References
- Sumida, K., Rogow, D. L., Mason, J. A., McDonald, T. M., Bloch, E. D., and Herm, Z. R., "Carbon Dioxide Capture in Metal-Organic Frameworks," Chem. Rev., 112, 724-781 (2012). https://doi.org/10.1021/cr2003272
- Li, J.-R., Sculley, J., and Zhou, H.-C., "Metal-Organic Frameworks for Separations," Chem. Rev., 112, 869-932 (2012). https://doi.org/10.1021/cr200190s
- Cohen, S. M., "Postsynthetic Methods for the Functionalization of Metal-Organic Frameworks," Chem. Rev., 112, 970-1000 (2012). https://doi.org/10.1021/cr200179u
- Corma, A., Garcia, H., and Xamena, F. X. L., "Engineering Metal-Organic Frameworks for Heterogeneous Catalysis," Chem. Rev., 110, 4606-4655 (2010). https://doi.org/10.1021/cr9003924
- Lee, J., Farha, O. K., Roberts, J., Scheidt, K. A., Nguyen, S. T., and Hupp, J. T., "Metal-Organic Framework Materials as Catalysts," Chem. Soc. Rev., 38, 1450-1459 (2009). https://doi.org/10.1039/b807080f
- Alaerts L., Seguin, E., Poelman, H., Thibault-Starzyk, F., Jacobs, P. A., and De Vos, D. E., "Probing the Lewis Acidity and Catalytic Activity of the Metal-Organic Framework [Cu3(btc)2] (BTC = Benzene-1,3,5-tricarboxylate)," Chem. Eur. J., 12, 7353-7363 (2006). https://doi.org/10.1002/chem.200600220
- Henschel, A., Gedrich, K., Kraehnert, R., and Kaskel, S., "Catalytic Properties of MIL-101," Chem. Commun., 4192-4194 (2008).
- Kurfirtova, L., Seo, Y.-K., Hwang, Y. K., Chang, J.-S., and Cejka, J., "High Activity of Iron Containing Metal-Organic Framework in Acylation of p-Xylene with Benzoyl Chloride," Catal. Today, 179, 85-90 (2012). https://doi.org/10.1016/j.cattod.2011.08.001
- Srirambalaji, R., Hong, S., Natarajan, R., Yoon, M., Hota, R., Kim, Y., Ko, Y. H., and Kim, K., "Tandem Catalysis with a Bifunctional Site-isolated Lewis Acid-Bronsted Base Metal-Organic Framework, NH2-MIL-101(Al)," Chem. Commun., 48, 11650-11652 (2012). https://doi.org/10.1039/c2cc36678a
- Akiyama, G., Matsuda, R., Sato, H., Takata, M., and Kitagawa, S. "Cellulose Hydrolysis by a New Porous Coordination Polymer Decorated with Sulfonic Acid Functional Groups," Adv. Mater., 23, 3294-3297 (2011). https://doi.org/10.1002/adma.201101356
- Vermoortele, F., Ameloot, R., Vimont, A., Serrec, C., and De Vos, D., "An Amino-modified Zr-terephthalate Metal-Organic Framework as an Acid-Bbase Catalyst for Cross-Aldol Condensation," Chem. Commun., 47, 1521-1523 (2011). https://doi.org/10.1039/c0cc03038d
- Prabhu, A. and Palanichamy, M., "Mesoporous Cubic la3d Materials for the Preparation of Fine Chemicals: Synthesis of Jasminaldehyde," Micro. Meso. Mater., 168, 126-131 (2013). https://doi.org/10.1016/j.micromeso.2012.09.020
- Climent, M. J., Corma, A., Garcia, H., Guil-Lopez, R., Iborra, S., and Fornes, V., "Acid-Base Bifunctional Catalysts for the Preparation of Fine Chemicals: Synthesis of Jasminaldehyde," J. Catal., 197, 385-393 (2001). https://doi.org/10.1006/jcat.2000.3086
- Yadav, G. D. and Aduri, P., "Aldol Condensation of Benzaldehyde with Heptanal to Jasminaldehyde over Novel Mg-Al Mixed Oxide on Hexagonal Mesoporous Silica," J. Mol. Catal. A: Chem., 355, 142-154 (2012). https://doi.org/10.1016/j.molcata.2011.12.008
-
Zlotea, C., Phanon, D., Mazaj, M., Heurtaux, D., Guillerm, V., Serre, C., Horcajada, P., Devic, T., Magnier, E., Cuevas, F., Ferey, G., Llewellyn. P. L., and Latroche, M., "Effect of
$NH_2$ and$CF_3$ Functionalization on the Hydrogen Sorption Properties of MOFs," Dalton Trans., 40, 4879-4881 (2011). https://doi.org/10.1039/c1dt10115c - Chung, Y.-M., Kim, H.-Y., and Ahn, W.-S., "Friedel-Crafts Acylation of p-Xylene over Sulfonated Zirconium Terephthalates," Catal. Lett., 144, 817-824 (2014). https://doi.org/10.1007/s10562-014-1242-4
- Kim, J., Lee, Y. R., and Ahn, W.-S., "Dry-gel Conversion Synthesis of Cr-MIL-101 Aided by Grinding: High Surface Area and High Yield Synthesis with Minimum Purification," Chem. Commun., 49, 7647-7649 (2013). https://doi.org/10.1039/c3cc44559c
-
Jiang, D., Keenan., L. L., Burrows, A. D., and Edler, K. J., "Synthesis and Post-synthetic Modification of MIL-101(Cr)-
$NH_2$ via a Tandem Diazotisation Process," Chem. Commun., 48, 12053-12055 (2012). https://doi.org/10.1039/c2cc36344e - Chung, Y.-M., Lee, Y.-R., and Ahn, W.-S., "A New Siteisolated Acid-base Bifunctional Metal-Organic Framework for One-pot Tandem Reaction," RSC Adv., 4, 23064-23067 (2014). https://doi.org/10.1039/c4ra02683g
- Sharma, S. K., Patel, H. A., and Jasra, R. V., "Synthesis of Jasminaldehyde using Magnesium Organo Silicate as a Solid Base Catalyst," J. Mol. Catal. A: Chem., 280, 61-67 (2008). https://doi.org/10.1016/j.molcata.2007.10.013
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