| Year |
Citation |
Score |
| 2016 |
Benson CR, Share AI, Marzo MG, Flood AH. Double Switching of Two Rings in Palindromic [3]Pseudorotaxanes: Cooperativity and Mechanism of Motion. Inorganic Chemistry. PMID 27050829 DOI: 10.1021/Acs.Inorgchem.5B02554 |
0.607 |
|
| 2014 |
Andersen SS, Share AI, Poulsen BL, Kørner M, Duedal T, Benson CR, Hansen SW, Jeppesen JO, Flood AH. Mechanistic evaluation of motion in redox-driven rotaxanes reveals longer linkers hasten forward escapes and hinder backward translations. Journal of the American Chemical Society. 136: 6373-84. PMID 24746239 DOI: 10.1021/Ja5013596 |
0.594 |
|
| 2014 |
Manck LE, Benson CR, Share AI, Park H, Griend DAV, Flood AH. Self-assembly snapshots of a 2 × 2 copper(I) grid Supramolecular Chemistry. 26: 267-279. DOI: 10.1080/10610278.2013.872780 |
0.577 |
|
| 2012 |
Stojanovi? S, Turner DA, Share AI, Flood AH, Hadad CM, Badji? JD. A stereodynamic and redox-switchable encapsulation-complex containing a copper ion held by a tris-quinolinyl basket. Chemical Communications (Cambridge, England). 48: 4429-31. PMID 22460128 DOI: 10.1039/C2Cc30339F |
0.579 |
|
| 2012 |
Hansen SW, Stein PC, Sørensen A, Share AI, Witlicki EH, Kongsted J, Flood AH, Jeppesen JO. Quantification of the π-π interactions that govern tertiary structure in donor-acceptor [2]pseudorotaxanes. Journal of the American Chemical Society. 134: 3857-63. PMID 22280483 DOI: 10.1021/Ja210861V |
0.633 |
|
| 2012 |
Benson CR, Share AI, Flood AH. Bioinspired Molecular Machines Bioinspiration and Biomimicry in Chemistry: Reverse-Engineering Nature. 71-119. DOI: 10.1002/9781118310083.ch4 |
0.489 |
|
| 2010 |
Trabolsi A, Fahrenbach AC, Dey SK, Share AI, Friedman DC, Basu S, Gasa TB, Khashab NM, Saha S, Aprahamian I, Khatib HA, Flood AH, Stoddart JF. A tristable [2]pseudo[2]rotaxane. Chemical Communications (Cambridge, England). 46: 871-3. PMID 20107634 DOI: 10.1039/B918321C |
0.587 |
|
| 2010 |
Share AI, Parimal K, Flood AH. Bilability is defined when one electron is used to switch between concerted and stepwise pathways in Cu(I)-based bistable [2/3]pseudorotaxanes. Journal of the American Chemical Society. 132: 1665-75. PMID 20070081 DOI: 10.1021/Ja908877D |
0.702 |
|
| 2010 |
Share AI, Flood AH. Supramolecular chemistry: Thinking inside and outside the box Nature Chemistry. 2: 349-350. DOI: 10.1038/Nchem.630 |
0.584 |
|
| 2009 |
McNitt KA, Parimal K, Share AI, Fahrenbach AC, Witlicki EH, Pink M, Bediako DK, Plaisier CL, Le N, Heeringa LP, Vander Griend DA, Flood AH. Reduction of a redox-active ligand drives switching in a Cu(I) pseudorotaxane by a bimolecular mechanism. Journal of the American Chemical Society. 131: 1305-13. PMID 19125582 DOI: 10.1021/Ja8085593 |
0.553 |
|
| Low-probability matches (unlikely to be authored by this person) |
| 2014 |
Ko SK, Kim SK, Share A, Lynch VM, Park J, Namkung W, Van Rossom W, Busschaert N, Gale PA, Sessler JL, Shin I. Synthetic ion transporters can induce apoptosis by facilitating chloride anion transport into cells. Nature Chemistry. 6: 885-92. PMID 25242483 DOI: 10.1038/Nchem.2021 |
0.095 |
|
| 2015 |
Park SH, Choi YP, Park J, Share A, Francesconi O, Nativi C, Namkung W, Sessler JL, Roelens S, Shin I. Synthetic aminopyrrolic receptors have apoptosis inducing activity. Chemical Science. 6: 7284-7292. PMID 28757987 DOI: 10.1039/C5Sc03200H |
0.092 |
|
| 2015 |
Park SH, Choi YP, Park J, Share A, Francesconi O, Nativi C, Namkung W, Sessler JL, Roelens S, Shin I. Synthetic aminopyrrolic receptors have apoptosis inducing activity Chemical Science. 6: 7284-7292. DOI: 10.1039/c5sc03200h |
0.073 |
|
| 2016 |
Share AI, Patel K, Nativi C, Cho EJ, Francesconi O, Busschaert N, Gale PA, Roelens S, Sessler JL. Chloride anion transporters inhibit growth of methicillin-resistant Staphylococcus aureus (MRSA) in vitro. Chemical Communications (Cambridge, England). PMID 27223254 DOI: 10.1039/C6Cc03645G |
0.032 |
|
| Hide low-probability matches. |