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(MeZn)2(μ‑η2:η2‑N6Ph2): A Powerful Starting Reagent for the Synthesis of Metal Hexazene Complexes

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Figshare2016-04-05 更新2026-04-29 收录
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https://figshare.com/articles/dataset/_MeZn_sub_2_sub__sup_2_sup_sup_2_sup_N_sub_6_sub_Ph_sub_2_sub_A_Powerful_Starting_Reagent_for_the_Synthesis_of_Metal_Hexazene_Complexes/3141883
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[(MeLDippZn)2(μ-η2:η2-PhN6Ph)] (3), which was synthesized by reaction of MeLDipp2Zn2 with PhN3, reacts with two equivalents of Me2Zn to give [(MeZn)2(μ-η2:η2-PhN6Ph)] (2). The reaction of 2 with pyridine gave [(MeZn)2­(μ-η2:η2-PhN6Ph)­(Py)2] (4), while reactions with H-acidic ligands (MeLMesH, MeLPhH) occurred with elimination of methane and formation of [(MeLMesZn)2­(μ-η2:η2-PhN6Ph)] (1) and [(MeLPhZn)2­(μ-η2:η2-PhN6Ph)] (5). The reaction of 1 with two equivalents of MeLi yielded the heterobimetallic hexazene complex [(MeZn)­(μ-η2:η2-PhN6Ph)­(Li)], which was found to undergo stepwise reaction with Me2AlCl to give [MeZn­(μ-η2:η2-PhN6Ph)­AlMe2] and finally [(Me2Al)2­(μ-η2:η2-PhN6Ph)­(thf)2] (6). Compounds 3–6 were characterized by elemental analysis, NMR spectroscopy, and single-crystal X-ray diffraction. Quantum chemical calculations were performed in order to investigate the electronic structure of 4′ and 6′ in more detail and to identify the absorption bands of the hexazene unit.
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2016-04-05
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