The structure and coordinative self-assembly of films based on a palladium compound of pyridyl-acetylene platinum and its application in Suzuki and Heck coupling reactions

被引:12
作者
Li, Xing [1 ,2 ]
Zhao, Xiuhua [1 ]
Gao, Shuiying [2 ]
Marques-Gonzalez, Santiago [3 ]
Yufit, Dmitry S. [3 ]
Howard, Judith A. K. [3 ]
Low, Paul J. [3 ]
Zhao, Yayun [1 ]
Gan, Ning [1 ]
Guo, Zhiyong [1 ]
机构
[1] Ningbo Univ, Fac Mat Sci & Chem Engn, Ningbo 315211, Zhejiang, Peoples R China
[2] Chinese Acad Sci, Fujian Inst Res Struct Matter, State Key Lab Struct Chem, Fuzhou 350002, Peoples R China
[3] Univ Durham, Dept Chem, Durham DH1 3LE, England
关键词
PHOTOPHYSICAL PROPERTIES; MOLECULAR ARCHITECTURE; PT-PT; COMPLEXES; MIYAURA; CATALYSTS; SURFACES; ADSORPTION; PHOSPHINE;
D O I
10.1039/c3ta11868a
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The platinum complex [Pt-2(C CPy)(2)(dppm)(2)] (Py = 4-pyridyl, dppm = bis(diphenylphosphino) methane) 1 has been prepared and characterized. Single crystal X-ray diffraction analysis reveals that the Pt-2(C CPy)(2) fragment of 1 exhibits an approximately linear molecular geometry, in which the Pt-Pt bond may be considered as having been inserted within the delocalized p-electron system of the 1,4-bis(4'-pyridyl) buta-1,3-diyne. The ability of the two terminal pyridyl nitrogen atoms of 1 to coordinate to other metal centers has enabled the use of 1 as a linking ligand in the layer-by-layer (LbL) growth of heterometallic films. The self-assembly behavior of 1 with Pd(II), supported by chloride counter ions, on poly(ethylenimine) (PEI) functionalized solid surfaces has been investigated. The resulting multilayer films of general composition and form (PdCl2/1)(n) have been characterized using UV-vis absorption spectroscopy, atomic force microscopy (AFM) and X-ray photoelectron spectroscopy (XPS). On the basis of the UV-vis spectroscopic data, it was shown that the (PdCl2/1)(n) multilayer films could be grown in a regular fashion, with film thickness increasing linearly with increasing deposition of the metal-ligand bilayers. Consistent with this metal ion dependent LbL growth, AFM images of the multilayer films exhibited island-shaped nanostructures with a mean diameter of about 25 nm. The catalytic properties of the (PdCl2/1)(n) multilayers were investigated, and (PdCl2/1)(n) film-loaded slides were used as a catalyst reservoir capable of liberating catalytic amounts of a highly active Pd species, which was suitable for promoting C-C bond formations. The catalyst loading was as low as 2.76 x 10(-6) mol% and gave high yields. The LbL catalyst and the technology presented in this work, show distinctive features that include extraordinarily low loading and high catalytic active characteristics.
引用
收藏
页码:9164 / 9172
页数:9
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