| Luminescent triarylborane-functionalized polystyrene: synthesis, photophysical characterization, and anion-binding studies K Parab, K Venkatasubbaiah, F Jäkle Journal of the American Chemical Society 128 (39), 12879-12885, 2006 | 333 | 2006 |
| A new route to organoboron polymers via highly selective polymer modification reactions Y Qin, G Cheng, O Achara, K Parab, F Jäkle Macromolecules 37 (19), 7123-7131, 2004 | 118 | 2004 |
| A thermodynamic and kinetic study of the heterolytic activation of hydrogen by frustrated borane–amine Lewis pairs A Karkamkar, K Parab, DM Camaioni, D Neiner, H Cho, TK Nielsen, ... Dalton Transactions, 2013 | 46 | 2013 |
| Synthesis, characterization, and anion binding of redox-active triarylborane polymers K Parab, F Jäkle Macromolecules 42 (12), 4002-4007, 2009 | 38 | 2009 |
| Luminescent diazaborolyl-functionalized polystyrene H Kuhtz, F Cheng, S Schwedler, L Böhling, A Brockhinke, L Weber, ... ACS Macro Letters 1 (5), 555-559, 2012 | 37 | 2012 |
| 3-Methyl-1, 2-BN-cyclopentane: a promising H2 storage material? D Neiner, A Karkamkar, K Parab, EB Garner III, DA Dixon, D Matson, ... Dalton Transactions, 2013 | 35 | 2013 |
| Catalytic reduction of polar substrates without metals: A thermodynamic and kinetic study of heterolytic activation of hydrogen by vacancies in frustrated Lewis pairs SM Whittemore, G Edvenson, DM Camaioni, A Karkamkar, D Neiner, ... Catalysis Today 251, 28-33, 2015 | 32 | 2015 |
| Synthesis and characterization of luminescent polystyrene derivatives with sterically protected fluorenyl-and carbazolylborane moieties K Parab, A Doshi, F Cheng, F Jäkle Macromolecules 44 (15), 5961-5967, 2011 | 25 | 2011 |
| Catalytic transesterification of ester compounds with groups reactive under transesterification conditions JM Sullivan, AS Palsule, PR Stevenson, KK Parab US Patent 9,416,091, 2016 | 20 | 2016 |
| Nucleophilicities and Lewis basicities of sterically hindered pyridines E Follet, H Zipse, S Lakhdar, AR Ofial, G Berionni Synthesis 49 (15), 3495-3504, 2017 | 18 | 2017 |
| Experimental and theoretical study of molecular response of amine bases in organic solvents SM Kathmann, H Cho, TM Chang, GK Schenter, K Parab, T Autrey The Journal of Physical Chemistry B 118 (18), 4883-4888, 2014 | 12 | 2014 |
| Lewis acidic organoboron polymers Y Qin, G Cheng, K Parab, A Sundararaman, F Jäkle Macromolecular Symposia 196 (1), 337-345, 2003 | 11 | 2003 |
| Blending materials composed of boron, nitrogen and carbon to transform approaches to liquid hydrogen stores SM Whittemore, M Bowden, A Karkamkar, K Parab, D Neiner, T Autrey, ... Dalton Transactions 45 (14), 6196-6203, 2016 | 10 | 2016 |
| Solution polymers including one or more 1, 1-disubstituted alkene compounds, solution polymerization methods, and polymer compositions A Palsule, AR Holzer, PR Stevenson, KK Parab, JM Sullivan US Patent 9,279,022, 2016 | 7 | 2016 |
| Solution polymers including one or more 1, 1-disubstituted alkene compounds, solution polymerization methods, and polymer compositions A Palsule, AR Holzer, PR Stevenson, KK Parab, JM Sullivan US Patent 9,279,022, 2016 | 7 | 2016 |
| Compositions containing 1, 1-disubstituted alkene compounds for preparing polymers having enhanced glass transition temperatures JM Sullivan, A Palsule, AR Holzer, KK Parab, A Doshi US Patent 9,315,597, 2016 | 5 | 2016 |
| Heterolysis of H2 Across a Classical Lewis Pair, 2, 6‐Lutidine⋅ BCl3: Synthesis, Characterization, and Mechanism B Ginovska, T Autrey, K Parab, ME Bowden, RG Potter, DM Camaioni Chemistry–A European Journal 21 (44), 15713-15719, 2015 | 5 | 2015 |
| Solution polymers including one or more 1, 1-disubstituted alkene compounds, solution polymerization methods, and polymer compositions A Palsule, AR Holzer, PR Stevenson, KK Parab, JM Sullivan US Patent 9,676,875, 2017 | 4 | 2017 |
| Polyester macromers containing 1, 1-dicarbonyl-substituted 1 alkenes A Palsule, JM Sullivan, KK Parab, E King, W Barrett US Patent 9,617,377, 2017 | 4 | 2017 |
| Polyester macromers containing 1, 1-dicarbonyl-substituted 1 alkenes A Palsule, JM Sullivan, KK Parab, E King, W Barrett US Patent 9,617,377, 2017 | 3 | 2017 |
