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Robotic Lepidoptery: Structural Characterization of (mostly) Unexpected Palladium Complexes Obtained from High-Throughput Catalyst Screening

机译:机器人鳞翅目:从高通量催化剂筛选获得的(大部分)意外钯配合物的结构表征

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In the course of a high-throughput search for optimal combinations of bidentate ligands with Pd(II) carboxylates to generate oxidation catalysts, we obtained and crystallographically characterized a number of crystalline products. While some combinations afforded the anticipated (L-L)Pd(OC(O)R)(2) structures (L-L = bipyridine, tmeda; R = CH3, CF3). many gave unusual oligometallic complexes resulting from reactions such as C-H activation (L-L = sparteine), P-C bond cleavage (L-L = 1,2-bis(diphenylphosphino)ethane, and C-C bond formation between solvent (acetone) and ligand (L-L = 1,4-bis(2,6-diisopropylphenyl)-1,4-diaza-1,3-butadiene). These findings illustrate potential pitfalls of screening procedures based on assuming uniform, in situ catalyst self-assembly.
机译:在高通量研究中,将双齿配体与Pd(II)羧酸酯进行最佳组合以生成氧化催化剂,我们获得了许多结晶产物并对其进行了结晶学表征。虽然某些组合提供了预期的(L-L)Pd(OC(O)R)(2)结构(L-L =联吡啶,tmeda; R = CH3,CF3)。许多化合物由于反应如CH活化(LL =斯巴地丁),PC键断裂(LL = 1,2-双(二苯基二膦基)乙烷以及在溶剂(丙酮)和配体之间形成CC键(LL = 1, 4-双(2,6-二异丙基苯基)-1,4-重氮-1,3-丁二烯)。这些发现说明了在假定催化剂均匀自组装的基础上筛选程序的潜在弊端。

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