Year |
Citation |
Score |
2015 |
Whittemore SM, Bowden M, Karkamkar A, Parab K, Neiner D, Autrey T, Ishibashi JS, Chen G, Liu SY, Dixon DA. Blending materials composed of boron, nitrogen and carbon to transform approaches to liquid hydrogen stores. Dalton Transactions (Cambridge, England : 2003). PMID 26629961 DOI: 10.1039/C5Dt04276C |
0.437 |
|
2015 |
Ginovska B, Autrey T, Parab K, Bowden ME, Potter RG, Camaioni DM. Heterolysis of H2 Across a Classical Lewis Pair, 2,6-Lutidine⋅BCl3 : Synthesis, Characterization, and Mechanism. Chemistry (Weinheim An Der Bergstrasse, Germany). 21: 15713-9. PMID 26493883 DOI: 10.1002/Chem.201501899 |
0.366 |
|
2015 |
Whittemore SM, Edvenson G, Camaioni DM, Karkamkar A, Neiner D, Parab K, Autrey T. Catalytic reduction of polar substrates without metals: A thermodynamic and kinetic study of heterolytic activation of hydrogen by vacancies in frustrated Lewis pairs Catalysis Today. 251: 28-33. DOI: 10.1016/J.Cattod.2014.10.040 |
0.35 |
|
2013 |
Karkamkar A, Parab K, Camaioni DM, Neiner D, Cho H, Nielsen TK, Autrey T. A thermodynamic and kinetic study of the heterolytic activation of hydrogen by frustrated borane-amine Lewis pairs. Dalton Transactions (Cambridge, England : 2003). 42: 615-9. PMID 22996636 DOI: 10.1039/C2Dt31628E |
0.341 |
|
2013 |
Luo W, Neiner D, Karkamkar A, Parab K, Garner EB, Dixon DA, Matson D, Autrey T, Liu SY. 3-Methyl-1,2-BN-cyclopentane: a promising H2 storage material? Dalton Transactions (Cambridge, England : 2003). 42: 611-4. PMID 22992627 DOI: 10.1039/C2Dt31617J |
0.449 |
|
2012 |
Kuhtz H, Cheng F, Schwedler S, Böhling L, Brockhinke A, Weber L, Parab K, Jäkle F. Luminescent Diazaborolyl-Functionalized Polystyrene. Acs Macro Letters. 1: 555-559. PMID 35607060 DOI: 10.1021/mz300071f |
0.31 |
|
2012 |
Kuhtz H, Cheng F, Schwedler S, Böhling L, Brockhinke A, Weber L, Parab K, Jäkle F. Luminescent diazaborolyl-functionalized polystyrene Acs Macro Letters. 1: 555-559. DOI: 10.1021/Mz300071F |
0.361 |
|
2011 |
Parab K, Doshi A, Cheng F, Jäkle F. Synthesis and characterization of luminescent polystyrene derivatives with sterically protected fluorenyl- and carbazolylborane moieties Macromolecules. 44: 5961-5967. DOI: 10.1021/Ma200358S |
0.377 |
|
2009 |
Parab K, Jäkle F. Synthesis, characterization, and anion binding of redox-active triarylborane polymers Macromolecules. 42: 4002-4007. DOI: 10.1021/Ma9001885 |
0.358 |
|
2006 |
Parab K, Venkatasubbaiah K, Jäkle F. Luminescent triarylborane-functionalized polystyrene: synthesis, photophysical characterization, and anion-binding studies. Journal of the American Chemical Society. 128: 12879-85. PMID 17002382 DOI: 10.1021/Ja063302V |
0.37 |
|
2004 |
Qin Y, Cheng G, Achara O, Parab K, Jäkle F. A new route to organoboron polymers via highly selective polymer modification reactions Macromolecules. 37: 7123-7131. DOI: 10.1021/Ma035880R |
0.353 |
|
2003 |
Qin Y, Cheng G, Parab K, Sundararaman A, Jäkle F. Lewis acidic organoboron polymers Macromolecular Symposia. 196: 337-345. DOI: 10.1002/Masy.200390172 |
0.332 |
|
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