BULLETIN OF THE
Note
KOREAN CHEMICAL SOCIETY
References
1
2
3
4
5
6
7
8
9
. E. Cariati, E. Lucenti, C. Botta, U. Giovanella, D. Marinotto,
S. Righetto, Coord. Chem. Rev. 2016, 306, 566.
. W. Liu, Y. Fang, G. Z. Wei, S. J. Teat, K. Xiong, Z. Hu,
W. P. Lustig, J. Li, J. Am. Chem. Soc. 2015, 137, 9400.
. W. Ji, J. Qu, S. Jing, D. Zhu, W. Huang, Dalton Trans. 2016,
4
5, 1016.
. S.-Q. Bai, L. Jiang, A. L. Tan, S. C. Yeo, D. J. Young,
T. S. A. Hor, Inorg. Chem. Front. 2015, 2, 1011.
. S. Cho, Y. Jeon, S. Lee, J. Kim, T. H. Kim, Chem. Eur. J.
2
015, 21, 1439.
. M. S. Deshmukh, A. Yadav, R. Pant, R. Boomishankar,
Inorg. Chem. 2015, 54, 1337.
. S. Cheon, T. H. Kim, Y. Jeon, J. Kim, K.-M. Park, CrystEng-
Comm. 2013, 15, 451.
. J.-C. Li, H.-X. Li, H.-Y. Li, W.-J. Gong, J.-P. Lang, Cryst.
Growth Des. 2016, 16, 1617.
. L. R. Hanton, R. M. Hellyer, M. D. Spicer, Inorg. Chim. Acta
Figure 4. Excitation and emission spectra of 1 in the solid state.
Emission spectrum at λex = 325 nm and excitation spectrum for
λ
em = 460 nm.
2
006, 359, 3659.
1
0. F. Wei, T. Zhang, X. Liu, X. Li, N. Jiang, Z. Liu, Z. Bian,
2
2
H, OCH ), 2.94 (t, 2H, CH S), 2.75 (m, H, SCH),
2 2
Y. Zhao, Z. Lu, C. Huang, Org. Electron. 2014, 15, 3292.
1
3
.1–1.25 (m, 10H, (CH ) ). C NMR (75.4 MHz, CDCl3):
2
5
11. R. Czerwieniec, H. Yersin, Inorg. Chem. 2015, 54, 4322.
12. F. Dumur, Org. Electron. 2015, 21, 27.
13. Q. Benito, X. F. Le Goff, G. Nocton, A. Fargues, A. Garcia,
A. Berhault, S. Kahlal, J.-Y. Saillard, C. Martineau,
J. Trébosc, T. Gacoin, J. -P. Boilot, S. Perruchas, Inorg.
Chem. 2015, 54, 4483.
δ = 154.71, 141.13, 137.88, 123.86, 121.19, 68.40, 43.99,
−
1
3
2
1
6
3.70, 28.81, 26.01, and 25.70. IR (KBr, ν, cm ): 3055 m,
927 s, 2852 s, 1707 w, 1576 s, 1475 s, 1425 s, 1263 s,
228 s, 1111 m, 1049 m, 1007 m, 887 m, 800 s, 708 s,
+
00 m, and 415 m. Mass spectrum m/z 237 (M , 4%).
1
4. Q. Benito, B. Baptiste, A. Polian, L. Delbes, L. Martinelli,
T. Gacoin, J.-P. Boilot, S. Perruchas, Inorg. Chem. 2015,
54, 9821.
Preparation of [CuIL] (1). An MeCN (10 mL) solution
n
of L (0.0237 g, 0.10 mmol) was permitted to react with
an MeCN (10 mL) solution of CuI (0.0195 g, 0.10 mmol).
Slow evaporation afforded crystals suitable for SCXRD.
Pale yellow crystals were washed with Et O/MeCN (2/1)
solution (0.0314 g, 73%). IR (KBr, ν, cm ): 3095 w,
1
1
1
1
5. T. H. Kim, Y. W. Shin, J. H. Jung, J. S. Kim, J. Kim, Angew.
Chem. Int. Ed. 2008, 47, 685.
6. G. Park, H. Yang, T. H. Kim, J. Kim, Inorg. Chem. 2011,
50, 961.
2
−
1
7. G. Kang, Y. Jeon, K. Y. Lee, J. Kim, T. H. Kim, Cryst.
Growth Des. 2015, 15, 5183.
8. T. H. Kim, H. Yang, G. Park, K. Y. Lee, J. Kim, Chem.
Asian J. 2010, 5, 252.
2
1
7
929 s, 2850 m, 1574 m, 1475 m, 1431 m, 1390 m,
281 s, 1236 s, 1119 m, 1049 m, 1011 m, 885 m, 800 m,
02 m, and 619 m. [CuIL]n Anal. Calcd for
C H CuINOS: C, 36.50; H, 4.48; N, 3.27; S, 7.50%.
1
3
19
19. Y. Jeon, S. Cheon, S. Cho, K. Y. Lee, T. H. Kim, J. Kim,
Measured: C, 36.48, H, 4.47, N, 3.11, S, 7.58%.
Cryst. Growth Des. 2014, 14, 2105.
2
2
2
2
0. T. H. Kim, G. Park, Y. W. Shin, K.-M. Park, M. Y. Choi,
J. Kim, Bull. Korean Chem. Soc 2008, 29, 499.
1. T. H. Kim, Y. W. Shin, S. S. Lee, J. Kim, Anal. Sci. 2006,
Acknowledgments. This work was supported by the
National Research Foundation of Korea, funded by the
Ministry of Education, Science and Technology (NRF-
2
2, x287.
2. S.-M. Zhang, T.-L. Hu, J.-L. Du, X.-H. Bu, Inorg. Chim. Acta
009, 362, 3915.
2014R1A1A4A01009105 and 2015R1D1A4A01020317).
2
3. H. Araki, K. Tsuge, Y. Sasaki, S. Ishizaka, N. Kitamura,
Supporting Information. Characterization details,
Inorg. Chem. 2005, 44, 9667.
selected bond distances, and angles for 1 are available in
the online version of this article.
24. M. Protiva, J. Pliml, P. Finglova, Chemicke Listy pro Vedu a
Prumysl 1953, 47, 1197.
Bull. Korean Chem. Soc. 2016
© 2016 Korean Chemical Society, Seoul & Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim
www.bkcs.wiley-vch.de
3