-
2
-
-
8444230517
-
-
Zhou Y.-F., Jiang F.-L., Yuan D.-Q., Wu B.-L., Wang R.-H., Lin Z.-Z., and Hong M.-C. Angew. Chem. Int. Ed. 43 (2004) 5665
-
(2004)
Angew. Chem. Int. Ed.
, vol.43
, pp. 5665
-
-
Zhou, Y.-F.1
Jiang, F.-L.2
Yuan, D.-Q.3
Wu, B.-L.4
Wang, R.-H.5
Lin, Z.-Z.6
Hong, M.-C.7
-
3
-
-
1642380376
-
-
Zhao B., Cheng P., Chen X., Cheng C., Shi W., Liao D., Yan S., and Jiang Z. J. Am. Chem. Soc. 126 (2004) 3012
-
(2004)
J. Am. Chem. Soc.
, vol.126
, pp. 3012
-
-
Zhao, B.1
Cheng, P.2
Chen, X.3
Cheng, C.4
Shi, W.5
Liao, D.6
Yan, S.7
Jiang, Z.8
-
5
-
-
0042365036
-
-
Fan J., Gan L., Kawaguchi H., Sun W.-Y., Yu K.B., and Tang X. Chem. Eur. J. 9 (2003) 3965
-
(2003)
Chem. Eur. J.
, vol.9
, pp. 3965
-
-
Fan, J.1
Gan, L.2
Kawaguchi, H.3
Sun, W.-Y.4
Yu, K.B.5
Tang, X.6
-
6
-
-
19844377625
-
-
Lin Z.-Z., Jiang F.-L., Yuan D.-Q., Chen L., Zhou Y.-F., and Hong M.-C. Eur. J. Inorg. Chem. (2005) 1927
-
(2005)
Eur. J. Inorg. Chem.
, pp. 1927
-
-
Lin, Z.-Z.1
Jiang, F.-L.2
Yuan, D.-Q.3
Chen, L.4
Zhou, Y.-F.5
Hong, M.-C.6
-
8
-
-
62649166348
-
-
Wang Y., Hu M.-C., Zhai Q.-G., Li S.-N., Jiang Y.-C., and Ji W.-J. Inorg. Chem. Commun. 12 (2009) 281
-
(2009)
Inorg. Chem. Commun.
, vol.12
, pp. 281
-
-
Wang, Y.1
Hu, M.-C.2
Zhai, Q.-G.3
Li, S.-N.4
Jiang, Y.-C.5
Ji, W.-J.6
-
10
-
-
33749040313
-
-
Fang Q.-R., Zhu G.-S., Jin Z., Xue M., Wei X., Wang D.-J., and Qiu S.-L. Angew. Chem. Int. Ed. 45 (2006) 6126
-
(2006)
Angew. Chem. Int. Ed.
, vol.45
, pp. 6126
-
-
Fang, Q.-R.1
Zhu, G.-S.2
Jin, Z.3
Xue, M.4
Wei, X.5
Wang, D.-J.6
Qiu, S.-L.7
-
13
-
-
0001412882
-
-
Seo J.S., Whang D., Lee H., Jun S.I., Oh J., Jeon Y.J., and Kim K. Nature 404 (2000) 982
-
(2000)
Nature
, vol.404
, pp. 982
-
-
Seo, J.S.1
Whang, D.2
Lee, H.3
Jun, S.I.4
Oh, J.5
Jeon, Y.J.6
Kim, K.7
-
18
-
-
0034735148
-
-
Graham P.M., Pike R.D., Sabat M., Bailey R.D., and Pennington W.T. Inorg. Chem. 39 (2000) 5121
-
(2000)
Inorg. Chem.
, vol.39
, pp. 5121
-
-
Graham, P.M.1
Pike, R.D.2
Sabat, M.3
Bailey, R.D.4
Pennington, W.T.5
-
19
-
-
37049111024
-
-
Healy P.C., Pakawatchai C., Raston C.L., Skelton B.W., and White A.H. J. Chem. Soc., Dalton Trans. (1983) 1905
-
(1983)
J. Chem. Soc., Dalton Trans.
, pp. 1905
-
-
Healy, P.C.1
Pakawatchai, C.2
Raston, C.L.3
Skelton, B.W.4
White, A.H.5
-
21
-
-
0000574393
-
-
Barron P.F., Dyason J.C., Engelhardt L.M., Healy P.C., and White A.H. Inorg. Chem. 23 (1984) 3766
-
(1984)
Inorg. Chem.
, vol.23
, pp. 3766
-
-
Barron, P.F.1
Dyason, J.C.2
Engelhardt, L.M.3
Healy, P.C.4
White, A.H.5
-
24
-
-
7244245663
-
-
Li G.-H., Shi Z., Liu X.-M., Dai Z.-M., and Feng S.-H. Inorg. Chem. 43 (2004) 6884
-
(2004)
Inorg. Chem.
, vol.43
, pp. 6884
-
-
Li, G.-H.1
Shi, Z.2
Liu, X.-M.3
Dai, Z.-M.4
Feng, S.-H.5
-
25
-
-
64349096860
-
-
Hu M.-C., Wang Y., Zhai Q.-G., Li S.-N., Jiang Y.-C., and Zhang Y. Inorg. Chem. 48 (2009) 1449
-
(2009)
Inorg. Chem.
, vol.48
, pp. 1449
-
-
Hu, M.-C.1
Wang, Y.2
Zhai, Q.-G.3
Li, S.-N.4
Jiang, Y.-C.5
Zhang, Y.6
-
27
-
-
72249119325
-
-
To the stirring colorless solution of bmt (0.15 g, 1 mmol) in MeOH (15 mL, CuI (0.38 g, 2 mmol) in MeCN (15 mL) was added. The reaction mixture turned to white suspension, and the mixture was kept stirring for 6 h and filtered. After filtration, the filter residue was resolved in DMF. The filtrate was allowed to stand at ambient temperatures for several days. Then colorless prism crystals of complex 1 suitable for single crystal X-ray analysis were obtained. Yield: 55, 0.067 g) based on Cu. Anal. Calc. for C20H26Cu4I4N6O2S2: C, 19.88; H, 2.17; N, 6.95; Found: C, 19.84; H, 2.20; N, 6.97, IR KBr pellet, 4000-400 cm-1, 3450m, 3276vs, 3050m, 2805w, 1645vs, 1618m, 1530w, 1497m, 1454m, 1361m, 1182m, 1003w, 960w, 738s
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-1): 3450m, 3276vs, 3050m, 2805w, 1645vs, 1618m, 1530w, 1497m, 1454m, 1361m, 1182m, 1003w, 960w, 738s.
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Crystal data for 1: C20H26Cu4I4N6O2S2, M, 1208.35, colorless prism crystal (0.20 × 0.15 × 0.10 mm, monoclinic, space group C2/m, a, 22.342(10, b, 6.479(3, c, 11.277(5) Å, β, 106.363(7)°, V, 1566.1(12) Å3, Z, 4, Dc, 2.562 g/cm3, F(0 0 0, 1128, μ, 6.785 mm-1, T, 293(2) K. 6021 reflections collected, 1920 unique (Rint, 0.0244, R1, 0.0293, wR2, 0.0801 and S, 1.044, based on 1660 reflections with I > 2σ(I, refinement on F2, Intensity data were collected on a Rigaku mercury CCD diffractometer with graphite-monochromated Mo Ka (λ, 0.71073 Å) radiation by using ω-2θ scan method at room temperature. The structure was solved by direct methods and refined by shelxtl-97 program. All non-hydrogen atoms were refined anisotropically. Positions of
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2). Intensity data were collected on a Rigaku mercury CCD diffractometer with graphite-monochromated Mo Ka (λ = 0.71073 Å) radiation by using ω-2θ scan method at room temperature. The structure was solved by direct methods and refined by shelxtl-97 program. All non-hydrogen atoms were refined anisotropically. Positions of the hydrogen atoms attached to carbon atoms were fixed at their ideal positions.
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-
-
-
29
-
-
19944394886
-
-
Xie H.-Y., Kinoshita I., Karasawa T., Kimura K., Nishioka T., Akai I., and Kanemoto K. J. Phys. Chem. B 109 (2005) 9339
-
(2005)
J. Phys. Chem. B
, vol.109
, pp. 9339
-
-
Xie, H.-Y.1
Kinoshita, I.2
Karasawa, T.3
Kimura, K.4
Nishioka, T.5
Akai, I.6
Kanemoto, K.7
-
30
-
-
33645460970
-
-
Bai Y., He G.-J., Zhao Y.-G., Duan C.-Y., Dang D.-B., and Meng Q.-J. Chem. Commun. (2006) 1530
-
(2006)
Chem. Commun.
, pp. 1530
-
-
Bai, Y.1
He, G.-J.2
Zhao, Y.-G.3
Duan, C.-Y.4
Dang, D.-B.5
Meng, Q.-J.6
-
32
-
-
20444460813
-
-
Cariati E., Roberto D., Ugo R., Ford P.C., Galli S., and Sironi A. Inorg. Chem. 44 (2005) 4077
-
(2005)
Inorg. Chem.
, vol.44
, pp. 4077
-
-
Cariati, E.1
Roberto, D.2
Ugo, R.3
Ford, P.C.4
Galli, S.5
Sironi, A.6
-
33
-
-
2442709420
-
-
Fu W.F., Gan X., Che C.M., Cao Q.Y., Zhou Z.Y., and Zhu N.N.Y. Chem. Eur. J. 10 (2004) 2228
-
(2004)
Chem. Eur. J.
, vol.10
, pp. 2228
-
-
Fu, W.F.1
Gan, X.2
Che, C.M.3
Cao, Q.Y.4
Zhou, Z.Y.5
Zhu, N.N.Y.6
-
34
-
-
31144468535
-
-
Hiromi A., Kiyoshi T., Yoichi S., Shoji I., and Noboru K. Inorg. Chem. 44 (2005) 9667
-
(2005)
Inorg. Chem.
, vol.44
, pp. 9667
-
-
Hiromi, A.1
Kiyoshi, T.2
Yoichi, S.3
Shoji, I.4
Noboru, K.5
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