Calden Carroll - Publications

Affiliations: 
2011 University of Oregon, Eugene, OR, United States 

6 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2013 Tresca BW, Zakharov LN, Carroll CN, Johnson DW, Haley MM. Aryl C-H···Cl(-) hydrogen bonding in a fluorescent anion sensor. Chemical Communications (Cambridge, England). 49: 7240-2. PMID 23843050 DOI: 10.1039/C3Cc44574G  0.502
2012 Engle JM, Carroll CN, Johnson DW, Haley MM. Synthesis and optoelectronic properties of 2,6-bis(2-anilinoethynyl)pyridine scaffolds. Chemical Science (Royal Society of Chemistry : 2010). 3: 1105-1110. PMID 25328662 DOI: 10.1039/C2Sc00975G  0.593
2011 Engle JM, Lakshminarayanan PS, Carroll CN, Zakharov LN, Haley MM, Johnson DW. Molecular Self Assembly: Solvent Guests Tune the Conformation of a Series of 2,6-Bis(2-anilinoethynyl)pyridine-Based Ureas. Crystal Growth & Design. 11: 5144-5152. PMID 22102795 DOI: 10.1021/Cg201074V  0.54
2011 Carroll CN, Coombs BA, McClintock SP, Johnson CA, Berryman OB, Johnson DW, Haley MM. Anion-dependent fluorescence in bis(anilinoethynyl)pyridine derivatives: switchable ON-OFF and OFF-ON responses. Chemical Communications (Cambridge, England). 47: 5539-41. PMID 21472189 DOI: 10.1039/C1Cc10947B  0.576
2010 Carroll CN, Naleway JJ, Haley MM, Johnson DW. Arylethynyl receptors for neutral molecules and anions: emerging applications in cellular imaging. Chemical Society Reviews. 39: 3875-88. PMID 20820467 DOI: 10.1039/B926231H  0.457
2009 Carroll CN, Berryman OB, Johnson CA, Zakharov LN, Haley MM, Johnson DW. Protonation activates anion binding and alters binding selectivity in new inherently fluorescent 2,6-bis(2-anilinoethynyl)pyridine bisureas. Chemical Communications (Cambridge, England). 2520-2. PMID 19532876 DOI: 10.1039/B901643K  0.429
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