Ferroelectric polarization and second harmonic generation in supramolecular co–crystals with two axes of charge–transfer, (A. Narayanan, D. Cao, L. Frazer, A. S. Tayi, A. K. Blackburn, A. C.–H. Sue, J. B. Ketterson, J. F. Stoddart, S. I. Stupp), J. Am. Chem. Soc.2017, 139, 9186—9191.
Functionalised cyclodextrin–based metal–organic frameworks, (K. J. Hartlieb, A. W. Peters, T. C. Wang, P. Deria, O. K. Farha, J. T. Hupp, J. F. Stoddart), Chem. Commun.2017, 53, 7561—7564.
Composite CD–MOF nanocrystals–containing microspheres for sustained drug delivery, (H. Li, N. Lv, X. Li, B. Liu, J. Feng, X. Ren, T. Guo, D. Chen, J. F. Stoddart, R. Gref, J. Zhang), Nanoscale2017, 9, 7454—7463.
Mastering the non-equilibrium assembly and operation of molecular machines, (C. Pezzato, C. Cheng, J. F. Stoddart, R. D. Astumian), Chem. Soc. Rev.2017, 46, 5491—5507.
A boat–shaped tetracationic macrocycle with a semiconducting organic framework, (M. T. Nguyen, M. D. Krzyaniak, M. Owczarek, D. P. Ferris, M. R. Wasielewski, J. F. Stoddart), Angew. Chem. Int. Ed.2017, 56, 5795—5800.
Surveying macrocyclic chemistry: From flexible crown ethers to rigid cyclophanes, (Z. Liu, S. K. M. Nalluri, J. F. Stoddart), Chem. Soc. Rev.2017, 46, 2459—2478.
Redox-active macrocycles for organic rechargeable batteries, (D. J. Kim, K.R. Hermann, A. Prokofjevs, M. T. Otley, C. Pezzato, M. Owczarek, J. F. Stoddart), J. Am. Chem. Soc.2017, 139, 6635—6643.
Encapsulation of Ibuprofen in CD–MOF and related bioavailability studies, (K. J. Hartlieb, D. P. Ferris, J. M. Holcroft, I. Kandela, C. L. Stern, M. S. Nassar, Y. Y. Botros, J. F. Stoddart), Mol. Pharm.2017, 14, 1831—1839.
Intramolecular energy and electron transfer within a diazaperopyrenium-based cyclophane, (X. Gong, R. M. Young, K. J. Hartlieb, C. Miller, Y. Wu, H. Xiao, P. Li, N. Hafezi, J. Zhou, L. Ma, T. Cheng, W. A. Goddard III, O. K Farha, J. T. Hupp, M. R. Wasielewski, J. F. Stoddart), J. Am. Chem. Soc.2017, 139, 4107—4116.
Size–matched radical multivalency, (M. C. Lipke, T. Chang, Y. Wu, H. Arslan, H. Xiao, M. R. Wasielewski, W. A. Goddard III, J. F. Stoddart), J. Am. Chem. Soc.2017, 139, 3986—3998.
Spin frustration in the triradical trianion of a naphthalenediimide molecular triangle, (Y. Wu, M. D. Krzyaniak, J. F. Stoddart, M. R. Wasielewski), J. Am. Chem. Soc.2017, 139, 2948—2951.
Radically promoted formation of a molecular lasso, (Y. Wang, J. Sun, Z. Liu, M. S. Nassar, Y. Y. Botros, J. F. Stoddart), Chem. Sci.2017, 8, 2562—2568.
Postsynthetic incorporation of a singlet oxygen photosensitizer in a metal–organic framework for fast and selective oxidative detoxification of sulfur mustard, (A. J. Howarth, C. T. Buru, Y. Liu, A. M. Ploskonka, K. J. Hartlieb, M. McEntee, J. J. Mahle, J. H. Buchanan, E. M. Durke, S. S. Al-Juaid, J. F. Stoddart, J. B. DeCoste, J. T. Hupp, O. K. Farha), Chem. Eur. J.2017, 23, 214—218.
Complex formation dynamics in a single–molecule electronic device, (H. Wen, W. Li, J. Chen, G. He, L. Li, M. A. Olson, A. C.-H. Sue, J. F. Stoddart, X. Guo), Sci. Adv.2016, 2, e1601113.
Optimized synthesis and crystalline stability of γ–cyclodextrin metal–organic frameworks for drug adsorption, (B. Liu, H. Li, X. Xu, X. Li, N. Lv, V. Singh, J. F. Stoddart, P. York, X. Xu, R. Gref, J. Zhang), Int. J. Pharm.2016, 514, 212—219.
A redox–active bistable molecular switch mounted inside a metal–organic framework, (Q. Chen, J. Sun, P. Li, I. Hod, P. Z. Moghadem, Z. Kean, R. Q. Snurr, J. T. Hupp, O. K. Farha, J. F. Stoddart), J. Am. Chem. Soc.2016, 138, 14242—14245.
In silico discovery of metal–organic frameworks for precombustion CO2 capture using a genetic algorithm, (Y. G. Chung, D. A. Gómez-Gualdrón, P. Li, K. T. Leperi, P. Deria, H. Zhang, N. A. Vermeulen, J. F. Stoddart, F. You, J. T. Hupp, O. K. Farha, R. Q. Snurr), Sci. Adv.2016, 2, e1600909.
Flexible ferroelectric organic crystals, (M. Owczarek, K. A. Hujsak, D. P. Ferris, A. Prokofjevs, I. Mayerz, P. Szklarz, H. Zhang, A. A. Sarjeant, C. L. Stern, R. Jakubas, S. Hong, V. P. Dravid, J. F. Stoddart), Nat. Commun.2016, 7, article 13108.
Supramolecular double helix formation by diastereoisomeric conformations of configurationally enantiomeric macrocycles, (A. Samanta, Z. Liu, S. K. M. Nalluri, Y. Zhang, G. C. Schatz, J. F. Stoddart), J. Am. Chem. Soc.2016, 138, 14469—14480.