-
2
-
-
0041691427
-
-
Artero V., Proust A., Herson P., Villain F., Moulin C., and Gouzerh P. J. Am. Chem. Soc. 125 (2003) 11156
-
(2003)
J. Am. Chem. Soc.
, vol.125
, pp. 11156
-
-
Artero, V.1
Proust, A.2
Herson, P.3
Villain, F.4
Moulin, C.5
Gouzerh, P.6
-
4
-
-
84875232895
-
-
Müller A. Nature 352 (1991) 115
-
(1991)
Nature
, vol.352
, pp. 115
-
-
Müller, A.1
-
6
-
-
34250354077
-
-
Lisnard L., Mialane P., Dolbecq A., Marrot J., Clemente-Juan J.M., Coronado E., Keita B., Oliveira P., Nadjo L., and Secheresse F. Chem. Eur. J. 13 (2007) 3525
-
(2007)
Chem. Eur. J.
, vol.13
, pp. 3525
-
-
Lisnard, L.1
Mialane, P.2
Dolbecq, A.3
Marrot, J.4
Clemente-Juan, J.M.5
Coronado, E.6
Keita, B.7
Oliveira, P.8
Nadjo, L.9
Secheresse, F.10
-
11
-
-
55049102894
-
-
Zou N., Chen W.L., Li Y.G., Liu W.L., and Wang E.B. Inorg. Chem. Commun. 11 (2008) 1367
-
(2008)
Inorg. Chem. Commun.
, vol.11
, pp. 1367
-
-
Zou, N.1
Chen, W.L.2
Li, Y.G.3
Liu, W.L.4
Wang, E.B.5
-
12
-
-
75149178976
-
-
Chen W.L., Chen B.W., Tan H.Q., Li Y.G., Wang Y.H., and Wang E.B. J. Solid State Chem. 183 (2009) 310
-
(2009)
J. Solid State Chem.
, vol.183
, pp. 310
-
-
Chen, W.L.1
Chen, B.W.2
Tan, H.Q.3
Li, Y.G.4
Wang, Y.H.5
Wang, E.B.6
-
13
-
-
75749108880
-
-
Lin S.W., Liu W.L., Li Y.G., Wu Q., Wang E.B., and Zhang Z.M. Dalton Trans. 39 (2010) 1740
-
(2010)
Dalton Trans.
, vol.39
, pp. 1740
-
-
Lin, S.W.1
Liu, W.L.2
Li, Y.G.3
Wu, Q.4
Wang, E.B.5
Zhang, Z.M.6
-
14
-
-
46749117185
-
-
Lin S.W., Chen W.L., Zhang Z.M., Liu W.L., and Wang E.B. Acta Cryst. E64 (2008) m954
-
(2008)
Acta Cryst.
, vol.E64
-
-
Lin, S.W.1
Chen, W.L.2
Zhang, Z.M.3
Liu, W.L.4
Wang, E.B.5
-
18
-
-
3242742075
-
-
Abbott A.P., Boothby D., Capper G., Davies D.L., and Rasheed R.K. J. Am. Chem. Soc. 126 (2004) 9142
-
(2004)
J. Am. Chem. Soc.
, vol.126
, pp. 9142
-
-
Abbott, A.P.1
Boothby, D.2
Capper, G.3
Davies, D.L.4
Rasheed, R.K.5
-
19
-
-
4344580408
-
-
Cooper E.R., Andrews C.D., Wheatley P.S., Webb P.B., Wormald P., and Morris R.E. Nature 430 (2004) 1012
-
(2004)
Nature
, vol.430
, pp. 1012
-
-
Cooper, E.R.1
Andrews, C.D.2
Wheatley, P.S.3
Webb, P.B.4
Wormald, P.5
Morris, R.E.6
-
22
-
-
70349784949
-
-
Zhang J., Wu T., Chen S.M., Feng P.Y., and Bu X.H. Angew. Chem. Int. Ed. 48 (2009) 3486
-
(2009)
Angew. Chem. Int. Ed.
, vol.48
, pp. 3486
-
-
Zhang, J.1
Wu, T.2
Chen, S.M.3
Feng, P.Y.4
Bu, X.H.5
-
23
-
-
77950020021
-
-
Wang S.M., Li Y.W., Feng X.J., Li Y.G., and Wang E.B. Inorg. Chim. Acta 363 (2010) 1556
-
(2010)
Inorg. Chim. Acta
, vol.363
, pp. 1556
-
-
Wang, S.M.1
Li, Y.W.2
Feng, X.J.3
Li, Y.G.4
Wang, E.B.5
-
24
-
-
77953872457
-
-
Synthesis of 1: Na2MoO4·2H2O (1.35 g, 5.58 mmol) was added to 8 mL choline chloride/urea eutectic mixture with stirring, after the Na2MoO4·2H2O was dissolved completely, NaIO4 (0.20 g, 0.94 mmol) was added to the solution. After ten minutes, the glacial acetic acid (0.5 mL) and water (0.4 mL) were added to above solution, stirring for 4 hours in air at 30 °C. The white suspension was filtered and the filterate was kept at room temperature. Colorless plate crystals of 1 were isolated after 3 days. The products were collected by filtration, washed with absolute alcohol and dried in vacuum desiccator at 80 °C for half an hour (yield: 64% based on Mo, Thermal gravimetric (TG) analyses were carried out to detect the thermal stability of 1 (Fig. S11, Elemental Anal. Calcd (found) for the compound 1 (wt, Mo 38.95 (39.14, C 8.12 (7.93, H 3.48 (3.31, N 1.89 (1.95, FT-IR data (cm-1, 3452(br, 1613(m, 1478(m, 1411(w, 1342(w, 1290(w, 1054(m, 946s, 9
-
-1): 3452(br), 1613(m), 1478(m), 1411(w), 1342(w), 1290(w), 1054(m), 946(s), 906(s), 690(s), 632(s), 455(s).
-
-
-
-
25
-
-
77953872641
-
-
Crystal data for 1: C10H34IMo6N2Na2O34, M, 1474.91, Monoclinic, space group C2/m, a, 21.012(4)Å, b, 12.907(3)Å, c, 7.3450(15)Å, β, 109.01(3)° V, 1883.4(7)Å3, Z, 2, Dcalc, 2.601 mg m-3, T, 150(2) K, R1, 0.0375
-
-3, T = 150(2) K, R1 = 0.0375.
-
-
-
-
26
-
-
33847747088
-
-
Honda D., Ikegami S., Inoue T., Ozeki T., and Yagasaki A. Inorg. Chem. 46 (2007) 1464
-
(2007)
Inorg. Chem.
, vol.46
, pp. 1464
-
-
Honda, D.1
Ikegami, S.2
Inoue, T.3
Ozeki, T.4
Yagasaki, A.5
-
28
-
-
77953871964
-
-
Crystal data for 2: C28H108Al2Mo12N20Na2O64, M, 3000.56, Monoclinic, space group C2, a, 24.786(5)Å, b, 9.819(2)Å, c, 21.285(4)Å, β, 120.32(3)° V, 4471.7(16)Å3, Z, 2, Dcalc, 2.228 mg m-3, T, 150(2) K, R1, 0.0581
-
-3, T = 150(2) K, R1 = 0.0581.
-
-
-
-
31
-
-
41949101509
-
-
Cao R.G., Liu S.X., Xie L.H., Pan Y.B., Cao J.F., and Liu Y. Inorg. Chim. Acta 361 (2008) 2013
-
(2008)
Inorg. Chim. Acta
, vol.361
, pp. 2013
-
-
Cao, R.G.1
Liu, S.X.2
Xie, L.H.3
Pan, Y.B.4
Cao, J.F.5
Liu, Y.6
-
32
-
-
60149089298
-
-
Zhang S.W., Li Y.X., Liu Y., Cao R.G., Sun C.Y., Ji H.M., and Liu S.X. J. Mol. Struct. 920 (2009) 284
-
(2009)
J. Mol. Struct.
, vol.920
, pp. 284
-
-
Zhang, S.W.1
Li, Y.X.2
Liu, Y.3
Cao, R.G.4
Sun, C.Y.5
Ji, H.M.6
Liu, S.X.7
-
33
-
-
34248347928
-
-
Cao R.G., Liu S.X., Xie L.H., Pan Y.B., Cao J.F., Ren Y.H., and Xu L. Inorg. Chem. 46 (2007) 3541
-
(2007)
Inorg. Chem.
, vol.46
, pp. 3541
-
-
Cao, R.G.1
Liu, S.X.2
Xie, L.H.3
Pan, Y.B.4
Cao, J.F.5
Ren, Y.H.6
Xu, L.7
-
36
-
-
77953869518
-
-
Crystal data for 3: C16H92Mo14N14Na8O75, M, 3208.12, Orthorhombic, space group Fdd2, a, 32.240(6)Å, b, 38.563(8)Å, c, 17.199(3)Å, V, 21384(7, Z, 8, Dcalc, 1.993 mg m-3, T, 150(2) K, R1, 0.0407
-
-3, T = 150(2) K, R1 = 0.0407.
-
-
-
-
37
-
-
0013109171
-
-
Gili P., Lorenzo-Luis P.A., Mederos A., Arrieta J.M., Germain G., Castiñeiras A., and Carballo R. Inorg. Chim. Acta 295 (1999) 106
-
(1999)
Inorg. Chim. Acta
, vol.295
, pp. 106
-
-
Gili, P.1
Lorenzo-Luis, P.A.2
Mederos, A.3
Arrieta, J.M.4
Germain, G.5
Castiñeiras, A.6
Carballo, R.7
-
38
-
-
34247143258
-
-
Coué V., Dessapt R., Bujoli-Doeuff M., Evain M., and Jobic S. Inorg. Chem. 46 (2007) 2824
-
(2007)
Inorg. Chem.
, vol.46
, pp. 2824
-
-
Coué, V.1
Dessapt, R.2
Bujoli-Doeuff, M.3
Evain, M.4
Jobic, S.5
-
39
-
-
77953870498
-
-
Compound 1 (0.005 g) was dissolved in 200 mL rhodamine B (RhB) solutions (2.0 × 10-5 mol/L, magnetically stirred in the dark for about 30 min. The solution was then exposed to UV irradiation from a 125 W Hg lamp with a distance of 4 5 cm between the liquid surface and the lamp. The solution was kept stirring during irradiation. Every 30 minutes intervals, 3 mL of samples were taken out from the beaker and subsequently analyzed by UV-visible spectroscopy. After the initial amount of RhB had degraded, the same amount of RhB was added into the system again, the RhB was degraded for the second cycle. Repeat the procedure for another three times. An identical procedure above-mentioned was used in the following experiments except compound 1, which was replaced by 0.012 g (2 × 10-5 mol/L) compound 2 and the 60 minutes time interval
-
-5 mol/L) compound 2 and the 60 minutes time interval.
-
-
-
|