Journal of Sulfur Chemistry
5
4.2.4. Bis(1-phenylethyl)carbonotrithioate (Table 2, Entry 9)
Yellow oil; IR (neat): 1069 (C S), 1449, 1493, 1596 cm−1; 1H NMR (400 MHz, CDCl3): δ 1.82
(d, J = 7.6 Hz, 6H), 5.39 (q, J = 7.6 Hz, 2H), 7.35–7.41 (m, 10H); 13C NMR (100 MHz, CDCl3):
δ 21.41, 50.10, 127.77, 128.44, 128.71, 141.13, 221.44.
=
4.2.5. 1,3-Dithiolane-2-thion (Table 2, Entry 11)
Yellow oil; IR (neat): 1075 (C S) cm−1; 1H NMR (400 MHz, CDCl3): δ 3.99 (s, 4H); 13C NMR
=
(100 MHz, CDCl3): δ 43.86, 228.68.
4.2.6. Diisopropyl trithiocarbonate (Table 2, Entry 13)
Light yellow oil; IR (neat): 1073 (C S) cm−1; 1H NMR (400 MHz, CDCl3): δ 1.42 (d, J = 7.2 Hz,
=
12H), 4.22 (sept, J = 7.2 Hz, 2H); 13C NMR (100 MHz, CDCl3): δ 22.07, 41.63, 223.48.
Acknowledgement
The authors thank the K. N. Toosi University of Technology Research Council for providing financial support for this
study.
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