Yuran Hua, Ph.D.
Affiliations: | 2012 | Chemistry | Indiana University, Bloomington, Bloomington, IN, United States |
Google:
"Yuran Hua"Mean distance: 9.46 | S | N | B | C | P |
Parents
Sign in to add mentorAmar H. Flood | grad student | 2012 | Indiana University | |
(Binding chloride with triazole-based receptors: Climbing the dielectric ladder.) |
BETA: Related publications
See more...
Publications
You can help our author matching system! If you notice any publications incorrectly attributed to this author, please sign in and mark matches as correct or incorrect. |
Lee S, Hua Y, Flood AH. (2014) β-sheet-like hydrogen bonds interlock the helical turns of a photoswitchable foldamer to enhance the binding and release of chloride. The Journal of Organic Chemistry. 79: 8383-96 |
Ramabhadran RO, Hua Y, Flood AH, et al. (2014) C vs N: which end of the cyanide anion is a better hydrogen bond acceptor? The Journal of Physical Chemistry. A. 118: 7418-23 |
Ramabhadran RO, Liu Y, Hua Y, et al. (2014) An overlooked yet ubiquitous fluoride congenitor: binding bifluoride in triazolophanes using computer-aided design. Journal of the American Chemical Society. 136: 5078-89 |
Hua Y, Liu Y, Chen CH, et al. (2013) Hydrophobic collapse of foldamer capsules drives picomolar-level chloride binding in aqueous acetonitrile solutions. Journal of the American Chemical Society. 135: 14401-12 |
McDonald KP, Hua Y, Lee S, et al. (2012) Shape persistence delivers lock-and-key chloride binding in triazolophanes. Chemical Communications (Cambridge, England). 48: 5065-75 |
Ramabhadran RO, Hua Y, Li YJ, et al. (2011) From atomic to molecular anions: a neutral receptor captures cyanide using strong C-H hydrogen bonds. Chemistry (Weinheim An Der Bergstrasse, Germany). 17: 9123-9 |
Hua Y, Ramabhadran RO, Karty JA, et al. (2011) Two levels of conformational pre-organization consolidate strong CH hydrogen bonds in chloride-triazolophane complexes. Chemical Communications (Cambridge, England). 47: 5979-81 |
Zahran EM, Hua Y, Lee S, et al. (2011) Ion-selective electrodes based on a pyridyl-containing triazolophane: altering halide selectivity by combining dipole-promoted cooperativity with hydrogen bonding. Analytical Chemistry. 83: 3455-61 |
Hua Y, Ramabhadran RO, Uduehi EO, et al. (2011) Aromatic and aliphatic CH hydrogen bonds fight for chloride while competing alongside ion pairing within triazolophanes. Chemistry (Weinheim An Der Bergstrasse, Germany). 17: 312-21 |
Hua Y, Flood AH. (2010) Flipping the switch on chloride concentrations with a light-active foldamer. Journal of the American Chemical Society. 132: 12838-40 |