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铑(I)(2,5-降冰片二烯)(联苯)((4-氟苯基)膦):苯乙炔立体定向(共)聚合引发剂的合成、表征及应用

Rh(I)(2,5-norbornadiene)(biphenyl)((4-fluorophenyl)phosphine): Synthesis, Characterization, and Application as an Initiator in the Stereoregular (Co)Polymerization of Phenylacetylenes.

作者信息

Loong Tan Nicholas Sheng, Nealon Gareth L, Turner Gemma F, Moggach Stephen A, Ogden Mark I, Massi Massimiliano, Lowe Andrew B

机构信息

Curtin Institute for Functional Molecules and Interfaces (CIFMI) and School of Molecular and Life Sciences (MLS), Curtin University, Kent Street, Bentley, Perth, Western Australia 6102, Australia.

Centre for Microscopy, Characterisation, and Analysis (CMCA) and School of Molecular Sciences, M310, University of Western Australia, 35 Stirling Highway, Perth, Western Australia 6009, Australia.

出版信息

ACS Macro Lett. 2020 Jan 21;9(1):56-60. doi: 10.1021/acsmacrolett.9b00975. Epub 2019 Dec 24.

Abstract

The synthesis of the Rh(I)-aryl complex, Rh(I)(nbd)(BiPh)(P(4-FCH)) is reported and its efficacy as an initiator for the (co)polymerization of phenylacetylenes established. The X-ray crystal structure indicates that the complex adopts a slightly distorted square planar geometry whose purity and structure was also confirmed by elemental analysis and H, C, P, F, Rh, and P-Rh{H} HMQC NMR spectroscopy. We demonstrate that Rh(I)(nbd)(BiPh)(P(4-FCH)) mediates the (co)polymerization of phenylacetylenes in a controlled fashion with initiation efficiencies as high as 0.98, as evidenced by the pseudo-first-order kinetic and number-average molecular weight versus conversion profiles. The ability to form well-defined AB diblock copolymers, in a stereoregular manner, by sequential monomer addition is verified in the block copolymerization of phenylacetylene with 4-fluorophenylacetylene with quantitative crossover efficiency, as determined by size exclusion chromatography.

摘要

报道了Rh(I)-芳基配合物Rh(I)(nbd)(BiPh)(P(4-FCH))的合成,并确定了其作为苯乙炔(共)聚合引发剂的有效性。X射线晶体结构表明该配合物采用略微扭曲的平面正方形几何结构,其纯度和结构也通过元素分析以及H、C、P、F、Rh和P-Rh{H} HMQC核磁共振光谱得到证实。我们证明,Rh(I)(nbd)(BiPh)(P(4-FCH))以可控方式介导苯乙炔的(共)聚合,引发效率高达0.98,这由准一级动力学以及数均分子量与转化率曲线所证明。通过尺寸排阻色谱法测定,在苯乙炔与4-氟苯乙炔的嵌段共聚中,通过顺序添加单体以立构规整方式形成明确的AB二嵌段共聚物的能力得到了验证,交叉效率为定量。

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