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. Author manuscript; available in PMC: 2014 Oct 17.
Published in final edited form as: Chem Sci. 2012 Apr;3(4):1105–1110. doi: 10.1039/C2SC00975G

Fig. 2.

Fig. 2

(a) 1H NMR spectrum of the 3d·TFA salt (top) in DMSO-d6 compared to the 1H NMR of 3d in its neutral state (bottom). When TFA is added to 3d while in solution the 1H NMR spectrum does not resolve, suggesting the presence of a kinetically stable aggregate. (b) 1H NMR titration of 3d with Bu4NCl in CD3CN. The 1H NMR titration shows resolved peaks prior to addition of Bu4NCl, but upon addition of ca. one equivalent Bu4NCl the sample forms insoluble aggregates. Upon addition of excess Bu4NCl the aggregation appears to dissipate and the 1H NMR spectra resolve.