536
K. Sada and K. Kokado
7. Yoon, M., Srirambalaji, R., Kim, K.: Homochiral metal-organic frameworks for asymmetric
heterogeneous catalysis. Chem. Rev. 112, 1196–1231 (2012)
8. Farrusseng, D., Aguado, S., Pinel, C.: Metal-Organic frameworks: opportunities for catalysis.
Angew. Chem. Int. Ed. 48, 7502–7513 (2009)
9. Della Rocca, J., Liu, D., Lin, W.: Nanoscale metal–organic frameworks for biomedical imaging
and drug delivery. Acc. Chem. Res. 44, 957–968 (2011)
10. Horcajada, P., Gref, R., Baati, T., Allan, P.K., Maurin, G., Couvreur, P., Férey, G., Morris, R.E.,
Serre, C.: Metal-organic frameworks in biomedicine. Chem. Rev. 112, 1232–1268 (2012)
11. Stavila, V., Talin, A.A., Allendorf, M.D.: MOF-based electronic and optoelectronic devices.
Chem. Soc. Rev. 43, 5994–6010 (2014)
12. Hu, Z., Deibert, B.J., Li, J.: Luminescent metal-organic frameworks for chemical sensing and
explosive detection. Chem. Soc. Rev. 43, 5815–5840 (2014)
13. Férey, G.: Hybrid porous solids: Past, present, future. Chem. Soc. Rev. 37, 191–214 (2008)
14. Kuppler, R.J., Timmons, D.J., Fang, Q.-R., Li, J.-R., Makal, T.A., Young, M.D., Yuan, D.,
Zhao, D., Zhuang, W., Zhou, H.-C.: Potential applications of metal-organic frameworks. Coord.
Chem. Rev. 253, 3042–3066 (2009)
15. Cohen, S.M.: Postsynthetic methods for the functionalization of metal-organic frameworks.
Chem. Rev. 112, 970–1000 (2012)
16. Cohen, S.M.: The postsynthetic renaissance in porous solids. J. Am. Chem. Soc. 139, 2855–
2863 (2017)
17. Tanabe, K.K., Cohen, S.M.: Postsynthetic modification of metal-organic frameworks—A
progress report. Chem. Soc. Rev. 40, 498–519 (2011)
18. Wang, Z., Cohen, S.M.: Postsynthetic covalent modification of a neutral metal-organic
framework. J. Am. Chem Soc. 129, 12368–12369 (2007)
19. Rostovtsev, V.V., Green, L.G., Fokin, V.V., Sharpless, K.B.: A stepwise huisgen cycloaddition
process: Copper(I)-catalyzed regioselective “ligation” of azides and terminal alkynes. Angew.
Chem. Int. Ed. 41, 2596–2599 (2002)
20. Kolb, H.C., Finn, M.G., Sharpless, K.B.: Click chemistry: Diverse chemical function from a
few good reactions. Angew. Chemie Int. Ed. 40, 2004–2021 (2001)
21. Wang, C., Ikhlef, D., Kahlal, S., Saillard, J.-Y., Astruc, D.: Metal-catalyzed azide-alkyne “click”
reactions: Mechanistic overview and recent trends. Coord. Chem. Rev. 316, 1–20 (2016)
22. Liang, L., Astruc, D.: The copper(I)-catalyzed alkyne-azide cycloaddition (CuAAC) “click”
reaction and its applications. An overview. Coord. Chem. Rev. 255, 2933–2945 (2011)
23. Binder, W.H., Sachsenhofer, R.: “Click” chemistry in polymer and materials science.
Macromol. Rapid Commun. 28, 15–54 (2007)
24. Doehler, D., Michael, P., Binder, W.H.: CuAAC-based click chemistry in self-healing polymers.
Acc. Chem. Res. 50, 2610–2620 (2017)
25. Li, P.-Z., Wang, X.-J., Zhao, Y.: Click chemistry as a versatile reaction for construction and
modification of metal-organic frameworks. Coord. Chem. Rev. 380, 484–518 (2019)
26. Goto, Y., Sato, H., Shinkai, S., Sada, K.: “Clickable” metal-organic framework. J. Am. Chem.
Soc. 130, 14354–14355 (2008)
27. Gadzikwa, T., Lu, G., Stern, C.L., Wilson, S.R., Hupp, J.T., Nguyen, S.T.: Covalent surface
modification of a metal-organic framework: Selective surface engineering via Cu I -catalyzed
Huisgen cycloaddition, Chem. Commun., 5493–5495 (2008)
28. Gadzikwa, T., Farha, O.K., Malliakas, C.D., Kanatzidis, M.G., Hupp, J.T., Nguyen, S.T.: Selective bifunctional modification of a non-catenated metal-organic framework material via “click”
chemistry. J. Am. Chem. Soc. 131, 13613–13615 (2009)
29. Savonnet, M., Bazer-Bachi, D., Bats, N., Perez-Pellitero, J., Jeanneau, E., Lecocq, V., Pinel,
C., Farrusseng, D.: Generic postfunctionalization route from amino-derived metal-organic
frameworks. J. Am. Chem. Soc. 132, 4518–4519 (2010)
30. Tuci, G., Rossin, A., Xu, X., Ranocchiari, M., van Bokhoven, J.A., Luconi, L., Manet,
I., Melucci, M., Giambastiani, G.: “Click” on MOFs: A versatile tool for the multimodal
derivatization of N-3-Decorated metal organic frameworks. Chem. Mater. 25, 2297–2308
(2013)
K. Sada and K. Kokado
7. Yoon, M., Srirambalaji, R., Kim, K.: Homochiral metal-organic frameworks for asymmetric
heterogeneous catalysis. Chem. Rev. 112, 1196–1231 (2012)
8. Farrusseng, D., Aguado, S., Pinel, C.: Metal-Organic frameworks: opportunities for catalysis.
Angew. Chem. Int. Ed. 48, 7502–7513 (2009)
9. Della Rocca, J., Liu, D., Lin, W.: Nanoscale metal–organic frameworks for biomedical imaging
and drug delivery. Acc. Chem. Res. 44, 957–968 (2011)
10. Horcajada, P., Gref, R., Baati, T., Allan, P.K., Maurin, G., Couvreur, P., Férey, G., Morris, R.E.,
Serre, C.: Metal-organic frameworks in biomedicine. Chem. Rev. 112, 1232–1268 (2012)
11. Stavila, V., Talin, A.A., Allendorf, M.D.: MOF-based electronic and optoelectronic devices.
Chem. Soc. Rev. 43, 5994–6010 (2014)
12. Hu, Z., Deibert, B.J., Li, J.: Luminescent metal-organic frameworks for chemical sensing and
explosive detection. Chem. Soc. Rev. 43, 5815–5840 (2014)
13. Férey, G.: Hybrid porous solids: Past, present, future. Chem. Soc. Rev. 37, 191–214 (2008)
14. Kuppler, R.J., Timmons, D.J., Fang, Q.-R., Li, J.-R., Makal, T.A., Young, M.D., Yuan, D.,
Zhao, D., Zhuang, W., Zhou, H.-C.: Potential applications of metal-organic frameworks. Coord.
Chem. Rev. 253, 3042–3066 (2009)
15. Cohen, S.M.: Postsynthetic methods for the functionalization of metal-organic frameworks.
Chem. Rev. 112, 970–1000 (2012)
16. Cohen, S.M.: The postsynthetic renaissance in porous solids. J. Am. Chem. Soc. 139, 2855–
2863 (2017)
17. Tanabe, K.K., Cohen, S.M.: Postsynthetic modification of metal-organic frameworks—A
progress report. Chem. Soc. Rev. 40, 498–519 (2011)
18. Wang, Z., Cohen, S.M.: Postsynthetic covalent modification of a neutral metal-organic
framework. J. Am. Chem Soc. 129, 12368–12369 (2007)
19. Rostovtsev, V.V., Green, L.G., Fokin, V.V., Sharpless, K.B.: A stepwise huisgen cycloaddition
process: Copper(I)-catalyzed regioselective “ligation” of azides and terminal alkynes. Angew.
Chem. Int. Ed. 41, 2596–2599 (2002)
20. Kolb, H.C., Finn, M.G., Sharpless, K.B.: Click chemistry: Diverse chemical function from a
few good reactions. Angew. Chemie Int. Ed. 40, 2004–2021 (2001)
21. Wang, C., Ikhlef, D., Kahlal, S., Saillard, J.-Y., Astruc, D.: Metal-catalyzed azide-alkyne “click”
reactions: Mechanistic overview and recent trends. Coord. Chem. Rev. 316, 1–20 (2016)
22. Liang, L., Astruc, D.: The copper(I)-catalyzed alkyne-azide cycloaddition (CuAAC) “click”
reaction and its applications. An overview. Coord. Chem. Rev. 255, 2933–2945 (2011)
23. Binder, W.H., Sachsenhofer, R.: “Click” chemistry in polymer and materials science.
Macromol. Rapid Commun. 28, 15–54 (2007)
24. Doehler, D., Michael, P., Binder, W.H.: CuAAC-based click chemistry in self-healing polymers.
Acc. Chem. Res. 50, 2610–2620 (2017)
25. Li, P.-Z., Wang, X.-J., Zhao, Y.: Click chemistry as a versatile reaction for construction and
modification of metal-organic frameworks. Coord. Chem. Rev. 380, 484–518 (2019)
26. Goto, Y., Sato, H., Shinkai, S., Sada, K.: “Clickable” metal-organic framework. J. Am. Chem.
Soc. 130, 14354–14355 (2008)
27. Gadzikwa, T., Lu, G., Stern, C.L., Wilson, S.R., Hupp, J.T., Nguyen, S.T.: Covalent surface
modification of a metal-organic framework: Selective surface engineering via Cu I -catalyzed
Huisgen cycloaddition, Chem. Commun., 5493–5495 (2008)
28. Gadzikwa, T., Farha, O.K., Malliakas, C.D., Kanatzidis, M.G., Hupp, J.T., Nguyen, S.T.: Selective bifunctional modification of a non-catenated metal-organic framework material via “click”
chemistry. J. Am. Chem. Soc. 131, 13613–13615 (2009)
29. Savonnet, M., Bazer-Bachi, D., Bats, N., Perez-Pellitero, J., Jeanneau, E., Lecocq, V., Pinel,
C., Farrusseng, D.: Generic postfunctionalization route from amino-derived metal-organic
frameworks. J. Am. Chem. Soc. 132, 4518–4519 (2010)
30. Tuci, G., Rossin, A., Xu, X., Ranocchiari, M., van Bokhoven, J.A., Luconi, L., Manet,
I., Melucci, M., Giambastiani, G.: “Click” on MOFs: A versatile tool for the multimodal
derivatization of N-3-Decorated metal organic frameworks. Chem. Mater. 25, 2297–2308
(2013)