Synthesis of six-component metallodendrimers via [3 + 3] coordination-driven self-assembly.

Synthesis of six-component metallodendrimers via [3 + 3] coordination-driven self-assembly.
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DOI:
10.1021/jo900067v
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发表时间:
2009-05-01
期刊:
The Journal of organic chemistry
影响因子:
--
通讯作者:
Stang PJ
Stang PJ
中科院分区:
其他
文献类型:
--
作者:
Yang HB;Northrop BH;Zheng YR;Ghosh K;Lyndon MM;Muddiman DC;Stang PJ

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设计并合成了一类新的120°树枝状双Pt(II)受体亚基,通过[3+3]配位驱动的自组装,与120°树枝状双吡啶供体形成六元六角金属树枝状大分子.所有金属树枝状大分子的结构都通过多核NMR,ESI-TOF-MS/ESI-FTMS和元素分析进行了确认。MMFF力场模拟表明,所有的金属树枝状聚合物有一个六边形的环,内半径约为1.4 nm。
A new class of 120° dendritic di-Pt(II) acceptor subunits has been designed and synthesized, from which six-component hexagonal metallodendrimers were easily formed with 120° dendritic dipyridine donors via [3+3] coordination-driven self-assembly. The structures of all metallodendrimers are confirmed by multinuclear NMR, ESI-TOF-MS/ESI-FTMS, and elemental analysis. MMFF force-field simulations indicates that all metallodendrimers have a hexagonal ring with an internal radius of approximately 1.4 nm.
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