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Klein Gebank, R. J. M.; Suijkerbuijk, B. M. J. M. Angew. Chem., Int. Ed. 2008, 47, 7396.
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(a) Arnold, D. P.; Sakata, Y.; Sugiura, K.; Worthington, E. I. Chem. Commun. 1998, 2331.
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Hodgson, M.J.1
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(e) Arnold, D. P.; Healy, P. C.; Hodgson, M. J.; Williams, M. L. J. Organomet. Chem. 2000, 607, 41.
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(a) Yamaguchi, S.; Katoh, T.; Shinokubo, H.; Osuka, A. J. Am. Chem. Soc 2007, 129, 6392.
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(a) Albrecht, M.; van Koten, G. Angew. Chem., Int. Ed. 2001, 40, 3750.
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Li, R.1
Jiang, L.2
Lu, W.3
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61449142675
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3 C-H dehydrogenated cross-coupling reaction has been reported. In the literature, the authors suggest that the coupling occurs via the Friedel-Crafts-type reaction mechanism, (a) Li, Z.; Li, C.-H. J. Am. Chem. Soc. 2005, 127, 6968. For related reactions, see:
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3 C-H dehydrogenated cross-coupling reaction has been reported. In the literature, the authors suggest that the coupling occurs via the Friedel-Crafts-type reaction mechanism, (a) Li, Z.; Li, C.-H. J. Am. Chem. Soc. 2005, 127, 6968. For related reactions, see:
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27544488753
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Murahashi, S.-I.1
Komiya, N.2
Terai, H.3
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Hata, H.; Shinokubo, H.; Osuka, A. J. Am. Chem. Soc. 2005, 127, 8264.
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Hata, H.1
Shinokubo, H.2
Osuka, A.3
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25
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61449150625
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Iv probably by air in the course of the reaction. The reaction under an inert atmosphere did not afford 4Ni. For an oxidant-promoted C-H bond activation reaction, see: Newman, C. P.; Casey-Green, K.; Clarkson, G. J.; Cave, G. W. V.; Errington, W.; Rourke, J. P. Dalton Trans. 2007, 3170.
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Iv probably by air in the course of the reaction. The reaction under an inert atmosphere did not afford 4Ni. For an oxidant-promoted C-H bond activation reaction, see: Newman, C. P.; Casey-Green, K.; Clarkson, G. J.; Cave, G. W. V.; Errington, W.; Rourke, J. P. Dalton Trans. 2007, 3170.
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26
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61449190886
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The reaction of 1Ni with a platinum(IV) salt in toluene/AcOH provided a platinum(IV)-bridged cofacial diporphyrin. See ref 3b. However, none of such diporphyrins was detected in the reaction in toluene/ DMF
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The reaction of 1Ni with a platinum(IV) salt in toluene/AcOH provided a platinum(IV)-bridged cofacial diporphyrin. See ref 3b. However, none of such diporphyrins was detected in the reaction in toluene/ DMF.
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27
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61449258464
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Crystallographic data for 4: C68H74ClN 5NiOPt·3CCl4, Mw, 1728.00, triclinic, space group Pl (No. 2, a, 11.841(5) Å, b, 16.521(5) Å, c, 19.620(5) Å, α, 99.387(5)°, β, 103.850(5)°, γ, 93.508(5)°, V, 3656(2) Å3, Z, 2, Dcalc, 1.569 Mg/cm 3, R, 0.0807 [I > 2.0σ(I, RW, 0.2353 (all data, GOF, 1.006 [I > 2.0σI
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W = 0.2353 (all data), GOF = 1.006 [I > 2.0σ(I)].
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28
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61449117949
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Crystallography data for 3Ni: C70OH80Cl 2N6NiOPt ·3C6H5Cl, Mw, 1683.75, triclinic, space group Pl (No. 2, a, 14.277(4) Å, b, 16.450(5) Å,c= 17.619(4) Å, α, 89.353(12)°, ß, 78.992(11)°, γ, 85.740(12)°, V, 4051(2) Å3, Z, 2, Dcalc, 1.380 Mg/cm3, T, 90 K, R, 0.0521 [1 > 2.0σ(I, RW, 0.1396 (all data, GOF, 1.047 [I > 2.0σ(Z, Crystallographic data for 3H2: C70H82Cl2N6OPt·4C 6H5Cl, Mw, 1739.61, triclinic, space group ZM (No. 2, a, 9.117(5) A, b, 16.014(5) Å, 31.276(5) Å, α, 78.593(5)°, β, 89.631(5)°, γ, 74.974(5)°, V, 43185
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w = 0.1505 (all data), GOF = 1.048 [I > 2.0σ(I)].
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