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85080514504
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The complex was prepared by reacting H3L (0.24 g, 0.5 mM) taken in a mixture of MeOH, EtOH, and MeCN (3:3:2, v/v, 20 mL) with Et 3N (0.2 mL, 1.5 mM) followed by the addition of Fe(NO 3)3·9H2O (0.20 g, 0.5 mM, The solution was stirred for 15 min followed by the addition of dpq (0.12 g, 0.5 mM, It was filtered after 10 min. The filtrate upon slow concentration gave dark-purple block-shaped crystals in analytically pure form [yield: 0.27 g (65, Anal. Calcd for C46H54N5O4Fe·MeCN: C, 69.34; H, 6.83; N, 8.79. Found: C, 69.16; H, 6.95; N, 9.21. ΛM, 10 S m2 M-1. FT-IR (KBr phase, 1670 cm-1 (νCOO, ESI-MS: mlz 797.3 (M, H, UV-visible in a 6% DMF/Tris-HCl buffer [λ max, nm (ε, M-1 cm-1, 253 (71 720, 282 (39 770, 325 (18 680, 340 16
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B.
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17
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85080570101
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Crystal data for 1·MeCN: C48H57N 6O4Fe, M, 837.85, monoclinic, P2 1/n, a, 14.907(6) Å, b, 13.736(6) Å, c, 21.759(9) Å, β, 92.844(9)°, V, 4450(3) Å3, Z, 4, ρ, 1.251 g cm-3, T, 293(2) K, 1.70 ≤ θ ≤ 5.25°, μ, 3.89 cm-1, F(000, 1780, goodness-of-fit(GOF, 1.042, R1, 0.0927, wR2, 0.1989 for 4526 reflections with I > 2σ(I) and 523 parameters [R1(F2, 0.1635 (all data, w, σ 2(F02, 0.0869P)2, 8.7803P]-1, where P, F02, 2Fc2]/3 (Bruker SMART APEX CCD diffractometer with a Mo Kα X-ray source, The structure was solved and refined using the SHELX program Sheldrick, G. M
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2]/3 (Bruker SMART APEX CCD diffractometer with a Mo Kα X-ray source). The structure was solved and refined using the SHELX program (Sheldrick, G. M. SHELX-97, Programs for Crystal Structure Solution and Refinement; University of Göttingen: Göttingen, Germany, 1997).
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18
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18944408052
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Shongwe, M. S.; Kaschula, C. H.; Adsetts, M. S.; Ainscough, E. W.; Brodie, A. M.; Morris, M. J. Inorg. Chem. 2005, 44, 3070.
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Shongwe, M.S.1
Kaschula, C.H.2
Adsetts, M.S.3
Ainscough, E.W.4
Brodie, A.M.5
Morris, M.J.6
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19
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85080614081
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DNA binding and cleavage experiments were carried out using CT DNA (ca. 310 μM NP) and SC pUC19 DNA (0.2 μg, 33.3 μM bp, respectively, in a 5 mM Tris-HCl/5 mM NaCl buffer (pH 7.2) containing 6% DMF. The light sources used were a UV lamp of 365 nm (12 W, tunable wavelength Spectra Physics Water-Cooled Mixed-Gas Ion Laser Stabilite 2018-RM with laser power meter model 407A (100 mW, CW beam diameter at 1/e2, 1.8 mm ± 10, beam divergence, 0.7 mrad ± 10, and a CW helium-neon laser of Research Electro-Optics make 632.8 nm, 12 mW, beam diameter, 0.88 mm, beam divergence, 0.92 mrad, The complex and reagent concentrations correspond to those in the 18 μL sample solution pathlength, 5 mm, The extent of DNA cleavage was measured from the intensities of the bands in agarose gels using a UVITECH Gel Documentation System
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2 = 1.8 mm ± 10%, beam divergence = 0.7 mrad ± 10%), and a CW helium-neon laser of Research Electro-Optics make (632.8 nm, 12 mW, beam diameter = 0.88 mm, beam divergence = 0.92 mrad). The complex and reagent concentrations correspond to those in the 18 μL sample volume (solution pathlength = 5 mm). The extent of DNA cleavage was measured from the intensities of the bands in agarose gels using a UVITECH Gel Documentation System.
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0024804717
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Murphy Jr., W.R.5
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23
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0026342061
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