-
2
-
-
0347088935
-
-
Yashima, E.; Maeda, K.; Nishimura, T. Chem.-Eur. J. 2004, 10, 42-51.
-
(2004)
Chem.-Eur. J
, vol.10
, pp. 42-51
-
-
Yashima, E.1
Maeda, K.2
Nishimura, T.3
-
8
-
-
33748758414
-
-
Wen, H.-R.; Wang, C.-F.; Li, Y.-Z.; Zuo, J.-L.; Song, Y.; You, X.-Z. Inorg. Chem. 2006, 45, 7032-7034.
-
(2006)
Inorg. Chem
, vol.45
, pp. 7032-7034
-
-
Wen, H.-R.1
Wang, C.-F.2
Li, Y.-Z.3
Zuo, J.-L.4
Song, Y.5
You, X.-Z.6
-
9
-
-
33748776809
-
-
Cucos, P.; Pascu, M.; Sessoli, R.; Avarvari, N.; Pointillart, F.; Andruh, M. Inorg. Chem. 2006, 45, 7035-7037.
-
(2006)
Inorg. Chem
, vol.45
, pp. 7035-7037
-
-
Cucos, P.1
Pascu, M.2
Sessoli, R.3
Avarvari, N.4
Pointillart, F.5
Andruh, M.6
-
10
-
-
0023335034
-
-
Lehn, J.-M.; Rigault, A.; Siegel, J.; Harrowfield, J.; Chevrier, B.; Moras, D. Proc. Natl. Acad. Sci. U.S.A. 1987, 84, 2565-2569.
-
(1987)
Proc. Natl. Acad. Sci. U.S.A
, vol.84
, pp. 2565-2569
-
-
Lehn, J.-M.1
Rigault, A.2
Siegel, J.3
Harrowfield, J.4
Chevrier, B.5
Moras, D.6
-
12
-
-
0033553103
-
-
Ezuhara, T.; Endo, K.; Aoyama, Y. J. Am. Chem. Soc. 1999, 121, 3279-3283.
-
(1999)
J. Am. Chem. Soc
, vol.121
, pp. 3279-3283
-
-
Ezuhara, T.1
Endo, K.2
Aoyama, Y.3
-
14
-
-
0037131931
-
-
Roitzsch, M.; Rother, I. B.; Willermann, M.; Erxleben, A.; Costisella, B.; Lippert, B. Inorg. Chem. 2002, 41, 5946-5953.
-
(2002)
Inorg. Chem
, vol.41
, pp. 5946-5953
-
-
Roitzsch, M.1
Rother, I.B.2
Willermann, M.3
Erxleben, A.4
Costisella, B.5
Lippert, B.6
-
16
-
-
0025868404
-
-
Chen, Y. C. J.; Hansske, F.; Janda, K. D.; Robins, M. J. J. Org. Chem. 1991, 56, 3410-3413.
-
(1991)
J. Org. Chem
, vol.56
, pp. 3410-3413
-
-
Chen, Y.C.J.1
Hansske, F.2
Janda, K.D.3
Robins, M.J.4
-
17
-
-
12644283523
-
-
Wentworth, P., Jr.; Wiemann, T.; Janda, K. D. J. Am. Chem. Soc. 1996, 118, 12521-12527.
-
(1996)
J. Am. Chem. Soc
, vol.118
, pp. 12521-12527
-
-
Wentworth Jr., P.1
Wiemann, T.2
Janda, K.D.3
-
19
-
-
0037462401
-
-
Chiba, J.; Tanaka, K.; Ohshiro, Y.; Miyake, R.; Hiraoka, S.; Shiro, M.; Shionoya, M. J. Org. Chem. 2003, 68, 331-338.
-
(2003)
J. Org. Chem
, vol.68
, pp. 331-338
-
-
Chiba, J.1
Tanaka, K.2
Ohshiro, Y.3
Miyake, R.4
Hiraoka, S.5
Shiro, M.6
Shionoya, M.7
-
20
-
-
17444396767
-
-
Gottschaldt, M.; Koth, D.; Görls, H. Org. Biomol. Chem. 2005, 3, 1170-1171.
-
(2005)
Org. Biomol. Chem
, vol.3
, pp. 1170-1171
-
-
Gottschaldt, M.1
Koth, D.2
Görls, H.3
-
21
-
-
33846172770
-
-
Synthetic details for 3′,5′-bis(salicylaldiminato)-3′, 5′-dideoxy-β-D-xylo-thymidine (1) are described in: Koth, D.; Gottschaldt, M.; Goerls, H. Beilstein J. Org. Chem. 2006, 2 (17).
-
Synthetic details for 3′,5′-bis(salicylaldiminato)-3′, 5′-dideoxy-β-D-xylo-thymidine (1) are described in: Koth, D.; Gottschaldt, M.; Goerls, H. Beilstein J. Org. Chem. 2006, 2 (17).
-
-
-
-
22
-
-
33846143622
-
-
Synthesis of Fe1: 58 mg of 1 was dispersed in 10 mL of acetonitrile and rapidly stirred while a solution of 46 mg of Fe 2(ClO4)2·6H2O was added dropwise and the color of the reaction mixture turned from pale yellow to black-purple. After being stirred for a few minutes, the ligand was completely dissolved. A solution of 10 mg of sodium thiocyanate in 2 mL of acetonitrile and three droplets of aqueous ammonia 25, were added, accompanied by a color change to blood-red and precipitation of some dark solid. After being stirred for 1 h at 50°C, the precipitate was almost completely redissolved. The mixture was allowed to cool down to room temperature and was filtered. After a few days of slow evaporation, flower-shaped aggregates of dark purple-red crystals were obtained that were suitable for single-crystal structure determination. A second crop of micro-crystalline complex was obtained after 2 more days of slow evapora
-
-1): 3061, 2925, 2043, 1696, 1605, 1544, 1470, 1445, 1294, 761, 611.
-
-
-
-
23
-
-
33846146437
-
-
Crystallographic data for Fe1: C29H28N 7O5SFe, M, 642.49 g mol-1, brown-red prism, size 0.04 x 0.04 x 0.03 cm3, tetragonal, space group P41, a, 10.0247(2) Å, b, 10.0247(2) Å, c, 29.1741(5) Å, α, β, γ, 90.00°, V, 2931.84(10) Å3, T, 183(2) K, Z, 4, ρcalcd, 1.456 g cm-1, μ, 0.638 cm-1, F(000, 1332, 16 491 reflections in h(-9/13, k(-11/13, l(-35/37, measured in the range 2.15° ≤ θ ≤ 27.48°, completeness θmax, 99.6, 6640 independent reflections, Rint, 0.0472, 5223 reflections with I ≥ 4σ(I, 391 parameters, 1 restraint, R1, 0.0659 and wR2, 0.0882 all data, R1, 0.0427 and wR
-
2 = 0.0798 (observed), GOF = 1.030, Flack parameter = -0.006(13).
-
-
-
|