6
Tetrahedron
ACCEPTED MANUSCRIPT
23.
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4H2O (3.86 mg, 0.0125 mmol) in 20 mL MeOH was added.
After refluxing for 10 hours at 70 . After cooling to room
temperature, the expectant product was deposited by NH4PF6 (20
times) which was filtered and washed with MeOH (3 × 20 mL)
24.
Campos-Fernández, C. S.; Schottel, B. L.; Chifotides, H.
T.; Bera, J. K.; Bacsa, J.; Koomen, J. M.; Russell, D. H.;
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1
and water thoroughly to give a solid (12.7 mg, 92%). H NMR
(400 MHz, CD3CN) δ (ppm): 9.04 (s, 12H), 8.92 (s, 6H), 8.82 (d,
12H), 8.36 (d, 12H), 8.24 (m, 24H), 8.20 (d, 6H), 8.13 (d, 12H),
8.06(d, 6H), 7.52 (t, 12H) (Fig. S3). ESI/MS (m/z): Found For:
575.8367 [L33Cd3-5PF6¯ ]5+ (Calcd. For: 575.9001), 756.0364
[L33Cd3-4PF6¯ ]4+ (Calcd. For: 756.1009), 1056.0194 [L33Cd3-
3PF6¯ ]3+ (Calcd. For: 1056.1006), respectively.
25.
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29.
Chan, Y.-T.; Moorefield, C. N.; Soler, M.; Newkome, G.
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Acknowledgments
Wu, T.; Yuan, G.; Liu, D.; Wang, M.; Li, Y.; Chen, M.;
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Chan, Y.-T.; Li, X.; Soler, M.; Wang, J.-L.; Wesdemiotis,
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Wang, J.-L.; Li, X.; Lu, X.; Chan, Y.-T.; Moorefield, C.
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This research was supported by the Fundamental Research Fu
nds of Central South University (2018zzts012), the Distinguished
Professor Research Fund from Guangzhou University. Authors
acknowledge the NMR measurements from The Modern
Analysis and Testing Center of CSU.
30.
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