作者: Jesús R. Berenguer , Elena Lalinde , M. Teresa Moreno , Patricia Montaño
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摘要: The reactivity of the Pt0 derivative [Pt2(dba)3] (dba = trans,trans-dibenzylideneacetone) towards PPh2C≡CR [R Ph, tolyl (Tol), C5H4N-2] and PPh2C≡CPPh2 (dppa) has been explored. Treatment with (8 equiv.) in THF gave tetrahedral complexes [Pt(PPh2C≡CR)4] Ph (1), Tol (3), C5H4N-2 (5)], whereas reactions a molar ratio 1:4 afforded binuclear derivatives [{Pt(PPh2C≡CR)(μ-κP:η2-PPh2C≡CR)}2] (2), (4) X-ray, (6)], which were shown to be generated through mononuclear 1, 3 5 as intermediate species. An analogous reaction using 4 equiv. [Pt2(PPh2C≡CPPh2)2(μ-κ2PP′-PPh2C≡CPPh2)3] (7), two “Pt(PPh2C≡CPPh2)” fragments are joined three bridging dppa ligands (μ-κ2PP′-PPh2C≡CPPh2). Attempts crystallize 7 at –30 °C crystals [Pt2{PPh2C≡CP(O)Ph2}2(μ-κ2PP′-PPh2C≡CPPh2)3] (8) by oxidation free end terminal ligands. compound was characterized X-ray diffraction.