Albrecht Christian, Schwieger Sebastian, Bruhn Clemens, Wagner Christoph, Kluge Ralph, Schmidt Harry, Steinborn Dirk
Institut für Anorganische Chemie, Martin-Luther-Universität Halle-Wittenberg, Kurt-Mothes-Strasse 2, D-06120 Halle, Germany.
J Am Chem Soc. 2007 Apr 18;129(15):4551-66. doi: 10.1021/ja068476r. Epub 2007 Mar 23.
Acetylplatinum(II) complexes trans-[Pt(COMe)Cl(L)2] (L = PPh3, 2a; P(4-FC6H4)3, 2b) were found to react with dialkyldisulfides R2S2 (R = Me, Et, Pr, Bu; Pr = n-propyl, Bu = n-butyl), yielding trinuclear 44 cve (cluster valence electrons) platinum clusters [(PtL)3(mu-SR)3]Cl (4). The analogous reaction of 2a-b with Ph2S2 gave SPh bridged dinuclear complexes trans-[{PtCl(L)}2(mu-SPh)2] (5), whereas the addition of Bn2S2 (Bn = benzyl) to 2a ended up in the formation of [{Pt(PPh3)}3(mu3-S)(mu-SBn)3]Cl (6). Theoretical studies based on the AIM theory revealed that type 4 complexes must be regarded as triangular platinum clusters with Pt-Pt bonds whereas complex 6 must be treated as a sulfur capped 48 ve (valence electrons) trinuclear platinum(II) complex without Pt-Pt bonding interactions. Phosphine ligands with a lower donor capability in clusters 4 proved to be subject to substitution by stronger donating monodentate phosphine ligands (L' = PMePh2, PMe2Ph, PBu3) yielding clusters [(PtL')3(mu-SR)3]Cl (9). In case of the reaction of clusters 4 and 9 with PPh2CH2PPh2 (dppm), a fragmentation reaction occurred, and the complexes [(PtL)2(mu-SMe)(mu-dppm)]Cl (12) and [Pt(mu-SMe)2(dppm)] (13) were isolated. Furthermore, oxidation reactions of cluster [{Pt(PPh3)}3(mu-SMe)3]Cl (4a) using halogens (Br2, I2) gave dimeric platinum(II) complexes cis-[{PtX(PPh3)}2(mu-SMe)2] (14, X = Br, I) whereas oxidation reactions using sulfur and selenium afforded chalcogen capped trinuclear 48 ve complexes [{Pt(PPh3)}3(mu3-E)(mu-SMe)3] (15, E = S, Se). All compounds were fully characterized by means of NMR and IR spectroscopy, microanalyses, and ESI mass spectrometry. Furthermore, X-ray diffraction analyses were performed for the triangular cluster 4a, the trinuclear complex 6, as well as for the dinuclear complexes trans-[{Pt(AsPh3)}2(mu-SPh)2] (5c), [{Pt(PPh3)}2(mu-SMe)(mu-dppm)]Cl (12a), and [{{PtBr(PPh3)}2(mu-SMe)2] (14a).
乙酰铂(II)配合物反式-[Pt(COMe)Cl(L)₂](L = PPh₃,2a;P(4-FC₆H₄)₃,2b)被发现可与二烷基二硫化物R₂S₂(R = Me、Et、Pr、Bu;Pr = 正丙基,Bu = 正丁基)反应,生成三核44个簇价电子(cluster valence electrons)的铂簇合物[(PtL)₃(μ-SR)₃]Cl(4)。2a - b与Ph₂S₂的类似反应生成了SPh桥连的双核配合物反式-[{PtCl(L)}₂(μ-SPh)₂](5),而将Bn₂S₂(Bn = 苄基)加入到2a中最终形成了[{Pt(PPh₃)}₃(μ₃-S)(μ-SBn)₃]Cl(6)。基于AIM理论的理论研究表明,4型配合物必须被视为具有Pt - Pt键的三角铂簇,而配合物6必须被视为一个硫封端的48个价电子(valence electrons)的三核铂(II)配合物,不存在Pt - Pt键相互作用。在簇合物4中供体能力较低的膦配体被更强供电子的单齿膦配体(L' = PMePh₂、PMe₂Ph、PBu₃)取代,生成簇合物[(PtL')₃(μ-SR)₃]Cl(9)。在簇合物4和9与PPh₂CH₂PPh₂(dppm)反应的情况下,发生了碎片化反应,并分离出了配合物[(PtL)₂(μ-SMe)(μ-dppm)]Cl(12)和[Pt(μ-SMe)₂(dppm)](13)。此外,使用卤素(Br₂、I₂)对簇合物[{Pt(PPh₃)}₃(μ-SMe)₃]Cl(4a)进行氧化反应得到二聚铂(II)配合物顺式-[{PtX(PPh₃)}₂(μ-SMe)₂](14,X = Br、I),而使用硫和硒进行氧化反应则得到硫属元素封端的三核48个价电子的配合物[{Pt(PPh₃)}₃(μ₃-E)(μ-SMe)₃](15,E = S、Se)。所有化合物都通过核磁共振和红外光谱、微量分析以及电喷雾电离质谱进行了全面表征。此外,对三角簇4a、三核配合物6以及双核配合物反式-[{Pt(AsPh₃)}₂(μ-SPh)₂](5c)、[{Pt(PPh₃)}₂(μ-SMe)(μ-dppm)]Cl(12a)和[{{PtBr(PPh₃)}₂(μ-SMe)₂](14a)进行了X射线衍射分析。