“DDT polymorphism and the lethality of crystal forms”, J. Yang, C. Hu, X. Zhu, Q. Zhu, M. D. Ward, B. Kahr, Angew. Chem. Int. Ed. 2017, 56, 10165-10169.
https://doi.org/10.1002/anie.201703028

“Polymeric peptide pigments with sequence-encoded properties”, A. Lampel, S. A. McPhee, H.-A. Park, G. G. Scott, S. Humagain, D. R. Hekstra, B. Yoo, P. W. J. M. Frederix, T.-D. Li, R. R. Abzalimov, S. G. Greenbaum, T. Tuttle, C. Hu, C. J. Bettinger, R. V. Ulijn, Science 2017, 356, 1064-1068.

https://doi.org/10.1126/science.aal5005

“The third ambient aspirin polymorph”, A. G. Shtukenberg, C. Hu, Q. Zhu, M. U. Schmidt, W. Xu, M. Tan, B. Kahr, Cryst. Growth Des. 2017, 17, 3562-3566.
http://dx.doi.org/10.1021/acs.cgd.7b00673

“Uncatalyzed carboboration of seven-membered-ring trans-alkenes: formation of air-stable trialkylboranes”, J. R. Sanzone, C. Hu, K. A. Woerpel, J. Am. Chem. Soc. 2017, 139, 8404-8407.
http://pubs.acs.org/doi/abs/10.1021/jacs.7b03986

“Structure of glycine dihydrate: its implications to crystallization of glycine from solution and its structure in outer space”, W. Xu, Q. Zhu, C. Hu, Angew. Chem. Int. Ed. 2017, 56, 2030-2034.
http://dx.doi.org/10.1002/anie.201610977

“Binuclear, high-valent nickel complexes: Ni-Ni bonds in aryl-halogen bond formation”, J. B. Diccianni, C. Hu, T. Diao, Angew. Chem. Int. Ed. 2017, 56, 3635-3639.
https://doi.org/10.1002/anie.201611572

“Structure and Isotope Effects of β-H Agostic (α-Diimine)Ni Cation as the Polymerization Intermediate”, H. Xu, P. B. White, C. Hu, T. Diao, Angew. Chem. Int. Ed. 2017, 56, 1535-1538.
http://dx.doi.org/10.1002/anie.201611282

“A Supramolecular ice growth inhibitor”, R. Drori, C. Li, C. Hu, P. Raiteri, A. L. Rohl, M. D. Ward, B. Kahr, J. Am. Chem. Soc. 2016, 138, 13396-13401.
http://pubs.acs.org/doi/abs/10.1021/jacs.6b08267

“Catalytic Carbonylative Spirolactonization of Hydroxycyclopropanols”, D. C. Davis, K. L. Walker, C. Hu, R. N. Zare, R. M. Waymouth, M. Dai, J. Am. Chem. Soc. 2016, 138, 10693-10699.
http://pubs.acs.org/doi/abs/10.1021/jacs.6b06573

“Structural and spectroscopic insight into the metal binding properties of the o-aminophenol-N,N,O-triacetic acid (APTRA) chelator: implications for design of metal indicators”, M. Brady, S. D. Piombo, C. Hu, D. Buccella, Dalton Trans. 2016, 45, 12458-12464.
https://doi.org/10.1039/c6dt01557c

“N–N bond forming reductive elimination via a mixed-valent nickel(II)–nickel(III) intermediate”, Angew. Chem. Int. Ed. 2016, 55, 7534-7538.
https://doi.org/10.1002/anie.201602566

“An alternative synthesis and X-ray crystallographic confirmation of (–)-stepholidine”, S. V. Gadhiya, C. Hu, W. W. Harding, Tetra. Lett. 2016, 57, 2090-2092.
https://doi.org/10.1016/j.tetlet.2016.03.108

“Bimetallic C−C bond-forming reductive elimination from nickel”, H. Xu, J. B. Diccianni, J. Katigbak, C. Hu, Y. Zhang, T. Diao, J. Am. Chem. Soc. 2016, 138, 4779-4786.
http://pubs.acs.org/doi/abs/10.1021/jacs.6b00016

“Discrete {Ni40} Coordination Cage: A Calixarene-Based Johnson-Type (J17) Hexadecahedron”, X. Hang, B. Liu, X. Zhu, S. Wang, H. Han, W. Liao, Y. Liu, C. Hu, J. Am. Chem. Soc. 2016, 138, 2969-2972.
http://pubs.acs.org/doi/abs/10.1021/jacs.6b00695

“p-SCN-Bn-HOPO: a superior bifunctional chelator for 89Zr immunoPET”, M. A. Deri, S. Ponnala, P. Kozlowski, B. P. Burton-Pye, H. T. Cicek, C. Hu, J. S. Lewis, L. C. Francesconi, Bioconjugate Chem. 2015, 26, 2579-2591.
http://pubs.acs.org/doi/full/10.1021/acs.bioconjchem.5b00572

“Redox-configurable ambidextrous catalysis: structural and mechanistic insight”, S. Mortezaei, N. R. Catarineu, X. Duan, C. Hu, J. W. Canary, Chemical Science, 2015, 6, 5904-5912.
http://dx.doi.org/10.1039/c5sc02144h

“Structure modeling, synthesis and X-ray diffraction determination of an extra-large calixarene-based coordination cage and its application in drug delivery”, S. Du, T.-Q. Yu, W. Liao, C. Hu, Dalton Trans. 2015, 44, 14394-14402.
https://doi.org/10.1039/c5dt01526j

“Cyclometalated iminophosphorane gold(III) and platinum(II) complexes. A highly permeable cationic platinum(II) compound with promising anticancer properties”, M. Frik, J. Fernández-Gallardo, O. Gonzalo, V. Mangas-Sanjuán, M. González-Alvarez, A. S. del Valle, C. Hu, I. González-Alvarez, M. Bermejo, I. Marzo, M. Contel, J. Med. Chem. 2015, 58, 5825-5841.
http://pubs.acs.org/doi/abs/10.1021/acs.jmedchem.5b00427

“Strong intermolecular electronic coupling of chromophores confined in hydrogen-bonded frameworks”, T. Adachi, D. M. Connors, W. Xiao, C. Hu, M. D. Ward, Cryst. Growth Des. 2015, 15, 3366-3373.
http://pubs.acs.org/doi/abs/10.1021/acs.cgd.5b00452

“Non-topotactic phase transformations in single crystals of β-glycine”, Q. Jiang, A. G. Shtukenberg, M. D. Ward, C. Hu, Cryst. Growth Des. 2015, 15, 2568-2573.
http://pubs.acs.org/doi/abs/10.1021/acs.cgd.5b00187

“Oxidation of carbon monoxide in basic solution catalyzed by nickel cyano carbonyls under ambient conditions and the prototype of a CO-powered alkaline fuel cell”, W. Lo, C. Hu, T. Berenson, N. Tracer, D. Shlian, M. Khaloo, A. Benhaima, J. Jiang, Chem. Commun. 2015, 51, 9432-9435. (Highlighted on the journal cover)
https://doi.org/10.1039/c5cc01872b

“Regulating the architectures of hydrogen-bonded frameworks through topological enforcement”, Y. Liu, W. Xiao, J. J. Yi, C. Hu, S.-J. Park, M. D. Ward, J. Am. Chem. Soc. 2015, 137, 3386-3392.
http://pubs.acs.org/doi/abs/10.1021/jacs.5b00534

“Structure and reactivity of an isolable seven-membered-ring trans-alkene”, B. Hurlocker, C. Hu, K. A. Woerpel, Angew. Chem. Int. Ed. 2015, 54, 4295-4298.
https://doi.org/10.1002/anie.201410752