. In this work, novel zeolitic imidazolate frameworks (ZIFs) have been synthesized by encapsulating N-doped carbon quantum dots (N-CDs) with a blue FL into the zeolitic imidazolate framework materials core-shell structure (ZIF-8@ZIF-67). The functionalized core-shell MOFs maintained their crystal structure, morphology, and enhanced UV-vis absorbance. The properties of these new composites exhibit excellent potential for different applications including sensing, photo-catalysis, and selective
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34

Son, Ye Rim, Minseok Kwak, Songyi Lee, and Hyun Sung Kim. "Strategy for Encapsulation of CdS Quantum Dots into Zeolitic Imidazole Frameworks for Photocatalytic Activity." Nanomaterials 10, no. 12 (2020): 2498. http://dx.doi.org/10.3390/nano10122498.

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Encapsulating CdS quantum dots (QDs) into zeolitic imidazole framework-8 (ZIF-8) can offer several advantages for photocatalysis. Various types of capping agents have been used to encapsulate QDs into ZIF-8 nanopores. An effective method for encapsulating CdS QDs into ZIF-8 is to use 2-mercaptoimidazole as the capping agent. This is because 2-mercaptoimidazole is similar to the imidazolate ligands of ZIFs and can used for capping active species with simultaneous encapsulation during the crystal growth of ZIF-8. Compared to other widely used capping agents such as polyvinylpyrrolidone (PVP), us
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35

Cui, Bo, Lirong Zhao, Jin Tong, Xiayan Wang, and Shuyan Yu. "Constructing Supramolecular Frameworks Based Imidazolate-Edge-Bridged Metallacalix[3]arenes via Hierarchical Self-Assemblies." Crystals 12, no. 2 (2022): 212. http://dx.doi.org/10.3390/cryst12020212.

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Hierarchical self-assembly of novel supramolecular structures has obtained increasing attention. Herein we design and synthesize the palladium(II)-based molecular basket-like structures, as structural analog of metallacalix[3]arene [M3L3]3+ (M = (dmbpy)Pd, (phen)Pd; dmbpy = 4,4’-dimethyl-bipyridine; phen = 1,10-phenanthroline), by coordination-driven self-assembly from imidazolate-containing ligand [4,5-bis(2,5-dimethylthiophen-3-yl)-1H-imidazole (HL) with palladium(II) nitrate precursors (dmbpy)Pd(NO3)2 and (phen)Pd(NO3)2. The difference of the palladium(II) nitrate precursors with π-surface
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36

Cui, Xue, Jianting Ma, Tingting Zeng, Junyu Xu, Youbin Li, and Xuesong Wang. "Metal-free cascade synthesis of unsymmetrical 2-aminopyrimidines from imidazolate enaminones." RSC Advances 11, no. 39 (2021): 24247–53. http://dx.doi.org/10.1039/d1ra04319f.

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37

Xiong, Mo, Neng Li, Guanchao Yin, Wai-Yim Ching, and Xiujian Zhao. "Effects of the halogenated imidazolate linker on the fundamental properties of amorphous zeolitic imidazolate frameworks." Journal of Non-Crystalline Solids 536 (May 2020): 120005. http://dx.doi.org/10.1016/j.jnoncrysol.2020.120005.

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38

Linder-Patton, Oliver M., Thomas J. de Prinse, Shuhei Furukawa, et al. "Influence of nanoscale structuralisation on the catalytic performance of ZIF-8: a cautionary surface catalysis study." CrystEngComm 20, no. 34 (2018): 4926–34. http://dx.doi.org/10.1039/c8ce00746b.

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39

Li, Yizhou, Yepeng Yang, Daomei Chen, et al. "Liquid-Phase Catalytic Oxidation of Limonene to Carvone over ZIF-67(Co)." Catalysts 9, no. 4 (2019): 374. http://dx.doi.org/10.3390/catal9040374.

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Liquid-phase catalytic oxidation of limonene was carried out under mild conditions, and carvone was produced in the presence of ZIF-67(Co), cobalt based zeolitic imidazolate framework, as catalyst, using t-butyl hydroperoxide (t-BHP) as oxidant and benzene as solvent. As a heterogeneous catalyst, the zeolitic imidazolate framework ZIF-67(Co) exhibited reasonable substrate–product selectivity (55.4%) and conversion (29.8%). Finally, the X-ray diffraction patterns of the catalyst before and after proved that ZIF-67(Co) acted as a heterogeneous catalyst, and can be reused without losing its activ
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40

Kaneshige, Takaya, Hikaru Sakamoto, and Masataka Ohtani. "Thermal crystal phase transition in zeolitic imidazolate frameworks induced by nanosizing the crystal." Chemical Communications 58, no. 29 (2022): 4588–91. http://dx.doi.org/10.1039/d2cc00486k.

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41

Baxter, Emma F., Thomas D. Bennett, Andrew B. Cairns, et al. "A comparison of the amorphization of zeolitic imidazolate frameworks (ZIFs) and aluminosilicate zeolites by ball-milling." Dalton Transactions 45, no. 10 (2016): 4258–68. http://dx.doi.org/10.1039/c5dt03477a.

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42

Butler, Keith T., Stephen D. Worrall, Christopher D. Molloy, et al. "Electronic structure design for nanoporous, electrically conductive zeolitic imidazolate frameworks." Journal of Materials Chemistry C 5, no. 31 (2017): 7726–31. http://dx.doi.org/10.1039/c7tc03150e.

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43

Zheng, Bin, Yihan Zhu, Fang Fu, Lian Li Wang, Jinlei Wang, and Huiling Du. "Theoretical prediction of the mechanical properties of zeolitic imidazolate frameworks (ZIFs)." RSC Advances 7, no. 66 (2017): 41499–503. http://dx.doi.org/10.1039/c7ra07242b.

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44

Chen, Binling, Zhuxian Yang, Yanqiu Zhu, and Yongde Xia. "Zeolitic imidazolate framework materials: recent progress in synthesis and applications." J. Mater. Chem. A 2, no. 40 (2014): 16811–31. http://dx.doi.org/10.1039/c4ta02984d.

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45

Jiang, Zhen, Weijun Lu, Zhengping Li, et al. "Synthesis of amorphous cobalt sulfide polyhedral nanocages for high performance supercapacitors." J. Mater. Chem. A 2, no. 23 (2014): 8603–6. http://dx.doi.org/10.1039/c3ta14430e.

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46

Fu, Xinwei, Zhangyou Yang, Tao Deng, et al. "A natural polysaccharide mediated MOF-based Ce6 delivery system with improved biological properties for photodynamic therapy." Journal of Materials Chemistry B 8, no. 7 (2020): 1481–88. http://dx.doi.org/10.1039/c9tb02482d.

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47

Gugin, Nikita, Jose A. Villajos, Ines Feldmann, and Franziska Emmerling. "Mix and wait – a relaxed way for synthesizing ZIF-8." RSC Advances 12, no. 15 (2022): 8940–44. http://dx.doi.org/10.1039/d2ra00740a.

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48

Henke, Sebastian, Michael T. Wharmby, Gregor Kieslich, et al. "Pore closure in zeolitic imidazolate frameworks under mechanical pressure." Chemical Science 9, no. 6 (2018): 1654–60. http://dx.doi.org/10.1039/c7sc04952h.

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Gómez-Álvarez, Paula, Said Hamad, Maciej Haranczyk, A. Rabdel Ruiz-Salvador, and Sofia Calero. "Comparing gas separation performance between all known zeolites and their zeolitic imidazolate framework counterparts." Dalton Transactions 45, no. 1 (2016): 216–25. http://dx.doi.org/10.1039/c5dt04012d.

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Li, Yang, Shumei Chen, Xin Wu, Huabin Zhang, and Jian Zhang. "A hybrid zeolitic imidazolate framework-derived ZnO/ZnMoO4 heterostructure for electrochemical hydrogen production." Dalton Transactions 50, no. 33 (2021): 11365–69. http://dx.doi.org/10.1039/d1dt01861b.

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