Year |
Citation |
Score |
2015 |
Basilio N, Morice AH, Marti G, Montagne G. High- and Low-Order Overtaking-Ability Affordances: Drivers Rely on the Maximum Velocity and Acceleration of Their Cars to Perform Overtaking Maneuvers. Human Factors. 57: 879-94. PMID 25947014 DOI: 10.1177/0018720815583581 |
0.535 |
|
2015 |
Basilio N, Morice AHP, Marti G, Montagne G. High- and Low-Order Overtaking-Ability Affordances: Drivers Rely on the Maximum Velocity and Acceleration of Their Cars to Perform Overtaking Maneuvers Human Factors. 57: 879-894. DOI: 10.1177/0018720815583581 |
0.66 |
|
2015 |
Morice AHP, Diaz GJ, Fajen BR, Basilio N, Montagne G. An Affordance-Based Approach to Visually Guided Overtaking Ecological Psychology. 27: 1-25. DOI: 10.1080/10407413.2015.991641 |
0.692 |
|
2013 |
Basilio N, Morice AHP, Marti G, Montagne G. Visually guided overtaking behavior understood in relation to the maximal acceleration of vehicle: an affordance-based approach Journal of Vision. 13: 946-946. DOI: 10.1167/13.9.946 |
0.587 |
|
Low-probability matches (unlikely to be authored by this person) |
2005 |
Basilio N, García-Río L, Leis JR, Mejuto JC, Pérez-Lorenzo M. Novel catalytic effects in ester aminolysis in chlorobenzene. Chemical Communications (Cambridge, England). 3817-9. PMID 16041427 DOI: 10.1039/b504629g |
0.134 |
|
2006 |
Basilio N, García-Río L, Mejuto JC, Pérez-Lorenzo M. A new reaction pathway in the ester aminolysis catalyzed by glymes and crown ethers. The Journal of Organic Chemistry. 71: 4280-5. PMID 16709072 DOI: 10.1021/jo060389u |
0.077 |
|
2010 |
Basilio N, García-Río L, Moreira JA, Pessêgo M. Supramolecular catalysis by cucurbit[7]uril and cyclodextrins: similarity and differences. The Journal of Organic Chemistry. 75: 848-55. PMID 20058896 DOI: 10.1021/jo902398z |
0.072 |
|
2012 |
Francisco V, Basilio N, García-Río L. Counterion exchange as a decisive factor in the formation of host:guest complexes by p-sulfonatocalix[4]arene. The Journal of Physical Chemistry. B. 116: 5308-15. PMID 22489553 DOI: 10.1021/jp301290u |
0.053 |
|
2013 |
Basilio N, Francisco V, Garcia-Rio L. Aggregation of p-Sulfonatocalixarene-Based Amphiphiles and Supra-Amphiphiles. International Journal of Molecular Sciences. 14: 3140-57. PMID 23380960 DOI: 10.3390/ijms14023140 |
0.051 |
|
2011 |
Pessêgo M, Basilio N, Moreira JA, García-Río L. Cucurbit[7]uril: surfactant host-guest complexes in equilibrium with micellar aggregates. Chemphyschem : a European Journal of Chemical Physics and Physical Chemistry. 12: 1342-50. PMID 21472839 DOI: 10.1002/cphc.201001045 |
0.044 |
|
2015 |
Fernández-Rosas J, Pessêgo M, Cepeda-Plaza M, Basilio N, Parajó M, Rodríguez-Dafonte P, García-Río L. γ-Cyclodextrin modulates the chemical reactivity by multiple complexation. Organic & Biomolecular Chemistry. 13: 1213-24. PMID 25429442 DOI: 10.1039/c4ob02113d |
0.027 |
|
2010 |
Basilio N, García-Río L, Martín-Pastor M. Counterion binding in solutions of p-sulfonatocalix[4]arene. The Journal of Physical Chemistry. B. 114: 7201-6. PMID 20446749 DOI: 10.1021/jp101474a |
0.026 |
|
2012 |
Basilio N, Martín-Pastor M, García-Río L. Insights into the structure of the supramolecular amphiphile formed by a sulfonated calix[6]arene and alkyltrimethylammonium surfactants. Langmuir : the Acs Journal of Surfaces and Colloids. 28: 6561-8. PMID 22448819 DOI: 10.1021/la3006794 |
0.021 |
|
2013 |
Basilio N, Gómez B, Garcia-Rio L, Francisco V. Using calixarenes to model polyelectrolyte surfactant nucleation sites. Chemistry (Weinheim An Der Bergstrasse, Germany). 19: 4570-6. PMID 23400939 DOI: 10.1002/chem.201203377 |
0.01 |
|
2010 |
Francisco V, Basilio N, Garcia-Rio L, Leis JR, Maques EF, Vázquez-Vázquez C. Novel catanionic vesicles from calixarene and single-chain surfactant. Chemical Communications (Cambridge, England). 46: 6551-3. PMID 20721387 DOI: 10.1039/c0cc01806f |
0.01 |
|
2009 |
Basilio N, García-Río L. Sulfonated calix[6]arene host-guest complexes induce surfactant self-assembly. Chemistry (Weinheim An Der Bergstrasse, Germany). 15: 9315-9. PMID 19658136 DOI: 10.1002/chem.200901065 |
0.01 |
|
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