Cucurbituril chemistry: a tale of supramolecular success E Masson, X Ling, R Joseph, L Kyeremeh-Mensah, X Lu Rsc Advances 2 (4), 1213-1247, 2012 | 1022 | 2012 |
2, 1213–1247; b) J. Lagona, P. Mukhopadhyay, S. Chakrabarti, L. Isaacs E Masson, X Ling, R Joseph, L Kyeremeh-Mensah, X Lu, R c Adv Angew. Chem 117, 4922-4949, 2005 | 329 | 2005 |
Comprehensive Supramolecular Chemistry II DE Fagnani, A Sotuyo, RK Castellano Elsevier, Amsterdam 1, 121-148, 2017 | 105 | 2017 |
Cucurbit [7] uril as a supramolecular artificial enzyme for Diels–Alder reactions A Palma, M Artelsmair, G Wu, X Lu, SJ Barrow, N Uddin, E Rosta, ... Angewandte Chemie 129 (49), 15894-15898, 2017 | 99 | 2017 |
Stabilization of cucurbituril/guest assemblies via long-range coulombic and CH··· O interactions R Joseph, A Nkrumah, RJ Clark, E Masson Journal of the American Chemical Society 136 (18), 6602-6607, 2014 | 89 | 2014 |
Formation and Stabilization of Silver Nanoparticles with Cucurbit[n]urils (n = 5−8) and Cucurbituril-Based Pseudorotaxanes in Aqueous Medium X Lu, E Masson Langmuir 27 (6), 3051-3058, 2011 | 88 | 2011 |
Silver-promoted desilylation catalyzed by ortho-and allosteric cucurbiturils X Lu, E Masson Organic Letters 12 (10), 2310-2313, 2010 | 78 | 2010 |
Torsional barriers of substituted biphenyls calculated using density functional theory: a benchmarking study E Masson Organic & biomolecular chemistry 11 (17), 2859-2871, 2013 | 69 | 2013 |
Kinetic vs thermodynamic self-sorting of cucurbit [6] uril, cucurbit [7] uril, and a spermine derivative E Masson, X Lu, X Ling, DL Patchell Organic Letters 11 (17), 3798-3801, 2009 | 66 | 2009 |
Cucurbituril slippage: Translation is a complex motion X Ling, EL Samuel, DL Patchell, E Masson Organic Letters 12 (12), 2730-2733, 2010 | 50 | 2010 |
Kinetics inside, outside and through cucurbiturils E Masson, M Raeisi, K Kotturi Israel Journal of Chemistry 58 (3-4), 413-434, 2018 | 46 | 2018 |
Cucurbituril slippage: Cations as supramolecular lubricants X Ling, E Masson Organic letters 14 (18), 4866-4869, 2012 | 41 | 2012 |
Directional Self‐Sorting with Cucurbit [8] uril Controlled by Allosteric π–π and Metal–Metal Interactions K Kotturi, E Masson Chemistry–A European Journal 24 (34), 8670-8678, 2018 | 38 | 2018 |
Water vs. cucurbituril rim: a fierce competition for guest solvation X Ling, S Saretz, L Xiao, J Francescon, E Masson Chemical Science 7 (6), 3569-3573, 2016 | 37 | 2016 |
Sequence-specific self-assembly of positive and negative monomers with cucurbit [8] uril linkers M Raeisi, K Kotturi, I Del Valle, J Schulz, P Dornblut, E Masson Journal of the American Chemical Society 140 (9), 3371-3377, 2018 | 33 | 2018 |
“Supramolecular circuitry”: three chemiluminescent, cucurbit [7] uril-controlled on/off switches E Masson, YM Shaker, JP Masson, ME Kordesch, C Yuwono Organic Letters 13 (15), 3872-3875, 2011 | 31 | 2011 |
Fluoronaphthalene building blocks via arynes: A solution to the problem of positional selectivity E Masson, M Schlosser European journal of organic chemistry 2005 (20), 4401-4405, 2005 | 27 | 2005 |
The Effect of Ring Size on Reactivity: The Diagnostic Value of ‘Rate Profiles’ E Masson, F Leroux Helvetica chimica acta 88 (6), 1375-1386, 2005 | 26 | 2005 |
π-Arene/metal binding: an issue not only of structure but also of reactivity E Masson, M Schlosser Organic letters 7 (10), 1923-1925, 2005 | 24 | 2005 |
Stuffed pumpkins: mechanochemical synthesis of host–guest complexes with cucurbit [7] uril M Dračínský, CS Hurtado, E Masson, J Kaleta Chemical Communications 57 (17), 2132-2135, 2021 | 21 | 2021 |