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Kluge, T.; Bette, M.; Vetter, C.; Schmidt, J.; Steinborn, D.;Synthesis and characterization of diacetyl platinum(II) complexes with two primary and secondary amine ligandsJ. Organomet. Chem.71593-101(2012)DOI: 10.1016/j.jorganchem.2012.05.043
[Pt(COMe)2(bpy)] (2; bpy = 2,2′-bipyridine) and [Pt(COMe)2{H(Me)dmg}] (5; H(Me)dmg = MeO–NC(Me)–C(Me)N–OH) were found to react with primary and secondary amines yielding diacetyl platinum(II) complexes with two monodendate amine ligands [Pt(COMe)2(NH2R)2] (R = Bn, 3a; CH2CH2Ph, 3b; Et, 3c; i-Pr, 3d; CH2CHCH2, 3e; Cy, 3f; Bn = benzyl, Cy = cyclohexyl) and [Pt(COMe)2(NHR2)2] (R = Me, 6a; Et, 6b), respectively. The equilibrium of these ligand exchange reactions was investigated by NMR experiments and DFT calculations showing that complex 5 is the more preferable starting complex and a large excess of the amine has to be used. The sterically demanding diisopropylamine was found to react with 5 yielding a thermally highly unstable dinuclear bis(acetyl) bridged complex [{Pt(COMe){NH(i-Pr)2}}2(μ-COMe)2] (7). Analogous reactions with ethylenediamine derivatives resulted in the formation of [Pt(COMe)2(N^N)] (N^N = ethylenediamine, en, 8a; N,N′-dimethylethylenediamine, 8b; N,N-dimethylethylenediamine, 8c; N,N,N′,N′-tetramethylethylenediamine, TMEDA, 8d). All complexes were fully characterized by microanalysis/high-resolution ESI mass spectrometry, by NMR (1H, 13C, 195Pt) and IR spectroscopies as well as by single-crystal X-ray diffraction measurements (3a/3d). Due to the high trans influence of the acetyl ligands, the Pt–N bonds were found to be relatively long (2.164(2)–2.182(3) Å). The resulting weak coordination of the amines gave rise to a decomposition of complexes 3 under CO extrusion yielding carbonyl–methyl complexes.
Publikation
Bette, M.; Rüffer, T.; Bruhn, C.; Schmidt, J.; Steinborn, D.;Synthesis, Characterization, and Reactivity of Diacetylplatinum(II) and -platinum(IV) Complexes Bearing κ2- and κ3-Coordinated Scorpionate LigandsOrganometallics313700-3710(2012)DOI: 10.1021/om3001907
Reactions of the dinuclear platina-β-diketone [Pt2{(COR)2H}2(μ-Cl)2] (1) with K[(pz)3BH] and K[(3,5-Me2pz)3BH] (pz = pyrazolyl; 3,5-Me2pz = 3,5-dimethylpyrazolyl) afforded neutral diacetyl(hydrido)platinum(IV) complexes [Pt(COMe)2H{(pz)3BH}] (4a) and [Pt(COMe)2H{(3,5-Me2pz)3BH}] (4b), bearing κ3-bonded tris(pyrazolyl)borate (scorpionate) ligands. These complexes were found to decompose in chloroform solution under formation of the respective chlorido complexes [Pt(COMe)2Cl{(pz)3BH}] (5a) and [Pt(COMe)2Cl{(3,5-Me2pz)3BH}] (5b) as the initial step. Diacetylplatinum(II) complexes with κ2-coordinated scorpionate ligands (K[Pt(COMe)2{(pz)3BH}], 6a; K[Pt(COMe)2{(3,5-Me2pz)3BH}], 6b; K[Pt(COMe)2{(pz)4B}], 7; K[{Pt(COMe)2}2{(pz)4B}], 8) were obtained in ligand exchange reactions of [Pt(COMe)2(NH2Bn)2] (3; Bn = benzyl) with the respective potassium (pyrazolyl)borates. The deprotonation of the hydrido complexes 4 with potassium methoxide led also to the formation of 6. Diacetylplatinum(II) complexes 6a and 7 were found to react in oxidative addition reactions with alkyl halides to yield diacetylplatinum(IV) complexes of the type [Pt(COMe)2R{(pz)3BH)}] (R = Me, 9a; Et, 9b; Bn, 9c) and [Pt(COMe)2R{(pz)4B}] (R = Me, 10a; Et, 10b; Bn, 10c), respectively, with κ3-bonded scorpionate ligands. The identities of all platinum complexes were unambiguously proved by microanalyses or by high-resolution mass spectrometric investigations, by NMR (1H, 13C, 195Pt) and IR spectroscopies, and by single-crystal X-ray diffraction analyses (4a, 5a, 7·(18C6), 9c; 18C6 = 18-crown-6). The reactivity of the complexes is discussed in terms of hemilability of the scorpionate ligands.