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New Mono- and Tricyclopalladated Dendritic Systems with Encapsulated Catalytic Sites

机译:具有密封催化位点的新型单环和三环钯树枝状体系

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摘要

The preparation of a series of new macrocyclic carbodiazasilane molecules functionalized with the monoanionic [2,6-(CH_2Nme_2)_2C_6H_3]~- (ident to) N,C,N-pincer ligand has been accomplished. Palladation of these systems was possible through oxidative addition with [Pd(dba)_2] affording exclusive formation of the meso diastereoisomer. The X-ray crystal structures of these novel ligands and of the palladium(II) complex 10 were determined and confirmed the stereo-chemistry of the organopalladium cage. Attachment of the para-OH functionalized carbodiazasilane macrocycle 16 to a central core led to the formation of the dendritic structure 18 which was palla-dated to afford the novel multimetallic dendritic system with encapsulated catalytic sites 1. This cyclopalladated carbosilane dendrimer (1) as well as the mononuclear organopalladium cage 10 can be conveniently converted into active Lewis acid catalysts for the aldol condensation reaction. The catalytic data showed higher reaction rates for the dendritic structure than for the corresponding mononuclear systems.
机译:已经完成了一系列由单阴离子[2,6-(CH_2Nme_2)_2C_6H_3]〜-(与N,C,N-钳子配体相同)官能化的新的大环碳二氮杂硅烷分子的制备。通过与[Pd(dba)_2]进行氧化添加,可以制得这些系统的钯,从而形成内消旋非对映异构体。确定了这些新颖的配体和钯(II)配合物10的X射线晶体结构,并证实了有机钯笼的立体化学。对羟基官能化的碳二氮杂硅烷大环16与中心核的连接导致树状结构18的形成,该树状结构被钯化以提供具有封装的催化位点1的新型多金属树状体系。该环钯化的碳硅烷树状大分子(1)也是如此因为单核有机钯笼10可以方便地转化为用于路易斯醇醛缩合反应的活性路易斯酸催化剂。催化数据表明,与相应的单核体系相比,树状结构的反应速率更高。

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