Year |
Citation |
Score |
2014 |
Lee S, Hua Y, Flood AH. 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. PMID 25157797 DOI: 10.1021/Jo501595K |
0.69 |
|
2014 |
Ramabhadran RO, Hua Y, Flood AH, Raghavachari K. C vs N: which end of the cyanide anion is a better hydrogen bond acceptor? The Journal of Physical Chemistry. A. 118: 7418-23. PMID 24707902 DOI: 10.1021/Jp412816W |
0.654 |
|
2014 |
Ramabhadran RO, Liu Y, Hua Y, Ciardi M, Flood AH, Raghavachari K. An overlooked yet ubiquitous fluoride congenitor: binding bifluoride in triazolophanes using computer-aided design. Journal of the American Chemical Society. 136: 5078-89. PMID 24559019 DOI: 10.1021/Ja500125R |
0.644 |
|
2013 |
Hua Y, Liu Y, Chen CH, Flood AH. Hydrophobic collapse of foldamer capsules drives picomolar-level chloride binding in aqueous acetonitrile solutions. Journal of the American Chemical Society. 135: 14401-12. PMID 24028552 DOI: 10.1021/Ja4074744 |
0.639 |
|
2012 |
McDonald KP, Hua Y, Lee S, Flood AH. Shape persistence delivers lock-and-key chloride binding in triazolophanes. Chemical Communications (Cambridge, England). 48: 5065-75. PMID 22252285 DOI: 10.1039/C2Cc17459F |
0.721 |
|
2011 |
Ramabhadran RO, Hua Y, Li YJ, Flood AH, Raghavachari K. 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. PMID 21710678 DOI: 10.1002/Chem.201100793 |
0.664 |
|
2011 |
Hua Y, Ramabhadran RO, Karty JA, Raghavachari K, Flood AH. Two levels of conformational pre-organization consolidate strong CH hydrogen bonds in chloride-triazolophane complexes. Chemical Communications (Cambridge, England). 47: 5979-81. PMID 21523308 DOI: 10.1039/C1Cc10428D |
0.647 |
|
2011 |
Zahran EM, Hua Y, Lee S, Flood AH, Bachas LG. 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. PMID 21456590 DOI: 10.1021/Ac200052Q |
0.706 |
|
2011 |
Hua Y, Ramabhadran RO, Uduehi EO, Karty JA, Raghavachari K, Flood AH. 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. PMID 21207627 DOI: 10.1002/Chem.201002340 |
0.689 |
|
2010 |
Hua Y, Flood AH. Flipping the switch on chloride concentrations with a light-active foldamer. Journal of the American Chemical Society. 132: 12838-40. PMID 20799723 DOI: 10.1021/Ja105793C |
0.554 |
|
2010 |
Lee S, Hua Y, Park H, Flood AH. Intramolecular hydrogen bonds preorganize an aryl-triazole receptor into a crescent for chloride binding. Organic Letters. 12: 2100-2. PMID 20373782 DOI: 10.1021/Ol1005856 |
0.71 |
|
2010 |
Hua Y, Flood AH. Click chemistry generates privileged CH hydrogen-bonding triazoles: the latest addition to anion supramolecular chemistry. Chemical Society Reviews. 39: 1262-71. PMID 20349532 DOI: 10.1039/B818033B |
0.706 |
|
2010 |
Zahran EM, Hua Y, Li Y, Flood AH, Bachas LG. Triazolophanes: a new class of halide-selective ionophores for potentiometric sensors. Analytical Chemistry. 82: 368-75. PMID 19994863 DOI: 10.1021/Ac902132D |
0.583 |
|
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