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Parkin SR

First name:
Parkin
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SR
Mertens, R. T., & Awuah, S. G. (2019). Synthesis and crystal structure of 1,3-bis-(4-hy-droxy-phen-yl)-1H-imidazol-3-ium chloride.. Acta Crystallographica. Section E, Crystallographic Communications, 75(Pt 9), 1311-1315. https://doi.org/10.1107/S2056989019011058 (Original work published 2019)
Anthony, J. E., & Eaton, D. L. (2002). A road map to stable, soluble, easily crystallized pentacene derivatives. Organic Letters, 4(1), 15-8. https://doi.org/10.1021/ol0167356 (Original work published 2002)
Anthony, J. E., Brooks, J. S., & Eaton, D. L. (2001). Functionalized pentacene: improved electronic properties from control of solid-state order. Journal Of The American Chemical Society, 123(38), 9482-3. https://doi.org/10.1021/ja0162459 (Original work published 2001)
Palmer, G. J., & Anthony, J. E. (2001). Synthesis of a Remarkably Stable Dehydro. Angewandte Chemie (International Ed. In English), 40(13), 2509-2512. (Original work published 2001)
Palmer, G. J., & Anthony, J. E. (2001). Synthesis of a Remarkably Stable Dehydro 14 annulene. Angewandte Chemie (International Ed. In English), 40(13), 2509-2512. https://doi.org/10.1002/1521-3773(20010702)40:13<2509::AID-ANIE2509>3.0.CO;2-F (Original work published 2001)
Casselman, M. D., Elliott, C. F., Modekrutti, S., Zhang, P. L., Risko, C., & Odom, S. A. (2017). Beyond the Hammett Effect: Using Strain to Alter the Landscape of Electrochemical Potentials. Chemphyschem : A European Journal Of Chemical Physics And Physical Chemistry, 18(16), 2142-2146. https://doi.org/10.1002/cphc.201700607 (Original work published 2017)
Kelsey, R. A., Miller, D. A., Liu, K., Remias, J. E., Yang, Y., Lightstone, F. C., et al. (2016). Carbonic anhydrase mimics for enhanced CO2 absorption in an amine-based capture solvent. Dalton Transactions (Cambridge, England : 2003), 45(1), 324-33. https://doi.org/10.1039/c5dt02943k (Original work published 2016)
Narayana, K. A., Casselman, M. D., Elliott, C. F., Ergun, S., Risko, C., & Odom, S. A. (2015). N-substituted phenothiazine derivatives: how the stability of the neutral and radical cation forms affects overcharge performance in lithium-ion batteries. Chemphyschem : A European Journal Of Chemical Physics And Physical Chemistry, 16(6), 1179-89. https://doi.org/10.1002/cphc.201402674 (Original work published 2015)
Ergun, S., Elliott, C. F., Kaur, A. P., & Odom, S. A. (2014). Overcharge performance of 3,7-disubstituted N-ethylphenothiazine derivatives in lithium-ion batteries. Chemical Communications (Cambridge, England), 50(40), 5339-41. https://doi.org/10.1039/c3cc47503d (Original work published 2014)
Thorley, K. J., Song, Y., & Anthony, J. E. (2020). In Situ Reduction and Functionalization of Polycyclic Quinones.. Organic Letters, 22(18), 7193-7196. https://doi.org/10.1021/acs.orglett.0c02529 (Original work published 2020)