Miami University

36. Dissipative assembly of aqueous carboxylic acid anhydrides fueled by carbodiimides
Lasith S. Kariyawasam and C. Scott Hartley*
J. Am. Chem. Soc. 2017, 139, 11949–11955

35. Twisted macrocycles with folded ortho-phenylene subunits
Zacharias J. Kinney and C. Scott Hartley*
J. Am. Chem. Soc. 2017, 139, 4821–4827

34. Solvent effects on the folding of ortho-phenylene oligomers
Gopi Nath Vemuri, Meng Chu, Han Dong, Brian J. Spinello, and C. Scott Hartley*
Org. Biomol. Chem. 2017, 15, 845–851

33. Two- and three-tiered stacked architectures by covalent assembly
Fengfeng Ren, Kody J. Day, and C. Scott Hartley*
Angew. Chem., Int. Ed. 2016, 55, 8620–8623
Selected by the editors at a "Hot Paper".

32. Folding of ortho-phenylenes
C. Scott Hartley*
Acc. Chem. Res. 2016, 49, 646–654

31. Smectic-A and hexatic-B liquid crystal phases of sanidic alkyl-substituted dibenzo[fg,op]naphthacenes
Paul J. Repasky, Deña M. Agra-Kooijman, Satyendra Kumar,* and C. Scott Hartley*
J. Phys. Chem. B 2016, 120, 2829–2837

30. Visualizing molecular chirality in the organic chemistry laboratory using cholesteric liquid crystals
Maia Popova, Stacey Lowery Bretz, and C. Scott Hartley*
J. Chem. Educ. 2016, 93, 1096–1099
Featured on the cover. Open access (available without a subscription).

29. Tetrabenzanthanthrenes by mitigation of rearrangements in the planarization of ortho-phenylene hexamers
Jian He, Sanyo Mathew, Zacharias J. Kinney, Rachel M. Warrell, James S. Molina, and C. Scott Hartley*
Chem. Commun. 2015, 51, 7245–7248

28. Enhanced helical folding of ortho-phenylenes through the control of aromatic stacking interactions
Sanyo Mathew, Laura A. Crandall, Christopher J. Ziegler, and C. Scott Hartley*
J. Am. Chem. Soc. 2014, 136, 16666–16675
Featured as a JACS Spotlight.

27. Solution-phase dimerization of an oblong shape-persistent macrocycle
Meng Chu, Ashley N. Scioneaux, and C. Scott Hartley*
J. Org. Chem. 2014, 79, 9009–9017

26. Intramolecular charge transfer in donor-bridge- acceptor compounds with paired linearly conjugated or cross-conjugated pathways
Nicole M. Dickson-Karn,* Courtney M. Olson, Wade C. W. Leu, and C. Scott Hartley
J. Phys. Org. Chem. 2014, 27, 661–669

25. Graphene synthesis: nanoribbons from the bottom-up (News & Views)
C. Scott Hartley*
Nat. Chem. 2014, 6, 91–92

24. Board-like dibenzo[fg,op]naphthacenes: synthesis, characterization, self-assembly, and liquid crystallinity
Jian He, Dena M. Agra-Kooijman, Gautam Singh, Chen Wang, Cherrelle Dugger, Jianbo Zeng, Ling Zang, Satyendra Kumar, and C. Scott Hartley*
J. Mater. Chem. C 2013, 15, 6714–6722

23. A push–pull macrocycle with both linearly conjugated and cross-conjugated bridges
Wade C. W. Leu and C. Scott Hartley*
Org. Lett. 2013, 15, 3762–3765

22. The role of arene–arene interactions in the folding of ortho-phenylenes
Sanyo M. Mathew, James T. Engle, Christopher J. Ziegler, and C. Scott Hartley*
J. Am. Chem. Soc. 2013, 135, 6714–6722
Please note a small correction published to the SI of this paper.

21. opp-Dibenzoporphyrins as a light-harvester for dye-sensitized solar cells
Rohit Deshpande, Bo Wang, Lin Dai, Lin Jiang, C. Scott Hartley, Shouzhong Zou, Hong Wang,* and Lei Kerr*
Chem. Asian. J. 2012, 11, 2662–2669

20. Water-soluble ionic benzoporphyrins
Lin Jiang, Ross A. Zaenglein, James T. Engle, Chris Mittal, C. Scott Hartley, Christopher J. Ziegler, and Hong Wang*
Chem. Commun. 2012, 48, 6927–6929

19. ortho-Phenylene oligomers with terminal push–pull subsitution
Jian He, Sanyo M. Mathew, Sarah D. Cornett, Stephan C. Grundy, and C. Scott Hartley*
Org. Biomol. Chem. 2012, 10, 3398–3405

18. Push–pull macrocycles: donor–acceptor compounds with paired linearly conjugated or cross-conjugated pathways
Wade C. W. Leu, Amanda E. Fritz, Katherine M. Digianantonio, and C. Scott Hartley*
J. Org. Chem. 2012, 77, 2285–2298

17. Excited-state behavior of ortho-phenylenes
C. Scott Hartley*
J. Org. Chem. 2011, 76, 9188–9191

16. Parent o-phenylene oligomers: synthesis, conformational behavior, and characterization
Sanyo M. Mathew and C. Scott Hartley*
Macromolecules 2011, 44, 8425–8432

15. Synthesis and characterization of self-assembled liquid crystals: p-alkoxybenzoic acids
Jana Jensen, Stephan C. Grundy, Stacey Lowery Bretz, and C. Scott Hartley*
J. Chem. Educ. 2011, 88, 1133–1136
Featured on the cover.

14. Triphenylene-fused porphyrins
Lin Jiang, James T. Engle, Laura Sirk, C. Scott Hartley, Christopher J. Ziegler, and Hong Wang*
Org. Lett. 2011, 13, 3020–3023

13. Conformational analysis of o-phenylenes: helical oligomers with frayed ends
C. Scott Hartley* and Jian He
J. Org. Chem. 2010, 75, 8627–8636

12. ortho-Phenylenes: unusual conjugated oligomers with a surprisingly long effective conjugation length
Jian He, Jason L. Crase, Shriya H. Wadumethrige, Khushabu Thakur, Lin Dai, Shouzhong Zou, Rajendra Rathore, and C. Scott Hartley*
J. Am. Chem. Soc. 2010, 132, 13848–13857

Postdoctoral Work at the University of Illinois

11. Covalent ladder formation becomes kinetically trapped beyond four rungs
Erin L. Elliott, C. Scott Hartley, and Jeffrey S. Moore*
Chem. Commun. 2011, 47, 5028–5030

10. Programmed dynamic covalent assembly of unsymmetrical macrocycles
C. Scott Hartley and Jeffrey S. Moore*
J. Am. Chem. Soc. 2007, 129, 11682–11683

9. Covalent assembly of molecular ladders
C. Scott Hartley, Erin L. Elliott, Jeffrey S. Moore*
J. Am. Chem. Soc. 2007, 129, 4512–4513

Graduate school at Queen's University

8. Formation of smectic phases in binary liquid crystal mixtures with a huge length ratio
Nadia Kapernaum,* Friederike Knecht, C. Scott Hartley, Jeffrey C. Roberts, Robert P. Lemieux, and Frank Giesselmann
Beilstein J. Org. Chem. 2012, 8, 1118–1125

7. Systematic variation of length ratio and the formation of smectic A and smectic C phases
Nadia Kapernaum, C. Scott Hartley, Jeffrey C. Roberts, Florian Schoerg, Daniel Krueerke, Robert P. Lemieux, and Frank Giesselmann*
ChemPhysChem 2010, 11, 2099–2107

6. Molecular length distribution and the formation of smectic phases
Nadia Kapernaum, C. Scott Hartley, Jeffrey C. Roberts, Robert P. Lemieux, and Frank Giesselmann*
Beilstein J. Org. Chem. 2009, 5, no. 65

5. Electroclinic effect in chiral SmA* liquid crystals induced by atropisomeric biphenyl dopants: amplification of the electroclinic coefficient using achiral additives
C. Scott Hartley, Nadia Kapernaum, Jeffrey C. Roberts, Frank Giesselmann, and Robert P. Lemieux*
J. Mater. Chem. 2006, 16, 2329–2337
Featured on the inside front cover.

4. Ferroelectric liquid crystals induced by atropisomeric biphenyl dopants: correlation between the sign of induced polarization and the absolute configuration
C. Scott Hartley, Ruiyao Wang, and Robert P. Lemieux*
Chem. Mater. 2004, 16, 5297–5303

3. Ferroelectric liquid crystals induced by atropisomeric biphenyl dopants: the effect of chiral perturbations on achiral dopants
C. Scott Hartley and Robert P. Lemieux*
Liq. Cryst. 2004, 31, 1101–1108

2. Detection of chiral perturbations in ferroelectric liquid crystals induced by an atropisomeric biphenyl dopant
C. Scott Hartley, Carmen Lazar, Michael D. Wand, and Robert P. Lemieux*
J. Am. Chem. Soc. 2002, 124, 13513–13518

1. Ferroelectric liquid crystals induced by atropisomeric biphenyl dopants: dependence of the polarization power on the nature of the symmetry-breaking groups
Despina Vizitiu, Carmen Lazar, Joshua P. Radke, C. Scott Hartley, Matthew A. Glaser, and Robert P. Lemieux*
Chem. Mater. 2001, 13, 1692–1699